Variant #0000950254 (NC_000014.8:g.58955530T>C, NM_014749.3:c.3491T>C (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.58955530T>C
DNA change (hg38) -
Published as KIAA0586(NM_001244189.1):c.3878T>C (p.(Leu1293Ser))
ISCN -
DB-ID KIAA0586_000052 See all 3 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) 0.0138 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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.3878T>C r.(?) p.(Leu1293Ser)
KIAA0586 NM_001329943.2 -?/. - c.3719T>C r.(?) p.(Leu1240Ser)
TIMM9 NM_012460.2 -?/. - c.-61724A>G r.(?) p.(=)
KIAA0586 NM_014749.3 -?/. - c.3491T>C r.(?) p.(Leu1164Ser)


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