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CATCCTTCTTGCCCTCCTCGAAGCC[A/G]GCGCACAGCATGTCATTCTTGATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611285 MIM: 608018 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCTD5 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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KCTD5 - potassium channel tetramerization domain containing 5 | ||||||
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There are no transcripts associated with this gene. |
PRSS27 - protease, serine 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318395.1 | 765 | Silent Mutation | GCC,GCT | A,A 113 | NP_001305324.1 | |
NM_031948.4 | 765 | Silent Mutation | GCC,GCT | A,A 215 | NP_114154.1 | |
XM_011522689.2 | 765 | Silent Mutation | GCC,GCT | A,A 113 | XP_011520991.1 |