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CCTGAGACCTCTTGCTCCCAGATCC[C/T]CTGAGGAGGAGACAGGTTGGCAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605857 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP6V1E2 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ATP6V1E2 - ATPase H+ transporting V1 subunit E2 | ||||||
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There are no transcripts associated with this gene. |
RHOQ - ras homolog family member Q | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012249.3 | Intron | NP_036381.2 | ||||
XM_005264229.2 | Intron | XP_005264286.1 | ||||
XM_011532726.2 | Intron | XP_011531028.1 | ||||
XM_011532728.2 | Intron | XP_011531030.1 | ||||
XM_017003716.1 | Intron | XP_016859205.1 |