Product Details

SNP ID

rs355613

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:180229564 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGCCCAGCCTCAGCCAGACGCGG[A/G]GGAGAGAGAGCAGGGGCTGGGAAGT

Phenotype

MIM: 602146

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LHX4 PubMed Links

Gene Details

Gene

LHX4

Gene Name

LIM homeobox 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033343.3		Intron			NP_203129.1
XM_011510105.2		Intron			XP_011508407.1
XM_011510106.2		Intron			XP_011508408.1
XM_011510108.2		Intron			XP_011508410.1
XM_017002755.1		Intron			XP_016858244.1

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