SSH3 slingshot protein phosphatase 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
not provided | 0 | 2 |
Uncertain significance | 0 | 104 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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112 |
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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
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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 |
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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 |
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MGeND data only
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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 |
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SYNONYM | SSH3L |
MIM | 606780 OMIM |
HGNC | HGNC:30581 HGNC |
Ensembl | ENSG00000172830 Ensembl |
AllianceGenome | HGNC:30581 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000308127.9 | hg38 | chr11 | 67,303,530 | 67,312,592 | 9,063 |
ENST00000376757.9 | hg38 | chr11 | 67,303,478 | 67,312,605 | 9,128 |
ENST00000308298.11 | hg38 | chr11 | 67,303,480 | 67,312,602 | 9,123 |
ENST00000376757.9 | hg19 | chr11 | 67,070,949 | 67,080,076 | 9,128 |
ENST00000308298.11 | hg19 | chr11 | 67,070,951 | 67,080,073 | 9,123 |
ENST00000308127.9 | hg19 | chr11 | 67,071,001 | 67,080,063 | 9,063 |
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