Product Details

SNP ID

rs200519924

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:32021878 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTACCTCCAGAACTCCGGGTGAA[C/T]GCAGATGAGCCTCCAGGGCCTCCTG

Phenotype

MIM: 616558

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LRRC37B PubMed Links

Gene Details

Gene

LRRC37B

Gene Name

leucine rich repeat containing 37B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321350.1	937	Silent Mutation	AAC,AAT	N162N	NP_001308279.1
NM_052888.2	937	Intron			NP_443120.2

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