Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAAGAGGACCAAGCTGCTGGCACA[A/C]CAGCCGCTCCCGGTGCACCAGCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608427 MIM: 602544 | ||||||||||||||||||||
Literature Links: |
PACRG 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 |
PACRG - PARK2 coregulated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080378.1 | 227 | Silent Mutation | CAA,CAC | Q,H 26 | NP_001073847.1 | |
NM_001080379.1 | 227 | Silent Mutation | CAA,CAC | Q,H 26 | NP_001073848.1 | |
NM_152410.2 | 227 | Silent Mutation | CAA,CAC | Q,H 26 | NP_689623.2 | |
XM_005266825.4 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_005266882.1 | |
XM_005266826.4 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_005266883.1 | |
XM_006715344.3 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_006715407.1 | |
XM_006715345.3 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_006715408.1 | |
XM_011535461.2 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533763.1 | |
XM_011535462.2 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533764.1 | |
XM_011535466.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533768.1 | |
XM_011535468.2 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533770.1 | |
XM_011535469.2 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533771.1 | |
XM_011535471.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_011533773.1 | |
XM_017010275.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865764.1 | |
XM_017010276.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865765.1 | |
XM_017010277.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865766.1 | |
XM_017010278.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865767.1 | |
XM_017010279.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865768.1 | |
XM_017010280.1 | 227 | Missense Mutation | CAA,CAC | Q,H 26 | XP_016865769.1 | |
XM_017010281.1 | 227 | Intron | XP_016865770.1 | |||
XM_017010282.1 | 227 | Intron | XP_016865771.1 |
PARK2 - parkin RBR E3 ubiquitin protein ligase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004562.2 | 227 | Intron | NP_004553.2 | |||
NM_013987.2 | 227 | Intron | NP_054642.2 | |||
NM_013988.2 | 227 | Intron | NP_054643.2 | |||
XM_011535863.1 | 227 | Intron | XP_011534165.1 | |||
XM_017010908.1 | 227 | Intron | XP_016866397.1 | |||
XM_017010909.1 | 227 | Intron | XP_016866398.1 |