Variant #0000853854 (NC_000014.8:g.58979320T>C, NM_014749.3:c.4176T>C (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.58979320T>C
DNA change (hg38) -
Published as KIAA0586(NM_001329943.2):c.4404T>C (p.S1468=)
ISCN -
DB-ID KIAA0586_000089
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) 0.00025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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.4563T>C r.(?) p.(Ser1521=)
KIAA0586 NM_001329943.2 -?/. - c.4404T>C r.(?) p.(Ser1468=)
TIMM9 NM_012460.2 -?/. - c.-85514A>G r.(?) p.(=)
KIAA0586 NM_014749.3 -?/. - c.4176T>C r.(?) p.(Ser1392=)


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