SLC6A4 solute carrier family 6 member 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 20 |
Likely benign | 0 | 46 |
Conflicting classifications of pathogenicity | 0 | 6 |
Uncertain significance | 0 | 198 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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8 |
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252 |
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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
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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 | 5-HTT |
SYNONYM | 5-HTTLPR |
SYNONYM | 5HTT |
SYNONYM | HTT |
SYNONYM | OCD1 |
SYNONYM | SERT |
SYNONYM | SERT1 |
SYNONYM | hSERT |
MIM | 182138 OMIM |
HGNC | HGNC:11050 HGNC |
Ensembl | ENSG00000108576 Ensembl |
AllianceGenome | HGNC:11050 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000650711.1 | hg38 | chr17 | 30,194,319 | 30,235,697 | 41,379 |
ENST00000401766.6 | hg38 | chr17 | 30,194,319 | 30,236,002 | 41,684 |
ENST00000261707.7 | hg38 | chr17 | 30,194,321 | 30,235,968 | 41,648 |
ENST00000650711.1 | hg19 | chr17 | 28,521,337 | 28,562,715 | 41,379 |
ENST00000401766.6 | hg19 | chr17 | 28,521,337 | 28,563,020 | 41,684 |
ENST00000261707.7 | hg19 | chr17 | 28,521,339 | 28,562,986 | 41,648 |
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