Variant #0000691679 (NC_000014.8:g.58924507C>T, NM_014749.3:c.1393C>T (KIAA0586))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.58924507C>T
DNA change (hg38) -
Published as KIAA0586(NM_001329943.2):c.1393C>T (p.P465S)
ISCN -
DB-ID KIAA0586_000059
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) 8.0E-5 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0586 NM_001244189.1 ?/. - c.1552C>T r.(?) p.(Pro518Ser)
KIAA0586 NM_001329943.2 ?/. - c.1393C>T r.(?) p.(Pro465Ser)
TIMM9 NM_012460.2 ?/. - c.-30701G>A r.(?) p.(=)
KIAA0586 NM_014749.3 ?/. - c.1393C>T r.(?) p.(Pro465Ser)


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