Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCTACAGCTACATCGCGCTCATCG[C/T]CATGGCGATCCAGGACGCGCCCGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602402 MIM: 603252 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXC2 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
|
FOXC2 - forkhead box C2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
FOXL1 - forkhead box L1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005250.2 | 391 | Missense Mutation | GCC,GTC | A,V 59 | NP_005241.1 |