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CACGCGCAGCAGGTTGGCTACACGT[A/T]TGGCCATGTCTAGAGAGAAAAACTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606372 MIM: 601021 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHRNA10 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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CHRNA10 - cholinergic receptor nicotinic alpha 10 subunit | ||||||
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There are no transcripts associated with this gene. |
NUP98 - nucleoporin 98 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005387.6 | 5394 | Intron | NP_005378.4 | |||
NM_016320.4 | 5394 | Missense Mutation | AAA,ATA | K,I 1732 | NP_057404.2 | |
NM_139131.4 | 5394 | Intron | NP_624357.1 | |||
NM_139132.3 | 5394 | Missense Mutation | AAA,ATA | K,I 1658 | NP_624358.2 |