RAP1B RAP1B, member of RAS oncogene family

Information
Symbol
RAP1B
Type
protein-coding
Description
RAP1B, member of RAS oncogene family
Entrez Gene ID
5908
Genome
hg19
Position
chr12:69,004,679-69,065,681
Genome
hg38
Position
chr12:68,610,899-68,671,901
MIM
179530 OMIM
HGNC
HGNC:9857 HGNC
Ensembl
ENSG00000127314 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 2
Benign 0 28
Likely benign 0 14
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
52
10
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 K-REV
SYNONYM RAL1B
SYNONYM THC11
MIM 179530 OMIM
HGNC HGNC:9857 HGNC
Ensembl ENSG00000127314 Ensembl
AllianceGenome HGNC:9857
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000542145.5 hg38 chr12 68,610,929 68,659,754 48,826
ENST00000539091.5 hg38 chr12 68,610,929 68,659,647 48,719
ENST00000541216.1 hg38 chr12 68,611,025 68,656,637 45,613
ENST00000378985.7 hg38 chr12 68,610,925 68,657,713 46,789
ENST00000450214.6 hg38 chr12 68,610,908 68,660,124 49,217
ENST00000250559.14 hg38 chr12 68,610,899 68,671,901 61,003
ENST00000393436.9 hg38 chr12 68,610,858 68,660,522 49,665
ENST00000537460.5 hg38 chr12 68,610,908 68,659,401 48,494
ENST00000341355.9 hg38 chr12 68,610,908 68,657,191 46,284
ENST00000543697.5 hg38 chr12 68,610,939 68,659,441 48,503
ENST00000543393.5 hg38 chr12 68,610,919 68,659,626 48,708
ENST00000540209.5 hg38 chr12 68,610,925 68,659,870 48,946
ENST00000393436.9 hg19 chr12 69,004,638 69,054,302 49,665
ENST00000250559.14 hg19 chr12 69,004,679 69,065,681 61,003
ENST00000341355.9 hg19 chr12 69,004,688 69,050,971 46,284
ENST00000537460.5 hg19 chr12 69,004,688 69,053,181 48,494
ENST00000378985.7 hg19 chr12 69,004,705 69,051,493 46,789
ENST00000450214.6 hg19 chr12 69,004,688 69,053,904 49,217
ENST00000539091.5 hg19 chr12 69,004,709 69,053,427 48,719
ENST00000540209.5 hg19 chr12 69,004,705 69,053,650 48,946
ENST00000541216.1 hg19 chr12 69,004,805 69,050,417 45,613
ENST00000542145.5 hg19 chr12 69,004,709 69,053,534 48,826
ENST00000543393.5 hg19 chr12 69,004,699 69,053,406 48,708
ENST00000543697.5 hg19 chr12 69,004,719 69,053,221 48,503
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