Variant #0000982824 (NC_000017.10:g.7606721dup, NM_000546.5:c.-16049dup (TP53))

Chromosome 17
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.7606721dup
DNA change (hg38) -
Published as WRAP53(NM_001143992.2):c.1564dup (p.(Ala522GlyfsTer8)), WRAP53(NM_018081.2):c.1564dupG (p.A522Gfs*8)
ISCN -
DB-ID EFNB3_000017 See all 2 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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ?/. - c.-16049dup r.(?) p.(=)
WRAP53 NM_001143992.1 ?/. - c.1564dup r.(?) p.(Ala522Glyfs*8)
EFNB3 NM_001406.3 ?/. - c.-2196dup r.(?) p.(=)


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