Variant #0000554810 (NC_000015.9:g.55497857_55497861del, NM_004580.4:c.514_518del (RAB27A))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55497857_55497861del
DNA change (hg38) g.55205659_55205663del
Published as RAB27A(NM_004580.4):c.514_518delCAAGC (p.Q172Nfs*2)
ISCN -
DB-ID RAB27A_000012
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 15:02:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB27A NM_004580.4 +/. - c.514_518del r.(?) p.(Gln172AsnfsTer2)


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