Variant #0000863070 (NC_000012.11:g.56115707T>C, NM_002905.3:c.545T>C (RDH5))

Chromosome 12
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.56115707T>C
DNA change (hg38) -
Published as RDH5(NM_002905.5):c.545T>C (p.L182P)
ISCN -
DB-ID BLOC1S1_000031
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:51:19 +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     
CD63 NM_001257389.1 ?/. - c.*3638A>G r.(=) p.(=)
BLOC1S1 NM_001487.3 ?/. - c.*2314T>C r.(=) p.(=)
RDH5 NM_002905.3 ?/. - c.545T>C r.(?) p.(Leu182Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.