Product Details

SNP ID

rs148510226

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:76336909 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGTGGATATTATTTTTCATTATC[C/G]TTTTCTGGGTGCTATGGGTGATCAT

Phenotype

MIM: 609481

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ISL2 PubMed Links

Gene Details

Gene

ISL2

Gene Name

ISL LIM homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145805.2	186	Missense Mutation	CCT,CGT	P9R	NP_665804.1
XM_017022505.1	186	Missense Mutation	CCT,CGT	P9R	XP_016877994.1

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