Variant #0000357008 (NC_000002.11:g.47998510_48020183del, MSH6(NM_000179.2):c.-11863_457+1921del)
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47998510_48020183del |
DNA change (hg38) |
g.47771371_47793044del |
Published as |
- |
ISCN |
- |
DB-ID |
MSH6_000002 See all 2 reported entries |
Variant remarks |
Insight class: 5 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
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 4.0 International |
Created by |
Julia Lopez |
Date created |
2018-03-08 19:39:55 +01:00 (CET) |
Date last edited |
2018-11-09 16:06:39 +01:00 (CET) |

Variant on transcripts
|
|