Product Details

SNP ID

rs4930409

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:67070494 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCGTGGGCTGCAAGACTGACCTG[C/T]GCAAGGACAAATCACTGGTGAACAA

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	485	Missense Mutation	CGC,TGC	R68C	NP_001287815.1
NM_014578.3	485	Missense Mutation	CGC,TGC	R134C	NP_055393.1

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