Variant #0000552715 (NC_000014.8:g.58895020del, NM_014749.3:c.38del (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.58895020del
DNA change (hg38) g.58428302del
Published as KIAA0586(NM_001329944.1):c.38delA (p.K13Rfs*6)
ISCN -
DB-ID KIAA0586_000026
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 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.74del r.(?) p.(Lys25ArgfsTer6)
KIAA0586 NM_001329943.2 +/. - c.38del r.(?) p.(Lys13ArgfsTer6)
TIMM9 NM_012460.2 +/. - c.-1207del r.(?) p.(=)
KIAA0586 NM_014749.3 +/. - c.38del r.(?) p.(Lys13ArgfsTer6)
TOMM20L NM_207377.2 +/. - c.*19720del r.(?) p.(=)


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