Variant #0001041693 (NC_000017.10:g.2203691T>A, NM_021947.1:c.-3625T>A (SRR))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2203691T>A
DNA change (hg38) -
Published as SMG6(NM_017575.5):c.356A>T (p.(Glu119Val))
ISCN -
DB-ID SRR_000032
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSR1 NM_018128.4 ?/. - c.*23799A>T r.(=) p.(=)
SRR NM_021947.1 ?/. - c.-3625T>A r.(?) p.(=)


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