Product Details

SNP ID: rs1298577
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.X:107153172 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTTCAATCTTTTTTCAGTTACTTAC[A/G]TCTCCACATGCTCCTCATCTGCATC
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	789	Missense Mutation			NP_060151.2