Variant #0000945969 (NC_000010.10:g.90700981C>G, NC_000010.10(NM_001613.2):c.616+5G>C (ACTA2))

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.90700981C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID ACTA2_000106
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1845842113
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-23 15:16:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTA2 NM_001613.2 ?/. - c.616+5G>C r.(?) p.(?)


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