RASGRP4 RAS guanyl releasing protein 4
Information
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 |
Type | ID |
---|---|
MIM | 607320 OMIM |
HGNC | HGNC:18958 HGNC |
Ensembl | ENSG00000171777 Ensembl |
AllianceGenome | HGNC:18958 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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