Variant #0001043161 (NC_000019.9:g.54637655_54637656del, NM_015629.3:c.*2792_*2793del (PRPF31))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54637655_54637656del
DNA change (hg38) -
Published as CNOT3(NM_014516.4):c.-4105_-4104del
ISCN -
DB-ID CNOT3_000049
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFPT NM_013342.3 -?/. - c.-19002_-19001del r.(?) p.(=)
CNOT3 NM_014516.3 -?/. - c.-4105_-4104del r.(?) p.(=)
PRPF31 NM_015629.3 -?/. - c.*2792_*2793del r.(=) p.(=)
LENG1 NM_024316.1 -?/. - c.*21808_*21809del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.