Variant #0000853849 (NC_000014.8:g.58910784G>A, NM_014749.3:c.698G>A (KIAA0586))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58910784G>A
DNA change (hg38) -
Published as KIAA0586(NM_001244189.2):c.857G>A (p.R286K), KIAA0586(NM_001329943.2):c.698G>A (p.R233K)
ISCN -
DB-ID KIAA0586_000082 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) 0.00172 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.857G>A r.(?) p.(Arg286Lys)
KIAA0586 NM_001329943.2 -?/. - c.698G>A r.(?) p.(Arg233Lys)
TIMM9 NM_012460.2 -?/. - c.-16978C>T r.(?) p.(=)
KIAA0586 NM_014749.3 -?/. - c.698G>A r.(?) p.(Arg233Lys)


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