Variant #0000294782 (NC_000012.11:g.56115030G>A, NM_002905.3:c.62G>A (RDH5))

Chromosome 12
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.56115030G>A
DNA change (hg38) g.55721246G>A
Published as RDH5(NM_001199771.3):c.62G>A (p.R21Q)
ISCN -
DB-ID RDH5_000205
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) 9.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD63 NM_001257389.1 -/. - c.*4315C>T r.(=) p.(=)
BLOC1S1 NM_001487.3 -/. - c.*1637G>A r.(=) p.(=)
RDH5 NM_002905.3 -/. - c.62G>A r.(?) p.(Arg21Gln)


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