Variant #0001047999 (NC_000020.10:g.36031762C>T, NM_198291.2:c.1591C>T (SRC))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36031762C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SRC_000011
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121913314
Origin Unknown
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 2025-09-16 08:45:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRC NM_198291.2 +?/. - c.1591C>T r.(?) p.(Gln531Ter)


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