Variant #0000563708 (NC_000017.10:g.79618706G>A, NM_002602.3:c.156C>T (PDE6G))

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.79618706G>A
DNA change (hg38) g.81651676G>A
Published as PDE6G(NM_002602.3):c.156C>T (p.D52=), PDE6G(NM_002602.4):c.156C>T (p.D52=)
ISCN -
DB-ID PDE6G_000001 See all 2 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) 0.00256 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6G NM_002602.3 -/. - c.156C>T r.(?) p.(Asp52=)
TSPAN10 NM_031945.3 -/. - c.*3382G>A r.(=) p.(=)


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