Variant #0000792234 (NC_000001.10:g.150316688C>T, NM_004698.2:c.1477C>T (PRPF3))

Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.150316688C>T
DNA change (hg38) -
Published as p.P493S
ISCN -
DB-ID PRPF3_000034 See all 9 reported entries
Variant remarks -
Reference PubMed: Tanackovic 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-08-02 20:37:33 +02:00 (CEST)
Date last edited 2024-02-09 15:16:32 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPF3 NM_004698.2 ?/. 11 c.1477C>T r.(?) p.(Pro493Ser)


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