RTL8C retrotransposon Gag like 8C
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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
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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Category | : |
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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 | CXX1 |
SYNONYM | FAM127A |
SYNONYM | MAR8C |
SYNONYM | MART8C |
SYNONYM | Mar8 |
SYNONYM | Mart8 |
SYNONYM | SIRH5 |
MIM | 300213 OMIM |
HGNC | HGNC:2569 HGNC |
Ensembl | ENSG00000134590 Ensembl |
AllianceGenome | HGNC:2569 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000257013.9 | hg38 | chrX | 135,032,355 | 135,033,546 | 1,192 |
ENST00000257013.9 | hg19 | chrX | 134,166,385 | 134,167,576 | 1,192 |
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