Variant #0000721517 (NC_000007.13:g.6043635_6043636dup, NM_000535.6:c.219_220dup (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.6043635_6043636dup
DNA change (hg38) -
Published as PMS2(NM_000535.5):c.219_220dupTG (p.Gly74Valfs*3), PMS2(NM_000535.7):c.219_220dupTG (p.G74Vfs*3)
ISCN -
DB-ID PMS2_000176 See all 16 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +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 +/. - c.219_220dup r.(?) p.(Gly74Valfs*3)


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