Product Details

SNP ID

hCV89212109

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:63155628 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATGCCAAATGATATACCTTCTGT[C/G]AGTCTGGCCTTTCCTCCTGTAGGCT

Phenotype

MIM: 612055

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RPS27L PubMed Links

Gene Details

Gene

RPS27L

Gene Name

ribosomal protein S27 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015920.3	356	Silent Mutation	CTC,CTG	L73L	NP_057004.1

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