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TTGGGGGAGCCCCCTACCAGGTGAC[A/G]GGCTGTGCCCTGGGTTTCTTCCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 614397 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MFSD2A 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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MFSD2A - major facilitator superfamily domain containing 2A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136493.2 | 325 | Silent Mutation | ACA,ACG | T,T 59 | NP_001129965.1 | |
NM_001287808.1 | 325 | Intron | NP_001274737.1 | |||
NM_001287809.1 | 325 | Intron | NP_001274738.1 | |||
NM_032793.4 | 325 | Silent Mutation | ACA,ACG | T,T 59 | NP_116182.2 | |
XM_005271285.1 | 325 | Silent Mutation | ACA,ACG | T,T 57 | XP_005271342.1 | |
XM_011542312.2 | 325 | Silent Mutation | ACA,ACG | T,T 59 | XP_011540614.1 |