Variant #0000291856 (NC_000017.10:g.56293498C>T, NM_017777.3:c.368G>A (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.56293498C>T
DNA change (hg38) g.58216137C>T
Published as MKS1(NM_017777.3):c.368G>A (p.R123Q), MKS1(NM_017777.4):c.368G>A (p.R123Q)
ISCN -
DB-ID MKS1_000054 See all 6 reported entries
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) 0.00043 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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     
MKS1 NM_017777.3 -?/. - c.368G>A r.(?) p.(Arg123Gln)


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