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CACAATTACTTATGAAGCAAACTGT[C/T]CTTCCCTTTTAGTAATTTGAGATTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
20 submissions
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Phenotype: |
MIM: 614904 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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SNX7 - sorting nexin 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015976.4 | Intron | NP_057060.2 | ||||
NM_152238.3 | Intron | NP_689424.2 | ||||
XM_006710677.2 | Intron | XP_006710740.1 | ||||
XM_006710678.2 | Intron | XP_006710741.1 | ||||
XM_011541564.2 | Intron | XP_011539866.1 | ||||
XM_017001425.1 | Intron | XP_016856914.1 | ||||
XM_017001426.1 | Intron | XP_016856915.1 | ||||
XM_017001427.1 | Intron | XP_016856916.1 | ||||
XM_017001428.1 | Intron | XP_016856917.1 |