Variant #0000356417 (NC_000003.11:g.37042515A>G, NM_000249.3:c.277A>G (MLH1))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
InSiGHT |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37042515A>G |
| DNA change (hg38) |
g.37001024A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MLH1_000967 See all 43 reported entries |
| Variant remarks |
Insight class: 3 |
| Reference |
InSiGHT |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| 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 |
2020-06-12 15:47:42 +02:00 (CEST) |

Variant on transcripts
|