Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGAACAAATTTCAATATTTTCAT[C/T]TTCATCTTCATGAATAGCCTATACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604588 | ||||||||||||||||||||
Literature Links: |
NEK1 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 |
NEK1 - NIMA related kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199397.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1245 | NP_001186326.1 | |
NM_001199398.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1201 | NP_001186327.1 | |
NM_001199399.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1148 | NP_001186328.1 | |
NM_001199400.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1173 | NP_001186329.1 | |
NM_012224.2 | 4229 | Missense Mutation | AAT,GAT | N,D 1217 | NP_036356.1 | |
XM_006714228.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1186 | XP_006714291.1 | |
XM_011532003.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1217 | XP_011530305.1 | |
XM_011532004.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1173 | XP_011530306.1 | |
XM_011532005.2 | 4229 | Intron | XP_011530307.1 | |||
XM_017008249.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1038 | XP_016863738.1 | |
XM_017008250.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1038 | XP_016863739.1 | |
XM_017008251.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1010 | XP_016863740.1 | |
XM_017008252.1 | 4229 | Missense Mutation | AAT,GAT | N,D 1010 | XP_016863741.1 | |
XM_017008253.1 | 4229 | Missense Mutation | AAT,GAT | N,D 861 | XP_016863742.1 | |
XM_017008254.1 | 4229 | Missense Mutation | AAT,GAT | N,D 793 | XP_016863743.1 |