Variant #0000546394 (NC_000012.11:g.110013805_110013952del, NC_000012.11(NM_000431.2):c.81_226+2del (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.110013805_110013952del
DNA change (hg38) g.109576000_109576147del
Published as MVK(NM_000431.2):c.79_226del (p.V27Sfs*16)
ISCN -
DB-ID MVK_000195
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 2020-07-03 09:19:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MVK NM_000431.2 +/. - c.81_226+2del r.spl? p.?
MMAB NM_052845.3 +/. - c.-2664_-2517del r.(?) p.(=)


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