Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGGTGGCCTCCTCCATGCTGGAGGC[C/T]GGCAGGATGACTGCAGGAAGACCAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||
Phenotype: |
MIM: 609298 | |||||||||||||||||||||||
Literature Links: |
SEMA5B PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SEMA5B - semaphorin 5B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031702.3 | 3494 | Silent Mutation | CCA,CCG | P,P 1019 | NP_001026872.2 | |
NM_001256346.1 | 3494 | Silent Mutation | CCA,CCG | P,P 1019 | NP_001243275.1 | |
NM_001256347.1 | 3494 | Silent Mutation | CCA,CCG | P,P 1073 | NP_001243276.1 | |
NM_001256348.1 | 3494 | Silent Mutation | CCA,CCG | P,P 925 | NP_001243277.1 | |
XM_017006638.1 | 3494 | Silent Mutation | CCA,CCG | P,P 985 | XP_016862127.1 | |
XM_017006639.1 | 3494 | Intron | XP_016862128.1 |