Variant #0000929360 (NC_000007.13:g.6026942G>T, NM_000535.6:c.1454C>A (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6026942G>T
DNA change (hg38) -
Published as PMS2(NM_000535.5):c.1454C>A (p.T485K), PMS2(NM_000535.7):c.1454C>A (p.T485K)
ISCN -
DB-ID PMS2_000138 See all 29 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.07975 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 -/. - c.1454C>A r.(?) p.(Thr485Lys)


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