Variant #0000346302 (NC_000007.13:g.6013049C>G, NM_000535.6:c.2570G>C (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.6013049C>G
DNA change (hg38) g.5973418C>G
Published as PMS2(NM_000535.5):c.2570G>C (p.G857A), PMS2(NM_000535.7):c.2570G>C (p.G857A)
ISCN -
DB-ID PMS2_000113 See all 27 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) 0.28559 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.2570G>C r.(?) p.(Gly857Ala)
RSPH10B NM_173565.3 -/. - c.-3006G>C r.(?) p.(=)


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