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Search Thermo Fisher Scientific
AAGCTAACTATTGGAAAGATCTGGC[A/G]ATGACCTACAAACAGAGGTCAGTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609449 | ||||||||||||||||||||
Literature Links: |
NDE1 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 |
NDE1 - nudE neurodevelopment protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143979.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | NP_001137451.1 | |
NM_017668.2 | 178 | Silent Mutation | GCA,GCG | A,A 22 | NP_060138.1 | |
XM_005255396.4 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_005255453.1 | |
XM_006720897.3 | 178 | Silent Mutation | GCA,GCG | A,A 54 | XP_006720960.1 | |
XM_006720900.3 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_006720963.1 | |
XM_011522553.2 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_011520855.1 | |
XM_017023349.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878838.1 | |
XM_017023350.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878839.1 | |
XM_017023351.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878840.1 | |
XM_017023352.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878841.1 | |
XM_017023353.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878842.1 | |
XM_017023354.1 | 178 | Intron | XP_016878843.1 | |||
XM_017023355.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878844.1 | |
XM_017023356.1 | 178 | Silent Mutation | GCA,GCG | A,A 22 | XP_016878845.1 | |
XM_017023357.1 | 178 | Intron | XP_016878846.1 |