HAR1B highly accelerated region 1B
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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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 | HAR1R |
SYNONYM | LINC00065 |
SYNONYM | NCRNA00065 |
MIM | 610557 OMIM |
HGNC | HGNC:33118 HGNC |
Ensembl | ENSG00000231133 Ensembl |
AllianceGenome | HGNC:33118 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000651861.1 | hg38 | chr20 | 63,092,256 | 63,102,371 | 10,116 |
ENST00000657642.1 | hg38 | chr20 | 63,093,378 | 63,102,631 | 9,254 |
ENST00000608031.5 | hg38 | chr20 | 63,095,493 | 63,102,319 | 6,827 |
ENST00000651861.1 | hg19 | chr20 | 61,723,608 | 61,733,723 | 10,116 |
ENST00000657642.1 | hg19 | chr20 | 61,724,730 | 61,733,983 | 9,254 |
ENST00000608031.5 | hg19 | chr20 | 61,726,845 | 61,733,671 | 6,827 |
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