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Search Thermo Fisher Scientific
CACACAGTTAAAACACAGGAATGCA[A/G]TTCAGGGAAGCAAATCCTCATTGTC
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 | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
PACRGL - PARK2 coregulated like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130727.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | NP_001124199.1 | |
NM_001258345.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | NP_001245274.1 | |
NM_001258346.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | NP_001245275.1 | |
NM_001317849.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | NP_001304778.1 | |
NM_145048.3 | 327 | Missense Mutation | ATT,GTT | I,V 36 | NP_659485.1 | |
XM_011513780.1 | 327 | Missense Mutation | ATT,GTT | I,V 84 | XP_011512082.1 | |
XM_011513781.1 | 327 | Missense Mutation | ATT,GTT | I,V 84 | XP_011512083.1 | |
XM_011513784.1 | 327 | Missense Mutation | ATT,GTT | I,V 84 | XP_011512086.1 | |
XM_011513785.1 | 327 | Missense Mutation | ATT,GTT | I,V 57 | XP_011512087.1 | |
XM_011513786.2 | 327 | Missense Mutation | ATT,GTT | I,V 84 | XP_011512088.1 | |
XM_011513787.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512089.1 | |
XM_011513788.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512090.1 | |
XM_011513791.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512093.1 | |
XM_011513792.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512094.1 | |
XM_011513794.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512096.1 | |
XM_011513795.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512097.1 | |
XM_011513796.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512098.1 | |
XM_011513797.2 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512099.1 | |
XM_011513798.2 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512100.1 | |
XM_011513804.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512106.1 | |
XM_011513805.2 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_011512107.1 | |
XM_017007747.1 | 327 | Missense Mutation | ATT,GTT | I,V 84 | XP_016863236.1 | |
XM_017007748.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863237.1 | |
XM_017007749.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863238.1 | |
XM_017007750.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863239.1 | |
XM_017007751.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863240.1 | |
XM_017007752.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863241.1 | |
XM_017007753.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863242.1 | |
XM_017007754.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863243.1 | |
XM_017007755.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863244.1 | |
XM_017007756.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863245.1 | |
XM_017007757.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863246.1 | |
XM_017007758.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863247.1 | |
XM_017007759.1 | 327 | Missense Mutation | ATT,GTT | I,V 36 | XP_016863248.1 |