Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTTGGCTATGTCAGCCAGCAGGG[A/G]GGGCAGCGCTCCACGCCCCTCATCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 613539 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FEM1B 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
|
FEM1B - fem-1 homolog B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015322.4 | 744 | Silent Mutation | GGA,GGG | G,G 43 | NP_056137.1 | |
XM_017021859.1 | 744 | Intron | XP_016877348.1 |