Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCTCTCTCTCCCACCTCAGCACC[C/T]GTCCGTCCCACTGGCTAACTGCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608077 MIM: 603752 | ||||||||||||||||||||
Literature Links: |
P2RX6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
P2RX6 - purinergic receptor P2X 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159554.1 | 1117 | Missense Mutation | CCG,CTG | P,L 105 | NP_001153026.1 | |
NM_005446.3 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | NP_005437.2 | |
XM_005261819.3 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | XP_005261876.1 | |
XM_011530498.2 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | XP_011528800.1 | |
XM_011530499.2 | 1117 | Missense Mutation | CCG,CTG | P,L 107 | XP_011528801.1 | |
XM_011530500.2 | 1117 | Missense Mutation | CCG,CTG | P,L 105 | XP_011528802.1 | |
XM_011530501.2 | 1117 | Intron | XP_011528803.1 | |||
XM_011530502.2 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | XP_011528804.1 | |
XM_017029066.1 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | XP_016884555.1 | |
XM_017029067.1 | 1117 | Missense Mutation | CCG,CTG | P,L 107 | XP_016884556.1 | |
XM_017029068.1 | 1117 | Missense Mutation | CCG,CTG | P,L 131 | XP_016884557.1 | |
XM_017029069.1 | 1117 | Missense Mutation | CCG,CTG | P,L 81 | XP_016884558.1 | |
XM_017029070.1 | 1117 | Intron | XP_016884559.1 | |||
XM_017029071.1 | 1117 | Intron | XP_016884560.1 | |||
XM_017029072.1 | 1117 | Intron | XP_016884561.1 | |||
XM_017029073.1 | 1117 | Intron | XP_016884562.1 | |||
XM_017029074.1 | 1117 | Intron | XP_016884563.1 | |||
XM_017029075.1 | 1117 | Intron | XP_016884564.1 | |||
XM_017029076.1 | 1117 | Intron | XP_016884565.1 |
SLC7A4 - solute carrier family 7 member 4 | ||||||
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There are no transcripts associated with this gene. |
TUBA3FP - tubulin alpha 3f pseudogene | ||||||
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There are no transcripts associated with this gene. |