Product Details

SNP ID

rs3775261

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:4862018 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGAAAAAGCCCATTAGAATAAAG[A/C]AGCCCCTCGTTCTCCGCTCCAGATG

Phenotype

MIM: 142983

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MSX1 PubMed Links

Gene Details

Gene

MSX1

Gene Name

msh homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002448.3		Intron			NP_002439.2

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