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Search Thermo Fisher Scientific
AAAAATAAAAAATGGAAAACACACC[G/T]TTAGTGAAGTAGAAGTATTTGAGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 120920 | ||||||||||||||||||||
Literature Links: |
CD46 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 |
CD46 - CD46 molecule | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002389.4 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_002380.3 | |
NM_153826.3 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_722548.1 | |
NM_172350.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758860.1 | |
NM_172351.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758861.1 | |
NM_172352.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758862.1 | |
NM_172353.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758863.1 | |
NM_172359.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758869.1 | |
NM_172361.2 | 698 | Missense Mutation | GTT,TTT | V,F 175 | NP_758871.1 | |
XM_011509563.1 | 698 | Missense Mutation | GTT,TTT | V,F 175 | XP_011507865.1 | |
XM_011509564.1 | 698 | Missense Mutation | GTT,TTT | V,F 175 | XP_011507866.1 | |
XM_017001308.1 | 698 | Missense Mutation | GTT,TTT | V,F 175 | XP_016856797.1 | |
XM_017001309.1 | 698 | Missense Mutation | GTT,TTT | V,F 175 | XP_016856798.1 | |
XM_017001310.1 | 698 | Missense Mutation | GTT,TTT | V,F 175 | XP_016856799.1 |