Product Details

SNP ID

rs62637020

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:41473545 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGTGGGGGCCTGCGCCCGCGCTT[C/G]TCCCGCCGCCTGCGCCTGCAGCACC

Phenotype

MIM: 300278

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NYX PubMed Links

Gene Details

Gene

NYX

Gene Name

nyctalopin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022567.2	190	Missense Mutation	TCT,TGT	S31C	NP_072089.1
XM_017029709.1	190	Missense Mutation	TCT,TGT	S31C	XP_016885198.1

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