Variant #0001001016 (NC_000014.8:g.50585064A>G, NM_006939.2:c.3997T>C (SOS2))

Chromosome 14
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.50585064A>G
DNA change (hg38) -
Published as SOS2(NM_006939.2):c.3997T>C (p.(Ter1333Argext*?))
ISCN -
DB-ID METTL21D_000015
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
SOS2 NM_006939.2 ?/. - c.3997T>C r.(?) p.(*1333Argext*2)
METTL21D NM_024558.2 ?/. - c.-1794T>C r.(?) p.(=)


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