Variant #0000982822 (NC_000017.10:g.7605066C>T, NM_000546.5:c.-14400G>A (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.7605066C>T
DNA change (hg38) -
Published as WRAP53(NM_001143992.2):c.914C>T (p.(Thr305Met))
ISCN -
DB-ID EFNB3_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) 5.0E-5 View details
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ?/. - c.-14400G>A r.(?) p.(=)
WRAP53 NM_001143992.1 ?/. - c.914C>T r.(?) p.(Thr305Met)
EFNB3 NM_001406.3 ?/. - c.-3851C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.