CXCL14 C-X-C motif chemokine ligand 14
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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 | |||||
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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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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 | BMAC |
SYNONYM | BRAK |
SYNONYM | KEC |
SYNONYM | KS1 |
SYNONYM | MIP-2g |
SYNONYM | MIP2G |
SYNONYM | NJAC |
SYNONYM | SCYB14 |
MIM | 604186 OMIM |
HGNC | HGNC:10640 HGNC |
Ensembl | ENSG00000145824 Ensembl |
AllianceGenome | HGNC:10640 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000337225.5 | hg38 | chr5 | 135,570,683 | 135,579,279 | 8,597 |
ENST00000512158.6 | hg38 | chr5 | 135,570,679 | 135,578,991 | 8,313 |
ENST00000512158.6 | hg19 | chr5 | 134,906,369 | 134,914,681 | 8,313 |
ENST00000337225.5 | hg19 | chr5 | 134,906,373 | 134,914,969 | 8,597 |
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