Product Details

SNP ID

rs202002402

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99613035 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTTCCATTCTTTCTTGCCCAGGG[A/G]AGGAGCGCTACATCTGCTGGTACTG

Phenotype

MIM: 616741

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PRDM13 PubMed Links

Gene Details

Gene

PRDM13

Gene Name

PR domain 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021620.3	661	Missense Mutation	AAG,GAG	K134E	NP_067633.2

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