Variant #0000994408 (NC_000004.11:g.660377G>A, NM_000283.3:c.2326G>A (PDE6B))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.660377G>A
DNA change (hg38) -
Published as PDE6B(NM_000283.3):c.2326G>A (p.D776N, p.(Asp776Asn)), PDE6B(NM_000283.4):c.2326G>A (p.D776N)
ISCN -
DB-ID PDE6B_000008 See all 13 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) 5.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6B NM_000283.3 ?/. - c.2326G>A r.(?) p.(Asp776Asn)


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