Variant #0000546413 (NC_000012.11:g.110029080T>C, NM_000431.2:c.803T>C (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.110029080T>C
DNA change (hg38) g.109591275T>C
Published as MVK(NM_000431.2):c.803T>C (p.I268T), MVK(NM_000431.4):c.803T>C (p.I268T)
ISCN -
DB-ID MVK_000115 See all 7 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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.803T>C r.(?) p.(Ile268Thr)


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