Variant #0000016633 (NC_000017.10:g.56293641_56293783del, NC_000017.10(NM_017777.3):c.262-179_262-37del (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.56293641_56293783del
DNA change (hg38) g.58216280_58216422del
Published as 262-37_179del
ISCN -
DB-ID MKS1_000019 See all 6 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) Retrieve
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 13:49:23 +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 +/. 3i c.262-179_262-37del r.[262_417del,262_417delins418-60_418-1] p.[Phe88_Glu139del,Phe88fs]


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