Variant #0000556212 (NC_000015.9:g.90627553G>A, NM_002168.2:c.1304C>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.90627553G>A
DNA change (hg38) g.90084321G>A
Published as IDH2(NM_001289910.1):c.1148C>T (p.(Thr383Met)), IDH2(NM_002168.3):c.1304C>T (p.T435M)
ISCN -
DB-ID IDH2_000004 See all 2 reported entries
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) 0.00366 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH2 NM_002168.2 -?/. - c.1304C>T r.(?) p.(Thr435Met)
ZNF710 NM_198526.2 -?/. - c.*4492G>A r.(=) p.(=)


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