Product Details

SNP ID: rs41303725
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:74739447 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAATGCGAGTCTCTTCTTCAAACAC[A/G]GGTAAAACCCAAAAGGTTGTTTCTG
Phenotype: MIM: 300524
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KIAA2022 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008537.2	5126	Silent Mutation	CCC,CCT	P1503P	NP_001008537.1