Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SNX31 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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SNX31 - sorting nexin 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152628.3 | 1514 | Missense Mutation | GAT,GGT | D,G 428 | NP_689841.3 | |
XM_005250815.3 | 1514 | Missense Mutation | GAT,GGT | D,G 329 | XP_005250872.1 | |
XM_011516899.1 | 1514 | Missense Mutation | GAT,GGT | D,G 362 | XP_011515201.1 | |
XM_017013153.1 | 1514 | Missense Mutation | GAT,GGT | D,G 427 | XP_016868642.1 | |
XM_017013154.1 | 1514 | Missense Mutation | GAT,GGT | D,G 427 | XP_016868643.1 | |
XM_017013155.1 | 1514 | Missense Mutation | GAT,GGT | D,G 426 | XP_016868644.1 | |
XM_017013156.1 | 1514 | Missense Mutation | GAT,GGT | D,G 409 | XP_016868645.1 | |
XM_017013157.1 | 1514 | Missense Mutation | GAT,GGT | D,G 390 | XP_016868646.1 | |
XM_017013158.1 | 1514 | Missense Mutation | GAT,GGT | D,G 389 | XP_016868647.1 | |
XM_017013159.1 | 1514 | Missense Mutation | GAT,GGT | D,G 371 | XP_016868648.1 | |
XM_017013160.1 | 1514 | Missense Mutation | GAT,GGT | D,G 360 | XP_016868649.1 | |
XM_017013161.1 | 1514 | Missense Mutation | GAT,GGT | D,G 345 | XP_016868650.1 | |
XM_017013162.1 | 1514 | Missense Mutation | GAT,GGT | D,G 322 | XP_016868651.1 | |
XM_017013163.1 | 1514 | Missense Mutation | GAT,GGT | D,G 223 | XP_016868652.1 | |
XM_017013164.1 | 1514 | Intron | XP_016868653.1 | |||
XM_017013165.1 | 1514 | Intron | XP_016868654.1 |
Set Membership: |
HapMap Validated |