Variant #0000469300 (NC_000003.11:g.37048539A>G, NM_000249.3:c.438A>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 |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37048539A>G |
DNA change (hg38) |
g.37007048A>G |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_001951 See all 5 reported entries |
Variant remarks |
Insight class: 2 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-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 |
2019-03-15 06:46:09 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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