Variant #0000552737 (NC_000014.8:g.59010649T>C, NC_000014.8(NM_014749.3):c.4267+3795T>C (KIAA0586))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.59010649T>C
DNA change (hg38) g.58543931T>C
Published as -
ISCN -
DB-ID KIAA0586_000046
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) 0.3788 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +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.4703T>C r.(?) p.(Leu1568Pro)
KIAA0586 NM_001329943.2 -/. - c.4495+3795T>C r.(=) p.(=)
TIMM9 NM_012460.2 -/. - c.-116843A>G r.(?) p.(=)
KIAA0586 NM_014749.3 -/. - c.4267+3795T>C r.(=) p.(=)


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