AFP alpha fetoprotein
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Likely pathogenic | 0 | 2 |
| Benign | 14 | 10 |
| Likely benign | 0 | 14 |
| Uncertain significance | 0 | 52 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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78 |
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2 |
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
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | AFPD |
| SYNONYM | FETA |
| SYNONYM | HPAFP |
| MIM | 104150 OMIM |
| HGNC | HGNC:317 HGNC |
| Ensembl | ENSG00000081051 Ensembl |
| AllianceGenome | HGNC:317 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000226359.2 | hg38 | chr4 | 73,436,247 | 73,455,743 | 19,497 |
| ENST00000395792.7 | hg38 | chr4 | 73,436,221 | 73,456,174 | 19,954 |
| ENST00000395792.7 | hg19 | chr4 | 74,301,938 | 74,321,891 | 19,954 |
| ENST00000226359.2 | hg19 | chr4 | 74,301,964 | 74,321,460 | 19,497 |
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