Variant #0000791699 (NC_000002.11:g.48032717T>A, NC_000002.11(NM_000179.2):c.3557-40T>A (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method InSiGHT
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48032717T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MSH6_000364 See all 6 reported entries
Variant remarks RNA DATA pCAS2 minigene splicing assay in HeLa cells 2 independent experiments (Inserm U1245, Rouen, France: No effect on exon 7 splicing
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00565 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2021-07-30 05:09:48 +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     
MSH6 NM_000179.2 -/. - c.3557-40T>A r.(=) p.(=)


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