Product Details

SNP ID: rs201018804
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:24310997 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACACTGGCTGCTGCAGGACTCTCAA[A/G]GGCTGTGTCTGGAGCTGGATCTGCT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SUPT20HL2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136233.1	2319	Silent Mutation			NP_001129705.1