Variant #0000679391 (NC_000012.11:g.110013909G>A, NM_000431.2:c.185G>A (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.110013909G>A
DNA change (hg38) -
Published as MVK(NM_000431.2):c.185G>A (p.W62*), MVK(NM_000431.4):c.185G>A (p.W62*)
ISCN -
DB-ID MVK_000025 See all 4 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +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.185G>A r.(?) p.(Trp62Ter)
MMAB NM_052845.3 +/. - c.-2624C>T r.(?) p.(=)


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