Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGCCAGACCCAGGCCGAGGAGGG[A/T]CAGGATGCCAGAGGTAGTGCCAACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 607252 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APOL2 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
|
APOL2 - apolipoprotein L2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030882.3 | 868 | Intron | NP_112092.2 | |||
NM_145637.2 | 868 | Missense Mutation | ACC,TCC | T,S 131 | NP_663612.2 | |
XM_011530074.1 | 868 | Intron | XP_011528376.1 | |||
XM_011530075.1 | 868 | Intron | XP_011528377.1 | |||
XM_011530076.2 | 868 | Intron | XP_011528378.1 | |||
XM_011530077.2 | 868 | Intron | XP_011528379.1 | |||
XM_011530078.1 | 868 | Intron | XP_011528380.1 | |||
XM_017028724.1 | 868 | Intron | XP_016884213.1 |