Variant #0000357688 (NC_000014.8:g.75515915C>G, NM_001040108.1:c.444G>C (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.75515915C>G |
DNA change (hg38) |
g.75049212C>G |
Published as |
- |
ISCN |
- |
DB-ID |
MLH3_000005 See all 3 reported entries |
Variant remarks |
- |
Reference |
copied from InSiGHT database |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0043 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 |
2018-03-09 13:27:44 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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