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CCTGTTTCCCACAGCAGCTACAGTC[C/T]GCGTGGAAAACCCTGGGTGTAAGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616731 | ||||||||||||||||||||
Literature Links: |
LOC107984562 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 |
LOC107984562 - serine/threonine-protein kinase Nek5-like | ||||||
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There are no transcripts associated with this gene. |
NEK5 - NIMA related kinase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_199289.2 | 2099 | Missense Mutation | CAG,CGG | Q,R 646 | NP_954983.1 | |
XM_006719808.3 | 2099 | Intron | XP_006719871.2 | |||
XM_011535066.2 | 2099 | Intron | XP_011533368.1 | |||
XM_011535068.2 | 2099 | Intron | XP_011533370.1 | |||
XM_017020555.1 | 2099 | Missense Mutation | CAG,CGG | Q,R 693 | XP_016876044.1 | |
XM_017020556.1 | 2099 | Intron | XP_016876045.1 | |||
XM_017020557.1 | 2099 | Missense Mutation | CAG,CGG | Q,R 718 | XP_016876046.1 |