DMRTC1 DMRT like family C1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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 |
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 | : | |
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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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MIM | 300878 OMIM |
HGNC | HGNC:13910 HGNC |
Ensembl | ENSG00000269502 Ensembl |
AllianceGenome | HGNC:13910 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000615063.2 | hg38 | chrX | 72,872,025 | 72,943,837 | 71,813 |
ENST00000596389.5 | hg38 | chrX | 72,872,029 | 72,877,864 | 5,836 |
ENST00000595412.5 | hg38 | chrX | 72,872,121 | 72,875,974 | 3,854 |
ENST00000615063.2 | hg19 | chrX | 72,091,859 | 72,163,679 | 71,821 |
ENST00000596389.5 | hg19 | chrX | 72,091,863 | 72,097,698 | 5,836 |
ENST00000595412.5 | hg19 | chrX | 72,091,955 | 72,095,808 | 3,854 |
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