Variant #0000979231 (NC_000010.10:g.90699271G>A, NM_000043.4:c.-51363G>A (FAS))

Chromosome 10
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.90699271G>A
DNA change (hg38) -
Published as ACTA2(NM_001141945.2):c.801C>T (p.S267=)
ISCN -
DB-ID FAS_000096
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAS NM_000043.4 -?/. - c.-51363G>A r.(?) p.(=)
ACTA2 NM_001613.2 -?/. - c.801C>T r.(?) p.(=)
STAMBPL1 NM_020799.3 -?/. - c.*16290G>A r.(=) p.(=)


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