Variant #0000436835 (NC_000002.11:g.39278343A>G, SOS1(NM_005633.3):c.806T>C)

Individual ID 00206156
Chromosome 2
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39278343A>G
DNA change (hg38) g.39051202A>G
Published as -
ISCN -
DB-ID SOS1_000004 See all 2 reported entries
Variant remarks -
Reference PubMed: Zenker 2007
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOS1 NM_005633.3 +/? 6 c.806T>C r.(?) p.(Met269Thr)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000207188 DNA SEQ - - SOS1 1 LOVD