Variant #0000562391 (NC_000017.10:g.56294075G>C, NM_017777.3:c.213C>G (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.56294075G>C
DNA change (hg38) g.58216714G>C
Published as MKS1(NM_001165927.1):c.183C>G (p.(Asp61Glu)), MKS1(NM_017777.3):c.213C>G (p.D71E), MKS1(NM_017777.4):c.213C>G (p.D71E)
ISCN -
DB-ID MKS1_000055 See all 4 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) 0.00314 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 2019-07-18 18:22:55 +02:00 (CEST)
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.213C>G r.(?) p.(Asp71Glu)


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