Product Details
- SNP ID
-
rs200127470
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:11321365 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCAGAGCCTGCTGCAGCAGCAGAGC[A/G]CTGCAGGCAGCCAGAAGGAAGGTAG
- Phenotype
-
MIM: 602538
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CELF2
PubMed Links
Gene Details
- Gene
- CELF2
- Gene Name
- CUGBP, Elav-like family member 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001025076.2 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001020247.1 |
NM_001025077.2 |
1560 |
Missense Mutation |
ACT,GCT |
T412A |
NP_001020248.1 |
NM_001083591.1 |
1560 |
Missense Mutation |
ACT,GCT |
T392A |
NP_001077060.1 |
NM_001326317.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
NP_001313246.1 |
NM_001326318.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313247.1 |
NM_001326319.1 |
1560 |
Missense Mutation |
ACT,GCT |
T412A |
NP_001313248.1 |
NM_001326320.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313249.1 |
NM_001326321.1 |
1560 |
Missense Mutation |
ACT,GCT |
T402A |
NP_001313250.1 |
NM_001326323.1 |
1560 |
Missense Mutation |
ACT,GCT |
T408A |
NP_001313252.1 |
NM_001326324.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313253.1 |
NM_001326325.1 |
1560 |
Missense Mutation |
ACT,GCT |
T443A |
NP_001313254.1 |
NM_001326326.1 |
1560 |
Missense Mutation |
ACT,GCT |
T424A |
NP_001313255.1 |
NM_001326327.1 |
1560 |
Missense Mutation |
ACT,GCT |
T430A |
NP_001313256.1 |
NM_001326328.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313257.1 |
NM_001326329.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
NP_001313258.1 |
NM_001326330.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313259.1 |
NM_001326331.1 |
1560 |
Missense Mutation |
ACT,GCT |
T418A |
NP_001313260.1 |
NM_001326332.1 |
1560 |
Missense Mutation |
ACT,GCT |
T412A |
NP_001313261.1 |
NM_001326333.1 |
1560 |
Missense Mutation |
ACT,GCT |
T190A |
NP_001313262.1 |
NM_001326334.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313263.1 |
NM_001326335.1 |
1560 |
Missense Mutation |
ACT,GCT |
T416A |
NP_001313264.1 |
NM_001326336.1 |
1560 |
Missense Mutation |
ACT,GCT |
T436A |
NP_001313265.1 |
NM_001326337.1 |
1560 |
Intron |
|
|
NP_001313266.1 |
NM_001326338.1 |
1560 |
Missense Mutation |
ACT,GCT |
T301A |
NP_001313267.1 |
NM_001326339.1 |
1560 |
Missense Mutation |
ACT,GCT |
T307A |
NP_001313268.1 |
NM_001326340.1 |
1560 |
Missense Mutation |
ACT,GCT |
T437A |
NP_001313269.1 |
NM_001326341.1 |
1560 |
Missense Mutation |
ACT,GCT |
T419A |
NP_001313270.1 |
NM_001326342.1 |
1560 |
Missense Mutation |
ACT,GCT |
T425A |
NP_001313271.1 |
NM_001326343.1 |
1560 |
Missense Mutation |
ACT,GCT |
T443A |
NP_001313272.1 |
NM_001326344.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
NP_001313273.1 |
NM_001326345.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313274.1 |
NM_001326346.1 |
1560 |
Missense Mutation |
ACT,GCT |
T184A |
NP_001313275.1 |
NM_001326347.1 |
1560 |
Missense Mutation |
ACT,GCT |
T400A |
NP_001313276.1 |
NM_001326348.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
NP_001313277.1 |
NM_001326349.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
