Product Details

SNP ID

rs185767086

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:67066846 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACAGCTTTGACAACATCTTTAACC[A/G]GGTAGGTACTGGGGGGCAGGGAGGC

Phenotype

MIM: 605781

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RHOD PubMed Links

Gene Details

Gene

RHOD

Gene Name

ras homolog family member D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300886.1	414	Intron			NP_001287815.1
NM_014578.3	414	Missense Mutation	CAG,CGG	Q110R	NP_055393.1

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