Product Details

SNP ID

rs11114623

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:80805293 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACTTGGTTTTCTTAGTGACTAGGC[G/T]GATAGTTTTCGTAATAATTCCCTGG

Phenotype

MIM: 603380

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LIN7A PubMed Links

Gene Details

Gene

LIN7A

Gene Name

lin-7 homolog A, crumbs cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324423.1		Intron			NP_001311352.1
NM_004664.3		Intron			NP_004655.1
XM_011538928.2		Intron			XP_011537230.1

View Full Product Details