RASSF10 Ras association domain family member 10

Information
Symbol
RASSF10
Type
protein-coding
Description
Ras association domain family member 10
Entrez Gene ID
644943
Genome
hg19
Position
chr11:13,030,863-13,033,666
Genome
hg38
Position
chr11:13,009,316-13,012,119
MIM
614713 OMIM
HGNC
HGNC:33984 HGNC
Ensembl
ENSG00000189431 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
52
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 :
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
MIM 614713 OMIM
HGNC HGNC:33984 HGNC
Ensembl ENSG00000189431 Ensembl
AllianceGenome HGNC:33984
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000529419.3 hg38 chr11 13,009,316 13,012,119 2,804
ENST00000529419.3 hg19 chr11 13,030,863 13,033,666 2,804
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