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TAAAACTGTTCTCTTTTTTACAGAT[A/C]TTTATTGATAGAGATCCAGCAGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 613272 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCTD3 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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KCTD3 - potassium channel tetramerization domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319294.1 | 687 | Silent Mutation | ATA,ATC | I,I 62 | NP_001306223.1 | |
NM_001319295.1 | 687 | UTR 5 | NP_001306224.1 | |||
NM_016121.4 | 687 | Silent Mutation | ATA,ATC | I,I 62 | NP_057205.2 | |
XM_005273158.1 | 687 | UTR 5 | XP_005273215.1 |