RASSF9 Ras association domain family member 9

Information
Symbol
RASSF9
Type
protein-coding
Description
Ras association domain family member 9
Entrez Gene ID
9182
Genome
hg19
Position
chr12:86,194,481-86,230,187
Genome
hg38
Position
chr12:85,800,703-85,836,409
MIM
610383 OMIM
HGNC
HGNC:15739 HGNC
Ensembl
ENSG00000198774 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
58
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM P-CIP1
SYNONYM PAMCI
SYNONYM PCIP1
MIM 610383 OMIM
HGNC HGNC:15739 HGNC
Ensembl ENSG00000198774 Ensembl
AllianceGenome HGNC:15739
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361228.5 hg38 chr12 85,800,703 85,836,409 35,707
ENST00000361228.5 hg19 chr12 86,194,481 86,230,187 35,707
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