Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGATCTTCTTCCTTTATGTTCCC[A/C]AAAACGCAGTCATCTTTAGCTATCT
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SNX31 - sorting nexin 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152628.3 | 1527 | Missense Mutation | TTG,TTT | L,F 432 | NP_689841.3 | |
XM_005250815.3 | 1527 | Missense Mutation | TTG,TTT | L,F 333 | XP_005250872.1 | |
XM_011516899.1 | 1527 | Missense Mutation | TTG,TTT | L,F 366 | XP_011515201.1 | |
XM_017013153.1 | 1527 | Missense Mutation | TTG,TTT | L,F 431 | XP_016868642.1 | |
XM_017013154.1 | 1527 | Missense Mutation | TTG,TTT | L,F 431 | XP_016868643.1 | |
XM_017013155.1 | 1527 | Missense Mutation | TTG,TTT | L,F 430 | XP_016868644.1 | |
XM_017013156.1 | 1527 | Missense Mutation | TTG,TTT | L,F 413 | XP_016868645.1 | |
XM_017013157.1 | 1527 | Missense Mutation | TTG,TTT | L,F 394 | XP_016868646.1 | |
XM_017013158.1 | 1527 | Missense Mutation | TTG,TTT | L,F 393 | XP_016868647.1 | |
XM_017013159.1 | 1527 | Missense Mutation | TTG,TTT | L,F 375 | XP_016868648.1 | |
XM_017013160.1 | 1527 | Missense Mutation | TTG,TTT | L,F 364 | XP_016868649.1 | |
XM_017013161.1 | 1527 | Missense Mutation | TTG,TTT | L,F 349 | XP_016868650.1 | |
XM_017013162.1 | 1527 | Missense Mutation | TTG,TTT | L,F 326 | XP_016868651.1 | |
XM_017013163.1 | 1527 | Missense Mutation | TTG,TTT | L,F 227 | XP_016868652.1 | |
XM_017013164.1 | 1527 | Intron | XP_016868653.1 | |||
XM_017013165.1 | 1527 | Intron | XP_016868654.1 |