Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTTGCAAAGGTGATGGAAGGCTCC[C/G]TGCTTTCAGTCCCTCCCAATTAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601591 | ||||||||||||||||||||
Literature Links: |
PRKG2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
PRKG2 - protein kinase, cGMP-dependent, type II | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282480.1 | 2713 | Missense Mutation | CGG,GGG | R,G 302 | NP_001269409.1 | |
NM_001282481.1 | 2713 | Missense Mutation | CGG,GGG | R,G 302 | NP_001269410.1 | |
NM_001282482.1 | 2713 | Missense Mutation | CGG,GGG | R,G 273 | NP_001269411.1 | |
NM_001282483.1 | 2713 | Missense Mutation | CGG,GGG | R,G 242 | NP_001269412.1 | |
NM_001282485.1 | 2713 | Missense Mutation | CGG,GGG | R,G 693 | NP_001269414.1 | |
NM_006259.2 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | NP_006250.1 | |
XM_005263126.3 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | XP_005263183.1 | |
XM_017008413.1 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | XP_016863902.1 | |
XM_017008414.1 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | XP_016863903.1 | |
XM_017008415.1 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | XP_016863904.1 | |
XM_017008416.1 | 2713 | Missense Mutation | CGG,GGG | R,G 722 | XP_016863905.1 | |
XM_017008417.1 | 2713 | Missense Mutation | CGG,GGG | R,G 693 | XP_016863906.1 | |
XM_017008418.1 | 2713 | Intron | XP_016863907.1 |