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TGCGCTTTGAGACACAATTGCGCAC[C/G]CTGTCGCTGTTTCCGGACACGCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176257 | ||||||||||||||||||||
Literature Links: |
KCNA6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
KCNA6 - potassium voltage-gated channel subfamily A member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002235.3 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | NP_002226.1 | |
XM_005253686.3 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | XP_005253743.1 | |
XM_011520955.2 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | XP_011519257.1 | |
XM_017019270.1 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | XP_016874759.1 | |
XM_017019271.1 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | XP_016874760.1 | |
XM_017019272.1 | 1040 | Silent Mutation | ACC,ACG | T,T 58 | XP_016874761.1 |