OR8H2 olfactory receptor family 8 subfamily H member 2
Information
- Symbol
- OR8H2
- Type
- protein-coding
- Description
- olfactory receptor family 8 subfamily H member 2
- Entrez Gene ID
- 390151
- Genome
- hg19
- Position
- chr11:55,871,163-55,875,134
- Genome
- hg38
- Position
- chr11:56,103,687-56,107,658
- HGNC
- HGNC:15308 HGNC
- Ensembl
- ENSG00000181767 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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
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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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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 | OR11-171 |
HGNC | HGNC:15308 HGNC |
Ensembl | ENSG00000181767 Ensembl |
AllianceGenome | HGNC:15308 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000313503.2 | hg38 | chr11 | 56,103,687 | 56,107,658 | 3,972 |
ENST00000618136.1 | hg38 | chr11 | 56,105,018 | 56,106,055 | 1,038 |
ENST00000641311.1 | hg38 | chr11 | 56,103,687 | 56,107,658 | 3,972 |
ENST00000313503.2 | hg19 | chr11 | 55,871,163 | 55,875,134 | 3,972 |
ENST00000641311.1 | hg19 | chr11 | 55,871,163 | 55,875,134 | 3,972 |
ENST00000618136.1 | hg19 | chr11 | 55,872,494 | 55,873,531 | 1,038 |
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