Variant #0000998605 (NC_000010.10:g.90695045T>C, NM_000043.4:c.-55589T>C (FAS))

Chromosome 10
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.90695045T>C
DNA change (hg38) -
Published as ACTA2(NM_001141945.2):c.1069A>G (p.M357V), ACTA2(NM_001613.2):c.1069A>G (p.(Met357Val))
ISCN -
DB-ID ACTA2_000005 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) 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 2024-08-28 13:16:32 +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.-55589T>C r.(?) p.(=)
ACTA2 NM_001613.2 ?/. - c.1069A>G r.(?) p.(Met357Val)
STAMBPL1 NM_020799.3 ?/. - c.*12064T>C r.(=) p.(=)


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