TDRD6 tudor domain containing 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 44 |
Uncertain significance | 0 | 274 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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318 |
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2 |
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
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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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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 | CT41.2 |
SYNONYM | NY-CO-45 |
SYNONYM | SPATA36 |
SYNONYM | TDR2 |
SYNONYM | bA446F17.4 |
MIM | 611200 OMIM |
HGNC | HGNC:21339 HGNC |
Ensembl | ENSG00000180113 Ensembl |
AllianceGenome | HGNC:21339 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000316081.11 | hg38 | chr6 | 46,687,885 | 46,704,319 | 16,435 |
ENST00000544460.5 | hg38 | chr6 | 46,687,875 | 46,704,319 | 16,445 |
ENST00000544460.5 | hg19 | chr6 | 46,655,612 | 46,672,056 | 16,445 |
ENST00000316081.11 | hg19 | chr6 | 46,655,622 | 46,672,056 | 16,435 |
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