Variant #0000235003 (NC_000002.11:g.27534767C>A, NM_002437.4:c.461G>T (MPV17))

Chromosome 2
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.27534767C>A
DNA change (hg38) g.27311899C>A
Published as -
ISCN -
DB-ID MPV17_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Hongzheng Dai
Database submission license No license selected
Created by Hongzheng Dai
Date created 2017-12-01 21:31:25 +01:00 (CET)
Date last edited 2017-12-04 14:12:31 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPV17 NM_002437.4 +/. 7 c.461G>T r.spl? p.(Arg154Met)



Screenings

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