Variant #0000259868 (NC_000010.10:g.90695096_90695097del, NM_000043.4:c.-55538_-55537del (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.90695096_90695097del
DNA change (hg38) g.88935339_88935340del
Published as ACTA2(NM_001141945.2):c.1019_1020delCT (p.S340Cfs*26)
ISCN -
DB-ID ACTA2_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-55538_-55537del r.(?) p.(=)
ACTA2 NM_001613.2 +/. - c.1019_1020del r.(?) p.(Ser340CysfsTer26)
STAMBPL1 NM_020799.3 +/. - c.*12115_*12116del r.(=) p.(=)


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