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ACACTCTACTGGGCAGTTCTGAGAG[A/G]GACTTTTTCTACCACCCAGAAACTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605410 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCND2 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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KCND2 - potassium voltage-gated channel subfamily D member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012281.2 | 1181 | Silent Mutation | AGA,AGG | R,R 72 | NP_036413.1 | |
XM_011516165.2 | 1181 | Silent Mutation | AGA,AGG | R,R 72 | XP_011514467.1 |