Product Details
- SNP ID
-
rs139722132
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
2
- Location
-
Chr.1:161229876 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGGATTTGGTACCCGTAGGCCTCA[A/T]TAATGCTCCGGAGCTCAGCCAGCAG
- Phenotype
-
MIM: 107670
MIM: 603881
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
APOA2
PubMed Links
Gene Details
- Gene
- APOA2
- Gene Name
- apolipoprotein A2
There are no transcripts associated with this gene.
- Gene
- MIR5187
- Gene Name
- microRNA 5187
There are no transcripts associated with this gene.
- Gene
- NR1I3
- Gene Name
- nuclear receptor subfamily 1 group I member 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001077469.2 |
2041 |
Intron |
|
|
NP_001070937.1 |
NM_001077470.2 |
2041 |
Missense Mutation |
AAT,ATT |
N255I |
NP_001070938.1 |
NM_001077471.2 |
2041 |
Missense Mutation |
AAT,ATT |
N284I |
NP_001070939.1 |
NM_001077472.2 |
2041 |
Missense Mutation |
AAT,ATT |
N299I |
NP_001070940.1 |
NM_001077473.2 |
2041 |
Intron |
|
|
NP_001070941.1 |
NM_001077474.2 |
2041 |
Intron |
|
|
NP_001070942.1 |
NM_001077475.2 |
2041 |
Intron |
|
|
NP_001070943.1 |
NM_001077476.2 |
2041 |
Intron |
|
|
NP_001070944.1 |
NM_001077477.2 |
2041 |
Intron |
|
|
NP_001070945.1 |
NM_001077478.2 |
2041 |
Intron |
|
|
NP_001070946.1 |
NM_001077479.2 |
2041 |
Missense Mutation |
AAT,ATT |
N294I |
NP_001070947.1 |
NM_001077480.2 |
2041 |
Missense Mutation |
AAT,ATT |
N327I |
NP_001070948.1 |
NM_001077481.2 |
2041 |
Missense Mutation |
AAT,ATT |
N289I |
NP_001070949.1 |
NM_001077482.2 |
2041 |
Missense Mutation |
AAT,ATT |
N332I |
NP_001070950.1 |
NM_005122.4 |
2041 |
Missense Mutation |
AAT,ATT |
N323I |
NP_005113.1 |
XM_005245693.4 |
2041 |
Missense Mutation |
AAT,ATT |
N404I |
XP_005245750.1 |
XM_005245694.4 |
2041 |
Missense Mutation |
AAT,ATT |
N399I |
XP_005245751.1 |
XM_005245697.4 |
2041 |
Missense Mutation |
AAT,ATT |
N328I |
XP_005245754.1 |
XM_011510237.2 |
2041 |
Missense Mutation |
AAT,ATT |
N361I |
XP_011508539.1 |
- Gene
- TOMM40L
- Gene Name
- translocase of outer mitochondrial membrane 40 like
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