STARD3NL STARD3 N-terminal like
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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
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 |
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 | MENTHO |
MIM | 611759 OMIM |
HGNC | HGNC:19169 HGNC |
Ensembl | ENSG00000010270 Ensembl |
AllianceGenome | HGNC:19169 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000009041.12 | hg38 | chr7 | 38,178,245 | 38,230,669 | 52,425 |
ENST00000434197.5 | hg38 | chr7 | 38,178,263 | 38,230,379 | 52,117 |
ENST00000396013.5 | hg38 | chr7 | 38,178,351 | 38,230,381 | 52,031 |
ENST00000009041.12 | hg19 | chr7 | 38,217,847 | 38,270,270 | 52,424 |
ENST00000434197.5 | hg19 | chr7 | 38,217,865 | 38,269,980 | 52,116 |
ENST00000396013.5 | hg19 | chr7 | 38,217,953 | 38,269,982 | 52,030 |
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