Product Details

SNP ID

rs150676565

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:38839562 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGCTGGGATTCAGACTAGATGGC[A/G]TTTCGTGGCGTGCCATTGTGTGTCA

Phenotype

MIM: 608267

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RRAGC PubMed Links

Gene Details

Gene

RRAGC

Gene Name

Ras related GTP binding C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271851.1	1266	Silent Mutation	AAC,AAT	N363N	NP_001258780.1
NM_022157.3	1266	Silent Mutation	AAC,AAT	N397N	NP_071440.1

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