Variant #0000930476 (NC_000015.9:g.90630421A>G, NM_002168.2:c.890T>C (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.90630421A>G
DNA change (hg38) -
Published as IDH2(NM_001289910.1):c.734T>C (p.(Val245Ala))
ISCN -
DB-ID IDH2_000021
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) 0.00016 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 2023-07-07 10:10:56 +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     
IDH2 NM_002168.2 -?/. - c.890T>C r.(?) p.(Val297Ala)
ZNF710 NM_198526.2 -?/. - c.*7360A>G r.(=) p.(=)


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