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TGTGCTTTCATGTATAGACCAACAG[C/T]AAAGCCTTTACTGCCAAGACTTCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614906 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX11 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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SNX11 - sorting nexin 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013323.2 | 405 | Silent Mutation | AGC,AGT | S,S 46 | NP_037455.2 | |
NM_152244.1 | 405 | Silent Mutation | AGC,AGT | S,S 46 | NP_689450.1 | |
XM_005257260.3 | 405 | Missense Mutation | AGC,AGT | S,S 46 | XP_005257317.1 | |
XM_005257261.3 | 405 | Missense Mutation | AGC,AGT | S,S 38 | XP_005257318.1 | |
XM_005257262.3 | 405 | Missense Mutation | AGC,AGT | S,S 38 | XP_005257319.1 | |
XM_011524697.2 | 405 | Silent Mutation | AGC,AGT | S,S 46 | XP_011522999.1 |