Variant #0001048988 (NC_000007.13:g.75689741G>A, NM_005918.2:c.480G>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.75689741G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MDH2_000013 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139959689
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00045 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-09 17:11:02 +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     
MDH2 NM_005918.2 -?/. - c.480G>A r.(?) p.(Val160=)


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