Variant #0000414226 (NC_000014.8:g.75515912A>G, NM_001040108.1:c.447T>C (MLH3))
Chromosome |
14 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75515912A>G |
DNA change (hg38) |
g.75049209A>G |
Published as |
561T>C (Tyr149Tyr) |
ISCN |
- |
DB-ID |
MLH3_000052 See all 3 reported entries |
Variant remarks |
- |
Reference |
PubMed: Lipkin 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
4/120 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2008-09-14 12:07:00 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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