Product Details

SNP ID

rs184264222

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:85805107 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCACTTGCAGCTTCCCCTTCCGC[A/T]TCTTCATTTATATCAATGCAAACAC

Phenotype

MIM: 610383

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

RASSF9 PubMed Links

Gene Details

Gene

RASSF9

Gene Name

Ras association domain family member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005447.3	1242	Missense Mutation	GAA,GAT	E301D	NP_005438.2
XM_011538988.2	1242	Missense Mutation	GAA,GAT	E280D	XP_011537290.1

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