Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607385 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MGAT4C 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)
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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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MGAT4C - MGAT4 family member C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013244.3 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | NP_037376.2 | |
XM_005268776.4 | 1565 | Silent Mutation | CTA,CTG | L,L 440 | XP_005268833.1 | |
XM_005268779.3 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_005268836.1 | |
XM_011538150.2 | 1565 | Silent Mutation | CTA,CTG | L,L 449 | XP_011536452.1 | |
XM_011538151.2 | 1565 | Silent Mutation | CTA,CTG | L,L 449 | XP_011536453.1 | |
XM_011538156.2 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_011536458.1 | |
XM_011538157.2 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_011536459.1 | |
XM_017019143.1 | 1565 | Silent Mutation | CTA,CTG | L,L 460 | XP_016874632.1 | |
XM_017019144.1 | 1565 | Silent Mutation | CTA,CTG | L,L 449 | XP_016874633.1 | |
XM_017019145.1 | 1565 | Silent Mutation | CTA,CTG | L,L 440 | XP_016874634.1 | |
XM_017019146.1 | 1565 | Silent Mutation | CTA,CTG | L,L 440 | XP_016874635.1 | |
XM_017019147.1 | 1565 | Silent Mutation | CTA,CTG | L,L 440 | XP_016874636.1 | |
XM_017019148.1 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_016874637.1 | |
XM_017019149.1 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_016874638.1 | |
XM_017019150.1 | 1565 | Silent Mutation | CTA,CTG | L,L 411 | XP_016874639.1 |
Set Membership: |
HapMap |