Variant #0000792228 (NC_000019.9:g.?, NM_015629.3:c.? (PRPF31))

Chromosome 19
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.?
DNA change (hg38) -
Published as p.R372
ISCN -
DB-ID NPHS1_000138 See all 111 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) Genomic location of variant could not be determined
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)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPF31 NM_015629.3 ?/. - c.? r.(?) p.?


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