Genomic variant #0000409127

Individual ID 00000001
Chromosome 10
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.71160828C>T
Reference -
DB-ID HK1_000077
dbSNP ID rs14006
Frequency 0.052
Allele Count 27
Allele Number 516
Combined Depth 8531
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.06312 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ./. - c.2691C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin