Variant #0000912193 (NC_000005.9:g.1221428C>T, NM_001003841.2:c.1701C>T (SLC6A19))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1221428C>T
DNA change (hg38) -
Published as SLC6A19(NM_001003841.3):c.1701C>T (p.Y567=)
ISCN -
DB-ID SLC6A18_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00364 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A19 NM_001003841.2 -/. - c.1701C>T r.(?) p.(Tyr567=)
SLC6A18 NM_182632.2 -/. - c.-4165C>T r.(?) p.(=)


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