Variant #0000016453 (NC_000004.11:g.15565108C>G, NM_001080522.2:c.3145C>G (CC2D2A))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15565108C>G |
| DNA change (hg38) |
g.15563485C>G |
| Published as |
Arg1049X |
| ISCN |
- |
| DB-ID |
CC2D2A_000011 See all 6 reported entries |
| Variant remarks |
1 Guadeloupean MKS6 family (hom) |
| Reference |
PubMed: Mougou-Zerelli et al. 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-15 14:05:58 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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