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TTCCGCTCCACCTTCTTCTTGCCCC[A/G]AGGCTGCCGCCTCCTGCCCTGGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615648 MIM: 613278 | ||||||||||||||||||||
Literature Links: |
NLRC3 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 |
NLRC3 - NLR family CARD domain containing 3 | ||||||
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There are no transcripts associated with this gene. |
SLX4 - SLX4 structure-specific endonuclease subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032444.2 | 5508 | Missense Mutation | CGG,TGG | R,W 1826 | NP_115820.2 | |
XM_011522715.2 | 5508 | Missense Mutation | CGG,TGG | R,W 1825 | XP_011521017.1 | |
XM_017023775.1 | 5508 | Missense Mutation | CGG,TGG | R,W 1552 | XP_016879264.1 |