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
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