Product Details

SNP ID

rs7183555

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:76337476 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTCCGCAGTGCCTGTGTATTTACT[C/T]TCTTCTTAGTTTCGTGTTTGCGTTT

Phenotype

MIM: 609481

Polymorphism

C/T, Transition 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		Intron			NP_665804.1
XM_017022505.1		Intron			XP_016877994.1

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