Variant #0000340614 (NC_000017.10:g.7606350T>C, TP53(NM_000546.5):c.-15684A>G)

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.7606350T>C
DNA change (hg38) g.7703032T>C
Published as WRAP53(NM_001143990.1):c.1308T>C (p.(Ala436=))
ISCN -
DB-ID WRAP53_000021 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) 0.01445 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 -?/. - c.-15684A>G r.(?) p.(=)
WRAP53 NM_001143992.1 -?/. - c.1308T>C r.(?) p.(Ala436=)
EFNB3 NM_001406.3 -?/. - c.-2567T>C r.(?) p.(=)