Variant #0000692405 (NC_000017.10:g.56281676T>G, NM_017777.3:c.*1764A>C (MKS1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56281676T>G
DNA change (hg38) g.58204315T>G
Published as EPX(NM_000502.5):c.2040T>G (p.G680=)
ISCN -
DB-ID MKS1_000088
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 2020-09-15 15:50:26 +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.2040T>G r.(?) p.(Gly680=)
MKS1 NM_017777.3 -?/. - c.*1764A>C r.(=) p.(=)


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