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Search Thermo Fisher Scientific
CCGGCGGCGGCGGCGCCAGGACATG[A/G]AGCTCGAGAACATCGTGGCCAACTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137026 MIM: 611526 | ||||||||||||||||||||
Literature Links: |
GRK4 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 |
GRK4 - G protein-coupled receptor kinase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004056.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | NP_001004056.1 | |
NM_001004057.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | NP_001004057.1 | |
NM_005307.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | NP_005298.2 | |
NM_182982.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | NP_892027.2 | |
XM_005247962.3 | 106 | UTR 5 | XP_005248019.1 | |||
XM_006713880.3 | 106 | UTR 5 | XP_006713943.1 | |||
XM_011513447.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511749.1 | |
XM_011513448.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511750.1 | |
XM_011513449.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511751.1 | |
XM_011513450.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511752.1 | |
XM_011513451.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511753.1 | |
XM_011513452.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511754.1 | |
XM_011513453.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511755.1 | |
XM_011513454.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511756.1 | |
XM_011513455.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511757.1 | |
XM_011513456.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511758.1 | |
XM_011513457.2 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_011511759.1 | |
XM_017008052.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863541.1 | |
XM_017008053.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863542.1 | |
XM_017008054.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863543.1 | |
XM_017008055.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863544.1 | |
XM_017008056.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863545.1 | |
XM_017008057.1 | 106 | Intron | XP_016863546.1 | |||
XM_017008058.1 | 106 | UTR 5 | XP_016863547.1 | |||
XM_017008059.1 | 106 | UTR 5 | XP_016863548.1 | |||
XM_017008060.1 | 106 | UTR 5 | XP_016863549.1 | |||
XM_017008061.1 | 106 | Intron | XP_016863550.1 | |||
XM_017008062.1 | 106 | UTR 5 | XP_016863551.1 | |||
XM_017008063.1 | 106 | Intron | XP_016863552.1 | |||
XM_017008064.1 | 106 | UTR 5 | XP_016863553.1 | |||
XM_017008065.1 | 106 | Missense Mutation | AAG,GAG | K,E 2 | XP_016863554.1 | |
XM_017008066.1 | 106 | UTR 5 | XP_016863555.1 |
NOP14 - NOP14 nucleolar protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291978.1 | 106 | Intron | NP_001278907.1 | |||
NM_001291979.1 | 106 | Intron | NP_001278908.1 | |||
NM_003703.2 | 106 | Intron | NP_003694.1 |