Variant #0000426683 (NC_000003.11:g.37034626_37034628del, MLH1(NM_000249.3):c.-413_-411del)
Individual ID |
00188414 |
Chromosome |
3 |
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.37034626_37034628del |
DNA change (hg38) |
g.36993135_36993137del |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001800 See all 2 reported entries |
Variant remarks |
Testing stopped when variant detected |
Reference |
PubMed: Ward (2013) |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Robyn Ward |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |

Variant on transcripts
Screenings
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