Product Details
- SNP ID
-
rs183356632
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:184757177 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATCTATCTGCGACCTGAAATAGTTC[C/T]GCAGCTCTGGCCTTTTCGCCTTCAT
- Phenotype
-
MIM: 152425
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ACSL1
PubMed Links
Gene Details
- Gene
- ACSL1
- Gene Name
- acyl-CoA synthetase long-chain family member 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001286708.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
NP_001273637.1 |
| NM_001286710.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
NP_001273639.1 |
| NM_001286711.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q648R |
NP_001273640.1 |
| NM_001286712.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q511R |
NP_001273641.1 |
| NM_001995.3 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
NP_001986.2 |
| XM_005262828.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_005262885.1 |
| XM_005262829.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_005262886.1 |
| XM_005262831.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_005262888.1 |
| XM_011531742.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_011530044.1 |
| XM_017007887.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_016863376.1 |
| XM_017007888.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_016863377.1 |
| XM_017007889.1 |
2230 |
Missense Mutation |
CAG,CGG |
Q682R |
XP_016863378.1 |
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