Variant #0000532659 (NC_000007.13:g.75692892dup, NM_005918.2:c.615dup (MDH2))

Chromosome 7
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.75692892dup
DNA change (hg38) g.76063574dup
Published as MDH2(NM_005918.2):c.615dupC (p.(Ile206fs))
ISCN -
DB-ID MDH2_000014
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MDH2 NM_005918.2 ?/. - c.615dup r.(?) p.(Ile206HisfsTer36)
STYXL1 NM_016086.2 ?/. - c.-15914dup r.(?) p.(=)


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