Product Details

SNP ID: rs150692380
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:8545728 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGTCTCTGAAAAATTTTGAGTGAA[A/G]TGAATAGATTTGGGCTTTTAGGTCC
Phenotype: MIM: 300836
Polymorphism: A/G, Transition 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