RASGRP4 RAS guanyl releasing protein 4

Information
Symbol
RASGRP4
Type
protein-coding
Description
RAS guanyl releasing protein 4
Entrez Gene ID
115727
Genome
hg19
Position
chr19:38,899,698-38,916,859
Genome
hg38
Position
chr19:38,409,058-38,426,219
MIM
607320 OMIM
HGNC
HGNC:18958 HGNC
Ensembl
ENSG00000171777 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
76
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 607320 OMIM
HGNC HGNC:18958 HGNC
Ensembl ENSG00000171777 Ensembl
AllianceGenome HGNC:18958
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000614135.4 hg38 chr19 38,409,058 38,426,305 17,248
ENST00000617966.4 hg38 chr19 38,409,058 38,426,305 17,248
ENST00000587753.5 hg38 chr19 38,409,058 38,426,305 17,248
ENST00000622174.4 hg38 chr19 38,409,058 38,426,305 17,248
ENST00000587738.2 hg38 chr19 38,409,840 38,426,162 16,323
ENST00000615439.5 hg38 chr19 38,409,058 38,426,219 17,162
ENST00000454404.6 hg38 chr19 38,409,058 38,426,305 17,248
ENST00000586305.5 hg38 chr19 38,409,055 38,426,187 17,133
ENST00000586305.5 hg19 chr19 38,899,695 38,916,827 17,133
ENST00000615439.5 hg19 chr19 38,899,698 38,916,859 17,162
ENST00000454404.6 hg19 chr19 38,899,698 38,916,945 17,248
ENST00000587753.5 hg19 chr19 38,899,698 38,916,945 17,248
ENST00000614135.4 hg19 chr19 38,899,698 38,916,945 17,248
ENST00000617966.4 hg19 chr19 38,899,698 38,916,945 17,248
ENST00000622174.4 hg19 chr19 38,899,698 38,916,945 17,248
ENST00000587738.2 hg19 chr19 38,900,480 38,916,802 16,323
Genome browser