RASSF3 Ras association domain family member 3

Information
Symbol
RASSF3
Type
protein-coding
Description
Ras association domain family member 3
Entrez Gene ID
283349
Genome
hg19
Position
chr12:65,004,275-65,091,344
Genome
hg38
Position
chr12:64,610,495-64,697,564
MIM
607019 OMIM
HGNC
HGNC:14271 HGNC
Ensembl
ENSG00000153179 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
24
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 RASSF5
MIM 607019 OMIM
HGNC HGNC:14271 HGNC
Ensembl ENSG00000153179 Ensembl
AllianceGenome HGNC:14271
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000637125.1 hg38 chr12 64,507,001 64,694,912 187,912
ENST00000542104.6 hg38 chr12 64,610,495 64,697,564 87,070
ENST00000637125.1 hg19 chr12 64,900,781 65,088,692 187,912
ENST00000542104.6 hg19 chr12 65,004,275 65,091,344 87,070
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