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GACATTGAGCCACTTGCCATCCCGA[C/T]GGTGCCAGACCCGGGTCTCTTCTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602123 MIM: 603268 | ||||||||||||||||||||
Literature Links: |
CAMK2G 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 |
CAMK2G - calcium/calmodulin dependent protein kinase II gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204492.1 | 1644 | Missense Mutation | CAT,CGT | H,R 518 | NP_001191421.1 | |
NM_001222.3 | 1644 | Missense Mutation | CAT,CGT | H,R 474 | NP_001213.2 | |
NM_001320898.1 | 1644 | Intron | NP_001307827.1 | |||
NM_172169.2 | 1644 | Missense Mutation | CAT,CGT | H,R 506 | NP_751909.1 | |
NM_172170.4 | 1644 | Missense Mutation | CAT,CGT | H,R 497 | NP_751910.1 | |
NM_172171.2 | 1644 | Missense Mutation | CAT,CGT | H,R 535 | NP_751911.1 | |
NM_172173.2 | 1644 | Missense Mutation | CAT,CGT | H,R 483 | NP_751913.1 | |
XM_005270195.1 | 1644 | Missense Mutation | CAT,CGT | H,R 556 | XP_005270252.1 | |
XM_005270197.1 | 1644 | Missense Mutation | CAT,CGT | H,R 544 | XP_005270254.1 | |
XM_005270198.1 | 1644 | Missense Mutation | CAT,CGT | H,R 542 | XP_005270255.1 | |
XM_005270199.1 | 1644 | Missense Mutation | CAT,CGT | H,R 533 | XP_005270256.1 | |
XM_005270200.1 | 1644 | Missense Mutation | CAT,CGT | H,R 523 | XP_005270257.1 | |
XM_005270201.1 | 1644 | Missense Mutation | CAT,CGT | H,R 521 | XP_005270258.1 | |
XM_005270203.1 | 1644 | Missense Mutation | CAT,CGT | H,R 508 | XP_005270260.1 | |
XM_005270205.1 | 1644 | Missense Mutation | CAT,CGT | H,R 495 | XP_005270262.1 | |
XM_006717993.1 | 1644 | Missense Mutation | CAT,CGT | H,R 567 | XP_006718056.1 | |
XM_006717996.1 | 1644 | Missense Mutation | CAT,CGT | H,R 546 | XP_006718059.1 | |
XM_006717997.1 | 1644 | Missense Mutation | CAT,CGT | H,R 529 | XP_006718060.1 | |
XM_006717998.1 | 1644 | Missense Mutation | CAT,CGT | H,R 515 | XP_006718061.1 | |
XM_011540225.2 | 1644 | Intron | XP_011538527.1 | |||
XM_017016716.1 | 1644 | Intron | XP_016872205.1 | |||
XM_017016717.1 | 1644 | Intron | XP_016872206.1 | |||
XM_017016718.1 | 1644 | Intron | XP_016872207.1 | |||
XM_017016719.1 | 1644 | Intron | XP_016872208.1 | |||
XM_017016720.1 | 1644 | Intron | XP_016872209.1 | |||
XM_017016721.1 | 1644 | Intron | XP_016872210.1 | |||
XM_017016722.1 | 1644 | Intron | XP_016872211.1 | |||
XM_017016723.1 | 1644 | Intron | XP_016872212.1 | |||
XM_017016724.1 | 1644 | Intron | XP_016872213.1 | |||
XM_017016725.1 | 1644 | Intron | XP_016872214.1 | |||
XM_017016726.1 | 1644 | Intron | XP_016872215.1 | |||
XM_017016727.1 | 1644 | Intron | XP_016872216.1 | |||
XM_017016728.1 | 1644 | Missense Mutation | CAT,CGT | H,R 527 | XP_016872217.1 | |
XM_017016729.1 | 1644 | Intron | XP_016872218.1 | |||
XM_017016730.1 | 1644 | Missense Mutation | CAT,CGT | H,R 494 | XP_016872219.1 | |
XM_017016731.1 | 1644 | Intron | XP_016872220.1 | |||
XM_017016732.1 | 1644 | Intron | XP_016872221.1 | |||
XM_017016733.1 | 1644 | Missense Mutation | CAT,CGT | H,R 489 | XP_016872222.1 | |
XM_017016734.1 | 1644 | Intron | XP_016872223.1 | |||
XM_017016735.1 | 1644 | Missense Mutation | CAT,CGT | H,R 485 | XP_016872224.1 | |
XM_017016736.1 | 1644 | Missense Mutation | CAT,CGT | H,R 485 | XP_016872225.1 | |
XM_017016737.1 | 1644 | Intron | XP_016872226.1 | |||
XM_017016738.1 | 1644 | Intron | XP_016872227.1 | |||
XM_017016739.1 | 1644 | Intron | XP_016872228.1 |
NDST2 - N-deacetylase and N-sulfotransferase 2 | ||||||
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There are no transcripts associated with this gene. |