Product Details

SNP ID

rs147403234

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:130668177 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCAGGTGTTCAATGAGGATGGCA[C/T]GGTGCGCTACTTCATCGATGCCAGC

Phenotype

MIM: 616458

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PRDM12 PubMed Links

Gene Details

Gene

PRDM12

Gene Name

PR domain 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021619.2	494	Missense Mutation	ACG,ATG	T145M	NP_067632.2

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