RASGRP1 RAS guanyl releasing protein 1

Information
Symbol
RASGRP1
Type
protein-coding
Description
RAS guanyl releasing protein 1
Entrez Gene ID
10125
Genome
hg19
Position
chr15:38,780,304-38,857,015
Genome
hg38
Position
chr15:38,488,103-38,564,814
MIM
603962 OMIM
HGNC
HGNC:9878 HGNC
Ensembl
ENSG00000172575 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 38
Likely pathogenic 0 8
Benign 0 46
Likely benign 0 338
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 330
Ranking
ClinVar
0
0
54
680
12
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
SYNONYM CALDAG-GEFI
SYNONYM CALDAG-GEFII
SYNONYM IMD64
SYNONYM RASGRP
MIM 603962 OMIM
HGNC HGNC:9878 HGNC
Ensembl ENSG00000172575 Ensembl
AllianceGenome HGNC:9878
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000558418.6 hg38 chr15 38,488,110 38,560,279 72,170
ENST00000558164.5 hg38 chr15 38,490,554 38,564,635 74,082
ENST00000558432.5 hg38 chr15 38,490,095 38,560,082 69,988
ENST00000561180.5 hg38 chr15 38,490,480 38,565,575 75,096
ENST00000559830.5 hg38 chr15 38,490,554 38,564,635 74,082
ENST00000310803.10 hg38 chr15 38,488,103 38,564,814 76,712
ENST00000450598.6 hg38 chr15 38,490,554 38,564,635 74,082
ENST00000561117.6 hg38 chr15 38,491,539 38,565,397 73,859
ENST00000697785.1 hg38 chr15 38,488,110 38,565,384 77,275
ENST00000697784.1 hg38 chr15 38,488,110 38,564,806 76,697
ENST00000697783.1 hg38 chr15 38,488,110 38,564,710 76,601
ENST00000697782.1 hg38 chr15 38,488,110 38,564,710 76,601
ENST00000697780.1 hg38 chr15 38,488,110 38,560,088 71,979
ENST00000310803.10 hg19 chr15 38,780,304 38,857,015 76,712
ENST00000558418.6 hg19 chr15 38,780,311 38,852,480 72,170
ENST00000559830.5 hg19 chr15 38,782,755 38,856,836 74,082
ENST00000558164.5 hg19 chr15 38,782,755 38,856,836 74,082
ENST00000450598.6 hg19 chr15 38,782,755 38,856,836 74,082
ENST00000558432.5 hg19 chr15 38,782,296 38,852,283 69,988
ENST00000561117.6 hg19 chr15 38,783,740 38,857,598 73,859
ENST00000561180.5 hg19 chr15 38,782,681 38,857,776 75,096
ENST00000697780.1 hg19 chr15 38,780,311 38,852,289 71,979
ENST00000697783.1 hg19 chr15 38,780,311 38,856,911 76,601
ENST00000697782.1 hg19 chr15 38,780,311 38,856,911 76,601
ENST00000697784.1 hg19 chr15 38,780,311 38,857,007 76,697
ENST00000697785.1 hg19 chr15 38,780,311 38,857,585 77,275
Genome browser