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AACTGAGAGAACATTCAGACCAACA[C/T]GTTAAAGGTAAGTGAAAATTTGATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611423 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CEP135 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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CEP135 - centrosomal protein 135 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025009.4 | 565 | Silent Mutation | CAC,CAT | H,H 99 | NP_079285.2 | |
XM_005265788.3 | 565 | UTR 5 | XP_005265845.1 | |||
XM_006714055.2 | 565 | Missense Mutation | CAC,CAT | H,H 99 | XP_006714118.1 | |
XM_011534412.2 | 565 | Intron | XP_011532714.1 |