Variant #0000978039 (NC_000008.10:g.126095371T>C, NM_014846.3:c.316A>G (KIAA0196))

Chromosome 8
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.126095371T>C
DNA change (hg38) -
Published as KIAA0196(NM_014846.3):c.316A>G (p.I106V), WASHC5(NM_014846.4):c.316A>G (p.(Ile106Val))
ISCN -
DB-ID KIAA0196_000033 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) 0.00059 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0196 NM_014846.3 -?/. - c.316A>G r.(?) p.(Ile106Val)


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