TAC1 tachykinin precursor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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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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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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 | Hs.2563 |
SYNONYM | NK2 |
SYNONYM | NKNA |
SYNONYM | NPK |
SYNONYM | TAC2 |
MIM | 162320 OMIM |
HGNC | HGNC:11517 HGNC |
Ensembl | ENSG00000006128 Ensembl |
AllianceGenome | HGNC:11517 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000346867.4 | hg38 | chr7 | 97,732,084 | 97,740,465 | 8,382 |
ENST00000350485.8 | hg38 | chr7 | 97,732,084 | 97,740,438 | 8,355 |
ENST00000319273.10 | hg38 | chr7 | 97,732,086 | 97,740,472 | 8,387 |
ENST00000350485.8 | hg19 | chr7 | 97,361,396 | 97,369,750 | 8,355 |
ENST00000346867.4 | hg19 | chr7 | 97,361,396 | 97,369,777 | 8,382 |
ENST00000319273.10 | hg19 | chr7 | 97,361,398 | 97,369,784 | 8,387 |
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