Product Details

SNP ID

rs77926367

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:32021754 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCTAGCTGAACGTTGGAGCCTTC[C/T]TGAGATTGTTGGGATTCCACACCAA

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	813	Missense Mutation	CCT,CTT	P121L	NP_001308279.1
NM_052888.2	813	Intron			NP_443120.2

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