SAA2 serum amyloid A2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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2 |
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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
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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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| 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 | SAA |
| SYNONYM | SAA1 |
| MIM | 104751 OMIM |
| HGNC | HGNC:10514 HGNC |
| Ensembl | ENSG00000134339 Ensembl |
| AllianceGenome | HGNC:10514 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000530400.5 | hg38 | chr11 | 18,240,203 | 18,248,019 | 7,817 |
| ENST00000528349.5 | hg38 | chr11 | 18,242,139 | 18,248,635 | 6,497 |
| ENST00000529528.5 | hg38 | chr11 | 18,245,238 | 18,248,639 | 3,402 |
| ENST00000526900.1 | hg38 | chr11 | 18,245,243 | 18,248,635 | 3,393 |
| ENST00000256733.9 | hg38 | chr11 | 18,245,240 | 18,248,668 | 3,429 |
| ENST00000414546.6 | hg38 | chr11 | 18,239,223 | 18,248,643 | 9,421 |
| ENST00000414546.6 | hg19 | chr11 | 18,260,770 | 18,270,190 | 9,421 |
| ENST00000530400.5 | hg19 | chr11 | 18,261,750 | 18,269,566 | 7,817 |
| ENST00000528349.5 | hg19 | chr11 | 18,263,686 | 18,270,182 | 6,497 |
| ENST00000529528.5 | hg19 | chr11 | 18,266,785 | 18,270,186 | 3,402 |
| ENST00000256733.9 | hg19 | chr11 | 18,266,787 | 18,270,215 | 3,429 |
| ENST00000526900.1 | hg19 | chr11 | 18,266,790 | 18,270,182 | 3,393 |
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