Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGGGGACTCGCCATTCACCATCCG[A/C]ACAGAAGGTACCTTGGTGGGGCAAG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 488 | Silent Mutation | CGA,CGC | R,R 58 | NP_001186101.1 | |
NM_144677.2 | 488 | Silent Mutation | CGA,CGC | R,R 58 | NP_653278.2 | |
NM_198955.1 | 488 | Silent Mutation | CGA,CGC | R,R 69 | NP_945193.1 | |
XM_006721707.3 | 488 | Missense Mutation | AAC,CAC | N,H 45 | XP_006721770.1 | |
XM_011524350.2 | 488 | Silent Mutation | CGA,CGC | R,R 21 | XP_011522652.1 | |
XM_011524352.2 | 488 | Silent Mutation | CGA,CGC | R,R 58 | XP_011522654.1 | |
XM_011524354.2 | 488 | Silent Mutation | CGA,CGC | R,R 58 | XP_011522656.1 | |
XM_017024200.1 | 488 | Silent Mutation | CGA,CGC | R,R 58 | XP_016879689.1 |