Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609559 MIM: 609557 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAMKMT PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
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Global
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Caucasian
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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CAMKMT - calmodulin-lysine N-methyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024766.4 | 89 | Intron | NP_079042.1 | |||
XM_011533111.2 | 89 | Intron | XP_011531413.1 | |||
XM_011533113.2 | 89 | Intron | XP_011531415.1 | |||
XM_017004970.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860459.1 | |
XM_017004971.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860460.1 | |
XM_017004972.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860461.1 | |
XM_017004973.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860462.1 | |
XM_017004974.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860463.1 | |
XM_017004975.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860464.1 | |
XM_017004976.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860465.1 | |
XM_017004977.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860466.1 | |
XM_017004978.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860467.1 | |
XM_017004979.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860468.1 | |
XM_017004980.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860469.1 | |
XM_017004981.1 | 89 | Missense Mutation | AAA,AGA | K,R 27 | XP_016860470.1 | |
XM_017004982.1 | 89 | Intron | XP_016860471.1 | |||
XM_017004983.1 | 89 | Intron | XP_016860472.1 |
PREPL - prolyl endopeptidase-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042385.2 | 89 | Intron | NP_001035844.1 | |||
NM_001042386.2 | 89 | Intron | NP_001035845.1 | |||
NM_001171603.1 | 89 | UTR 5 | NP_001165074.1 | |||
NM_001171606.1 | 89 | Intron | NP_001165077.1 | |||
NM_001171613.1 | 89 | Intron | NP_001165084.1 | |||
NM_001171617.1 | 89 | UTR 5 | NP_001165088.1 | |||
NM_006036.4 | 89 | Intron | NP_006027.2 | |||
XM_011533198.1 | 89 | UTR 5 | XP_011531500.1 | |||
XM_011533200.1 | 89 | Intron | XP_011531502.1 | |||
XM_011533202.1 | 89 | Intron | XP_011531504.1 | |||
XM_017005384.1 | 89 | Intron | XP_016860873.1 | |||
XM_017005385.1 | 89 | Intron | XP_016860874.1 |
Set Membership: |
HapMap Validated |