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ATCCAGAGAGATTTGATCTGCAACT[C/T]TGACTGGAACCAAGTTAAATAAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600580 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLCN3 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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CLCN3 - chloride voltage-gated channel 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243372.1 | Intron | NP_001230301.1 | ||||
NM_001243374.1 | Intron | NP_001230303.1 | ||||
NM_001829.3 | Intron | NP_001820.2 | ||||
NM_173872.3 | Intron | NP_776297.2 | ||||
XM_005262726.2 | Intron | XP_005262783.1 | ||||
XM_011531586.2 | Intron | XP_011529888.1 |