Variant #0000562375 (NC_000017.10:g.56285347C>T, NM_017777.3:c.1181G>A (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.56285347C>T
DNA change (hg38) g.58207986C>T
Published as MKS1(NM_017777.3):c.1181G>A (p.W394*)
ISCN -
DB-ID MKS1_000073
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPX NM_000502.4 +/. - c.*3262C>T r.(=) p.(=)
MKS1 NM_017777.3 +/. - c.1181G>A r.(?) p.(Trp394Ter)


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