Genomic variant #0000641689

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.7578146T>C
Reference -
DB-ID TP53_000014
dbSNP ID rs34949160
Frequency 0.007752
Allele Count 4
Allele Number 516
Combined Depth 5183
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00369 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ./. - c.672+31A>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin