Product Details

SNP ID

rs78129995

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:87332065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCCGCCCCCGGTGACGGCCGGCT[C/G]CCTCTCCTGGAAGCGGTGCGCAGGC

Phenotype

MIM: 603129

Polymorphism

C/G, 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	3000	Missense Mutation	TCC,TGC	S17C	NP_006760.1
XM_005271291.3	3000	Missense Mutation	TCC,TGC	S17C	XP_005271348.1

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