Product Details

SNP ID

rs150284621

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:4862702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTTTTTTTCTTTCGGCCCTCAGG[G/T]CGGCTGAGCCCCCCAGCCTGCACCC

Phenotype

MIM: 142983

Polymorphism

G/T, 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	706	Silent Mutation	AGG,AGT	R157S	NP_002439.2

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