Variant #0000966675 (NC_000012.11:g.110013843G>A, NM_000431.2:c.119G>A (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>A
DNA change (hg38) -
Published as MVK(NM_000431.4):c.119G>A (p.R40Q)
ISCN -
DB-ID MVK_000239
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MVK NM_000431.2 ?/. - c.119G>A r.(?) p.(Arg40Gln)
MMAB NM_052845.3 ?/. - c.-2558C>T r.(?) p.(=)


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