Variant #0000415488 (NC_000007.13:g.6026556T>A, NM_000535.6:c.1840A>T (PMS2))

Chromosome 7
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.6026556T>A
DNA change (hg38) g.5986925T>A
Published as -
ISCN -
DB-ID PMS2_000124 See all 7 reported entries
Variant remarks ICCON data, Prince of Wales Hospital, NSW
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2016-07-07 12:00:00 +02:00 (CEST)
Date last edited 2018-11-09 14:54:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 +/. 11 c.1840A>T r.(?) p.(Lys614*)


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