Variant #0000261806 (NC_000010.10:g.90707140C>T, NM_000043.4:c.-43494C>T (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.90707140C>T
DNA change (hg38) g.88947383C>T
Published as ACTA2(NM_001613.2):c.133G>A (p.V45M)
ISCN -
DB-ID ACTA2_000077
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAS NM_000043.4 ?/. - c.-43494C>T r.(?) p.(=)
ACTA2 NM_001613.2 ?/. - c.133G>A r.(?) p.(Val45Met)
STAMBPL1 NM_020799.3 ?/. - c.*24159C>T r.(=) p.(=)


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