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AATAGAAGGTCTCAGAATTGTCACT[G/T]TCCTTTCCCTTTGGAAGTTAATTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 611541 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX27 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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SNX27 - sorting nexin family member 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030918.5 | Intron | NP_112180.4 | ||||
XM_005245509.2 | Intron | XP_005245566.1 | ||||
XM_005245510.3 | Intron | XP_005245567.1 | ||||
XM_005245511.4 | Intron | XP_005245568.1 | ||||
XM_011510024.2 | Intron | XP_011508326.1 | ||||
XM_011510025.2 | Intron | XP_011508327.1 | ||||
XM_011510026.2 | Intron | XP_011508328.1 | ||||
XM_017002417.1 | Intron | XP_016857906.1 |