Variant #0000623145 (NC_000014.8:g.58897417_58897421del, NM_014749.3:c.322_326del (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.58897417_58897421del
DNA change (hg38) g.58430699_58430703del
Published as KIAA0586(NM_001329944.2):c.322_326delGAGAA (p.E108Qfs*7)
ISCN -
DB-ID KIAA0586_000048
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-06 12:43:26 +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.358_362del r.(?) p.(Glu120GlnfsTer7)
KIAA0586 NM_001329943.2 +/. - c.322_326del r.(?) p.(Glu108GlnfsTer7)
TIMM9 NM_012460.2 +/. - c.-3611_-3607del r.(?) p.(=)
KIAA0586 NM_014749.3 +/. - c.322_326del r.(?) p.(Glu108GlnfsTer7)
TOMM20L NM_207377.2 +/. - c.*22117_*22121del r.(=) p.(=)


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