Variant #0001024467 (NC_000002.11:g.209108284T>C, NM_005896.2:c.565A>G (IDH1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.209108284T>C
DNA change (hg38) -
Published as IDH1(NM_005896.2):c.565A>G (p.(Ile189Val)), IDH1(NM_005896.4):c.565A>G (p.I189V)
ISCN -
DB-ID IDH1_000018 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) 0.00036 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH1 NM_005896.2 ?/. - c.565A>G r.(?) p.(Ile189Val)


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