Product Details
- SNP ID
-
rs199602272
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:111123885 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAGCCACAAGGTAATCCTGAAGGCA[A/G]TCACGGAGGTGAAGGGGACAGCTGC
- Phenotype
-
MIM: 603827
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ACOXL
PubMed Links
Gene Details
- Gene
- ACOXL
- Gene Name
- acyl-CoA oxidase-like
There are no transcripts associated with this gene.
- Gene
- BCL2L11
- Gene Name
- BCL2 like 11
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001204106.1 |
428 |
Intron |
|
|
NP_001191035.1 |
NM_001204107.1 |
428 |
Intron |
|
|
NP_001191036.1 |
NM_001204108.1 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_001191037.1 |
NM_001204109.1 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_001191038.1 |
NM_001204110.1 |
428 |
Intron |
|
|
NP_001191039.1 |
NM_001204111.1 |
428 |
Intron |
|
|
NP_001191040.1 |
NM_001204112.1 |
428 |
Intron |
|
|
NP_001191041.1 |
NM_001204113.1 |
428 |
Intron |
|
|
NP_001191042.1 |
NM_006538.4 |
428 |
Intron |
|
|
NP_006529.1 |
NM_138621.4 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_619527.1 |
NM_138622.3 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_619528.1 |
NM_138623.3 |
428 |
Intron |
|
|
NP_619529.1 |
NM_138624.3 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_619530.1 |
NM_138625.3 |
428 |
Intron |
|
|
NP_619531.1 |
NM_138626.3 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
NP_619532.1 |
NM_138627.3 |
428 |
Intron |
|
|
NP_619533.1 |
NM_207002.3 |
428 |
Intron |
|
|
NP_996885.1 |
NM_207003.2 |
428 |
Intron |
|
|
NP_996886.1 |
XM_005263550.3 |
428 |
Missense Mutation |
AAT,AGT |
N141S |
XP_005263607.1 |
XM_005263551.2 |
428 |
Missense Mutation |
AAT,AGT |
N141S |
XP_005263608.1 |
XM_005263552.3 |
428 |
Intron |
|
|
XP_005263609.1 |
XM_005263553.2 |
428 |
Intron |
|
|
XP_005263610.1 |
XM_005263554.2 |
428 |
Missense Mutation |
AAT,AGT |
N141S |
XP_005263611.1 |
XM_005263555.3 |
428 |
Intron |
|
|
XP_005263612.1 |
XM_005263556.3 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
XP_005263613.1 |
XM_005263557.4 |
428 |
Missense Mutation |
AAT,AGT |
N47S |
XP_005263614.1 |
XM_005263559.2 |
428 |
Intron |
|
|
XP_005263616.1 |
XM_005263561.3 |
428 |
Intron |
|
|
XP_005263618.1 |
XM_011510461.2 |
428 |
Missense Mutation |
AAT,AGT |
N141S |
XP_011508763.1 |
XM_011510464.2 |
428 |
Intron |
|
|
XP_011508766.1 |
XM_017003101.1 |
428 |
Intron |
|
|
XP_016858590.1 |
XM_017003102.1 |
428 |
Intron |
|
|
XP_016858591.1 |
- Gene
- LOC400997
- Gene Name
- uncharacterized LOC400997
There are no transcripts associated with this gene.
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