GALP galanin like peptide
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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 | GAL |
MIM | 611178 OMIM |
HGNC | HGNC:24840 HGNC |
Ensembl | ENSG00000197487 Ensembl |
AllianceGenome | HGNC:24840 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000357330.7 | hg38 | chr19 | 56,176,008 | 56,185,775 | 9,768 |
ENST00000590002.1 | hg38 | chr19 | 56,177,109 | 56,182,234 | 5,126 |
ENST00000440823.1 | hg38 | chr19 | 56,176,020 | 56,185,775 | 9,756 |
ENST00000357330.7 | hg19 | chr19 | 56,687,377 | 56,697,144 | 9,768 |
ENST00000440823.1 | hg19 | chr19 | 56,687,389 | 56,697,144 | 9,756 |
ENST00000590002.1 | hg19 | chr19 | 56,688,478 | 56,693,603 | 5,126 |
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