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CTGCTCCTTCTTGAGCTCCAGGTAG[C/G]AGTGGGAGAAGGTGTGGAAGATAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607603 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNG4 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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KCNG4 - potassium voltage-gated channel modifier subfamily G member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_172347.2 | 1500 | Missense Mutation | TCC,TGC | S,C 460 | NP_758857.1 |