Product Details

SNP ID: rs1207577
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:24363270 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCAGGCATATTCTTCTACGTCCAAC[C/G]ATGCAGACTTTAGCCCATGATGTGA
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: SUPT20HL1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136234.1	510	Silent Mutation	ACC,ACG	T170T	NP_001129706.1