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Search Thermo Fisher Scientific
CCCCTTCCTGGTGTCCACAGAAGCC[C/A]AACGTCACTAGCTGGGGTGTGTATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605956 | ||||||||||||||||||||
Literature Links: |
NOD2 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 |
NOD2 - nucleotide binding oligomerization domain containing 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001293557.1 | Intron | NP_001280486.1 | ||||
NM_022162.2 | Intron | NP_071445.1 | ||||
XM_005256084.3 | Intron | XP_005256141.1 | ||||
XM_006721242.3 | Intron | XP_006721305.1 | ||||
XM_006721243.3 | Intron | XP_006721306.1 | ||||
XM_011523259.2 | Intron | XP_011521561.1 | ||||
XM_011523260.2 | Intron | XP_011521562.1 | ||||
XM_011523261.1 | Intron | XP_011521563.1 | ||||
XM_017023535.1 | Intron | XP_016879024.1 | ||||
XM_017023536.1 | Intron | XP_016879025.1 | ||||
XM_017023537.1 | Intron | XP_016879026.1 | ||||
XM_017023538.1 | Intron | XP_016879027.1 |