Variant #0000691389 (NC_000012.11:g.56115021T>C, NM_002905.3:c.53T>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.56115021T>C
DNA change (hg38) -
Published as RDH5(NM_001199771.1):c.53T>C (p.L18P)
ISCN -
DB-ID BLOC1S1_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD63 NM_001257389.1 ?/. - c.*4324A>G r.(=) p.(=)
BLOC1S1 NM_001487.3 ?/. - c.*1628T>C r.(=) p.(=)
RDH5 NM_002905.3 ?/. - c.53T>C r.(?) p.(Leu18Pro)


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