Product Details

SNP ID

rs201728682

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:75073695 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCCCCAGCCCCGGCCCGCTCAGCC[A/G]CCGCCCCAGCCGAGCCCCAGCCACC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RCC1L PubMed Links

Gene Details

Gene

RCC1L

Gene Name

RCC1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281441.1	187	Missense Mutation	CGG,TGG	R15W	NP_001268370.1
NM_030798.4	187	Missense Mutation	CGG,TGG	R15W	NP_110425.2
NM_148842.2	187	Missense Mutation	CGG,TGG	R15W	NP_683682.1

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