Product Details

SNP ID

rs185607856

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:67065920 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGCTACACCCCCACGGTGTTTGAG[C/T]GGTACATGGTCAACCTGCAAGTGAA

Phenotype

MIM: 605781

Polymorphism

C/T, 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	242	Intron			NP_001287815.1
NM_014578.3	242	Missense Mutation	CGG,TGG	R53W	NP_055393.1

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