Variant #0000306900 (NC_000012.11:g.56115626G>A, NM_002905.3:c.464G>A (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.56115626G>A
DNA change (hg38) g.55721842G>A
Published as RDH5(NM_001199771.1):c.464G>A (p.R155Q)
ISCN -
DB-ID RDH5_000208
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) 6.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*3719C>T r.(=) p.(=)
BLOC1S1 NM_001487.3 ?/. - c.*2233G>A r.(=) p.(=)
RDH5 NM_002905.3 ?/. - c.464G>A r.(?) p.(Arg155Gln)


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