Variant #0000935187 (NC_000002.11:g.39281787A>C, NM_005633.3:c.688T>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.39281787A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOS1_000220
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397517177
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-10-17 22:55:02 +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     
SOS1 NM_005633.3 ?/. - c.688T>G r.(?) p.(Phe230Val)


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