SCARF1 scavenger receptor class F member 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 108 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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122 |
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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 | SREC |
SYNONYM | SREC-I |
SYNONYM | SREC1 |
MIM | 607873 OMIM |
HGNC | HGNC:16820 HGNC |
Ensembl | ENSG00000074660 Ensembl |
AllianceGenome | HGNC:16820 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000263071.9 | hg38 | chr17 | 1,633,858 | 1,645,732 | 11,875 |
ENST00000571272.5 | hg38 | chr17 | 1,634,390 | 1,645,744 | 11,355 |
ENST00000263071.9 | hg19 | chr17 | 1,537,152 | 1,549,026 | 11,875 |
ENST00000571272.5 | hg19 | chr17 | 1,537,684 | 1,549,038 | 11,355 |
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