Variant #0001030913 (NC_000002.11:g.39283897T>C, NM_005633.3:c.456A>G (SOS1))

Chromosome 2
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.39283897T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOS1_000243
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1671228114
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 2025-04-24 17:03:01 +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.456A>G r.(?) p.(Ile152Met)


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