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CAGCCCCAGGGACCTGCCCTGCTCC[A/G]CGTGGGCTCTCAGAAGCCCAGCAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
40 submissions
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Phenotype: |
MIM: 614612 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KANK4 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KANK4 - KN motif and ankyrin repeat domains 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320269.1 | 1591 | Missense Mutation | GCG,GTG | A,V 359 | NP_001307198.1 | |
NM_181712.4 | 1591 | Missense Mutation | GCG,GTG | A,V 987 | NP_859063.3 | |
XM_011540843.2 | 1591 | Missense Mutation | GCG,GTG | A,V 987 | XP_011539145.1 | |
XM_011540845.2 | 1591 | Missense Mutation | GCG,GTG | A,V 963 | XP_011539147.1 | |
XM_017000483.1 | 1591 | Missense Mutation | GCG,GTG | A,V 920 | XP_016855972.1 | |
XM_017000484.1 | 1591 | Missense Mutation | GCG,GTG | A,V 359 | XP_016855973.1 | |
XM_017000485.1 | 1591 | Missense Mutation | GCG,GTG | A,V 343 | XP_016855974.1 |