Variant #0000891820 (NC_000014.8:g.58941425C>T, NM_014749.3:c.2507C>T (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.58941425C>T
DNA change (hg38) -
Published as KIAA0586(NM_001244189.2):c.2894C>T (p.P965L)
ISCN -
DB-ID KIAA0586_000097
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) 0.00098 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 2022-11-01 13:01:21 +01:00 (CET)
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.2894C>T r.(?) p.(Pro965Leu)
KIAA0586 NM_001329943.2 -?/. - c.2735C>T r.(?) p.(Pro912Leu)
TIMM9 NM_012460.2 -?/. - c.-47619G>A r.(?) p.(=)
KIAA0586 NM_014749.3 -?/. - c.2507C>T r.(?) p.(Pro836Leu)


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