Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAGGTTATGCAGCGCGTGAACATG[A/T]TCATGGCAGAATCACCAGGCCTCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 300746 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
F9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
F9 - coagulation factor IX | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000133.3 | 64 | Missense Mutation | ATC,TTC | I,F 7 | NP_000124.1 | |
NM_001313913.1 | 64 | Missense Mutation | ATC,TTC | I,F 7 | NP_001300842.1 | |
XM_005262397.4 | 64 | Missense Mutation | ATC,TTC | I,F 7 | XP_005262454.1 |