Variant #0001064087 (NC_000003.11:g.148880043G>A, NM_032383.3:c.2215G>A (HPS3))

Chromosome 3
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.148880043G>A
DNA change (hg38) -
Published as HPS3(NM_032383.5):c.2215G>A (p.(Gly739Arg))
ISCN -
DB-ID HPS3_000023 See all 2 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) 0.00965 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 -/. - c.*11458C>T r.(=) p.(=)
HPS3 NM_032383.3 -/. - c.2215G>A r.(?) p.(Gly739Arg)


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