Variant #0000863069 (NC_000012.11:g.56115687C>T, NM_002905.3:c.525C>T (RDH5))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56115687C>T
DNA change (hg38) -
Published as RDH5(NM_001199771.1):c.525C>T (p.Y175=), RDH5(NM_001199771.3):c.525C>T (p.Y175=)
ISCN -
DB-ID BLOC1S1_000013 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) 0.00027 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 2022-05-09 15:51:19 +02:00 (CEST)
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.*3658G>A r.(=) p.(=)
BLOC1S1 NM_001487.3 -?/. - c.*2294C>T r.(=) p.(=)
RDH5 NM_002905.3 -?/. - c.525C>T r.(?) p.(Tyr175=)


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