Product Details

SNP ID
rs146491681
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:22279403 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCCGTCCATGGATCCTTTCCGAC[C/G]ATCGTTCAGGGGCCAGTCTCCTATC
Phenotype
MIM: 610312
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LOC100507071 PubMed Links

Gene Details

Gene
LOC100507071
Gene Name
uncharacterized LOC100507071
There are no transcripts associated with this gene.

Gene
PIWIL2
Gene Name
piwi like RNA-mediated gene silencing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135721.1 146 Missense Mutation CCA,CGA P6R NP_001129193.1
NM_018068.3 146 Missense Mutation CCA,CGA P6R NP_060538.2
XM_005273550.4 146 Missense Mutation CCA,CGA P6R XP_005273607.1
XM_005273551.3 146 Missense Mutation CCA,CGA P6R XP_005273608.1

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