Variant #0000433534 (NC_000003.11:g.37035112T>C, NM_000249.3:c.74T>C (MLH1))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37035112T>C |
| DNA change (hg38) |
g.36993621T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MLH1_000050 See all 17 reported entries |
| Variant remarks |
Authors describe this as non-pathogenic and to have an association with HNPCC. NOTE: Functional assay was done on the corresponding yeast allele I22T. |
| Reference |
PubMed: Wanat 2007 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Michael Woods |
| Database submission license |
No license selected |
| Created by |
Michael Woods |
| Date created |
2007-03-07 12:00:00 +01:00 (CET) |
| Date last edited |
2019-02-20 13:06:39 +01:00 (CET) |

Variant on transcripts
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