Variant #0000253452 (NC_000007.13:g.6013153A>G, NM_000535.6:c.2466T>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.6013153A>G
DNA change (hg38) g.5973522A>G
Published as PMS2(NM_000535.5):c.2466T>C (p.L822=), PMS2(NM_000535.7):c.2466T>C (p.L822=)
ISCN -
DB-ID PMS2_000111 See all 23 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) 0.11085 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.2466T>C r.(?) p.(Leu822=)
RSPH10B NM_173565.3 -/. - c.-3110T>C r.(?) p.(=)


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