Variant #0000433507 (NC_000003.11:g.37034626_37034628del, NM_000249.3:c.-413_-411del (MLH1))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37034626_37034628del |
DNA change (hg38) |
g.36993135_36993137del |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001800 See all 2 reported entries |
Variant remarks |
77% and 89% activity relative to wild-type promoter in HCT116 and HEK293 cells, respectively. |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Robyn Ward |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2016-08-31 04:26:49 +02:00 (CEST) |
Date last edited |
2018-11-09 18:15:18 +01:00 (CET) |

Variant on transcripts
|