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GCTCTCCAGTTTTCAGGTTGGAGAC[A/T]TTAGATGGAGGCCAAGAAGATGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606676 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRPV2 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
|
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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TRPV2 - transient receptor potential cation channel subfamily V member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016113.4 | 441 | Silent Mutation | ACA,ACT | T,T 14 | NP_057197.2 | |
XM_005256676.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_005256733.1 | |
XM_005256677.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_005256734.1 | |
XM_005256678.4 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_005256735.1 | |
XM_006721541.3 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_006721604.1 | |
XM_006721543.3 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_006721606.1 | |
XM_011523922.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_011522224.1 | |
XM_011523923.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_011522225.1 | |
XM_011523925.2 | 441 | Intron | XP_011522227.1 | |||
XM_017024730.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_016880219.1 | |
XM_017024731.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_016880220.1 | |
XM_017024732.1 | 441 | Silent Mutation | ACA,ACT | T,T 14 | XP_016880221.1 |