SNRPG small nuclear ribonucleoprotein polypeptide G
Information
- Symbol
- SNRPG
- Type
- protein-coding
- Description
- small nuclear ribonucleoprotein polypeptide G
- Entrez Gene ID
- 6637
- Genome
- hg19
- Position
- chr2:70,508,639-70,520,843
- Genome
- hg38
- Position
- chr2:70,281,507-70,293,711
- MIM
- 603542 OMIM
- HGNC
- HGNC:11163 HGNC
- Ensembl
- ENSG00000143977 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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6 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | SMG |
SYNONYM | Sm-G |
MIM | 603542 OMIM |
HGNC | HGNC:11163 HGNC |
Ensembl | ENSG00000143977 Ensembl |
AllianceGenome | HGNC:11163 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000272348.7 | hg38 | chr2 | 70,281,362 | 70,293,740 | 12,379 |
ENST00000413456.6 | hg38 | chr2 | 70,281,507 | 70,293,224 | 11,718 |
ENST00000454893.1 | hg38 | chr2 | 70,281,507 | 70,293,711 | 12,205 |
ENST00000438261.5 | hg38 | chr2 | 70,281,505 | 70,293,448 | 11,944 |
ENST00000449935.6 | hg38 | chr2 | 70,281,507 | 70,292,776 | 11,270 |
ENST00000482975.6 | hg38 | chr2 | 70,281,504 | 70,293,438 | 11,935 |
ENST00000272348.7 | hg19 | chr2 | 70,508,494 | 70,520,872 | 12,379 |
ENST00000482975.6 | hg19 | chr2 | 70,508,636 | 70,520,570 | 11,935 |
ENST00000438261.5 | hg19 | chr2 | 70,508,637 | 70,520,580 | 11,944 |
ENST00000449935.6 | hg19 | chr2 | 70,508,639 | 70,519,908 | 11,270 |
ENST00000413456.6 | hg19 | chr2 | 70,508,639 | 70,520,356 | 11,718 |
ENST00000454893.1 | hg19 | chr2 | 70,508,639 | 70,520,843 | 12,205 |
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