Product Details

SNP ID
rs149775642
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:55617807 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCATGATGGATGATGTTTCAGCTTT[A/G]GATTTTGTTTGCCTTTTAATGAAAG
Phenotype
MIM: 613261
Polymorphism
A/G, 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 5933 UTR 3 NP_776175.2
XM_011521459.1 5933 Intron XP_011519761.1
XM_011521460.1 5933 Intron XP_011519762.1
XM_017022081.1 5933 UTR 3 XP_016877570.1
XM_017022082.1 5933 Intron XP_016877571.1

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