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GTGTTTGTTGTTACTGGGAAAGTAG[A/C]ACTCGTAGAGCCAGAAAGTCATTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SNX29 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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SNX29 - sorting nexin 29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032167.4 | Intron | NP_115543.3 | ||||
XM_005255682.3 | Intron | XP_005255739.1 | ||||
XM_005255683.3 | Intron | XP_005255740.1 | ||||
XM_011522738.2 | Intron | XP_011521040.1 | ||||
XM_011522741.2 | Intron | XP_011521043.1 | ||||
XM_011522743.2 | Intron | XP_011521045.1 | ||||
XM_011522744.2 | Intron | XP_011521046.1 | ||||
XM_017023871.1 | Intron | XP_016879360.1 | ||||
XM_017023872.1 | Intron | XP_016879361.1 | ||||
XM_017023873.1 | Intron | XP_016879362.1 | ||||
XM_017023874.1 | Intron | XP_016879363.1 | ||||
XM_017023875.1 | Intron | XP_016879364.1 | ||||
XM_017023876.1 | Intron | XP_016879365.1 | ||||
XM_017023877.1 | Intron | XP_016879366.1 | ||||
XM_017023878.1 | Intron | XP_016879367.1 |