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AGCAGCTCAGCCAGGATGAGTTGAG[C/G]AAGTTCAAGTATCTGATCACGACCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609364 MIM: 609661 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NLRP2 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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NLRP2 - NLR family pyrin domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174081.1 | 214 | Missense Mutation | AGC,AGG | S,R 24 | NP_001167552.1 | |
NM_001174082.1 | 214 | Missense Mutation | AGC,AGG | S,R 24 | NP_001167553.1 | |
NM_001174083.1 | 214 | Missense Mutation | AGC,AGG | S,R 24 | NP_001167554.1 | |
NM_017852.3 | 214 | Missense Mutation | AGC,AGG | S,R 24 | NP_060322.1 |
NLRP7 - NLR family pyrin domain containing 7 | ||||||
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There are no transcripts associated with this gene. |