Variant #0000313480 (NC_000017.10:g.7579579C>T, TP53(NM_000546.5):c.108G>A)

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.7579579C>T
DNA change (hg38) g.7676261C>T
Published as TP53(NM_000546.5):c.108G>A (p.P36=, p.(Pro36=)), TP53(NM_001126114.2):c.108G>A (p.P36=)
ISCN -
DB-ID TP53_010050 See all 11 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) 0.01324 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 -/. - c.108G>A r.(?) p.(Pro36=)