Product Details

SNP ID

rs729832

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:75135547 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGGTATCTTGCCTGGTGCTTCCA[A/G]AGGGAGGGAGAAGGGGAGGCGAACA

Phenotype

MIM: 604425

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LHX8 PubMed Links

Gene Details

Gene

LHX8

Gene Name

LIM homeobox 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001933.1		Intron			NP_001001933.1
NM_001256114.1		Intron			NP_001243043.1

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