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SNP ID

rs11810270

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:38846119 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAAAGAAAGTACTATTCATTACAG[A/G]TTTCCCATCTAGGCATCTGCCACAT

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		Intron			NP_001258780.1
NM_022157.3		Intron			NP_071440.1

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