Variant #0000268553 (NC_000003.11:g.148901407C>A, HPS3(NM_032383.3):c.*11398C>A)

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.148901407C>A
DNA change (hg38) g.149183620C>A
Published as CP(NM_000096.3):c.2286-15G>T, CP(NM_000096.4):c.2286-15G>T
ISCN -
DB-ID CP_000025 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02385 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 -/. - c.2286-15G>T r.(=) p.(=)
HPS3 NM_032383.3 -/. - c.*11398C>A r.(=) p.(=)