Variant #0000805847 (NC_000012.11:g.56118322T>C, NM_002905.3:c.950T>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.56118322T>C
DNA change (hg38) -
Published as RDH5(NM_001199771.1):c.950T>C (p.V317A)
ISCN -
DB-ID BLOC1S1_000023
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 2021-09-17 14:40:49 +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.*1023A>G r.(=) p.(=)
BLOC1S1 NM_001487.3 ?/. - c.*4929T>C r.(=) p.(=)
RDH5 NM_002905.3 ?/. - c.950T>C r.(?) p.(Val317Ala)


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