Product Details
- SNP ID
-
rs144702884
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:26385210 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACAGAGGAGCAGATGGAGGAGTACC[A/G]GGGAAGAATCACCTTTGTGAGCAAA
- Phenotype
-
MIM: 613591
MIM: 613594
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
BTN2A2
PubMed Links
Gene Details
- Gene
- BTN2A2
- Gene Name
- butyrophilin subfamily 2 member A2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001197237.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
NP_001184166.1 |
NM_001197238.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
NP_001184167.1 |
NM_001197239.1 |
392 |
Intron |
|
|
NP_001184168.1 |
NM_001197240.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
NP_001184169.1 |
NM_006995.4 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
NP_008926.2 |
NM_181531.2 |
392 |
Intron |
|
|
NP_853509.1 |
XM_005248797.3 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_005248854.1 |
XM_005248798.4 |
392 |
Intron |
|
|
XP_005248855.1 |
XM_006714953.3 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_006715016.1 |
XM_006714955.3 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_006715018.1 |
XM_011514228.2 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_011512530.1 |
XM_011514229.2 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_011512531.1 |
XM_011514231.2 |
392 |
Intron |
|
|
XP_011512533.1 |
XM_017010166.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_016865655.1 |
XM_017010167.1 |
392 |
Intron |
|
|
XP_016865656.1 |
XM_017010168.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_016865657.1 |
XM_017010169.1 |
392 |
Missense Mutation |
CAG,CGG |
Q97R |
XP_016865658.1 |
- Gene
- BTN3A2
- Gene Name
- butyrophilin subfamily 3 member A2
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