Variant #0000356455 (NC_000003.11:g.37045873A>G, NC_000003.11(NM_000249.3):c.307-19A>G (MLH1))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Classification method |
InSiGHT |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37045873A>G |
DNA change (hg38) |
g.37004382A>G |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001681 See all 14 reported entries |
Variant remarks |
Insight class: 2 |
Reference |
InSiGHT |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00025 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 |
2018-03-05 12:40:48 +01:00 (CET) |
Date last edited |
2018-11-09 18:15:18 +01:00 (CET) |

Variant on transcripts
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