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GGTCACCCGCCATGTCGACCTTGCT[A/G]GACATTAAGAGCAGCGTGCTCAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604009 | ||||||||||||||||||||
Literature Links: |
BAIAP3 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 |
BAIAP3 - BAI1 associated protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199096.1 | 773 | Silent Mutation | CTA,CTG | L,L 5 | NP_001186025.1 | |
NM_001199097.1 | 773 | Silent Mutation | CTA,CTG | L,L 5 | NP_001186026.1 | |
NM_001199098.1 | 773 | Silent Mutation | CTA,CTG | L,L 5 | NP_001186027.1 | |
NM_001199099.1 | 773 | Silent Mutation | CTA,CTG | L,L 5 | NP_001186028.1 | |
NM_001286464.1 | 773 | Silent Mutation | CTA,CTG | L,L 5 | NP_001273393.1 | |
NM_003933.4 | 773 | Silent Mutation | CTA,CTG | L,L 40 | NP_003924.2 | |
XM_011522728.1 | 773 | Silent Mutation | CTA,CTG | L,L 40 | XP_011521030.1 | |
XM_011522729.1 | 773 | Silent Mutation | CTA,CTG | L,L 40 | XP_011521031.1 | |
XM_011522730.2 | 773 | Silent Mutation | CTA,CTG | L,L 40 | XP_011521032.1 |