SARNP SAP domain containing ribonucleoprotein
Information
- Symbol
- SARNP
- Type
- protein-coding
- Description
- SAP domain containing ribonucleoprotein
- Entrez Gene ID
- 84324
- Genome
- hg19
- Position
- chr12:56,151,054-56,211,508
- Genome
- hg38
- Position
- chr12:55,757,270-55,817,724
- MIM
- 610049 OMIM
- HGNC
- HGNC:24432 HGNC
- Ensembl
- ENSG00000205323 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
20 |
 |
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 | CIP29 |
| SYNONYM | HCC1 |
| SYNONYM | HSPC316 |
| SYNONYM | THO1 |
| MIM | 610049 OMIM |
| HGNC | HGNC:24432 HGNC |
| Ensembl | ENSG00000205323 Ensembl |
| AllianceGenome | HGNC:24432 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000552080.1 | hg38 | chr12 | 55,760,424 | 55,817,709 | 57,286 |
| ENST00000336133.8 | hg38 | chr12 | 55,757,270 | 55,817,724 | 60,455 |
| ENST00000336133.8 | hg19 | chr12 | 56,151,054 | 56,211,508 | 60,455 |
| ENST00000552080.1 | hg19 | chr12 | 56,154,208 | 56,211,493 | 57,286 |
Genome browser