Genomic variant #0000641681

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.7576841A>G
Reference -
DB-ID TP53_000002
dbSNP ID rs1800899
Frequency 0.023
Allele Count 12
Allele Number 516
Combined Depth 8374
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.01891 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ./. - c.993+12T>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin