TMEM161A transmembrane protein 161A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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72 |
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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 |
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 | : | |
Filtering | : |
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 | AROS-29 |
SYNONYM | AROS29 |
MIM | 618966 OMIM |
HGNC | HGNC:26020 HGNC |
Ensembl | ENSG00000064545 Ensembl |
AllianceGenome | HGNC:26020 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000587583.6 | hg38 | chr19 | 19,119,660 | 19,138,447 | 18,788 |
ENST00000162044.14 | hg38 | chr19 | 19,119,169 | 19,138,478 | 19,310 |
ENST00000450333.6 | hg38 | chr19 | 19,119,169 | 19,138,466 | 19,298 |
ENST00000450333.6 | hg19 | chr19 | 19,229,978 | 19,249,275 | 19,298 |
ENST00000162044.14 | hg19 | chr19 | 19,229,978 | 19,249,287 | 19,310 |
ENST00000587583.6 | hg19 | chr19 | 19,230,469 | 19,249,256 | 18,788 |
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