Variant #0001047191 (NC_000007.13:g.75689696T>C, NM_005918.2:c.435T>C (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.75689696T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MDH2_000031
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1585408408
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-06 17:22:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MDH2 NM_005918.2 -?/. - c.435T>C r.(?) p.(Asn145=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.