ATP6V1F ATPase H+ transporting V1 subunit F
Information
- Symbol
- ATP6V1F
- Type
- protein-coding
- Description
- ATPase H+ transporting V1 subunit F
- Entrez Gene ID
- 9296
- Genome
- hg19
- Position
- chr7:128,502,958-128,505,898
- Genome
- hg38
- Position
- chr7:128,862,904-128,865,844
- MIM
- 607160 OMIM
- HGNC
- HGNC:16832 HGNC
- Ensembl
- ENSG00000128524 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | ATP6S14 |
| SYNONYM | VATF |
| SYNONYM | Vma7 |
| MIM | 607160 OMIM |
| HGNC | HGNC:16832 HGNC |
| Ensembl | ENSG00000128524 Ensembl |
| AllianceGenome | HGNC:16832 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000249289.5 | hg38 | chr7 | 128,862,856 | 128,865,847 | 2,992 |
| ENST00000492758.1 | hg38 | chr7 | 128,862,904 | 128,865,844 | 2,941 |
| ENST00000249289.5 | hg19 | chr7 | 128,502,910 | 128,505,901 | 2,992 |
| ENST00000492758.1 | hg19 | chr7 | 128,502,958 | 128,505,898 | 2,941 |
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