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CGACATGGCCTCGGGCGCTCAGCTC[C/T]CGCCGCAGCCGTCGAGCTCAGAGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604683 MIM: 608418 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCNI2 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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CCNI2 - cyclin I family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039780.3 | 116 | Missense Mutation | CCG,TCG | P,S 8 | NP_001034869.1 | |
NM_001287252.1 | 116 | Missense Mutation | CCG,TCG | P,S 8 | NP_001274181.1 | |
NM_001287253.1 | 116 | Missense Mutation | CCG,TCG | P,S 8 | NP_001274182.1 | |
XM_017009725.1 | 116 | Missense Mutation | CCG,TCG | P,S 8 | XP_016865214.1 |
KIF3A - kinesin family member 3A | ||||||
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There are no transcripts associated with this gene. |
SEPT8 - septin 8 | ||||||
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There are no transcripts associated with this gene. |