Variant #0000546391 (NC_000012.11:g.110012656C>T, NM_000431.2:c.29C>T (MVK))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110012656C>T
DNA change (hg38) g.109574851C>T
Published as MVK(NM_000431.2):c.29C>T (p.A10V)
ISCN -
DB-ID MVK_000194
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MVK NM_000431.2 +/. - c.29C>T r.(?) p.(Ala10Val)
MMAB NM_052845.3 +/. - c.-1371G>A r.(?) p.(=)


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