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CCTCCAATCTTCATTCTCTCCCAGT[C/G]CCGCAAAGGCTTTTCCCCCTCCGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 188410 | ||||||||||||||||||||
Literature Links: |
CD1D 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 |
CD1D - CD1d molecule | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319145.1 | 377 | Silent Mutation | GTC,GTG | V,V 21 | NP_001306074.1 | |
NM_001766.3 | 377 | Silent Mutation | GTC,GTG | V,V 21 | NP_001757.1 | |
XM_005245583.1 | 377 | Intron | XP_005245640.1 | |||
XM_006711621.1 | 377 | Intron | XP_006711684.1 | |||
XM_011510125.1 | 377 | Silent Mutation | GTC,GTG | V,V 21 | XP_011508427.1 | |
XM_011510127.1 | 377 | UTR 5 | XP_011508429.1 |