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TAATTACTATACATTGTGACCTCAA[C/T]GGACTGCTAATCTATATGAAATTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616105 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SNX14 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SNX14 - sorting nexin 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297614.2 | Intron | NP_001284543.1 | ||||
NM_001304479.1 | Intron | NP_001291408.1 | ||||
NM_020468.5 | Intron | NP_065201.1 | ||||
NM_153816.5 | Intron | NP_722523.1 | ||||
XM_005248738.3 | Intron | XP_005248795.1 | ||||
XM_005248740.3 | Intron | XP_005248797.1 | ||||
XM_011535977.2 | Intron | XP_011534279.1 | ||||
XM_011535979.1 | Intron | XP_011534281.1 | ||||
XM_017011090.1 | Intron | XP_016866579.1 | ||||
XM_017011091.1 | Intron | XP_016866580.1 | ||||
XM_017011092.1 | Intron | XP_016866581.1 | ||||
XM_017011093.1 | Intron | XP_016866582.1 | ||||
XM_017011094.1 | Intron | XP_016866583.1 | ||||
XM_017011095.1 | Intron | XP_016866584.1 | ||||
XM_017011096.1 | Intron | XP_016866585.1 | ||||
XM_017011097.1 | Intron | XP_016866586.1 | ||||
XM_017011098.1 | Intron | XP_016866587.1 | ||||
XM_017011099.1 | Intron | XP_016866588.1 | ||||
XM_017011100.1 | Intron | XP_016866589.1 | ||||
XM_017011101.1 | Intron | XP_016866590.1 |
Set Membership: |
HapMap |