Product Details

SNP ID

rs200479309

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:24017520 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACTGTCCACGGGCTCATCGTGTCC[A/G]GCGCCCACAGACCCCACAGGTGCGA

Phenotype

Polymorphism

A/G, Transition 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	1781	Missense Mutation	AGC,GGC	S205G	NP_001073942.1
XM_005264301.4	1781	Missense Mutation	AGC,GGC	S205G	XP_005264358.1
XM_017004063.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859552.1
XM_017004064.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859553.1
XM_017004065.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859554.1
XM_017004066.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859555.1
XM_017004067.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859556.1
XM_017004068.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859557.1
XM_017004069.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859558.1
XM_017004070.1	1781	Missense Mutation	AGC,GGC	S236G	XP_016859559.1

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