Variant #0000806867 (NC_000015.9:g.64680161T>G, NM_016213.4:c.99T>G (TRIP4))

Chromosome 15
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.64680161T>G
DNA change (hg38) -
Published as TRIP4(NM_001321924.1):c.-676T>G (p.(=))
ISCN -
DB-ID KIAA0101_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0101 NM_014736.4 -?/. - c.-6591A>C r.(?) p.(=)
TRIP4 NM_016213.4 -?/. - c.99T>G r.(?) p.(Ile33Met)


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