chr16:69740899:> Detail (hg19) (NQO1)

Information

Genome

Assembly Position
hg19 chr16:69,740,899-69,760,571
hg38 chr16:69,706,996-69,726,668 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
DCPIP (redox dye 2,6-dichlorophenolindophenol) apoptogenicity observed in the human melanoma cell li... MMMP Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr16:69,740,899-69,760,571
Variant Type
snv
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