chr9:21967751:> Detail (hg19) (CDKN2A)

Information

Genome

Assembly Position
hg19 chr9:21,967,751-21,995,300
hg38 chr9:21,967,752-21,995,301 

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
Melanoma cells lacking p16 are more sensitive than those expressing p16. Flavopiridol inhibits CDK a... MMMP Detail
Isolated limb infusion model. p16INK4a expression and absence of activated B-RAF are independent pre... 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
chr9:21,967,751-21,995,300
Variant Type
snv
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