Variant #0000523895 (NC_000005.9:g.1201960C>T, NM_001003841.2:c.195C>T (SLC6A19))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1201960C>T
DNA change (hg38) g.1201845C>T
Published as SLC6A19(NM_001003841.2):c.195C>T (p.H65=), SLC6A19(NM_001003841.3):c.195C>T (p.H65=)
ISCN -
DB-ID SLC6A19_000025 See all 2 reported entries
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) 0.00012 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A19 NM_001003841.2 -?/. - c.195C>T r.(?) p.(His65=)


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