Variant #0000414232 (NC_000014.8:g.75516082G>C, NM_001040108.1:c.277C>G (MLH3))
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75516082G>C |
DNA change (hg38) |
g.75049379G>C |
Published as |
- |
ISCN |
- |
DB-ID |
MLH3_000002 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
0.01 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
6.0E-5 View details |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2009-08-17 12:46:00 +02:00 (CEST) |
Date last edited |
2021-09-09 14:48:34 +02:00 (CEST) |

Variant on transcripts
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