Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TRAF3IP3 (Hsa)
(GRCh38)1:209760047G>T
(Homo sapiens)Allele/Variant
Source: rs762916063
Genes: TRAF3IP3 (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)1:209760047G>T
(GRCh38)1:209780484G>A
(Homo sapiens)Allele/Variant
Source: rs758375285
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780484G>A
(GRCh38)1:209782089G>A
(Homo sapiens)Allele/Variant
Source: rs141902362
Genes: TRAF3IP3 (Hsa), C1orf74 (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)1:209782089G>A
(GRCh38)1:209780592G>A
(Homo sapiens)Allele/Variant
Source: rs1032979701
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780592G>A
(GRCh38)1:209781403G>A
(Homo sapiens)Allele/Variant
Source: rs771216589
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781403G>A
(GRCh38)1:209760152A>G
(Homo sapiens)Allele/Variant
Source: rs150652900
Genes: TRAF3IP3 (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)1:209760152A>G
(GRCh38)1:209760289G>A
(Homo sapiens)Allele/Variant
Source: rs768119914
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209760289G>A
(GRCh38)1:209772974G>C
(Homo sapiens)Allele/Variant
Source: rs769254539
Genes: TRAF3IP3 (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)1:209772974G>C
(GRCh38)1:209760080G>A
(Homo sapiens)Allele/Variant
Source: rs778963231
Genes: TRAF3IP3 (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)1:209760080G>A
(GRCh38)1:209775703G>C
(Homo sapiens)Allele/Variant
Source: rs377426065
Genes: TRAF3IP3 (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)1:209775703G>C
(GRCh38)1:209775600G>A
(Homo sapiens)Allele/Variant
Source: rs200380274
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209775600G>A
(GRCh38)1:209781421G>A
(Homo sapiens)Allele/Variant
Source: rs544408933
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781421G>A
(GRCh38)1:209762584T>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.209762584T>G
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209762584T>G
(GRCh38)1:209760055C>T
(Homo sapiens)Allele/Variant
Source: rs151094826
Genes: TRAF3IP3 (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)1:209760055C>T
(GRCh38)1:209760304C>A
(Homo sapiens)Allele/Variant
Source: rs138676697
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209760304C>A
(GRCh38)1:209762826G>C
(Homo sapiens)Allele/Variant
Source: rs1366526238
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209762826G>C
(GRCh38)1:209781373A>G
(Homo sapiens)Allele/Variant
Source: rs1306183518
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781373A>G
(GRCh38)1:209760275C>T
(Homo sapiens)Allele/Variant
Source: rs12732140
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209760275C>T
(GRCh38)1:209760067C>T
(Homo sapiens)Allele/Variant
Source: rs2077218893
Genes: TRAF3IP3 (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)1:209760067C>T
(GRCh38)1:209777359A>G
(Homo sapiens)Allele/Variant
Source: rs751004054
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209777359A>G
(GRCh38)1:209777484C>A
(Homo sapiens)Allele/Variant
Source: rs1031910707
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209777484C>A
(GRCh38)1:209780527G>A
(Homo sapiens)Allele/Variant
Source: rs1180866483
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780527G>A
(GRCh38)1:209772988C>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.209772988C>G
Genes: TRAF3IP3 (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)1:209772988C>G
(GRCh38)1:209760056C>T
(Homo sapiens)Allele/Variant
Source: rs756391768
Genes: TRAF3IP3 (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)1:209760056C>T
(GRCh38)1:209760146G>A
(Homo sapiens)Allele/Variant
Source: rs144580950
Genes: TRAF3IP3 (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)1:209760146G>A
(GRCh38)1:209760167G>A
(Homo sapiens)Allele/Variant
Source: rs368107878
Genes: TRAF3IP3 (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)1:209760167G>A
(GRCh38)1:209760167G>T
(Homo sapiens)Allele/Variant
Source: rs368107878
Genes: TRAF3IP3 (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)1:209760167G>T