Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTACACTTTATTTAAGCAGTTACT[A/T]GTTTAAAAGCACCTGTAATAACACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606831 MIM: 611148 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NLRC4 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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NLRC4 - NLR family CARD domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199138.1 | 3206 | Missense Mutation | CAA,CTA | Q,L 1021 | NP_001186067.1 | |
NM_001199139.1 | 3206 | Missense Mutation | CAA,CTA | Q,L 1021 | NP_001186068.1 | |
NM_001302504.1 | 3206 | Missense Mutation | CAA,CTA | Q,L 356 | NP_001289433.1 | |
NM_021209.4 | 3206 | Missense Mutation | CAA,CTA | Q,L 1021 | NP_067032.3 | |
XM_017004619.1 | 3206 | Intron | XP_016860108.1 |
SLC30A6 - solute carrier family 30 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_006712048.3 | 3206 | UTR 3 | XP_006712111.1 | |||
XM_011532959.2 | 3206 | UTR 3 | XP_011531261.1 | |||
XM_011532960.2 | 3206 | UTR 3 | XP_011531262.1 | |||
XM_011532961.2 | 3206 | UTR 3 | XP_011531263.1 | |||
XM_011532962.2 | 3206 | UTR 3 | XP_011531264.1 | |||
XM_011532963.2 | 3206 | Intron | XP_011531265.1 | |||
XM_017004462.1 | 3206 | UTR 3 | XP_016859951.1 | |||
XM_017004463.1 | 3206 | Intron | XP_016859952.1 | |||
XM_017004464.1 | 3206 | Intron | XP_016859953.1 | |||
XM_017004465.1 | 3206 | Intron | XP_016859954.1 | |||
XM_017004466.1 | 3206 | Intron | XP_016859955.1 |