Variant #0000003962 (NC_000002.12:g.47403074T>C, MSH2(NM_000251.2):c.-118T>C)

Individual ID 00000498
Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.47403074T>C
Reference -
DB-ID MSH2_000016 See all 6 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jose Llugdar-Instituto Oulton
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

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Co_ocurrence     

Review status     
MSH2 NM_000251.2 -/- 5'UTR c.-118T>C r.(=) p.(=) Homo no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000562 DNA SEQ-NG Clinica Universitaria Reina Fabiola - 5-mar-2018 - EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2 37 Jose Llugdar-Instituto Oulton