Product Details

SNP ID: rs141240078
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:46574648 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCGTGGCGATACGCGCCCTGGAGGC[A/C]GAGTGCCGAAAGTACCCGGTGGTGG
Phenotype: MIM: 300375
Polymorphism: A/C, Transversion 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	962	Silent Mutation	GCA,GCC	A239A	NP_063939.2