Variant #0001038092 (NC_000010.10:g.90699258G>A, NM_000043.4:c.-51376G>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.90699258G>A
DNA change (hg38) -
Published as ACTA2(NM_001613.4):c.808+6C>T
ISCN -
DB-ID FAS_000104
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAS NM_000043.4 -?/. - c.-51376G>A r.(?) p.(=)
ACTA2 NM_001613.2 -?/. - c.808+6C>T r.(=) p.(=)
STAMBPL1 NM_020799.3 -?/. - c.*16277G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.