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AGGAGGAACCTGCTTCCCAGATGCA[C/T]GTTAAGGACCCAGGTCCTCCAAGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609526 MIM: 600477 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCTD19 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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KCTD19 - potassium channel tetramerization domain containing 19 | ||||||
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There are no transcripts associated with this gene. |
PLEKHG4 - pleckstrin homology and RhoGEF domain containing G4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001129727.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | NP_001123199.1 | |
NM_001129728.1 | 471 | Silent Mutation | CAC,CAT | H,H 42 | NP_001123200.1 | |
NM_001129729.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | NP_001123201.1 | |
NM_001129731.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | NP_001123203.1 | |
XM_011522985.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | XP_011521287.1 | |
XM_011522986.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | XP_011521288.1 | |
XM_011522987.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | XP_011521289.1 | |
XM_011522988.2 | 471 | Silent Mutation | CAC,CAT | H,H 42 | XP_011521290.1 |
SLC9A5 - solute carrier family 9 member A5 | ||||||
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There are no transcripts associated with this gene. |