ERAS ES cell expressed Ras

Information
Symbol
ERAS
Type
protein-coding
Description
ES cell expressed Ras
Entrez Gene ID
3266
Genome
hg19
Position
chrX:48,687,283-48,688,548
Genome
hg38
Position
chrX:48,828,873-48,830,138
MIM
300437 OMIM
HGNC
HGNC:5174 HGNC
Ensembl
ENSG00000187682 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
not provided 6 0
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
18
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
SYNONYM HRAS2
SYNONYM HRASP
MIM 300437 OMIM
HGNC HGNC:5174 HGNC
Ensembl ENSG00000187682 Ensembl
AllianceGenome HGNC:5174
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000338270.1 hg38 chrX 48,828,873 48,830,138 1,266
ENST00000636362.1 hg38 chrX 48,826,513 48,829,869 3,357
ENST00000636362.1 hg19 chrX 48,684,923 48,688,279 3,357
ENST00000338270.1 hg19 chrX 48,687,283 48,688,548 1,266
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