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TGTGGAAATAAGGTTTCTAAAAAGC[C/T]TTCCAAGAAGACATAAACCATTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606589 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX13 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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SNX13 - sorting nexin 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015132.4 | 2884 | Missense Mutation | AGC,GGC | S,G 914 | NP_055947.1 | |
XM_005249672.1 | 2884 | Missense Mutation | AGC,GGC | S,G 925 | XP_005249729.1 | |
XM_005249673.4 | 2884 | Intron | XP_005249730.1 | |||
XM_011515229.1 | 2884 | Missense Mutation | AGC,GGC | S,G 871 | XP_011513531.1 | |
XM_011515230.2 | 2884 | Missense Mutation | AGC,GGC | S,G 845 | XP_011513532.1 | |
XM_011515231.2 | 2884 | Missense Mutation | AGC,GGC | S,G 845 | XP_011513533.1 | |
XM_011515233.2 | 2884 | Missense Mutation | AGC,GGC | S,G 823 | XP_011513535.1 | |
XM_017011893.1 | 2884 | Missense Mutation | AGC,GGC | S,G 860 | XP_016867382.1 | |
XM_017011894.1 | 2884 | Missense Mutation | AGC,GGC | S,G 845 | XP_016867383.1 | |
XM_017011895.1 | 2884 | Missense Mutation | AGC,GGC | S,G 812 | XP_016867384.1 | |
XM_017011896.1 | 2884 | Missense Mutation | AGC,GGC | S,G 796 | XP_016867385.1 | |
XM_017011897.1 | 2884 | Missense Mutation | AGC,GGC | S,G 962 | XP_016867386.1 |