Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCATCAAGCACACAGTTAAAACA[C/G]AGGAATGCAGTTCAGGGAAGCAAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PACRGL 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 |
PACRGL - PARK2 coregulated like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130727.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | NP_001124199.1 | |
NM_001258345.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | NP_001245274.1 | |
NM_001258346.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | NP_001245275.1 | |
NM_001317849.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | NP_001304778.1 | |
NM_145048.3 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | NP_659485.1 | |
XM_011513780.1 | 317 | Missense Mutation | CAC,CAG | H,Q 80 | XP_011512082.1 | |
XM_011513781.1 | 317 | Missense Mutation | CAC,CAG | H,Q 80 | XP_011512083.1 | |
XM_011513784.1 | 317 | Missense Mutation | CAC,CAG | H,Q 80 | XP_011512086.1 | |
XM_011513785.1 | 317 | Missense Mutation | CAC,CAG | H,Q 53 | XP_011512087.1 | |
XM_011513786.2 | 317 | Missense Mutation | CAC,CAG | H,Q 80 | XP_011512088.1 | |
XM_011513787.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512089.1 | |
XM_011513788.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512090.1 | |
XM_011513791.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512093.1 | |
XM_011513792.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512094.1 | |
XM_011513794.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512096.1 | |
XM_011513795.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512097.1 | |
XM_011513796.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512098.1 | |
XM_011513797.2 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512099.1 | |
XM_011513798.2 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512100.1 | |
XM_011513804.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512106.1 | |
XM_011513805.2 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_011512107.1 | |
XM_017007747.1 | 317 | Missense Mutation | CAC,CAG | H,Q 80 | XP_016863236.1 | |
XM_017007748.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863237.1 | |
XM_017007749.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863238.1 | |
XM_017007750.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863239.1 | |
XM_017007751.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863240.1 | |
XM_017007752.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863241.1 | |
XM_017007753.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863242.1 | |
XM_017007754.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863243.1 | |
XM_017007755.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863244.1 | |
XM_017007756.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863245.1 | |
XM_017007757.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863246.1 | |
XM_017007758.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863247.1 | |
XM_017007759.1 | 317 | Missense Mutation | CAC,CAG | H,Q 32 | XP_016863248.1 |