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ATCACAACACACCTGATTCTGTTCT[C/G]TAAAGTGTCTATATGAAGTTGCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614903 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX16 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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SNX16 - sorting nexin 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022133.3 | 1066 | Missense Mutation | CAG,GAG | Q,E 269 | NP_071416.2 | |
NM_152836.2 | 1066 | Missense Mutation | CAG,GAG | Q,E 269 | NP_690049.1 | |
NM_152837.2 | 1066 | Missense Mutation | CAG,GAG | Q,E 240 | NP_690050.1 | |
XM_005251282.4 | 1066 | Missense Mutation | CAG,GAG | Q,E 240 | XP_005251339.1 | |
XM_005251283.2 | 1066 | Missense Mutation | CAG,GAG | Q,E 240 | XP_005251340.1 | |
XM_011517574.2 | 1066 | Missense Mutation | CAG,GAG | Q,E 112 | XP_011515876.1 |