Variant #0000554313 (NC_000015.9:g.43762080_43762085del, NM_014444.2:c.*64668_*64673del (TUBGCP4))

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.43762080_43762085del
DNA change (hg38) g.43469882_43469887del
Published as TP53BP1(NM_001141979.1):c.1362_1367del (p.(Ile455_Pro456del))
ISCN -
DB-ID TP53BP1_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53BP1 NM_001141979.1 -?/. - c.1362_1367del r.(?) p.(Ile455_Pro456del)
TUBGCP4 NM_014444.2 -?/. - c.*64668_*64673del r.(=) p.(=)


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