Variant #0000982637 (NC_000017.10:g.56283391G>T, NM_017777.3:c.*49C>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.56283391G>T
DNA change (hg38) -
Published as MKS1(NM_001321269.2):c.1646C>A (p.(Ser549Tyr))
ISCN -
DB-ID MKS1_000137
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.*1306G>T r.(=) p.(=)
MKS1 NM_017777.3 ?/. - c.*49C>A r.(=) p.(=)


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