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TTCTTCGGGATCACTGGATTGCTGA[C/T]GGCAGCCCTCTCAGGTAGGCCCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186720 | ||||||||||||||||||||
Literature Links: |
CD6 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 |
CD6 - CD6 molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001254750.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | NP_001241679.1 | |
NM_001254751.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | NP_001241680.1 | |
NM_006725.4 | 260 | Missense Mutation | ACG,ATG | T,M 12 | NP_006716.3 | |
XM_006718738.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_006718801.1 | |
XM_006718739.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_006718802.1 | |
XM_006718740.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_006718803.1 | |
XM_006718741.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_006718804.1 | |
XM_011545360.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_011543662.1 | |
XM_011545362.1 | 260 | Missense Mutation | ACG,ATG | T,M 12 | XP_011543664.1 |