Product Details
- SNP ID
-
rs147425392
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:151032382 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACAGGGTAGACGCCAGGTGTATTCC[A/G]GCTGCGACAAAACTGGTGCTTAATA
- Phenotype
-
MIM: 138321
MIM: 607714
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GPX3
PubMed Links
Gene Details
- Gene
- GPX3
- Gene Name
- glutathione peroxidase 3
There are no transcripts associated with this gene.
- Gene
- TNIP1
- Gene Name
- TNFAIP3 interacting protein 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001252385.1 |
1887 |
Missense Mutation |
CGG,TGG |
R600W |
NP_001239314.1 |
NM_001252386.1 |
1887 |
Missense Mutation |
CCG,CTG |
P541L |
NP_001239315.1 |
NM_001252390.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_001239319.1 |
NM_001252391.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_001239320.1 |
NM_001252392.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_001239321.1 |
NM_001252393.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_001239322.1 |
NM_001258454.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_001245383.1 |
NM_001258455.1 |
1887 |
Missense Mutation |
CCG,CTG |
P530L |
NP_001245384.1 |
NM_001258456.1 |
1887 |
Intron |
|
|
NP_001245385.1 |
NM_006058.4 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
NP_006049.3 |
XM_005268355.1 |
1887 |
Missense Mutation |
CGG,TGG |
R600W |
XP_005268412.1 |
XM_006714751.1 |
1887 |
Missense Mutation |
CCG,CTG |
P530L |
XP_006714814.1 |
XM_006714752.2 |
1887 |
Missense Mutation |
CCG,CTG |
P530L |
XP_006714815.1 |
XM_017008945.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
XP_016864434.1 |
XM_017008946.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
XP_016864435.1 |
XM_017008947.1 |
1887 |
Missense Mutation |
CCG,CTG |
P594L |
XP_016864436.1 |
XM_017008948.1 |
1887 |
Missense Mutation |
CCG,CTG |
P541L |
XP_016864437.1 |
XM_017008949.1 |
1887 |
Missense Mutation |
CCG,CTG |
P530L |
XP_016864438.1 |
XM_017008950.1 |
1887 |
Missense Mutation |
CGG,TGG |
R600W |
XP_016864439.1 |
XM_017008951.1 |
1887 |
Missense Mutation |
CCG,CTG |
P541L |
XP_016864440.1 |
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