Variant #0000347335 (NC_000014.8:g.58937416T>C, NM_014749.3:c.2300T>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.58937416T>C
DNA change (hg38) g.58470698T>C
Published as -
ISCN -
DB-ID KIAA0586_000019
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) 0.99328 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 2018-01-15 20:58:59 +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.2687T>C r.(?) p.(Leu896Pro)
KIAA0586 NM_001329943.2 -/. - c.2528T>C r.(?) p.(Leu843Pro)
TIMM9 NM_012460.2 -/. - c.-43610A>G r.(?) p.(=)
KIAA0586 NM_014749.3 -/. - c.2300T>C r.(?) p.(Leu767Pro)


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