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AGGTCTCTGAGCTGGCATTATAGTC[C/T]ACATTCACTTCCGGCATGCTGAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 608162 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VTCN1 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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VTCN1 - V-set domain containing T cell activation inhibitor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001253849.1 | 886 | Intron | NP_001240778.1 | |||
NM_001253850.1 | 886 | Intron | NP_001240779.1 | |||
NM_024626.3 | 886 | Intron | NP_078902.2 | |||
XM_011542143.2 | 886 | Silent Mutation | GTA,GTG | V,V 207 | XP_011540445.2 | |
XM_017002335.1 | 886 | Silent Mutation | GTA,GTG | V,V 162 | XP_016857824.1 |