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TGCCTGGTTTGTTTTCTTCCAGGCA[C/T]GGATTAGAATAAACTTCAGACCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607925 | ||||||||||||||||||||
Literature Links: |
BTLA PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
BTLA - B and T lymphocyte associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085357.1 | 941 | Silent Mutation | CCA,CCG | P,P 198 | NP_001078826.1 | |
NM_181780.3 | 941 | Silent Mutation | CCA,CCG | P,P 246 | NP_861445.3 | |
XM_011512447.2 | 941 | Silent Mutation | CCA,CCG | P,P 252 | XP_011510749.1 | |
XM_017005748.1 | 941 | Silent Mutation | CCA,CCG | P,P 246 | XP_016861237.1 |