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Search Thermo Fisher Scientific
CGAGTACGACACGCCGCGCATCGTG[C/T]TCATCCGCAGCCGCAAAGTGGGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600846 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
P2RX4 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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P2RX4 - purinergic receptor P2X 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256796.1 | 368 | Missense Mutation | CTC,TTC | L,F 22 | NP_001243725.1 | |
NM_001261397.1 | 368 | Missense Mutation | CTC,TTC | L,F 22 | NP_001248326.1 | |
NM_001261398.1 | 368 | Missense Mutation | CTC,TTC | L,F 22 | NP_001248327.1 | |
NM_002560.2 | 368 | Missense Mutation | CTC,TTC | L,F 22 | NP_002551.2 | |
XM_011538416.2 | 368 | Missense Mutation | CTC,TTC | L,F 22 | XP_011536718.1 |