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TGTAGCCTGATGCCCAGCCTATGCC[A/G]GGAACTCAGTACATAACAGCCAATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613537 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NLRC5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
NLRC5 - NLR family CARD domain containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032206.4 | Intron | NP_115582.4 | ||||
XM_005256193.2 | Intron | XP_005256250.1 | ||||
XM_005256194.3 | Intron | XP_005256251.1 | ||||
XM_005256195.2 | Intron | XP_005256252.1 | ||||
XM_005256196.2 | Intron | XP_005256253.1 | ||||
XM_005256197.2 | Intron | XP_005256254.1 | ||||
XM_005256199.3 | Intron | XP_005256256.1 | ||||
XM_005256201.3 | Intron | XP_005256258.1 | ||||
XM_006721297.2 | Intron | XP_006721360.1 | ||||
XM_006721298.2 | Intron | XP_006721361.1 | ||||
XM_006721300.2 | Intron | XP_006721363.1 | ||||
XM_011523373.2 | Intron | XP_011521675.1 | ||||
XM_011523375.2 | Intron | XP_011521677.1 | ||||
XM_011523376.2 | Intron | XP_011521678.1 | ||||
XM_017023766.1 | Intron | XP_016879255.1 | ||||
XM_017023767.1 | Intron | XP_016879256.1 | ||||
XM_017023768.1 | Intron | XP_016879257.1 | ||||
XM_017023769.1 | Intron | XP_016879258.1 | ||||
XM_017023770.1 | Intron | XP_016879259.1 | ||||
XM_017023771.1 | Intron | XP_016879260.1 |