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CTGGAGCTTCAGGGTTCTCGGGATT[C/T]GAGTCCTGGCCCTGCTGCTTGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602451 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
P2RY6 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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P2RY6 - pyrimidinergic receptor P2Y6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277204.1 | 106 | UTR 5 | NP_001264133.1 | |||
NM_001277205.1 | 106 | Intron | NP_001264134.1 | |||
NM_001277206.1 | 106 | Intron | NP_001264135.1 | |||
NM_001277207.1 | 106 | Intron | NP_001264136.1 | |||
NM_001277208.1 | 106 | Missense Mutation | TCG,TTG | S,L 17 | NP_001264137.1 | |
NM_176796.2 | 106 | Intron | NP_789766.1 | |||
NM_176797.2 | 106 | Intron | NP_789767.1 | |||
NM_176798.2 | 106 | Intron | NP_789768.1 | |||
XM_005274022.3 | 106 | Intron | XP_005274079.1 | |||
XM_006718571.3 | 106 | Intron | XP_006718634.1 | |||
XM_011545076.2 | 106 | Intron | XP_011543378.1 | |||
XM_011545077.2 | 106 | Intron | XP_011543379.1 | |||
XM_011545079.2 | 106 | Intron | XP_011543381.1 |