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CCGGCAACAGGAAGCGCCCGTCCAG[C/T]GTGAAGGCCATGATGTAGGAGGCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613165 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CANT1 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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CANT1 - calcium activated nucleotidase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159772.1 | 1552 | Silent Mutation | NP_001153244.1 | |||
NM_001159773.1 | 1552 | Silent Mutation | NP_001153245.1 | |||
NM_138793.3 | 1552 | Silent Mutation | NP_620148.1 | |||
XM_005257021.1 | 1552 | Silent Mutation | XP_005257078.1 | |||
XM_005257022.1 | 1552 | Silent Mutation | XP_005257079.1 | |||
XM_006721683.1 | 1552 | Silent Mutation | XP_006721746.1 | |||
XM_011524291.1 | 1552 | Silent Mutation | XP_011522593.1 | |||
XM_011524293.1 | 1552 | Silent Mutation | XP_011522595.1 | |||
XM_011524294.1 | 1552 | Silent Mutation | XP_011522596.1 | |||
XM_011524295.2 | 1552 | Silent Mutation | XP_011522597.1 |