RASSF3 Ras association domain family member 3
Information
- Symbol
- RASSF3
- Type
- protein-coding
- Description
- Ras association domain family member 3
- Entrez Gene ID
- 283349
- Genome
- hg19
- Position
- chr12:65,004,275-65,091,344
- Genome
- hg38
- Position
- chr12:64,610,495-64,697,564
- MIM
- 607019 OMIM
- HGNC
- HGNC:14271 HGNC
- Ensembl
- ENSG00000153179 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
24 |
![]() |
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 |
---|---|
SYNONYM | RASSF5 |
MIM | 607019 OMIM |
HGNC | HGNC:14271 HGNC |
Ensembl | ENSG00000153179 Ensembl |
AllianceGenome | HGNC:14271 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000637125.1 | hg38 | chr12 | 64,507,001 | 64,694,912 | 187,912 |
ENST00000542104.6 | hg38 | chr12 | 64,610,495 | 64,697,564 | 87,070 |
ENST00000637125.1 | hg19 | chr12 | 64,900,781 | 65,088,692 | 187,912 |
ENST00000542104.6 | hg19 | chr12 | 65,004,275 | 65,091,344 | 87,070 |
Genome browser