Variant #0000357542 (NC_000002.11:g.(?_48010373)_(48032167_48032756)del, NC_000002.11(NM_000179.2):c.(?_-1)_(3556+1_3557-1)del (MSH6))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_48010373)_(48032167_48032756)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH6_000084 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
DUPLICATE – to be removed |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2018-03-08 19:39:55 +01:00 (CET) |
| Date last edited |
2018-11-09 16:06:39 +01:00 (CET) |

Variant on transcripts
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