LHFPL7 LHFPL tetraspan subfamily member 7
Information
- Symbol
- LHFPL7
- Type
- protein-coding
- Description
- LHFPL tetraspan subfamily member 7
- Entrez Gene ID
- 255349
- Genome
- hg19
- Position
- chr22:25,331,065-25,342,661
- Genome
- hg38
- Position
- chr22:24,935,098-24,946,694
- HGNC
- HGNC:33725 HGNC
- Ensembl
- ENSG00000206069 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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 | : |
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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 |
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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SYNONYM | TMEM211 |
SYNONYM | bA9F11.1 |
HGNC | HGNC:33725 HGNC |
Ensembl | ENSG00000206069 Ensembl |
AllianceGenome | HGNC:33725 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000640159.2 | hg38 | chr22 | 24,935,098 | 24,946,694 | 11,597 |
ENST00000407886.1 | hg38 | chr22 | 24,935,110 | 24,946,695 | 11,586 |
ENST00000640159.2 | hg19 | chr22 | 25,331,065 | 25,342,661 | 11,597 |
ENST00000407886.1 | hg19 | chr22 | 25,331,077 | 25,342,662 | 11,586 |
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