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CAATCCTCCCTAGCCTTGAGCTCCC[A/G]GAGGTGGCGCAGGCCTGGAATGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613037 MIM: 612854 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INPP5E 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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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INPP5E - inositol polyphosphate-5-phosphatase E | ||||||
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There are no transcripts associated with this gene. |
SEC16A - SEC16 homolog A, endoplasmic reticulum export factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276418.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2317 | NP_001263347.1 | |
NM_014866.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2340 | NP_055681.1 | |
XM_005266134.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2362 | XP_005266191.1 | |
XM_011519246.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2362 | XP_011517548.1 | |
XM_011519247.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2362 | XP_011517549.1 | |
XM_011519248.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2362 | XP_011517550.1 | |
XM_011519249.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2359 | XP_011517551.1 | |
XM_011519250.2 | 7174 | Intron | XP_011517552.1 | |||
XM_011519251.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2342 | XP_011517553.1 | |
XM_011519252.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2340 | XP_011517554.1 | |
XM_011519253.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2339 | XP_011517555.1 | |
XM_011519254.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2337 | XP_011517556.1 | |
XM_011519255.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2320 | XP_011517557.1 | |
XM_011519256.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2317 | XP_011517558.1 | |
XM_011519257.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2315 | XP_011517559.1 | |
XM_011519258.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2315 | XP_011517560.1 | |
XM_011519259.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2295 | XP_011517561.1 | |
XM_011519260.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2362 | XP_011517562.1 | |
XM_011519261.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2213 | XP_011517563.1 | |
XM_011519262.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2125 | XP_011517564.1 | |
XM_011519263.2 | 7174 | Silent Mutation | TCC,TCT | S,S 2083 | XP_011517565.1 | |
XM_011519264.2 | 7174 | Intron | XP_011517566.1 | |||
XM_017015363.1 | 7174 | Silent Mutation | TCC,TCT | S,S 2334 | XP_016870852.1 | |
XM_017015364.1 | 7174 | Intron | XP_016870853.1 |