Variant #0000877961 (NC_000009.11:g.13188953A>T, NM_001378778.1:c.2194T>A (MPDZ))

Chromosome 9
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.13188953A>T
DNA change (hg38) g.13188954A>T
Published as -
ISCN -
DB-ID MPDZ_000026 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs200475640
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0012 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-09-10 08:05:01 +02:00 (CEST)
Date last edited 2024-02-19 09:52:53 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPDZ NM_001378778.1 ?/. - c.2194T>A r.(?) p.(Ser732Thr)


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