Variant #0000074622 (NC_000007.13:g.6042268C>T, NC_000007.13(NM_000535.6):c.354-1G>A (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.6042268C>T
DNA change (hg38) g.6002637C>T
Published as -
ISCN -
DB-ID PMS2_000285 See all 4 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 2020-06-22 14:23:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 +?/+? 4i c.354-1G>A r.spl p.?


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