Genomic variant #0000641702

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.7579548G>A
Reference -
DB-ID TP53_000027
dbSNP ID rs1800371
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 9530
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00515 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ./. - c.139C>T r.(?) p.(Pro47Ser)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin