Variant #0000726530 (NC_000017.10:g.56285505_56285509dup, NM_017777.3:c.1122_1126dup (MKS1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56285505_56285509dup
DNA change (hg38) g.58208144_58208148dup
Published as MKS1(NM_017777.3):c.1122_1126dupATTCA (p.T376Nfs*56)
ISCN -
DB-ID MKS1_000093
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPX NM_000502.4 +/. - c.*3420_*3424dup r.(=) p.(=)
MKS1 NM_017777.3 +/. - c.1122_1126dup r.(?) p.(Thr376Asnfs*56)


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