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Search Thermo Fisher Scientific
GGGGAGTTCAGAGCCAGGGAGTGAC[A/G]CTGCAGAGCTTAAAACCTGCCGAGG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 7118 | Intron | NP_001263347.1 | |||
NM_014866.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2270 | NP_055681.1 | |
XM_005266134.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_005266191.1 | |
XM_011519246.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517548.1 | |
XM_011519247.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517549.1 | |
XM_011519248.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517550.1 | |
XM_011519249.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2289 | XP_011517551.1 | |
XM_011519250.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517552.1 | |
XM_011519251.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517553.1 | |
XM_011519252.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2270 | XP_011517554.1 | |
XM_011519253.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2289 | XP_011517555.1 | |
XM_011519254.1 | 7118 | Intron | XP_011517556.1 | |||
XM_011519255.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2270 | XP_011517557.1 | |
XM_011519256.1 | 7118 | Intron | XP_011517558.1 | |||
XM_011519257.1 | 7118 | Intron | XP_011517559.1 | |||
XM_011519258.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2245 | XP_011517560.1 | |
XM_011519259.1 | 7118 | Intron | XP_011517561.1 | |||
XM_011519260.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2292 | XP_011517562.1 | |
XM_011519261.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2143 | XP_011517563.1 | |
XM_011519262.1 | 7118 | Missense Mutation | GCG,GTG | A,V 2055 | XP_011517564.1 | |
XM_011519263.2 | 7118 | Missense Mutation | GCG,GTG | A,V 2033 | XP_011517565.1 | |
XM_011519264.2 | 7118 | Intron | XP_011517566.1 | |||
XM_017015363.1 | 7118 | Intron | XP_016870852.1 | |||
XM_017015364.1 | 7118 | Intron | XP_016870853.1 |