IGLV6-57 immunoglobulin lambda variable 6-57
Information
- Symbol
- IGLV6-57
- Type
- other
- Description
- immunoglobulin lambda variable 6-57
- Entrez Gene ID
- 28778
- Genome
- hg19
- Position
- chr22:22,550,199-22,550,676
- Genome
- hg38
- Position
- chr22:22,195,799-22,196,276
- HGNC
- HGNC:5927 HGNC
- Ensembl
- ENSG00000211640 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Ranking
ClinVar | |
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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
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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Category | : |
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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 | IGLV657 |
SYNONYM | V1-22 |
HGNC | HGNC:5927 HGNC |
Ensembl | ENSG00000211640 Ensembl |
IMGT/GENE-DB | IGLV6-57 |
AllianceGenome | HGNC:5927 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000390285.4 | hg38 | chr22 | 22,195,799 | 22,196,276 | 478 |
ENST00000390285.4 | hg19 | chr22 | 22,550,199 | 22,550,676 | 478 |
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