IGHV1-69 immunoglobulin heavy variable 1-69
Information
- Symbol
- IGHV1-69
- Type
- other
- Description
- immunoglobulin heavy variable 1-69
- Entrez Gene ID
- 28461
- Genome
- hg19
- Position
- chr14:107,169,931-107,170,428
- Genome
- hg38
- Position
- chr14:106,714,684-106,715,181
- HGNC
- HGNC:5558 HGNC
- Ensembl
- ENSG00000211973 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | IGHV1-E |
| SYNONYM | IGHV169 |
| SYNONYM | IGHV1E |
| HGNC | HGNC:5558 HGNC |
| Ensembl | ENSG00000211973 Ensembl |
| IMGT/GENE-DB | IGHV1-69 |
| AllianceGenome | HGNC:5558 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000390633.2 | hg38 | chr14 | 106,714,684 | 106,715,181 | 498 |
| ENST00000390633.2 | hg19 | chr14 | 107,169,931 | 107,170,428 | 498 |
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