S100A8 S100 calcium binding protein A8
Information
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 6 |
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 |
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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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SYNONYM | 60B8AG |
SYNONYM | CAGA |
SYNONYM | CFAG |
SYNONYM | CGLA |
SYNONYM | CP-10 |
SYNONYM | L1Ag |
SYNONYM | MA387 |
SYNONYM | MIF |
SYNONYM | MRP8 |
SYNONYM | NIF |
SYNONYM | P8 |
SYNONYM | S100-A8 |
MIM | 123885 OMIM |
HGNC | HGNC:10498 HGNC |
Ensembl | ENSG00000143546 Ensembl |
AllianceGenome | HGNC:10498 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368733.4 | hg38 | chr1 | 153,390,032 | 153,391,073 | 1,042 |
ENST00000368732.5 | hg38 | chr1 | 153,390,032 | 153,390,976 | 945 |
ENST00000368732.5 | hg19 | chr1 | 153,362,508 | 153,363,452 | 945 |
ENST00000368733.4 | hg19 | chr1 | 153,362,508 | 153,363,549 | 1,042 |
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