Variant #0000277757 (NC_000011.9:g.18309204T>C, NM_181507.1:c.2595A>G (HPS5))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18309204T>C
DNA change (hg38) g.18287657T>C
Published as HPS5(NM_181507.2):c.2595A>G (p.R865=)
ISCN -
DB-ID HPS5_000018
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAA1 NM_000331.4 -/. - c.*17802T>C r.(=) p.(=)
HPS5 NM_181507.1 -/. - c.2595A>G r.(?) p.(Arg865=)


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