Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCTGCAGCTGGGGAGCACCGTAGA[C/T]GCGGGCGAGGAAATCTCGGTCATAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 160995 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MGAT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MGAT1 - mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114617.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | NP_001108089.1 | |
NM_001114618.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | NP_001108090.1 | |
NM_001114619.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | NP_001108091.1 | |
NM_001114620.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | NP_001108092.1 | |
NM_002406.3 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | NP_002397.2 | |
XM_005265915.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_005265972.1 | |
XM_005265916.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_005265973.1 | |
XM_006714866.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_006714929.1 | |
XM_011534559.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_011532861.1 | |
XM_011534560.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_011532862.1 | |
XM_011534561.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_011532863.1 | |
XM_011534562.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_011532864.1 | |
XM_011534563.2 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_011532865.1 | |
XM_017009486.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_016864975.1 | |
XM_017009487.1 | 1850 | Missense Mutation | ATC,GTC | I,V 362 | XP_016864976.1 |