Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTCAGTAAAGGATGGTTGAAATG[C/T]CAGATCAGATATGTGCAGATTTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
FSTL5 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 |
FSTL5 - follistatin like 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128427.2 | 2660 | Missense Mutation | ACA,GCA | T,A 742 | NP_001121899.1 | |
NM_001128428.2 | 2660 | Missense Mutation | ACA,GCA | T,A 733 | NP_001121900.1 | |
NM_020116.4 | 2660 | Missense Mutation | ACA,GCA | T,A 743 | NP_064501.2 | |
XM_011532126.1 | 2660 | Missense Mutation | ACA,GCA | T,A 734 | XP_011530428.1 |