Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAAAAGCACCTGTAATAACACTGAG[A/C]TCATCATCATCAAATTGCCACCCAA
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 |
---|---|---|
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 |
NLRC4 - NLR family CARD domain containing 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199138.1 | 3177 | Missense Mutation | GAG,GAT | E,D 1011 | NP_001186067.1 | |
NM_001199139.1 | 3177 | Missense Mutation | GAG,GAT | E,D 1011 | NP_001186068.1 | |
NM_001302504.1 | 3177 | Missense Mutation | GAG,GAT | E,D 346 | NP_001289433.1 | |
NM_021209.4 | 3177 | Missense Mutation | GAG,GAT | E,D 1011 | NP_067032.3 | |
XM_017004619.1 | 3177 | Intron | XP_016860108.1 |
SLC30A6 - solute carrier family 30 member 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_006712048.3 | 3177 | UTR 3 | XP_006712111.1 | |||
XM_011532959.2 | 3177 | UTR 3 | XP_011531261.1 | |||
XM_011532960.2 | 3177 | UTR 3 | XP_011531262.1 | |||
XM_011532961.2 | 3177 | UTR 3 | XP_011531263.1 | |||
XM_011532962.2 | 3177 | UTR 3 | XP_011531264.1 | |||
XM_011532963.2 | 3177 | Intron | XP_011531265.1 | |||
XM_017004462.1 | 3177 | UTR 3 | XP_016859951.1 | |||
XM_017004463.1 | 3177 | Intron | XP_016859952.1 | |||
XM_017004464.1 | 3177 | Intron | XP_016859953.1 | |||
XM_017004465.1 | 3177 | Intron | XP_016859954.1 | |||
XM_017004466.1 | 3177 | Intron | XP_016859955.1 |