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TTTTTGTCCTGGGCATCGGCTTCTT[C/T]ACTCTCTGCTTCCTGATGACGTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612441 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MGAT5B 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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MGAT5B - mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199172.1 | 410 | Silent Mutation | TTC,TTT | F,F 32 | NP_001186101.1 | |
NM_144677.2 | 410 | Silent Mutation | TTC,TTT | F,F 32 | NP_653278.2 | |
NM_198955.1 | 410 | Silent Mutation | TTC,TTT | F,F 43 | NP_945193.1 | |
XM_006721707.3 | 410 | Missense Mutation | CAC,TAC | H,Y 19 | XP_006721770.1 | |
XM_011524350.2 | 410 | UTR 5 | XP_011522652.1 | |||
XM_011524352.2 | 410 | Silent Mutation | TTC,TTT | F,F 32 | XP_011522654.1 | |
XM_011524354.2 | 410 | Silent Mutation | TTC,TTT | F,F 32 | XP_011522656.1 | |
XM_017024200.1 | 410 | Silent Mutation | TTC,TTT | F,F 32 | XP_016879689.1 |