Variant #0000724803 (NC_000014.8:g.58895076dup, NM_014749.3:c.94dup (KIAA0586))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.58895076dup
DNA change (hg38) -
Published as KIAA0586(NM_001329943.2):c.94dupC (p.H32Pfs*8)
ISCN -
DB-ID KIAA0586_000061 See all 2 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.130dup r.(?) p.(His44Profs*8)
KIAA0586 NM_001329943.2 +/. - c.94dup r.(?) p.(His32Profs*8)
TIMM9 NM_012460.2 +/. - c.-1270dup r.(?) p.(=)
KIAA0586 NM_014749.3 +/. - c.94dup r.(?) p.(His32Profs*8)
TOMM20L NM_207377.2 +/. - c.*19776dup r.(?) p.(=)


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