DMC1 DNA meiotic recombinase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 2 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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6 |
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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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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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 | DMC1H |
SYNONYM | LIM15 |
SYNONYM | dJ199H16.1 |
MIM | 602721 OMIM |
HGNC | HGNC:2927 HGNC |
Ensembl | ENSG00000100206 Ensembl |
AllianceGenome | HGNC:2927 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000216024.7 | hg38 | chr22 | 38,518,948 | 38,570,183 | 51,236 |
ENST00000428462.6 | hg38 | chr22 | 38,518,949 | 38,568,409 | 49,461 |
ENST00000216024.7 | hg19 | chr22 | 38,914,953 | 38,966,188 | 51,236 |
ENST00000428462.6 | hg19 | chr22 | 38,914,954 | 38,964,414 | 49,461 |
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