Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGTAGATTTCCTCAGTATCAGGA[G/T]AGTAGCAGTAAAGCGCCCTGAACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613774 | ||||||||||||||||||||
Literature Links: |
CAMSAP1 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 |
CAMSAP1 - calmodulin regulated spectrin associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015447.3 | 4115 | Missense Mutation | TAT,TCT | Y,S 1530 | NP_056262.3 | |
XM_005263396.3 | 4115 | Missense Mutation | TAT,TCT | Y,S 1541 | XP_005263453.1 | |
XM_005263397.1 | 4115 | Missense Mutation | TAT,TCT | Y,S 1252 | XP_005263454.1 | |
XM_011518272.1 | 4115 | Missense Mutation | TAT,TCT | Y,S 1397 | XP_011516574.1 | |
XM_011518273.2 | 4115 | Missense Mutation | TAT,TCT | Y,S 1342 | XP_011516575.1 | |
XM_011518274.1 | 4115 | Missense Mutation | TAT,TCT | Y,S 1331 | XP_011516576.1 | |
XM_017014301.1 | 4115 | Missense Mutation | TAT,TCT | Y,S 1397 | XP_016869790.1 | |
XM_017014302.1 | 4115 | Missense Mutation | TAT,TCT | Y,S 1397 | XP_016869791.1 |