Variant #0000791699 (NC_000002.11:g.48032717T>A, NC_000002.11(NM_000179.2):c.3557-40T>A (MSH6))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
InSiGHT |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48032717T>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH6_000364 See all 6 reported entries |
| Variant remarks |
RNA DATA pCAS2 minigene splicing assay in HeLa cells 2 independent experiments (Inserm U1245, Rouen, France: No effect on exon 7 splicing |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00565 View details |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
InSiGHT - John-Paul Plazzer |
| Date created |
2021-07-30 05:09:48 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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