Variant #0000806433 (NC_000014.8:g.58899157del, NM_014749.3:c.392del (KIAA0586))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.58899157del
DNA change (hg38) -
Published as KIAA0586(NM_001244189.1):c.428delG (p.(Arg143Lysfs*4)), KIAA0586(NM_001244189.2):c.428delG (p.R143Kfs*4), KIAA0586(NM_001329944.1):c.392delG (p.R1...)
ISCN -
DB-ID KIAA0586_000016 See all 18 reported entries
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) 0.00306 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0586 NM_001244189.1 +/. - c.428del r.(?) p.(Arg143LysfsTer4)
KIAA0586 NM_001329943.2 +/. - c.392del r.(?) p.(Arg131LysfsTer4)
TIMM9 NM_012460.2 +/. - c.-5351del r.(?) p.(=)
KIAA0586 NM_014749.3 +/. - c.392del r.(?) p.(Arg131LysfsTer4)
TOMM20L NM_207377.2 +/. - c.*23857del r.(?) p.(=)


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