Variant #0001039974 (NC_000014.8:g.50585575_50585576insC, NC_000014.8(NM_006939.2):c.3490-5_3490-4insG (SOS2))

Chromosome 14
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.50585575_50585576insC
DNA change (hg38) -
Published as SOS2(NM_006939.4):c.3490-5_3490-4insG
ISCN -
DB-ID METTL21D_000016
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.3490-5_3490-4insG r.spl? p.?
METTL21D NM_024558.2 -?/. - c.-2306_-2305insG r.(?) p.(=)


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