Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGCGGGTCTCCTCAGACTGGCTGG[G/T]GCGGGGCCGGCCCTGCCCGTCAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607707 MIM: 606209 | ||||||||||||||||||||
Literature Links: |
CAMK2B 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 |
CAMK2B - calcium/calmodulin dependent protein kinase II beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220.4 | 2115 | Missense Mutation | ACC,CCC | T,P 634 | NP_001211.3 | |
NM_001293170.1 | 2115 | Missense Mutation | ACC,CCC | T,P 510 | NP_001280099.1 | |
NM_172078.2 | 2115 | Missense Mutation | ACC,CCC | T,P 510 | NP_742075.1 | |
NM_172079.2 | 2115 | Missense Mutation | ACC,CCC | T,P 486 | NP_742076.1 | |
NM_172080.2 | 2115 | Missense Mutation | ACC,CCC | T,P 485 | NP_742077.1 | |
NM_172081.2 | 2115 | Missense Mutation | ACC,CCC | T,P 471 | NP_742078.1 | |
NM_172082.2 | 2115 | Missense Mutation | ACC,CCC | T,P 460 | NP_742079.1 | |
NM_172083.2 | 2115 | Missense Mutation | ACC,CCC | T,P 447 | NP_742080.1 | |
NM_172084.2 | 2115 | Missense Mutation | ACC,CCC | T,P 417 | NP_742081.1 | |
XM_005249862.3 | 2115 | Missense Mutation | ACC,CCC | T,P 495 | XP_005249919.1 | |
XM_005249864.3 | 2115 | Missense Mutation | ACC,CCC | T,P 462 | XP_005249921.1 | |
XM_006715781.2 | 2115 | Missense Mutation | ACC,CCC | T,P 594 | XP_006715844.1 | |
XM_006715784.2 | 2115 | Missense Mutation | ACC,CCC | T,P 486 | XP_006715847.1 | |
XM_011515547.1 | 2115 | Missense Mutation | ACC,CCC | T,P 677 | XP_011513849.1 | |
XM_011515549.1 | 2115 | Missense Mutation | ACC,CCC | T,P 662 | XP_011513851.1 | |
XM_011515550.1 | 2115 | Missense Mutation | ACC,CCC | T,P 653 | XP_011513852.1 | |
XM_011515551.1 | 2115 | Missense Mutation | ACC,CCC | T,P 653 | XP_011513853.1 | |
XM_011515552.1 | 2115 | Missense Mutation | ACC,CCC | T,P 652 | XP_011513854.1 | |
XM_011515553.1 | 2115 | Missense Mutation | ACC,CCC | T,P 639 | XP_011513855.1 | |
XM_011515554.1 | 2115 | Missense Mutation | ACC,CCC | T,P 637 | XP_011513856.1 | |
XM_011515555.1 | 2115 | Missense Mutation | ACC,CCC | T,P 634 | XP_011513857.1 | |
XM_011515556.1 | 2115 | Missense Mutation | ACC,CCC | T,P 629 | XP_011513858.1 | |
XM_011515557.1 | 2115 | Missense Mutation | ACC,CCC | T,P 628 | XP_011513859.1 | |
XM_011515558.2 | 2115 | Intron | XP_011513860.1 | |||
XM_011515559.1 | 2115 | Missense Mutation | ACC,CCC | T,P 548 | XP_011513861.1 | |
XM_017012660.1 | 2115 | Missense Mutation | ACC,CCC | T,P 638 | XP_016868149.1 | |
XM_017012661.1 | 2115 | Missense Mutation | ACC,CCC | T,P 624 | XP_016868150.1 | |
XM_017012662.1 | 2115 | Missense Mutation | ACC,CCC | T,P 571 | XP_016868151.1 | |
XM_017012663.1 | 2115 | Missense Mutation | ACC,CCC | T,P 524 | XP_016868152.1 | |
XM_017012664.1 | 2115 | Missense Mutation | ACC,CCC | T,P 470 | XP_016868153.1 | |
XM_017012665.1 | 2115 | Missense Mutation | ACC,CCC | T,P 461 | XP_016868154.1 | |
XM_017012666.1 | 2115 | Missense Mutation | ACC,CCC | T,P 381 | XP_016868155.1 | |
XM_017012667.1 | 2115 | Missense Mutation | ACC,CCC | T,P 366 | XP_016868156.1 | |
XM_017012668.1 | 2115 | Missense Mutation | ACC,CCC | T,P 357 | XP_016868157.1 | |
XM_017012669.1 | 2115 | Missense Mutation | ACC,CCC | T,P 357 | XP_016868158.1 | |
XM_017012670.1 | 2115 | Missense Mutation | ACC,CCC | T,P 342 | XP_016868159.1 |
YKT6 - YKT6 v-SNARE homolog (S. cerevisiae) | ||||||
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There are no transcripts associated with this gene. |