SERINC4 serine incorporator 4
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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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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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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MIM | 614550 OMIM |
HGNC | HGNC:32237 HGNC |
Ensembl | ENSG00000184716 Ensembl |
AllianceGenome | HGNC:32237 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000319327.7 | hg38 | chr15 | 43,794,162 | 43,800,220 | 6,059 |
ENST00000299969.10 | hg38 | chr15 | 43,794,162 | 43,800,132 | 5,971 |
ENST00000299969.10 | hg19 | chr15 | 44,086,360 | 44,092,330 | 5,971 |
ENST00000319327.7 | hg19 | chr15 | 44,086,360 | 44,092,418 | 6,059 |
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