Product Details

SNP ID

rs200937927

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99613123 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTGCGTTTCCACTGCGTGTTCA[C/G]CGGCGGTGGAGGCGGCGCCTTCCTG

Phenotype

MIM: 616741

Polymorphism

C/G, Transversion 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	749	Missense Mutation	ACC,AGC	T163S	NP_067633.2

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