Variant #0000247900 (NC_000010.10:g.90701645A>G, NM_000043.4:c.-48989A>G (FAS))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90701645A>G
DNA change (hg38) g.88941888A>G
Published as ACTA2(NM_001141945.2):c.370-19T>C, ACTA2(NM_001141945.3):c.370-19T>C, ACTA2(NM_001613.2):c.370-19T>C
ISCN -
DB-ID ACTA2_000053 See all 3 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) 0.12017 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.-48989A>G r.(?) p.(=)
ACTA2 NM_001613.2 -/. - c.370-19T>C r.(=) p.(=)
STAMBPL1 NM_020799.3 -/. - c.*18664A>G r.(=) p.(=)


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