Product Details

SNP ID
rs138181911
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:95275982 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATGCGCTGTGATCGCGGGCCTCT[A/G]CCTGCTGCTGGTGCCCACTGCCGGG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PROM2 PubMed Links

Gene Details

Gene
PROM2
Gene Name
prominin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001165977.2 469 Missense Mutation TAC,TGC Y116C NP_001159449.1
NM_001165978.2 469 Missense Mutation TAC,TGC Y116C NP_001159450.1
NM_001321070.1 469 UTR 5 NP_001307999.1
NM_144707.3 469 Missense Mutation TAC,TGC Y116C NP_653308.2
XM_006712301.2 469 Intron XP_006712364.1
XM_011510672.2 469 Missense Mutation TAC,TGC Y116C XP_011508974.1

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