Variant #0001055073 (NC_000015.9:g.43692262A>G, NM_014444.2:c.1439A>G (TUBGCP4))

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.43692262A>G
DNA change (hg38) -
Published as TUBGCP4(NM_014444.5):c.1439A>G (p.(Tyr480Cys))
ISCN -
DB-ID TP53BP1_000019
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53BP1 NM_001141979.1 ?/. - c.*7319T>C r.(=) p.(=)
TUBGCP4 NM_014444.2 ?/. - c.1439A>G r.(?) p.(Tyr480Cys)


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