Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SLC6A6 (Hsa)
(GRCh38)3:14481692G>A
(Homo sapiens)Allele/Variant
Source: rs554946637
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14481692G>A
(GRCh38)3:14484958A>G
(Homo sapiens)Allele/Variant
Source: rs151175565
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484958A>G
(GRCh38)3:14472304G>T
(Homo sapiens)Allele/Variant
Source: rs1700769766
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14472304G>T
(GRCh38)3:14477307A>C
(Homo sapiens)Allele/Variant
Source: rs141131824
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14477307A>C
(GRCh38)3:14447606T>C
(Homo sapiens)Allele/Variant
Source: rs1400077213
Genes: SLC6A6 (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)3:14447606T>C
(GRCh38)3:14478473T>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.14478473T>G
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14478473T>G
(GRCh38)3:14484934C>T
(Homo sapiens)Allele/Variant
Source: rs938126566
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484934C>T
(GRCh38)3:14479129C>T
(Homo sapiens)Allele/Variant
Source: rs770780822
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14479129C>T
(GRCh38)3:14443750C>T
(Homo sapiens)Allele/Variant
Source: rs571621473
Genes: SLC6A6 (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)3:14443750C>T
(GRCh38)3:14472217C>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.14472217C>T
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14472217C>T
(GRCh38)3:14484904G>A
(Homo sapiens)Allele/Variant
Source: rs376586731
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484904G>A
(GRCh38)3:14445827G>A
(Homo sapiens)Allele/Variant
Source: rs368267241
Genes: SLC6A6 (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)3:14445827G>A
(GRCh38)3:14481701G>A
(Homo sapiens)Allele/Variant
Source: rs141254266
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14481701G>A
(GRCh38)3:14484960G>A
(Homo sapiens)Allele/Variant
Source: rs146953899
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484960G>A
(GRCh38)3:14445720C>A
(Homo sapiens)Allele/Variant
Source: rs754954058
Genes: SLC6A6 (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)3:14445720C>A
(GRCh38)3:14458065G>A
(Homo sapiens)Allele/Variant
Source: rs201094151
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14458065G>A
(GRCh38)3:14481735C>G
(Homo sapiens)Allele/Variant
Source: rs1259512423
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14481735C>G
(GRCh38)3:14468191A>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.14468191A>G
Genes: SLC6A6 (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)3:14468191A>G
(GRCh38)3:14443779G>A
(Homo sapiens)Allele/Variant
Source: rs1364177670
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14443779G>A
(GRCh38)3:14466597G>A
(Homo sapiens)Allele/Variant
Source: rs761829964
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14466597G>A
(GRCh38)3:14479117A>G
(Homo sapiens)Allele/Variant
Source: rs777593198
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14479117A>G
(GRCh38)3:14443702G>C
(Homo sapiens)Allele/Variant
Source: rs56135743
Genes: SLC6A6 (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)3:14443702G>C
(GRCh38)3:14447652C>T
(Homo sapiens)Allele/Variant
Source: rs267599635
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14447652C>T
(GRCh38)3:14447747G>A
(Homo sapiens)Allele/Variant
Source: rs554039615
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14447747G>A
(GRCh38)3:14484951G>A
(Homo sapiens)Allele/Variant
Source: rs200861169
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484951G>A
(GRCh38)3:14447599G>A
(Homo sapiens)Allele/Variant
Source: rs62233560
Genes: SLC6A6 (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)3:14447599G>A
(GRCh38)3:14467918G>A
(Homo sapiens)Allele/Variant
Source: rs146878732
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14467918G>A
(GRCh38)3:14479159G>A
(Homo sapiens)Allele/Variant
Source: rs772252157
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14479159G>A
(GRCh38)3:14484945C>G
(Homo sapiens)Allele/Variant
Source: rs748074723
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484945C>G
(GRCh38)3:14447775C>G
(Homo sapiens)Allele/Variant
Source: rs1335864670
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14447775C>G
(GRCh38)3:14447780C>A
(Homo sapiens)Allele/Variant
Source: rs774906046
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14447780C>A
(GRCh38)3:14458072C>G
(Homo sapiens)Allele/Variant
Source: rs757701813
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14458072C>G
(GRCh38)3:14484946G>A
(Homo sapiens)Allele/Variant
Source: rs200063855
Genes: SLC6A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:14484946G>A