Variant #0000541673 (NC_000010.10:g.95422842A>C, NM_006204.3:c.2425A>C (PDE6C))

Chromosome 10
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.95422842A>C
DNA change (hg38) g.93663085A>C
Published as PDE6C(NM_006204.3):c.2425A>C (p.R809=), PDE6C(NM_006204.4):c.2425A>C (p.R809=)
ISCN -
DB-ID PDE6C_000156 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) 0.00127 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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6C NM_006204.3 -/. - c.2425A>C r.(?) p.(Arg809=)
FRA10AC1 NM_145246.4 -/. - c.*6741T>G r.(=) p.(=)


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