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AGTGTTGCTCTGTAACGCATCTGCC[A/C]GCTGGGCAGTCCCCTTAGCTGTGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605980 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NOD1 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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NOD1 - nucleotide binding oligomerization domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006092.2 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | NP_006083.1 | |
XM_005249568.1 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_005249625.1 | |
XM_005249572.1 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_005249629.1 | |
XM_005249576.1 | 3184 | Missense Mutation | CGG,CTG | R,L 668 | XP_005249633.1 | |
XM_006715633.2 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_006715696.1 | |
XM_011515079.1 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_011513381.1 | |
XM_011515080.2 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_011513382.1 | |
XM_011515081.2 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_011513383.1 | |
XM_011515083.1 | 3184 | Missense Mutation | CGG,CTG | R,L 900 | XP_011513385.1 | |
XM_011515084.1 | 3184 | Missense Mutation | CGG,CTG | R,L 888 | XP_011513386.1 | |
XM_011515085.1 | 3184 | Missense Mutation | CGG,CTG | R,L 832 | XP_011513387.1 | |
XM_011515087.1 | 3184 | Intron | XP_011513389.1 | |||
XM_011515088.2 | 3184 | Intron | XP_011513390.1 | |||
XM_017011674.1 | 3184 | Missense Mutation | CGG,CTG | R,L 916 | XP_016867163.1 | |
XM_017011675.1 | 3184 | Missense Mutation | CGG,CTG | R,L 888 | XP_016867164.1 |