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Search Thermo Fisher Scientific
GCCGCCCCTGGGGAACAGGCCGTCG[C/T]GGGCCCTGCCCCCTCGACTGTCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605232 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
WNK1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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WNK1 - WNK lysine deficient protein kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184985.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | NP_001171914.1 | |
NM_014823.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | NP_055638.2 | |
NM_018979.3 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | NP_061852.3 | |
NM_213655.4 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | NP_998820.3 | |
XM_006719003.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_006719066.1 | |
XM_011520997.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519299.1 | |
XM_011520998.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519300.1 | |
XM_011520999.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519301.1 | |
XM_011521000.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519302.1 | |
XM_011521001.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519303.1 | |
XM_011521002.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519304.1 | |
XM_011521003.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519305.1 | |
XM_011521004.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519306.1 | |
XM_011521005.2 | 1414 | Intron | XP_011519307.1 | |||
XM_011521006.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519308.1 | |
XM_011521007.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519309.1 | |
XM_011521008.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519310.1 | |
XM_011521009.2 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_011519311.1 | |
XM_017019834.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875323.1 | |
XM_017019835.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875324.1 | |
XM_017019836.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875325.1 | |
XM_017019837.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875326.1 | |
XM_017019838.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875327.1 | |
XM_017019839.1 | 1414 | Missense Mutation | GCG,GTG | A,V 149 | XP_016875328.1 |
Set Membership: |
HapMap |