Variant #0000417441 (NC_000002.11:g.(?_48010221)_(48034092_?)del, MSH6(NM_000179.2):c.(?_-152)_(*93_?)del)
Individual ID |
00201416 |
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.(?_48010221)_(48034092_?)del |
DNA change (hg38) |
- |
Published as |
(?_-152)_(*93_?)del/Del exon 1-10 |
ISCN |
- |
DB-ID |
MSH6_000911 See all 5 reported entries |
Variant remarks |
- |
Reference |
{PMID:Nilbert Fam Cancer. 2009;8(1):75-83.:18566915} |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Thomas Hansen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |

Variant on transcripts
Screenings
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