Version: 8.0.0
Date: Tue Jan 28 2025
2,528 results for tarbp1

(GRCh38)1:234433438T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234433438T>C
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234433438T>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234437297A>T

(Homo sapiens)
Allele/Variant
Source: rs755927320
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234437297A>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234446863G>A

(Homo sapiens)
Allele/Variant
Source: rs373406252
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234446863G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234393660G>A

(Homo sapiens)
Allele/Variant
Source: rs200047728
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234393660G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234410500G>A

(Homo sapiens)
Allele/Variant
Source: rs188908188
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234410500G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234420733G>A

(Homo sapiens)
Allele/Variant
Source: rs140244260
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234420733G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234427376A>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234427376A>C
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234427376A>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234433447G>A

(Homo sapiens)
Allele/Variant
Source: rs1204437140
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234433447G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234460372C>T

(Homo sapiens)
Allele/Variant
Source: rs374015042
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234460372C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234467528G>T

(Homo sapiens)
Allele/Variant
Source: rs772457334
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234467528G>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234393724G>C

(Homo sapiens)
Allele/Variant
Source: rs754758365
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234393724G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234429218G>A

(Homo sapiens)
Allele/Variant
Source: rs775990802
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234429218G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234430102G>A

(Homo sapiens)
Allele/Variant
Source: rs1369991638
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234430102G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234478833G>A

(Homo sapiens)
Allele/Variant
Source: rs899772721
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234478833G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234405950A>G

(Homo sapiens)
Allele/Variant
Source: rs150036379
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234405950A>G
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234418207C>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234418207C>A
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234418207C>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234450559T>C

(Homo sapiens)
Allele/Variant
Source: rs200989209
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234450559T>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234460365C>T

(Homo sapiens)
Allele/Variant
Source: rs147838280
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234460365C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234405907C>T

(Homo sapiens)
Allele/Variant
Source: rs1304457447
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234405907C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234460271G>C

(Homo sapiens)
Allele/Variant
Source: rs201485197
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234460271G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234405994C>T

(Homo sapiens)
Allele/Variant
Source: rs778478690
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234405994C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234418134G>A

(Homo sapiens)
Allele/Variant
Source: rs750843942
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234418134G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234430270A>G

(Homo sapiens)
Allele/Variant
Source: rs375836600
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234430270A>G
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234433510T>C

(Homo sapiens)
Allele/Variant
Source: rs748004189
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234433510T>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234401239C>T

(Homo sapiens)
Allele/Variant
Source: rs201389692
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234401239C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234405966A>C

(Homo sapiens)
Allele/Variant
Source: rs1485012450
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234405966A>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234418183G>A

(Homo sapiens)
Allele/Variant
Source: rs12087572
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234418183G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234406060A>T

(Homo sapiens)
Allele/Variant
Source: rs906796654
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234406060A>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234457713A>G

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234457713A>G
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234457713A>G
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234393807G>A

(Homo sapiens)
Allele/Variant
Source: rs199534808
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234393807G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234478322C>G

(Homo sapiens)
Allele/Variant
Source: rs750114756
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234478322C>G
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234420717G>A

(Homo sapiens)
Allele/Variant
Source: rs267598421
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234420717G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234457689C>T

(Homo sapiens)
Allele/Variant
Source: rs374991542
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234457689C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234401205G>C

(Homo sapiens)
Allele/Variant
Source: rs144896311
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234401205G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234418220C>T

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234418220C>T
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234418220C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234398552G>C

(Homo sapiens)
Allele/Variant
Source: rs780957119
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234398552G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234391666G>A

(Homo sapiens)
Allele/Variant
Source: rs560732693
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234391666G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234398396G>C

(Homo sapiens)
Allele/Variant
Source: rs763362097
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234398396G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234398531C>T

(Homo sapiens)
Allele/Variant
Source: rs139118500
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234398531C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234427657C>T

(Homo sapiens)
Allele/Variant
Source: rs765575331
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234427657C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234478440C>G

(Homo sapiens)
Allele/Variant
Source: rs774577647
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234478440C>G
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234479031G>C

(Homo sapiens)
Allele/Variant
Source: rs746141862
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234479031G>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234429439A>T

(Homo sapiens)
Allele/Variant
Source: rs750995425
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234429439A>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234429523C>T

(Homo sapiens)
Allele/Variant
Source: rs563481719
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234429523C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234478732C>T

(Homo sapiens)
Allele/Variant
Source: rs1669834390
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234478732C>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234478763G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234478763G>A
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234478763G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234430199G>T

(Homo sapiens)
Allele/Variant
Source: rs138023326
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234430199G>T
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234430262T>C

(Homo sapiens)
Allele/Variant
Source: rs555089732
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234430262T>C
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234430129G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.234430129G>A
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234430129G>A
Gene Synonyms: probable methyltransferase TARBP1

(GRCh38)1:234429234A>G

(Homo sapiens)
Allele/Variant
Source: rs1664126821
Genes: TARBP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:234429234A>G
Gene Synonyms: probable methyltransferase TARBP1