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SNP ID

rs11621203

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:74241441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATCTGCCCGGGGGCCTTGGCGTC[C/G]GCACCGGTTGAGCAGGATGAGTGGC

Phenotype

MIM: 142993

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

VSX2 PubMed Links

Gene Details

Gene

VSX2

Gene Name

visual system homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182894.2		Intron			NP_878314.1

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