TMEM43 transmembrane protein 43
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 1 | 4 |
Likely pathogenic | 0 | 4 |
Benign | 10 | 152 |
Likely benign | 0 | 642 |
Conflicting classifications of pathogenicity | 0 | 162 |
Uncertain significance | 0 | 984 |
Ranking
ClinVar | |
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0 |
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0 |
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658 |
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1,050 |
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6 |
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 |
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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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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 | ARVC5 |
SYNONYM | ARVD5 |
SYNONYM | AUNA3 |
SYNONYM | EDMD7 |
SYNONYM | EDMD7; AUNA2 |
SYNONYM | LUMA |
MIM | 612048 OMIM |
HGNC | HGNC:28472 HGNC |
Ensembl | ENSG00000170876 Ensembl |
AllianceGenome | HGNC:28472 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000306077.5 | hg38 | chr3 | 14,125,052 | 14,143,680 | 18,629 |
ENST00000306077.5 | hg19 | chr3 | 14,166,552 | 14,185,180 | 18,629 |
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