ANKRD24 ankyrin repeat domain 24
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 18 |
Uncertain significance | 0 | 156 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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172 |
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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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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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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 | 620234 OMIM |
HGNC | HGNC:29424 HGNC |
Ensembl | ENSG00000089847 Ensembl |
AllianceGenome | HGNC:29424 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000318934.9 | hg38 | chr19 | 4,182,689 | 4,224,814 | 42,126 |
ENST00000600132.5 | hg38 | chr19 | 4,183,354 | 4,224,814 | 41,461 |
ENST00000262970.9 | hg38 | chr19 | 4,198,140 | 4,224,505 | 26,366 |
ENST00000318934.9 | hg19 | chr19 | 4,182,686 | 4,224,811 | 42,126 |
ENST00000600132.5 | hg19 | chr19 | 4,183,351 | 4,224,811 | 41,461 |
ENST00000262970.9 | hg19 | chr19 | 4,198,137 | 4,224,502 | 26,366 |
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