Variant #0000286742 (NC_000012.11:g.110013843G>T, NM_000431.2:c.119G>T (MVK))

Chromosome 12
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.110013843G>T
DNA change (hg38) g.109576038G>T
Published as MVK(NM_000431.2):c.119G>T (p.R40L)
ISCN -
DB-ID MVK_000019
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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.119G>T r.(?) p.(Arg40Leu)
MMAB NM_052845.3 ?/. - c.-2558C>A r.(?) p.(=)


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