Variant #0000074673 (NC_000007.13:g.6029588T>C, NC_000007.13(NM_000535.6):c.989-2A>G (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6029588T>C
DNA change (hg38) g.5989957T>C
Published as -
ISCN -
DB-ID PMS2_000249 See all 2 reported entries
Variant remarks Insight class: 4
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
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 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2015-07-20 15:58:19 +02:00 (CEST)
Date last edited 2019-02-22 12:22:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 +?/+? 9i c.989-2A>G r.989_1144del p.(Glu330_Glu381del)


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