Product Details

SNP ID

rs16917051

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:27496576 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACAGTAGCAAGCTAAACTACTGTA[C/T]TTGGCTCCTTTGAGCTACCCTTATT

Phenotype

MIM: 612332

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LIN7C PubMed Links

Gene Details

Gene

LIN7C

Gene Name

lin-7 homolog C, crumbs cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018362.3	2694	UTR 3			NP_060832.1

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