Variant #0000000060 (NC_000001.10:g.150316692C>T, PRPF3(NM_004698.2):c.1481C>T)

Individual ID 00000081
Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.150316692C>T
Reference -
DB-ID PRPF3_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
PRPF3 NM_004698.2 +/+ - c.1481C>T r.(?) p.(Thr494Met) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000082 DNA SEQ-NG PRPF3 1 variome.ir