TMEM258 transmembrane protein 258
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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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 | C11orf10 |
SYNONYM | Kud |
SYNONYM | Kuduk |
MIM | 617615 OMIM |
HGNC | HGNC:1164 HGNC |
Ensembl | ENSG00000134825 Ensembl |
AllianceGenome | HGNC:1164 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000543510.1 | hg38 | chr11 | 61,789,131 | 61,792,802 | 3,672 |
ENST00000537328.6 | hg38 | chr11 | 61,788,949 | 61,792,599 | 3,651 |
ENST00000537328.6 | hg19 | chr11 | 61,556,421 | 61,560,071 | 3,651 |
ENST00000543510.1 | hg19 | chr11 | 61,556,603 | 61,560,274 | 3,672 |
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