Product Details

SNP ID

rs28729140

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:43642109 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCCATGTCAATGCTTAGGCTAGC[C/T]AGGGTGTAACTCCAGGGACCCCAGC

Phenotype

MIM: 600147

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MEOX1 PubMed Links

Gene Details

Gene

MEOX1

Gene Name

mesenchyme homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040002.1		Intron			NP_001035091.1
NM_004527.3		Intron			NP_004518.1
NM_013999.3		Intron			NP_054705.1
XM_011524818.1		Intron			XP_011523120.1

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