Product Details

SNP ID: rs5978898
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:8547243 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AACAAAATCCAAGCTTCCTGGCATA[A/C]CATATAAGCTTCTCCATCACTTGAC
Phenotype: MIM: 300836
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ANOS1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000216.3		Intron			NP_000207.2
XM_005274501.4		Intron			XP_005274558.1