Variant #0000615639 (NC_000015.9:g.90628537G>A, NM_002168.2:c.1050C>T (IDH2))

Chromosome 15
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.90628537G>A
DNA change (hg38) g.90085305G>A
Published as IDH2(NM_002168.2):c.1050C>T (p.(=))
ISCN -
DB-ID IDH2_000006
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) 0.03427 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH2 NM_002168.2 -?/. - c.1050C>T r.(?) p.(Thr350=)
ZNF710 NM_198526.2 -?/. - c.*5476G>A r.(=) p.(=)


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