Variant #0001081344 (NC_000002.11:g.39278343A>G, NM_005633.3:c.806T>C (SOS1))

Chromosome 2
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.39278343A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOS1_000004 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs137852813
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 2026-07-30 11:44:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOS1 NM_005633.3 +/. - c.806T>C r.(?) p.(Met269Thr)


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