Variant #0000853848 (NC_000014.8:g.58896138T>C, NM_014749.3:c.257T>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.58896138T>C
DNA change (hg38) -
Published as KIAA0586(NM_001244189.2):c.293T>C (p.M98T)
ISCN -
DB-ID KIAA0586_000001
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) 0.00155 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 2022-05-09 15:40:45 +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.293T>C r.(?) p.(Met98Thr)
KIAA0586 NM_001329943.2 -/. - c.257T>C r.(?) p.(Met86Thr)
TIMM9 NM_012460.2 -/. - c.-2332A>G r.(?) p.(=)
KIAA0586 NM_014749.3 -/. - c.257T>C r.(?) p.(Met86Thr)
TOMM20L NM_207377.2 -/. - c.*20838T>C r.(=) p.(=)


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