Variant #0000433798 (NC_000003.11:g.37042537G>A, NM_000249.3:c.299G>A (MLH1))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37042537G>A |
DNA change (hg38) |
g.37001046G>A |
Published as |
R100Q |
ISCN |
- |
DB-ID |
MLH1_000129 See all 6 reported entries |
Variant remarks |
- |
Reference |
PubMed: Ellison 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Rolf Sijmons |
Database submission license |
No license selected |
Created by |
Rolf Sijmons |
Date created |
2009-02-06 12:00:00 +01:00 (CET) |
Date last edited |
2019-02-20 13:06:39 +01:00 (CET) |

Variant on transcripts
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