CCL4L2 C-C motif chemokine ligand 4 like 2
Clinical Significance
MGeND | ClinVar | |
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Likely benign | 0 | 1 |
Ranking
ClinVar | |
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0 |
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1 |
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0 |
Frequency
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 | |||||
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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 | AT744.2 |
SYNONYM | CCL4L |
SYNONYM | SCYA4L |
SYNONYM | SCYQ4L2 |
MIM | 610757 OMIM |
HGNC | HGNC:24066 HGNC |
Ensembl | ENSG00000276070 Ensembl |
AllianceGenome | HGNC:24066 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000617416.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000620576.5 | hg38 | chr17 | 36,211,063 | 36,212,873 | 1,811 |
ENST00000613173.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000615418.4 | hg38 | chr17 | 36,210,924 | 36,212,878 | 1,955 |
ENST00000620250.1 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000610565.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000620055.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000620098.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
ENST00000617405.5 | hg38 | chr17 | 36,211,063 | 36,212,873 | 1,811 |
ENST00000620732.4 | hg38 | chr17 | 36,211,063 | 36,212,878 | 1,816 |
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