Variant #0000417728 (NC_000002.11:g.48030647dup, NM_000179.2:c.3261dup (MSH6))
| Chromosome |
2 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48030647dup |
| DNA change (hg38) |
g.47803508dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH6_000077 See all 48 reported entries |
| Variant remarks |
These mutations in the exon 5 C(8) track were found in the MIN-positive colon cancer cell line HCT116 when the mutated MLH1 gene was corrected. |
| Reference |
PubMed: Weiss 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Michael Woods |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
InSiGHT - John-Paul Plazzer |
| Date created |
2006-12-01 12:00:00 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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