Variant #0000925889 (NC_000014.8:g.58895204del, NC_000014.8(NM_014749.3):c.199+23del (KIAA0586))

Chromosome 14
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.58895204del
DNA change (hg38) -
Published as KIAA0586(NM_001244189.2):c.235+23delT
ISCN -
DB-ID KIAA0586_000101
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.235+23del r.(=) p.(=)
KIAA0586 NM_001329943.2 -?/. - c.199+23del r.(=) p.(=)
TIMM9 NM_012460.2 -?/. - c.-1394del r.(?) p.(=)
KIAA0586 NM_014749.3 -?/. - c.199+23del r.(=) p.(=)
TOMM20L NM_207377.2 -?/. - c.*19904del r.(?) p.(=)


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