MS4A3 membrane spanning 4-domains A3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 10 | 0 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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
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 |
Search Word
Target data | : |
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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Search word | : | |
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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 | CD20L |
SYNONYM | HTM4 |
MIM | 606498 OMIM |
HGNC | HGNC:7317 HGNC |
Ensembl | ENSG00000149516 Ensembl |
AllianceGenome | HGNC:7317 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000278865.8 | hg38 | chr11 | 60,056,665 | 60,071,115 | 14,451 |
ENST00000395032.6 | hg38 | chr11 | 60,056,587 | 60,070,595 | 14,009 |
ENST00000358152.6 | hg38 | chr11 | 60,056,628 | 60,071,114 | 14,487 |
ENST00000395032.6 | hg19 | chr11 | 59,824,060 | 59,838,068 | 14,009 |
ENST00000358152.6 | hg19 | chr11 | 59,824,101 | 59,838,587 | 14,487 |
ENST00000278865.8 | hg19 | chr11 | 59,824,138 | 59,838,588 | 14,451 |
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