Product Details

SNP ID
rs491014
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:55616005 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAACTGATGCAAACCTCTGTCATTG[C/T]TCCCAATGTTGGCATTGCTCGTTTC
Phenotype
MIM: 613261
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PRTG PubMed Links

Gene Details

Gene
PRTG
Gene Name
protogenin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173814.5 7735 UTR 3 NP_776175.2
XM_011521459.1 7735 Intron XP_011519761.1
XM_011521460.1 7735 Intron XP_011519762.1
XM_017022081.1 7735 UTR 3 XP_016877570.1
XM_017022082.1 7735 Intron XP_016877571.1

View Full Product Details