S100A6 S100 calcium binding protein A6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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 |
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Target data | : |
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 | 2A9 |
SYNONYM | 5B10 |
SYNONYM | CABP |
SYNONYM | CACY |
SYNONYM | PRA |
SYNONYM | S10A6 |
MIM | 114110 OMIM |
HGNC | HGNC:10496 HGNC |
Ensembl | ENSG00000197956 Ensembl |
AllianceGenome | HGNC:10496 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368720.6 | hg38 | chr1 | 153,534,599 | 153,536,244 | 1,646 |
ENST00000496817.5 | hg38 | chr1 | 153,534,599 | 153,536,215 | 1,617 |
ENST00000368719.9 | hg38 | chr1 | 153,534,599 | 153,535,991 | 1,393 |
ENST00000368719.9 | hg19 | chr1 | 153,507,075 | 153,508,467 | 1,393 |
ENST00000496817.5 | hg19 | chr1 | 153,507,075 | 153,508,691 | 1,617 |
ENST00000368720.6 | hg19 | chr1 | 153,507,075 | 153,508,720 | 1,646 |
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