Product Details

SNP ID: rs6909333
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:42759057 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTACAGCATCCTAATGCCCCTTGA[A/G]TAAATCTGAATCTCTGGGAGTGGGG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GLTSCR1L PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318819.1		Intron			NP_001305748.1
NM_015349.2		Intron			NP_056164.1