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CGTGGGCCATGGCCGTGTGGATCTT[C/T]GCTGCGATCAACAGGAGAGACCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
8 submissions
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Phenotype: |
MIM: 606416 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NLRP3 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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NLRP3 - NLR family pyrin domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079821.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | NP_001073289.1 | |
NM_001127461.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | NP_001120933.1 | |
NM_001127462.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | NP_001120934.1 | |
NM_001243133.1 | 971 | Silent Mutation | TTC,TTT | F,F 73 | NP_001230062.1 | |
NM_004895.4 | 971 | Silent Mutation | TTC,TTT | F,F 75 | NP_004886.3 | |
NM_183395.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | NP_899632.1 | |
XM_011544048.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_011542350.1 | |
XM_011544053.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_011542355.1 | |
XM_011544055.2 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_011542357.1 | |
XM_017000181.1 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_016855670.1 | |
XM_017000182.1 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_016855671.1 | |
XM_017000183.1 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_016855672.1 | |
XM_017000184.1 | 971 | Silent Mutation | TTC,TTT | F,F 75 | XP_016855673.1 |