Variant #0000533753 (NC_000008.10:g.126091044G>A, NM_014846.3:c.647C>T (KIAA0196))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.126091044G>A
DNA change (hg38) g.125078802G>A
Published as KIAA0196(NM_014846.3):c.647C>T (p.P216L, p.(Pro216Leu)), WASHC5(NM_014846.4):c.647C>T (p.P216L)
ISCN -
DB-ID KIAA0196_000030 See all 4 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) 0.00111 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0196 NM_014846.3 ?/. - c.647C>T r.(?) p.(Pro216Leu)


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