Product Details

SNP ID

rs148156721

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:87332034 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGACCATGGTGAATCCGGGCAGC[A/T]GCTCGCAGCCGCCCCCGGTGACGGC

Phenotype

MIM: 603129

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

LMO4 PubMed Links

Gene Details

Gene

LMO4

Gene Name

LIM domain only 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006769.3	2969	Missense Mutation	AGC,TGC	S7C	NP_006760.1
XM_005271291.3	2969	Missense Mutation	AGC,TGC	S7C	XP_005271348.1

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