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TGACAGAGCCTAAGATGTCCCTGTC[A/G]AAGGCTGTGTCCCCAGAGATCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300680 | ||||||||||||||||||||
Literature Links: |
PNCK 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 |
PNCK - pregnancy up-regulated nonubiquitous CaM kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039582.3 | 876 | Silent Mutation | TTC,TTT | F,F 359 | NP_001034671.3 | |
NM_001135740.1 | 876 | Silent Mutation | TTC,TTT | F,F 293 | NP_001129212.1 | |
XM_005274651.2 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_005274708.1 | |
XM_006724809.3 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_006724872.1 | |
XM_011531107.2 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_011529409.2 | |
XM_011531108.2 | 876 | Silent Mutation | TTC,TTT | F,F 294 | XP_011529410.1 | |
XM_011531110.2 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_011529412.1 | |
XM_011531111.2 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_011529413.1 | |
XM_011531112.2 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_011529414.1 | |
XM_017029277.1 | 876 | Silent Mutation | TTC,TTT | F,F 359 | XP_016884766.1 | |
XM_017029278.1 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_016884767.1 | |
XM_017029279.1 | 876 | Silent Mutation | TTC,TTT | F,F 276 | XP_016884768.1 | |
XM_017029280.1 | 876 | Intron | XP_016884769.1 |