Product Details
- SNP ID
-
rs200325557
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:54575897 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGACCCTGCTGTGTCAGTCACGGG[A/G]GCAGTTCCACACTTTCCTTCTGACC
- Phenotype
-
MIM: 604812
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
LILRA2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7249811] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- LILRA2
- Gene Name
- leukocyte immunoglobulin like receptor A2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001130917.2 |
1627 |
Missense Mutation |
GAG,GGG |
E348G |
NP_001124389.2 |
NM_001290270.1 |
1627 |
Missense Mutation |
GAG,GGG |
E336G |
NP_001277199.1 |
NM_001290271.1 |
1627 |
Missense Mutation |
GAG,GGG |
E348G |
NP_001277200.1 |
NM_006866.3 |
1627 |
Missense Mutation |
GAG,GGG |
E348G |
NP_006857.2 |
XM_006722986.1 |
1627 |
Missense Mutation |
GAG,GGG |
E348G |
XP_006723049.1 |
XM_011526385.1 |
1627 |
Missense Mutation |
GAG,GGG |
E348G |
XP_011524687.1 |
XM_011526386.1 |
1627 |
Missense Mutation |
GAG,GGG |
E336G |
XP_011524688.1 |
XM_011526387.1 |
1627 |
Missense Mutation |
GAG,GGG |
E336G |
XP_011524689.1 |
XM_011526388.1 |
1627 |
Missense Mutation |
GAG,GGG |
E336G |
XP_011524690.1 |
XM_011526389.1 |
1627 |
Missense Mutation |
GAG,GGG |
E242G |
XP_011524691.1 |
XM_011526390.1 |
1627 |
Silent Mutation |
GGA,GGG |
G336G |
XP_011524692.1 |
XM_011526391.1 |
1627 |
Silent Mutation |
GGA,GGG |
G237G |
XP_011524693.1 |
XM_017026224.1 |
1627 |
Missense Mutation |
GAG,GGG |
E249G |
XP_016881713.1 |
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