Variant #0000417766 (NC_000002.11:g.48033421_48033433del, NM_000179.2:c.3725_3737del (MSH6))

Chromosome 2
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.48033421_48033433del
DNA change (hg38) g.47806282_47806294del
Published as -
ISCN -
DB-ID MSH6_000099 See all 6 reported entries
Variant remarks ICCON data, Prince of Wales Hospital, NSW
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2016-07-07 12:00:00 +02:00 (CEST)
Date last edited 2019-02-22 11:58:46 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 +/. 8 c.3725_3737del r.(?) p.(Arg1242Glnfs*7)


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