Product Details

SNP ID: rs4472366
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.6:122997156 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: TAAAAATAGCGTCTTTGAATAAGTA[C/G]AGGGAGAAATAATCTCCTTTCTCCC
Phenotype: MIM: 616945
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CLVS2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010852.3		Intron			NP_001010852.2
XM_017010266.1		Intron			XP_016865755.1