Variant #0000909807 (NC_000002.11:g.39216456C>T, NC_000002.11(NM_005633.3):c.3347-1G>A (SOS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39216456C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOS1_000129 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs141565234
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-01-05 18:11:01 +01:00 (CET)
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.3347-1G>A r.(?) p.(?)


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