Variant #0000417698 (NC_000002.11:g.48018236G>T, NM_000179.2:c.431G>T (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.48018236G>T |
| DNA change (hg38) |
g.47791097G>T |
| Published as |
S144I |
| ISCN |
- |
| DB-ID |
MSH6_000923 See all 37 reported entries |
| Variant remarks |
ClustalW AA not conserved |
| Reference |
PubMed: Barnetson 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In silico |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00097 View details |
| Owner |
Rolf Sijmons |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
InSiGHT - John-Paul Plazzer |
| Date created |
2009-04-24 17:16:00 +02:00 (CEST) |
| Date last edited |
2020-07-14 22:01:51 +02:00 (CEST) |

Variant on transcripts
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