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 InternationalCreative Commons License
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MKS1 NM_017777.3 +/. 4 c.417G>A r.262_417del p.Phe88_Glu139del


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