Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTCAGTCAGTGGAAGGTACGAGT[C/G]TATGCTTGTTCTGTATCCAGAGGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606037 | ||||||||||||||||||||
Literature Links: |
CD96 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 |
CD96 - CD96 molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318889.1 | 523 | Missense Mutation | TCT,TGT | S,C 118 | NP_001305818.1 | |
NM_005816.4 | 523 | Missense Mutation | TCT,TGT | S,C 118 | NP_005807.1 | |
NM_198196.2 | 523 | Missense Mutation | TCT,TGT | S,C 118 | NP_937839.1 | |
XM_005247063.3 | 523 | Missense Mutation | TCT,TGT | S,C 118 | XP_005247120.1 | |
XM_006713469.3 | 523 | Missense Mutation | TCT,TGT | S,C 118 | XP_006713532.1 | |
XM_006713470.3 | 523 | Missense Mutation | TCT,TGT | S,C 118 | XP_006713533.1 | |
XM_017005521.1 | 523 | Missense Mutation | TCT,TGT | S,C 118 | XP_016861010.1 | |
XM_017005522.1 | 523 | Missense Mutation | TCT,TGT | S,C 118 | XP_016861011.1 |