Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACAGCTCCTCTGCCTCTGTCTTC[A/C]CACTCTGGATCCGGGCACCCTGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
MIM: 614994 MIM: 150310 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAMK1G 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CAMK1G - calcium/calmodulin dependent protein kinase IG | ||||||
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There are no transcripts associated with this gene. |
LAMB3 - laminin subunit beta 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000228.2 | 3467 | Missense Mutation | GGG,GTG | G,V 1108 | NP_000219.2 | |
NM_001017402.1 | 3467 | Missense Mutation | GGG,GTG | G,V 1108 | NP_001017402.1 | |
NM_001127641.1 | 3467 | Missense Mutation | GGG,GTG | G,V 1108 | NP_001121113.1 | |
XM_005273124.4 | 3467 | Missense Mutation | GGG,GTG | G,V 1108 | XP_005273181.1 | |
XM_017001272.1 | 3467 | Missense Mutation | GGG,GTG | G,V 1044 | XP_016856761.1 |
MIR4260 - microRNA 4260 | ||||||
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There are no transcripts associated with this gene. |