Variant #0000016466 (NC_000004.11:g.15513014_15513016del, NM_001080522.2:c.685_687del (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.15513014_15513016del |
| DNA change (hg38) |
g.15511391_15511393del |
| Published as |
685_7delGAA (E229del) |
| ISCN |
- |
| DB-ID |
CC2D2A_000024 |
| Variant remarks |
1 British MKS6 family (com-het) |
| Reference |
PubMed: Otto et al. 2011 |
| 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 |
2020-06-16 12:40:18 +02:00 (CEST) |

Variant on transcripts
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