Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTCAGGATGTGTTCTGGGCCAAGT[A/G]CACAGGTGAGCACCGGGAAGGATTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 176930 | ||||||||||||||||||||
Literature Links: |
F2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
F2 - coagulation factor II, thrombin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000506.4 | 282 | Missense Mutation | TAC,TGC | Y,C 87 | NP_000497.1 | |
NM_001311257.1 | 282 | Missense Mutation | TAC,TGC | Y,C 71 | NP_001298186.1 |