Genomic variant #0000641707

Individual ID 00000001
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.7579644_7579659del
Reference -
DB-ID TP53_000030
dbSNP ID rs1376609066
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 3622
Homozygous 0
Heterozygote 1
Average frequency (large NGS studies) 0.74891 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ./. - c.96+41_97-54del r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin