GH1 growth hormone 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 42 |
Likely pathogenic | 0 | 10 |
Benign | 12 | 26 |
Likely benign | 0 | 72 |
Conflicting classifications of pathogenicity | 0 | 26 |
Uncertain significance | 0 | 124 |
Ranking
ClinVar | |
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0 |
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0 |
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64 |
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164 |
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30 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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Variants
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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 | GH |
SYNONYM | GH-N |
SYNONYM | GHB5 |
SYNONYM | GHN |
SYNONYM | IGHD1A |
SYNONYM | IGHD1B |
SYNONYM | IGHD2 |
SYNONYM | hGH-N |
MIM | 139250 OMIM |
HGNC | HGNC:4261 HGNC |
Ensembl | ENSG00000259384 Ensembl |
AllianceGenome | HGNC:4261 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000458650.6 | hg38 | chr17 | 63,917,203 | 63,918,817 | 1,615 |
ENST00000323322.10 | hg38 | chr17 | 63,917,203 | 63,918,839 | 1,637 |
ENST00000351388.8 | hg38 | chr17 | 63,917,200 | 63,918,818 | 1,619 |
ENST00000342364.8 | hg38 | chr17 | 63,917,203 | 63,918,838 | 1,636 |
ENST00000617086.1 | hg38 | chr17 | 63,917,203 | 63,918,838 | 1,636 |
ENST00000351388.8 | hg19 | chr17 | 61,994,560 | 61,996,178 | 1,619 |
ENST00000458650.6 | hg19 | chr17 | 61,994,563 | 61,996,177 | 1,615 |
ENST00000342364.8 | hg19 | chr17 | 61,994,563 | 61,996,198 | 1,636 |
ENST00000617086.1 | hg19 | chr17 | 61,994,563 | 61,996,198 | 1,636 |
ENST00000323322.10 | hg19 | chr17 | 61,994,563 | 61,996,199 | 1,637 |
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