Variant #0000313102 (NC_000017.10:g.7606722C>G, TP53(NM_000546.5):c.-16056G>C)

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7606722C>G
DNA change (hg38) g.7703404C>G
Published as WRAP53(NM_018081.2):c.1565C>G (p.A522G)
ISCN -
DB-ID WRAP53_000015 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.298 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 -/. - c.-16056G>C r.(?) p.(=)
WRAP53 NM_001143992.1 -/. - c.1565C>G r.(?) p.(Ala522Gly)
EFNB3 NM_001406.3 -/. - c.-2195C>G r.(?) p.(=)