TRA2A transformer 2 alpha homolog
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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 |
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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 | AWMS1 |
SYNONYM | HSU53209 |
MIM | 602718 OMIM |
HGNC | HGNC:16645 HGNC |
Ensembl | ENSG00000164548 Ensembl |
AllianceGenome | HGNC:16645 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000392502.8 | hg38 | chr7 | 23,504,784 | 23,532,041 | 27,258 |
ENST00000621813.4 | hg38 | chr7 | 23,504,784 | 23,532,041 | 27,258 |
ENST00000297071.9 | hg38 | chr7 | 23,504,780 | 23,531,981 | 27,202 |
ENST00000297071.9 | hg19 | chr7 | 23,544,399 | 23,571,600 | 27,202 |
ENST00000392502.8 | hg19 | chr7 | 23,544,403 | 23,571,660 | 27,258 |
ENST00000621813.4 | hg19 | chr7 | 23,544,403 | 23,571,660 | 27,258 |
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