Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGAGGAGCTGCGGCCGGGCTCCC[A/T]GGAGAGGGAGTGCAAGGAGGAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613878 | ||||||||||||||||||||
Literature Links: |
F7 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 |
F7 - coagulation factor VII | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000131.4 | 206 | Missense Mutation | CAG,CTG | Q,L 73 | NP_000122.1 | |
NM_001267554.1 | 206 | Intron | NP_001254483.1 | |||
NM_019616.3 | 206 | Missense Mutation | CAG,CTG | Q,L 51 | NP_062562.1 | |
XM_006719963.3 | 206 | Missense Mutation | CAG,CTG | Q,L 66 | XP_006720026.2 | |
XM_011537474.2 | 206 | Missense Mutation | CAG,CTG | Q,L 66 | XP_011535776.2 | |
XM_011537475.2 | 206 | Intron | XP_011535777.2 | |||
XM_011537476.2 | 206 | Intron | XP_011535778.1 |