Variant #0001001015 (NC_000014.8:g.50582635A>C, NM_006939.2:c.*2427T>G (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.50582635A>C
DNA change (hg38) -
Published as VCPKMT(NM_024558.2):c.378-6T>G (p.?)
ISCN -
DB-ID METTL21D_000014
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) 6.0E-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.*2427T>G r.(=) p.(=)
METTL21D NM_024558.2 -?/. - c.378-6T>G r.(=) p.(=)


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