Variant #0000877960 (NC_000009.11:g.13121734A>C, NC_000009.11(NM_001378778.1):c.5231+4T>G (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.13121734A>C
DNA change (hg38) g.13121735A>C
Published as -
ISCN -
DB-ID MPDZ_000047 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs199870788
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00093 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-09-10 08:04:01 +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.5231+4T>G r.spl? p.?


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