Variant #0000612774 (NC_000010.10:g.90708573G>A, NM_000043.4:c.-42061G>A (FAS))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.90708573G>A
DNA change (hg38) g.88948816G>A
Published as ACTA2(NM_001141945.2):c.115C>T (p.R39C)
ISCN -
DB-ID ACTA2_000085 See all 3 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAS NM_000043.4 +/. - c.-42061G>A r.(?) p.(=)
ACTA2 NM_001613.2 +/. - c.115C>T r.(?) p.(Arg39Cys)
STAMBPL1 NM_020799.3 +/. - c.*25592G>A r.(=) p.(=)


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