Product Details

SNP ID: rs1285565
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:107136398 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGAAACAGATAATCTGAATAGTCCT[A/G]GAAACATTAAAGAAATTCCATTTGT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NUP62CL PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017681.2		Intron			NP_060151.2