MMP3 matrix metallopeptidase 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 46 |
Likely benign | 0 | 20 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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14 |
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106 |
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2 |
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 | CHDS6 |
SYNONYM | MMP-3 |
SYNONYM | SL-1 |
SYNONYM | STMY |
SYNONYM | STMY1 |
SYNONYM | STR1 |
MIM | 185250 OMIM |
HGNC | HGNC:7173 HGNC |
Ensembl | ENSG00000149968 Ensembl |
AllianceGenome | HGNC:7173 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000299855.10 | hg38 | chr11 | 102,835,801 | 102,843,609 | 7,809 |
ENST00000299855.10 | hg19 | chr11 | 102,706,532 | 102,714,340 | 7,809 |
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