Variant #0000016621 (NC_000017.10:g.56293449C>T, NM_017777.3:c.417G>A (MKS1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56293449C>T |
DNA change (hg38) |
g.58216088C>T |
Published as |
E139E |
ISCN |
- |
DB-ID |
MKS1_000007 See all 18 reported entries |
Variant remarks |
RNA exon 4 skipping |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00013 View details |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-12-04 16:05:24 +01:00 (CET) |
Date last edited |
2023-11-29 13:53:43 +01:00 (CET) |

Variant on transcripts
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