Variant #0000417672 (NC_000002.11:g.48026308C>G, NM_000179.2:c.1186C>G (MSH6))
Chromosome |
2 |
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.48026308C>G |
DNA change (hg38) |
g.47799169C>G |
Published as |
1186C>G |
ISCN |
- |
DB-ID |
MSH6_000118 See all 34 reported entries |
Variant remarks |
MMR activity, repair efficiency (G.T heteroduplex), 89,8% versus 100% |
Reference |
Drost Hum Mutat 2012 33: 488-494. |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00551 View details |
Owner |
INSiGHT group |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
INSiGHT group |
Date created |
2012-12-01 12:00:00 +01:00 (CET) |
Date last edited |
2020-07-14 21:54:44 +02:00 (CEST) |

Variant on transcripts
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