Variant #0000563648 (NC_000017.10:g.7917236C>T, NM_000180.3:c.2302C>T (GUCY2D))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7917236C>T
DNA change (hg38) g.8013918C>T
Published as GUCY2D(NM_000180.3):c.2302C>T (p.R768W), GUCY2D(NM_000180.4):c.2302C>T (p.R768W, p.(Arg768Trp))
ISCN -
DB-ID GUCY2D_000055 See all 38 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) 0.00016 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUCY2D NM_000180.3 +/. - c.2302C>T r.(?) p.(Arg768Trp)


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