Product Details

SNP ID

rs76271227

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:85804953 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCAGGAGTTCATATTCTTTTGCTT[T/G]CATCTGAAGCAATGAGTCACTGTAT

Phenotype

MIM: 610383

Polymorphism

T/G, 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	1396	Missense Mutation	AAA,CAA	K353Q	NP_005438.2
XM_011538988.2	1396	Missense Mutation	AAA,CAA	K332Q	XP_011537290.1

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