Variant #0001064732 (NC_000007.13:g.75694276G>A, NC_000007.13(NM_005918.2):c.885+5G>A (MDH2))

Chromosome 7
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.75694276G>A
DNA change (hg38) -
Published as MDH2(NM_005918.4):c.885+5G>A
ISCN -
DB-ID MDH2_000034
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) 2.0E-5 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 2026-01-20 18:57:21 +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     
MDH2 NM_005918.2 -?/. - c.885+5G>A r.spl? p.?
STYXL1 NM_016086.2 -?/. - c.-17298C>T r.(?) p.(=)


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