Variant #0000801329 (NC_000003.11:g.52548457G>A, NM_015136.2:c.3623G>A (STAB1))

Chromosome 3
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.52548457G>A
DNA change (hg38) -
Published as STAB1(NM_015136.3):c.3623G>A (p.R1208H)
ISCN -
DB-ID STAB1_000012
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-08-04 19:29:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAB1 NM_015136.2 ?/. - c.3623G>A r.(?) p.(Arg1208His)
NT5DC2 NM_022908.2 ?/. - c.*10029C>T r.(=) p.(=)


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