Product Details

SNP ID: rs6521125
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:46582440 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AACATAGATTTGATTTCATTTTTTC[A/G]TCTTGGCCAGTTTGATGAATGGAAA
Phenotype: MIM: 300375
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CHST7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019886.3		Intron			NP_063939.2