RAP2C RAP2C, member of RAS oncogene family

Information
Symbol
RAP2C
Type
protein-coding
Description
RAP2C, member of RAS oncogene family
Entrez Gene ID
57826
Genome
hg19
Position
chrX:131,337,053-131,353,475
Genome
hg38
Position
chrX:132,203,025-132,219,447
MIM
301016 OMIM
HGNC
HGNC:21165 HGNC
Ensembl
ENSG00000123728 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 6 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
6
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
MIM 301016 OMIM
HGNC HGNC:21165 HGNC
Ensembl ENSG00000123728 Ensembl
AllianceGenome HGNC:21165
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000342983.6 hg38 chrX 132,203,025 132,218,124 15,100
ENST00000620646.4 hg38 chrX 132,203,024 132,219,480 16,457
ENST00000370874.2 hg38 chrX 132,203,025 132,219,447 16,423
ENST00000620646.4 hg19 chrX 131,337,052 131,353,508 16,457
ENST00000342983.6 hg19 chrX 131,337,053 131,352,152 15,100
ENST00000370874.2 hg19 chrX 131,337,053 131,353,475 16,423
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