Variant #0000681040 (NC_000017.10:g.7604965C>T, TP53(NM_000546.5):c.-14299G>A)

Chromosome 17
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.7604965C>T
DNA change (hg38) -
Published as WRAP53(NM_001143990.1):c.823-10C>T (p.(=)), WRAP53(NM_018081.2):c.823-10C>T
ISCN -
DB-ID WRAP53_000009 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) 0.00331 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 -?/. - c.-14299G>A r.(?) p.(=)
WRAP53 NM_001143992.1 -?/. - c.823-10C>T r.(=) p.(=)
EFNB3 NM_001406.3 -?/. - c.-3952C>T r.(?) p.(=)