SNRPD3 small nuclear ribonucleoprotein D3 polypeptide
Information
- Symbol
- SNRPD3
- Type
- protein-coding
- Description
- small nuclear ribonucleoprotein D3 polypeptide
- Entrez Gene ID
- 6634
- Genome
- hg19
- Position
- chr22:24,951,967-24,970,939
- Genome
- hg38
- Position
- chr22:24,555,999-24,574,971
- MIM
- 601062 OMIM
- HGNC
- HGNC:11160 HGNC
- Ensembl
- ENSG00000100028 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 7 | 0 |
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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
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| 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
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| Category | : |
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| 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 | SMD3 |
| SYNONYM | Sm-D3 |
| MIM | 601062 OMIM |
| HGNC | HGNC:11160 HGNC |
| Ensembl | ENSG00000100028 Ensembl |
| AllianceGenome | HGNC:11160 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000402849.5 | hg38 | chr22 | 24,556,007 | 24,582,052 | 26,046 |
| ENST00000215829.8 | hg38 | chr22 | 24,555,999 | 24,574,971 | 18,973 |
| ENST00000215829.8 | hg19 | chr22 | 24,951,967 | 24,970,939 | 18,973 |
| ENST00000402849.5 | hg19 | chr22 | 24,951,975 | 24,978,020 | 26,046 |
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