Product Details

SNP ID: rs12007674
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:100592861 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCTTTTTCAGGCTTTTAGTTTCCCA[A/G]ATTTTTTTCATAAGGAAAAATGAAC
Phenotype: MIM: 300459
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TNMD PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022144.2		Intron			NP_071427.2