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CTTCCTCCAACAGCTTCTTGATTTC[C/T]AAATTAGTTTCATAGGTCTTCAACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604530 MIM: 609661 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCR1 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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NCR1 - natural cytotoxicity triggering receptor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145457.2 | 3524 | Intron | NP_001138929.2 | |||
NM_001145458.2 | 3524 | Intron | NP_001138930.2 | |||
NM_001242356.2 | 3524 | Intron | NP_001229285.1 | |||
NM_001242357.2 | 3524 | Intron | NP_001229286.1 | |||
NM_004829.6 | 3524 | Intron | NP_004820.2 | |||
XM_011527528.2 | 3524 | Intron | XP_011525830.1 | |||
XM_011527529.2 | 3524 | Intron | XP_011525831.1 | |||
XM_011527530.2 | 3524 | Intron | XP_011525832.1 |
NLRP7 - NLR family pyrin domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127255.1 | 3524 | Silent Mutation | TTA,TTG | L,L 1002 | NP_001120727.1 | |
NM_139176.3 | 3524 | Silent Mutation | TTA,TTG | L,L 974 | NP_631915.2 | |
NM_206828.3 | 3524 | Silent Mutation | TTA,TTG | L,L 945 | NP_996611.2 | |
XM_006723075.3 | 3524 | Silent Mutation | TTA,TTG | L,L 1002 | XP_006723138.1 | |
XM_006723076.3 | 3524 | Silent Mutation | TTA,TTG | L,L 1002 | XP_006723139.1 | |
XM_011526596.2 | 3524 | Silent Mutation | TTA,TTG | L,L 1030 | XP_011524898.1 | |
XM_011526599.2 | 3524 | Silent Mutation | TTA,TTG | L,L 1002 | XP_011524901.1 | |
XM_011526601.2 | 3524 | Silent Mutation | TTA,TTG | L,L 973 | XP_011524903.1 |