Variant #0000518252 (NC_000003.11:g.148899775C>T, HPS3(NM_032383.3):c.*9766C>T)

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.148899775C>T
DNA change (hg38) g.149181988C>T
Published as CP(NM_000096.3):c.2554+17G>A
ISCN -
DB-ID CP_000017 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) 0.03136 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 -/. - c.2554+17G>A r.(=) p.(=)
HPS3 NM_032383.3 -/. - c.*9766C>T r.(=) p.(=)