Product Details

SNP ID

rs113325124

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:32879237 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCCAGCAGGTCTGCCTGAGAGAC[A/G]CCATTGAGGCTGGGGGCAACCAGAG

Phenotype

MIM: 615470 MIM: 604144

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CEP89 PubMed Links

Gene Details

Gene

CEP89

Gene Name

centrosomal protein 89

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032816.4	2432	Silent Mutation			NP_116205.3
XM_005259344.3	2432	Silent Mutation			XP_005259401.1
XM_011527425.2	2432	Silent Mutation			XP_011525727.1
XM_017027398.1	2432	Intron			XP_016882887.1

Gene

SLC7A9

Gene Name

solute carrier family 7 member 9

There are no transcripts associated with this gene.

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