Variant #0000806769 (NC_000015.9:g.55497812G>A, NM_004580.4:c.559C>T (RAB27A))

Chromosome 15
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.55497812G>A
DNA change (hg38) -
Published as RAB27A(NM_004580.4):c.559C>T (p.R187W), RAB27A(NM_004580.5):c.559C>T (p.R187W)
ISCN -
DB-ID RAB27A_000020 See all 4 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) 0.00016 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB27A NM_004580.4 ?/. - c.559C>T r.(?) p.(Arg187Trp)


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