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See other CAMK2G GT Assays ›
SNP ID:
rs199634557
Gene
CAMK2G NDST2
Gene Name
Set Membership:
-
Chromosome Location:
Chr.10: 73815116 - 73815116 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

ACCCGGGTCTCTTCTGACTGGCTGG[G/T]GCGAGGCCGACCCTGCCCGTCGATG

Assay ID C_189590929_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 602123 MIM: 603268

Literature Links:

 CAMK2G PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
CAMK2G - calcium/calmodulin dependent protein kinase II gamma
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001204492.1 1610 Missense Mutation ACC,CCC T,P 507 NP_001191421.1
NM_001222.3 1610 Missense Mutation ACC,CCC T,P 463 NP_001213.2
NM_001320898.1 1610 Intron NP_001307827.1
NM_172169.2 1610 Missense Mutation ACC,CCC T,P 495 NP_751909.1
NM_172170.4 1610 Missense Mutation ACC,CCC T,P 486 NP_751910.1
NM_172171.2 1610 Missense Mutation ACC,CCC T,P 524 NP_751911.1
NM_172173.2 1610 Missense Mutation ACC,CCC T,P 472 NP_751913.1
XM_005270195.1 1610 Missense Mutation ACC,CCC T,P 545 XP_005270252.1
XM_005270197.1 1610 Missense Mutation ACC,CCC T,P 533 XP_005270254.1
XM_005270198.1 1610 Missense Mutation ACC,CCC T,P 531 XP_005270255.1
XM_005270199.1 1610 Missense Mutation ACC,CCC T,P 522 XP_005270256.1
XM_005270200.1 1610 Missense Mutation ACC,CCC T,P 512 XP_005270257.1
XM_005270201.1 1610 Missense Mutation ACC,CCC T,P 510 XP_005270258.1
XM_005270203.1 1610 Missense Mutation ACC,CCC T,P 497 XP_005270260.1
XM_005270205.1 1610 Missense Mutation ACC,CCC T,P 484 XP_005270262.1
XM_006717993.1 1610 Missense Mutation ACC,CCC T,P 556 XP_006718056.1
XM_006717996.1 1610 Missense Mutation ACC,CCC T,P 535 XP_006718059.1
XM_006717997.1 1610 Missense Mutation ACC,CCC T,P 518 XP_006718060.1
XM_006717998.1 1610 Missense Mutation ACC,CCC T,P 504 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 T,P 516 XP_016872217.1
XM_017016729.1 1610 Intron XP_016872218.1
XM_017016730.1 1610 Missense Mutation ACC,CCC T,P 483 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 T,P 478 XP_016872222.1
XM_017016734.1 1610 Intron XP_016872223.1
XM_017016735.1 1610 Missense Mutation ACC,CCC T,P 474 XP_016872224.1
XM_017016736.1 1610 Missense Mutation ACC,CCC T,P 474 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
NDST2 - N-deacetylase and N-sulfotransferase 2
There are no transcripts associated with this gene.

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