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TCTGCAACCGTTTCCTTAAGAAATC[G/T]GAACCTCCAGGCTTTTGTCCCAGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605487 | ||||||||||||||||||||
Literature Links: |
ARPP19 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 |
ARPP19 - cAMP regulated phosphoprotein 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306191.1 | 436 | Silent Mutation | TCA,TCC | S,S 65 | NP_001293120.1 | |
NM_001306195.1 | 436 | Intron | NP_001293124.1 | |||
NM_001306196.1 | 436 | Silent Mutation | TCA,TCC | S,S 65 | NP_001293125.1 | |
NM_006628.5 | 436 | Silent Mutation | TCA,TCC | S,S 46 | NP_006619.1 | |
XM_017021868.1 | 436 | Intron | XP_016877357.1 | |||
XM_017021869.1 | 436 | Silent Mutation | TCA,TCC | S,S 46 | XP_016877358.1 | |
XM_017021870.1 | 436 | Intron | XP_016877359.1 | |||
XM_017021871.1 | 436 | Silent Mutation | TCA,TCC | S,S 30 | XP_016877360.1 |