Product Details
- SNP ID
-
rs199634557
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:73815116 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCCGGGTCTCTTCTGACTGGCTGG[G/T]GCGAGGCCGACCCTGCCCGTCGATG
- Phenotype
-
MIM: 602123
MIM: 603268
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CAMK2G
PubMed Links
Gene Details
- Gene
- CAMK2G
- Gene Name
- calcium/calmodulin dependent protein kinase II gamma
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001204492.1 |
1610 |
Missense Mutation |
ACC,CCC |
T507P |
NP_001191421.1 |
NM_001222.3 |
1610 |
Missense Mutation |
ACC,CCC |
T463P |
NP_001213.2 |
NM_001320898.1 |
1610 |
Intron |
|
|
NP_001307827.1 |
NM_172169.2 |
1610 |
Missense Mutation |
ACC,CCC |
T495P |
NP_751909.1 |
NM_172170.4 |
1610 |
Missense Mutation |
ACC,CCC |
T486P |
NP_751910.1 |
NM_172171.2 |
1610 |
Missense Mutation |
ACC,CCC |
T524P |
NP_751911.1 |
NM_172173.2 |
1610 |
Missense Mutation |
ACC,CCC |
T472P |
NP_751913.1 |
XM_005270195.1 |
1610 |
Missense Mutation |
ACC,CCC |
T545P |
XP_005270252.1 |
XM_005270197.1 |
1610 |
Missense Mutation |
ACC,CCC |
T533P |
XP_005270254.1 |
XM_005270198.1 |
1610 |
Missense Mutation |
ACC,CCC |
T531P |
XP_005270255.1 |
XM_005270199.1 |
1610 |
Missense Mutation |
ACC,CCC |
T522P |
XP_005270256.1 |
XM_005270200.1 |
1610 |
Missense Mutation |
ACC,CCC |
T512P |
XP_005270257.1 |
XM_005270201.1 |
1610 |
Missense Mutation |
ACC,CCC |
T510P |
XP_005270258.1 |
XM_005270203.1 |
1610 |
Missense Mutation |
ACC,CCC |
T497P |
XP_005270260.1 |
XM_005270205.1 |
1610 |
Missense Mutation |
ACC,CCC |
T484P |
XP_005270262.1 |
XM_006717993.1 |
1610 |
Missense Mutation |
ACC,CCC |
T556P |
XP_006718056.1 |
XM_006717996.1 |
1610 |
Missense Mutation |
ACC,CCC |
T535P |
XP_006718059.1 |
XM_006717997.1 |
1610 |
Missense Mutation |
ACC,CCC |
T518P |
XP_006718060.1 |
XM_006717998.1 |
1610 |
Missense Mutation |
ACC,CCC |
T504P |
XP_006718061.1 |
XM_011540225.2 |
1610 |
Intron |
|
|
XP_011538527.1 |
XM_017016716.1 |
1610 |
Intron |
|
|
XP_016872205.1 |
XM_017016717.1 |
1610 |
Intron |
|
|
XP_016872206.1 |
XM_017016718.1 |
1610 |
Intron |
|
|
XP_016872207.1 |
XM_017016719.1 |
1610 |
Intron |
|
|
XP_016872208.1 |
XM_017016720.1 |
1610 |
Intron |
|
|
XP_016872209.1 |
XM_017016721.1 |
1610 |
Intron |
|
|
XP_016872210.1 |
XM_017016722.1 |
1610 |
Intron |
|
|
XP_016872211.1 |
XM_017016723.1 |
1610 |
Intron |
|
|
XP_016872212.1 |
XM_017016724.1 |
1610 |
Intron |
|
|
XP_016872213.1 |
XM_017016725.1 |
1610 |
Intron |
|
|
XP_016872214.1 |
XM_017016726.1 |
1610 |
Intron |
|
|
XP_016872215.1 |
XM_017016727.1 |
1610 |
Intron |
|
|
XP_016872216.1 |
XM_017016728.1 |
1610 |
Missense Mutation |
ACC,CCC |
T516P |
XP_016872217.1 |
XM_017016729.1 |
1610 |
Intron |
|
|
XP_016872218.1 |
XM_017016730.1 |
1610 |
Missense Mutation |
ACC,CCC |
T483P |
XP_016872219.1 |
XM_017016731.1 |
1610 |
Intron |
|
|
XP_016872220.1 |
XM_017016732.1 |
1610 |
Intron |
|
|
XP_016872221.1 |
XM_017016733.1 |
1610 |
Missense Mutation |
ACC,CCC |
T478P |
XP_016872222.1 |
XM_017016734.1 |
1610 |
Intron |
|
|
XP_016872223.1 |
XM_017016735.1 |
1610 |
Missense Mutation |
ACC,CCC |
T474P |
XP_016872224.1 |
XM_017016736.1 |
1610 |
Missense Mutation |
ACC,CCC |
T474P |
XP_016872225.1 |
XM_017016737.1 |
1610 |
Intron |
|
|
XP_016872226.1 |
XM_017016738.1 |
1610 |
Intron |
|
|
XP_016872227.1 |
XM_017016739.1 |
1610 |
Intron |
|
|
XP_016872228.1 |
- Gene
- NDST2
- Gene Name
- N-deacetylase and N-sulfotransferase 2
There are no transcripts associated with this gene.
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