Product Details
- SNP ID
-
rs201504913
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:113455785 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTTTTGCCACAAAGAGGTGCCTCC[C/T]GAGAAGTTTTCTTTCCCATTTGGAA
- Phenotype
-
MIM: 607708
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CAMK2D
PubMed Links
Gene Details
- Gene
- CAMK2D
- Gene Name
- calcium/calmodulin dependent protein kinase II delta
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001221.3 |
2368 |
Silent Mutation |
TCA,TCG |
S490S |
NP_001212.2 |
NM_001321566.1 |
2368 |
Silent Mutation |
TCA,TCG |
S504S |
NP_001308495.1 |
NM_001321567.1 |
2368 |
Intron |
|
|
NP_001308496.1 |
NM_001321568.1 |
2368 |
Intron |
|
|
NP_001308497.1 |
NM_001321569.1 |
2368 |
Silent Mutation |
TCA,TCG |
S524S |
NP_001308498.1 |
NM_001321570.1 |
2368 |
Intron |
|
|
NP_001308499.1 |
NM_001321571.1 |
2368 |
Silent Mutation |
TCA,TCG |
S524S |
NP_001308500.1 |
NM_001321572.1 |
2368 |
Intron |
|
|
NP_001308501.1 |
NM_001321573.1 |
2368 |
Silent Mutation |
TCA,TCG |
S515S |
NP_001308502.1 |
NM_001321574.1 |
2368 |
Silent Mutation |
TCA,TCG |
S489S |
NP_001308503.1 |
NM_001321575.1 |
2368 |
Intron |
|
|
NP_001308504.1 |
NM_001321576.1 |
2368 |
Intron |
|
|
NP_001308505.1 |
NM_001321577.1 |
2368 |
Intron |
|
|
NP_001308506.1 |
NM_001321578.1 |
2368 |
Intron |
|
|
NP_001308507.1 |
NM_001321579.1 |
2368 |
Intron |
|
|
NP_001308508.1 |
NM_001321580.1 |
2368 |
Silent Mutation |
TCA,TCG |
S510S |
NP_001308509.1 |
NM_001321581.1 |
2368 |
Intron |
|
|
NP_001308510.1 |
NM_001321582.1 |
2368 |
Intron |
|
|
NP_001308511.1 |
NM_001321583.1 |
2368 |
Intron |
|
|
NP_001308512.1 |
NM_001321584.1 |
2368 |
Intron |
|
|
NP_001308513.1 |
NM_001321585.1 |
2368 |
Intron |
|
|
NP_001308514.1 |
NM_001321586.1 |
2368 |
Intron |
|
|
NP_001308515.1 |
NM_001321587.1 |
2368 |
Intron |
|
|
NP_001308516.1 |
NM_001321588.1 |
2368 |
Silent Mutation |
TCA,TCG |
S503S |
NP_001308517.1 |
NM_001321589.1 |
2368 |
Intron |
|
|
NP_001308518.1 |
NM_001321590.1 |
2368 |
Intron |
|
|
NP_001308519.1 |
NM_001321591.1 |
2368 |
Intron |
|
|
NP_001308520.1 |
NM_001321592.1 |
2368 |
Intron |
|
|
NP_001308521.1 |
NM_172114.1 |
2368 |
Intron |
|
|
NP_742112.1 |
NM_172115.2 |
2368 |
Intron |
|
|
NP_742113.1 |
NM_172127.2 |
2368 |
Intron |
|
|
NP_742125.1 |
NM_172128.2 |
2368 |
Intron |
|
|
NP_742126.1 |
NM_172129.1 |
2368 |
Intron |
|
|
NP_742127.1 |
XM_005263253.3 |
2368 |
Silent Mutation |
TCA,TCG |
S523S |
XP_005263310.1 |
XM_005263254.3 |
2368 |
Silent Mutation |
TCA,TCG |
S523S |
XP_005263311.1 |
XM_006714330.2 |
2368 |
Intron |
|
|
XP_006714393.1 |
XM_011532289.1 |
2368 |
Silent Mutation |
TCA,TCG |
S501S |
XP_011530591.1 |
XM_011532290.1 |
2368 |
Silent Mutation |
TCA,TCG |
S500S |
XP_011530592.1 |
XM_011532291.1 |
2368 |
Intron |
|
|
XP_011530593.1 |
XM_011532292.2 |
2368 |
Silent Mutation |
TCA,TCG |
S395S |
XP_011530594.1 |
XM_011532295.1 |
2368 |
Silent Mutation |
TCA,TCG |
S501S |
XP_011530597.1 |
XM_017008672.1 |
2368 |
Silent Mutation |
TCA,TCG |
S504S |
XP_016864161.1 |
XM_017008673.1 |
2368 |
Silent Mutation |
TCA,TCG |
S503S |
XP_016864162.1 |
XM_017008674.1 |
2368 |
Intron |
|
|
XP_016864163.1 |
XM_017008675.1 |
2368 |
Silent Mutation |
TCA,TCG |
S485S |
XP_016864164.1 |
XM_017008676.1 |
2368 |
Silent Mutation |
TCA,TCG |
S485S |
XP_016864165.1 |
XM_017008677.1 |
2368 |
Intron |
|
|
XP_016864166.1 |
XM_017008678.1 |
2368 |
Intron |
|
|
XP_016864167.1 |
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