Product Details

SNP ID

rs150134152

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:13475948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGAAGAAGCTGGAGATGATGGC[C/T]GCAATGGACACGGCCACACCGGAGA

Phenotype

MIM: 615212

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LRRC38 PubMed Links

Gene Details

Gene

LRRC38

Gene Name

leucine rich repeat containing 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010847.1	937	Silent Mutation	GCA,GCG	A261A	NP_001010847.1

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