Variant #0000074664 (NC_000007.13:g.6035206_6035207del, NM_000535.6:c.862_863del (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6035206_6035207del
DNA change (hg38) g.5995575_5995576del
Published as -
ISCN -
DB-ID PMS2_000193 See all 3 reported entries
Variant remarks Insight class: 5
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 2020-06-22 14:12:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 +/+ 8 c.862_863del r.(?) p.(Gln288Valfs*10)


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