Product Details

SNP ID

rs200264629

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:87504277 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTGTTCCAGCCTGGACACTGACC[A/G]TTGAAAAATAGATGCCTTTCTGTGC

Phenotype

MIM: 171050

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ABCB1 PubMed Links

Gene Details

Gene

ABCB1

Gene Name

ATP binding cassette subfamily B member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000927.4	4302	Missense Mutation	ACG,ATG	T1270M	NP_000918.2

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