Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 160995 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MGAT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
MGAT1 - mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114617.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | NP_001108089.1 | |
NM_001114618.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | NP_001108090.1 | |
NM_001114619.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | NP_001108091.1 | |
NM_001114620.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | NP_001108092.1 | |
NM_002406.3 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | NP_002397.2 | |
XM_005265915.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_005265972.1 | |
XM_005265916.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_005265973.1 | |
XM_006714866.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_006714929.1 | |
XM_011534559.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_011532861.1 | |
XM_011534560.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_011532862.1 | |
XM_011534561.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_011532863.1 | |
XM_011534562.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_011532864.1 | |
XM_011534563.2 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_011532865.1 | |
XM_017009486.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_016864975.1 | |
XM_017009487.1 | 1907 | Silent Mutation | CTG,TTG | L,L 381 | XP_016864976.1 |
Set Membership: |
HapMap |