Product Details

SNP ID

rs146491803

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:174728295 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCCCCTGACATTTACATTTATGG[A/G]CTAGCTAATTTTTCCCTTCGTCTTA

Phenotype

MIM: 123101

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MSX2 PubMed Links

Gene Details

Gene

MSX2

Gene Name

msh homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002449.4		Intron			NP_002440.2
XM_017009489.1		Intron			XP_016864978.1

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