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Search Thermo Fisher Scientific
ATAGACCAACAGCAAAGCCTTTACT[A/G]CCAAGACTTCCTGTGTGCGGCGCCG
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 |
---|---|---|
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 |
SNX11 - sorting nexin 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013323.2 | 418 | Missense Mutation | ACC,GCC | T,A 51 | NP_037455.2 | |
NM_152244.1 | 418 | Missense Mutation | ACC,GCC | T,A 51 | NP_689450.1 | |
XM_005257260.3 | 418 | Missense Mutation | ACC,GCC | T,A 51 | XP_005257317.1 | |
XM_005257261.3 | 418 | Missense Mutation | ACC,GCC | T,A 43 | XP_005257318.1 | |
XM_005257262.3 | 418 | Missense Mutation | ACC,GCC | T,A 43 | XP_005257319.1 | |
XM_011524697.2 | 418 | Missense Mutation | ACC,GCC | T,A 51 | XP_011522999.1 |