Product Details

SNP ID
rs6686999
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:39965897 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGGGCACAGTGCTGGGCACGGC[A/G]ATCCAGGGACAAATCGTGGGCCAAG
Phenotype
MIM: 614397
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MFSD2A PubMed Links

Gene Details

Gene
MFSD2A
Gene Name
major facilitator superfamily domain containing 2A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136493.2 667 Silent Mutation GCA,GCG A212A NP_001129965.1
NM_001287808.1 667 Silent Mutation GCA,GCG A43A NP_001274737.1
NM_001287809.1 667 Silent Mutation GCA,GCG A162A NP_001274738.1
NM_032793.4 667 Silent Mutation GCA,GCG A199A NP_116182.2
XM_005271285.1 667 Silent Mutation GCA,GCG A197A XP_005271342.1
XM_011542312.2 667 Silent Mutation GCA,GCG A199A XP_011540614.1

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