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ACTCCCCAGCGTTAATCTCTGTGTC[A/G]TGCACATCCTAAGCCTTACGGCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601774 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MGAT5 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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MGAT5 - mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002410.4 | Intron | NP_002401.1 | ||||
XM_005263668.4 | Intron | XP_005263725.1 | ||||
XM_005263669.4 | Intron | XP_005263726.1 | ||||
XM_005263670.3 | Intron | XP_005263727.1 | ||||
XM_006712534.3 | Intron | XP_006712597.1 | ||||
XM_011511199.2 | Intron | XP_011509501.1 | ||||
XM_011511200.1 | Intron | XP_011509502.1 | ||||
XM_011511201.2 | Intron | XP_011509503.1 | ||||
XM_011511202.1 | Intron | XP_011509504.1 | ||||
XM_011511204.2 | Intron | XP_011509506.1 | ||||
XM_017004147.1 | Intron | XP_016859636.1 | ||||
XM_017004148.1 | Intron | XP_016859637.1 | ||||
XM_017004149.1 | Intron | XP_016859638.1 |
MIR3679 - microRNA 3679 | ||||||
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There are no transcripts associated with this gene. |