Genomic variant #0000409126

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.71160750C>T
Reference -
DB-ID HK1_000076
dbSNP ID rs34616021
Frequency 0.016
Allele Count 8
Allele Number 516
Combined Depth 8667
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.01622 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ./. - c.2613C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin