Variant #0000016629 (NC_000017.10:g.56292145G>A, NM_017777.3:c.472C>T (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.56292145G>A
DNA change (hg38) g.58214784G>A
Published as -
ISCN -
DB-ID MKS1_000015 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 10:37:55 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MKS1 NM_017777.3 +/. 6i c.472C>T r.472c>u) p.(Arg158*)


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