Product Details

SNP ID

rs148320729

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:24017481 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGATGACTGTGGAGATGGCGGGA[A/T]CACTGATGGGGGCCACTGTCCACGG

Phenotype

Polymorphism

A/T, 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	1742	Missense Mutation	ACA,TCA	T192S	NP_001073942.1
XM_005264301.4	1742	Missense Mutation	ACA,TCA	T192S	XP_005264358.1
XM_017004063.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859552.1
XM_017004064.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859553.1
XM_017004065.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859554.1
XM_017004066.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859555.1
XM_017004067.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859556.1
XM_017004068.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859557.1
XM_017004069.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859558.1
XM_017004070.1	1742	Missense Mutation	ACA,TCA	T223S	XP_016859559.1

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