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TTTACCTGCTTGTTGAGTACTGGTT[C/G]CTGTAAGCCATCAAACAGAAGTCTG
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 | 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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SNX14 - sorting nexin 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297614.2 | 2874 | Missense Mutation | CAA,GAA | Q,E 900 | NP_001284543.1 | |
NM_001304479.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 857 | NP_001291408.1 | |
NM_020468.5 | 2874 | Missense Mutation | CAA,GAA | Q,E 856 | NP_065201.1 | |
NM_153816.5 | 2874 | Missense Mutation | CAA,GAA | Q,E 909 | NP_722523.1 | |
XM_005248738.3 | 2874 | Missense Mutation | CAA,GAA | Q,E 908 | XP_005248795.1 | |
XM_005248740.3 | 2874 | Missense Mutation | CAA,GAA | Q,E 865 | XP_005248797.1 | |
XM_011535977.2 | 2874 | Intron | XP_011534279.1 | |||
XM_011535979.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 813 | XP_011534281.1 | |
XM_017011090.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 856 | XP_016866579.1 | |
XM_017011091.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 899 | XP_016866580.1 | |
XM_017011092.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 864 | XP_016866581.1 | |
XM_017011093.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 856 | XP_016866582.1 | |
XM_017011094.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 812 | XP_016866583.1 | |
XM_017011095.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 559 | XP_016866584.1 | |
XM_017011096.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 524 | XP_016866585.1 | |
XM_017011097.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 524 | XP_016866586.1 | |
XM_017011098.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 524 | XP_016866587.1 | |
XM_017011099.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 524 | XP_016866588.1 | |
XM_017011100.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 524 | XP_016866589.1 | |
XM_017011101.1 | 2874 | Missense Mutation | CAA,GAA | Q,E 515 | XP_016866590.1 |