RASSF7 Ras association domain family member 7

Information
Symbol
RASSF7
Type
protein-coding
Description
Ras association domain family member 7
Entrez Gene ID
8045
Genome
hg19
Position
chr11:560,970-564,025
Genome
hg38
Position
chr11:560,970-564,025
MIM
143023 OMIM
HGNC
HGNC:1166 HGNC
Ensembl
ENSG00000099849 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
Uncertain significance 0 88
Ranking
ClinVar
0
0
0
98
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 :
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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 C11orf13
SYNONYM CFAP88
SYNONYM FAP88
SYNONYM HRAS1
SYNONYM HRC1
MIM 143023 OMIM
HGNC HGNC:1166 HGNC
Ensembl ENSG00000099849 Ensembl
AllianceGenome HGNC:1166
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000431809.5 hg38 chr11 560,404 563,993 3,590
ENST00000454668.2 hg38 chr11 561,450 564,021 2,572
ENST00000397582.7 hg38 chr11 560,956 564,012 3,057
ENST00000397583.8 hg38 chr11 560,970 564,025 3,056
ENST00000431809.5 hg19 chr11 560,404 563,993 3,590
ENST00000397582.7 hg19 chr11 560,956 564,012 3,057
ENST00000397583.8 hg19 chr11 560,970 564,025 3,056
ENST00000454668.2 hg19 chr11 561,450 564,021 2,572
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