NP_001313278.1 |
NM_006561.3 |
1560 |
Missense Mutation |
ACT,GCT |
T425A |
NP_006552.3 |
XM_005252354.4 |
1560 |
Missense Mutation |
ACT,GCT |
T418A |
XP_005252411.1 |
XM_005252357.4 |
1560 |
Missense Mutation |
ACT,GCT |
T184A |
XP_005252414.1 |
XM_005252358.3 |
1560 |
Missense Mutation |
ACT,GCT |
T184A |
XP_005252415.1 |
XM_006717373.2 |
1560 |
Missense Mutation |
ACT,GCT |
T307A |
XP_006717436.1 |
XM_011519294.2 |
1560 |
Missense Mutation |
ACT,GCT |
T412A |
XP_011517596.1 |
XM_011519297.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
XP_011517599.1 |
XM_017015542.1 |
1560 |
Missense Mutation |
ACT,GCT |
T398A |
XP_016871031.1 |
XM_017015543.1 |
1560 |
Missense Mutation |
ACT,GCT |
T429A |
XP_016871032.1 |
XM_017015544.1 |
1560 |
Missense Mutation |
ACT,GCT |
T425A |
XP_016871033.1 |
XM_017015545.1 |
1560 |
Missense Mutation |
ACT,GCT |
T423A |
XP_016871034.1 |
XM_017015546.1 |
1560 |
Missense Mutation |
ACT,GCT |
T423A |
XP_016871035.1 |
XM_017015547.1 |
1560 |
Missense Mutation |
ACT,GCT |
T422A |
XP_016871036.1 |
XM_017015548.1 |
1560 |
Missense Mutation |
ACT,GCT |
T419A |
XP_016871037.1 |
XM_017015549.1 |
1560 |
Missense Mutation |
ACT,GCT |
T419A |
XP_016871038.1 |
XM_017015550.1 |
1560 |
Missense Mutation |
ACT,GCT |
T418A |
XP_016871039.1 |
XM_017015551.1 |
1560 |
Missense Mutation |
ACT,GCT |
T416A |
XP_016871040.1 |
XM_017015552.1 |
1560 |
Missense Mutation |
ACT,GCT |
T398A |
XP_016871041.1 |
XM_017015553.1 |
1560 |
Missense Mutation |
ACT,GCT |
T394A |
XP_016871042.1 |
XM_017015554.1 |
1560 |
Missense Mutation |
ACT,GCT |
T388A |
XP_016871043.1 |
XM_017015555.1 |
1560 |
Intron |
|
|
XP_016871044.1 |
XM_017015556.1 |
1560 |
Missense Mutation |
ACT,GCT |
T311A |
XP_016871045.1 |
XM_017015557.1 |
1560 |
Missense Mutation |
ACT,GCT |
T311A |
XP_016871046.1 |
XM_017015558.1 |
1560 |
Missense Mutation |
ACT,GCT |
T311A |
XP_016871047.1 |
XM_017015559.1 |
1560 |
Missense Mutation |
ACT,GCT |
T307A |
XP_016871048.1 |
XM_017015560.1 |
1560 |
Missense Mutation |
ACT,GCT |
T307A |
XP_016871049.1 |
XM_017015561.1 |
1560 |
Missense Mutation |
ACT,GCT |
T307A |
XP_016871050.1 |
XM_017015562.1 |
1560 |
Missense Mutation |
ACT,GCT |
T301A |
XP_016871051.1 |
XM_017015563.1 |
1560 |
Missense Mutation |
ACT,GCT |
T301A |
XP_016871052.1 |
XM_017015564.1 |
1560 |
Missense Mutation |
ACT,GCT |
T194A |
XP_016871053.1 |
XM_017015565.1 |
1560 |
Missense Mutation |
ACT,GCT |
T194A |
XP_016871054.1 |
XM_017015566.1 |
1560 |
Missense Mutation |
ACT,GCT |
T190A |
XP_016871055.1 |
XM_017015567.1 |
1560 |
Missense Mutation |
ACT,GCT |
T190A |
XP_016871056.1 |
XM_017015568.1 |
1560 |
Missense Mutation |
ACT,GCT |
T190A |
XP_016871057.1 |
XM_017015569.1 |
1560 |
Missense Mutation |
ACT,GCT |
T188A |
XP_016871058.1 |
XM_017015570.1 |
1560 |
Missense Mutation |
ACT,GCT |
T188A |
XP_016871059.1 |
XM_017015571.1 |
1560 |
Missense Mutation |
ACT,GCT |
T184A |
XP_016871060.1 |
XM_017015572.1 |
1560 |
Missense Mutation |
ACT,GCT |
T184A |
XP_016871061.1 |
- Gene
- CELF2-AS1
- Gene Name
- CELF2 antisense RNA 1
There are no transcripts associated with this gene.
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