Product Details

SNP ID

rs138338692

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:59269076 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTCAGACGCAGCGCCGCGATGCT[A/G]CTGTTGCGCGGGTCCGCCTCGTCCA

Phenotype

MIM: 601881

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RAX PubMed Links

Gene Details

Gene

RAX

Gene Name

retina and anterior neural fold homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013435.2	1156	Silent Mutation	AGC,AGT	S323S	NP_038463.2

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