Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606715 MIM: 610405 MIM: 610991 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASIC4 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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ASIC4 - acid sensing ion channel subunit family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182847.2 | 1707 | Intron | NP_878267.2 | |||
XM_005246671.2 | 1707 | Intron | XP_005246728.2 | |||
XM_017004439.1 | 1707 | Intron | XP_016859928.1 |
CHPF - chondroitin polymerizing factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195731.1 | 1707 | Missense Mutation | GCT,GGT | A,G 488 | NP_001182660.1 | |
NM_024536.5 | 1707 | Missense Mutation | GCT,GGT | A,G 650 | NP_078812.2 | |
XM_011511838.2 | 1707 | Missense Mutation | GCT,GGT | A,G 359 | XP_011510140.1 |
MIR3132 - microRNA 3132 | ||||||
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There are no transcripts associated with this gene. |
OBSL1 - obscurin like 1 | ||||||
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There are no transcripts associated with this gene. |
TMEM198 - transmembrane protein 198 | ||||||
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There are no transcripts associated with this gene. |