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AGGCAAGAGATCCGTGAAAGCCGCC[A/G]CTGCCGTCCCAATGTGACCACTTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
8 submissions
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Phenotype: |
MIM: 608255 | ||||||||||||||||||||
Literature Links: |
TRAF3IP3 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 |
TRAF3IP3 - TRAF3 interacting protein 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287754.1 | 538 | Intron | NP_001274683.1 | |||
NM_001320143.1 | 538 | Missense Mutation | CAC,CGC | H,R 34 | NP_001307072.1 | |
NM_001320144.1 | 538 | Missense Mutation | CAC,CGC | H,R 34 | NP_001307073.1 | |
NM_025228.3 | 538 | Missense Mutation | CAC,CGC | H,R 34 | NP_079504.2 | |
XM_005273279.4 | 538 | Intron | XP_005273336.1 | |||
XM_005273280.2 | 538 | Intron | XP_005273337.1 | |||
XM_011510018.2 | 538 | Missense Mutation | CAC,CGC | H,R 34 | XP_011508320.1 | |
XM_011510019.1 | 538 | Missense Mutation | CAC,CGC | H,R 34 | XP_011508321.1 | |
XM_017002399.1 | 538 | Missense Mutation | CAC,CGC | H,R 34 | XP_016857888.1 | |
XM_017002400.1 | 538 | Missense Mutation | CAC,CGC | H,R 34 | XP_016857889.1 |