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TTCTTTTCCCTTTACCTCTCCCAAA[C/T]TGTAGAGTGATGCTCTTCAGTTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607296 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP6V1G1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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ATP6V1G1 - ATPase H+ transporting V1 subunit G1 | ||||||
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There are no transcripts associated with this gene. |
TMEM268 - transmembrane protein 268 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153045.3 | Intron | NP_694590.2 | ||||
XM_006716997.1 | Intron | XP_006717060.1 | ||||
XM_011518350.1 | Intron | XP_011516652.1 | ||||
XM_011518351.2 | Intron | XP_011516653.1 | ||||
XM_011518352.1 | Intron | XP_011516654.1 | ||||
XM_011518353.1 | Intron | XP_011516655.1 | ||||
XM_011518354.1 | Intron | XP_011516656.1 | ||||
XM_011518355.1 | Intron | XP_011516657.1 | ||||
XM_017014429.1 | Intron | XP_016869918.1 | ||||
XM_017014430.1 | Intron | XP_016869919.1 |