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TGCGGCTGGCACGCTCTGCTGCTCC[A/C]GCCGAACCTCTGTGGGGAAGGCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612685 MIM: 610850 | ||||||||||||||||||||
Literature Links: |
CAMSAP3 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 |
CAMSAP3 - calmodulin regulated spectrin associated protein family member 3 | ||||||
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There are no transcripts associated with this gene. |
MIR6792 - microRNA 6792 | ||||||
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There are no transcripts associated with this gene. |
XAB2 - XPA binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020196.2 | 2542 | Missense Mutation | CGG,CTG | R,L 839 | NP_064581.2 |