Product Details

SNP ID
rs60606664
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:24013295 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTGTCTCCTCCAGGACAGCAGAG[A/C]CGGTCGCCTCTCATTCTGTACAAAG
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MFSD2B PubMed Links

Gene Details

Gene
MFSD2B
Gene Name
major facilitator superfamily domain containing 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080473.1 1182 Missense Mutation GAC,GCC D36A NP_001073942.1
XM_005264301.4 1182 Missense Mutation GAC,GCC D36A XP_005264358.1
XM_017004063.1 1182 Missense Mutation GAC,GCC D36A XP_016859552.1
XM_017004064.1 1182 Missense Mutation GAC,GCC D36A XP_016859553.1
XM_017004065.1 1182 Missense Mutation GAC,GCC D36A XP_016859554.1
XM_017004066.1 1182 Missense Mutation GAC,GCC D36A XP_016859555.1
XM_017004067.1 1182 Missense Mutation GAC,GCC D36A XP_016859556.1
XM_017004068.1 1182 Missense Mutation GAC,GCC D36A XP_016859557.1
XM_017004069.1 1182 Missense Mutation GAC,GCC D36A XP_016859558.1
XM_017004070.1 1182 Missense Mutation GAC,GCC D36A XP_016859559.1

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