Variant #0000623721 (NC_000017.10:g.56284567A>T, NM_017777.3:c.1286T>A (MKS1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56284567A>T
DNA change (hg38) g.58207206A>T
Published as MKS1(NM_017777.4):c.1286T>A (p.L429Q)
ISCN -
DB-ID MKS1_000084
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPX NM_000502.4 ?/. - c.*2482A>T r.(=) p.(=)
MKS1 NM_017777.3 ?/. - c.1286T>A r.(?) p.(Leu429Gln)


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