Variant #0000555132 (NC_000015.9:g.64680168G>A, NC_000015.9(NM_016213.4):c.101+5G>A (TRIP4))

Chromosome 15
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.64680168G>A
DNA change (hg38) g.64387969G>A
Published as -
ISCN -
DB-ID KIAA0101_000001
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 15:21:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0101 NM_014736.4 ?/. - c.-6598C>T r.(?) p.(=)
TRIP4 NM_016213.4 ?/. - c.101+5G>A r.spl? p.?


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