Variant #0000355607 (NC_000003.11:g.(?_37034841)_(37045966_37048481)del, MLH1(NM_000249.3):c.(?_-198)_(380+1_381-1)del)
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
InSiGHT |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_37034841)_(37045966_37048481)del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001570 See all 2 reported entries |
Variant remarks |
Insight class: 5 |
Reference |
InSiGHT |
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-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-03-05 12:40:48 +01:00 (CET) |
Date last edited |
2018-11-09 18:15:18 +01:00 (CET) |

Variant on transcripts
|
|