Product Details

SNP ID
rs80000029
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:130343084 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGACGGCAGAGAGGAACAGCAGGAG[A/G]AACAGCCAAGTCACAAGGTGAAGAG
Phenotype
MIM: 605571
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PIWIL1 PubMed Links

Gene Details

Gene
PIWIL1
Gene Name
piwi like RNA-mediated gene silencing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190971.1 387 Missense Mutation GAA,GGA E58G NP_001177900.1
NM_004764.4 387 Missense Mutation GAA,GGA E58G NP_004755.2
XM_011539002.2 387 Missense Mutation GAA,GGA E58G XP_011537304.1
XM_011539003.2 387 Missense Mutation GAA,GGA E58G XP_011537305.1
XM_011539004.2 387 Missense Mutation GAA,GGA E58G XP_011537306.1
XM_011539005.1 387 Missense Mutation GAA,GGA E58G XP_011537307.1
XM_011539006.2 387 Intron XP_011537308.1
XM_017020229.1 387 Missense Mutation GAA,GGA E58G XP_016875718.1

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