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GCAACCTCAACGAGTTCCGCTTTAG[C/T]CAAGTCTCCAAGAATGACCTGTATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602866 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASIC1 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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ASIC1 - acid sensing ion channel subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001095.3 | 382 | Silent Mutation | AGC,AGT | S,S 101 | NP_001086.2 | |
NM_001256830.1 | 382 | Intron | NP_001243759.1 | |||
NM_020039.3 | 382 | Silent Mutation | AGC,AGT | S,S 101 | NP_064423.2 | |
XM_011538350.1 | 382 | Silent Mutation | AGC,AGT | S,S 101 | XP_011536652.1 | |
XM_011538351.2 | 382 | Silent Mutation | AGC,AGT | S,S 101 | XP_011536653.1 | |
XM_011538352.1 | 382 | Silent Mutation | AGC,AGT | S,S 101 | XP_011536654.1 |