Variant #0000433823 (NC_000003.11:g.37045896T>A, NM_000249.3:c.311T>A (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.37045896T>A |
DNA change (hg38) |
g.37004405T>A |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001012 See all 3 reported entries |
Variant remarks |
- |
Reference |
PubMed: Ellison 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Michael Woods |
Database submission license |
No license selected |
Created by |
Michael Woods |
Date created |
2005-11-17 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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