Variant #0000614964 (NC_000014.8:g.50585521_50585523dup, NM_006939.2:c.3546_3548dup (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.50585521_50585523dup
DNA change (hg38) g.50118803_50118805dup
Published as SOS2(NM_006939.4):c.3546_3548dupTCC (p.P1183dup)
ISCN -
DB-ID METTL21D_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOS2 NM_006939.2 -?/. - c.3546_3548dup r.(?) p.(Pro1183dup)
METTL21D NM_024558.2 -?/. - c.-2245_-2243dup r.(?) p.(=)


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