Variant #0000563627 (NC_000017.10:g.7906519G>T, NM_000180.3:c.154G>T (GUCY2D))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7906519G>T
DNA change (hg38) g.8003201G>T
Published as GUCY2D(NM_000180.3):c.154G>T (p.A52S), GUCY2D(NM_000180.4):c.154G>T (p.A52S)
ISCN -
DB-ID GUCY2D_000001 See all 12 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) 0.4168 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 2021-09-17 14:40:49 +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.154G>T r.(?) p.(Ala52Ser)


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