Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCCCGGCCACCTTCCTGCCCCAGG[C/T]GGGGTCGCTAAGGCCTCAGGAGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 613878 MIM: 609499 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
F7 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
|
F7 - coagulation factor VII | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000131.4 | 120 | Silent Mutation | GGC,GGT | G,G 22 | NP_000122.1 | |
NM_001267554.1 | 120 | Intron | NP_001254483.1 | |||
NM_019616.3 | 120 | Intron | NP_062562.1 | |||
XM_006719963.3 | 120 | Intron | XP_006720026.2 | |||
XM_011537474.2 | 120 | Intron | XP_011535776.2 | |||
XM_011537475.2 | 120 | Intron | XP_011535777.2 | |||
XM_011537476.2 | 120 | Intron | XP_011535778.1 |
MCF2L - MCF.2 cell line derived transforming sequence like | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |