Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTCTGATTGCTGAGGAGAGCAGA[A/T]CCAAGATGCTGACAATAGAAAGGCA
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 |
---|---|---|
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 |
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 | 3374 | Intron | NP_001138929.2 | |||
NM_001145458.2 | 3374 | Intron | NP_001138930.2 | |||
NM_001242356.2 | 3374 | Intron | NP_001229285.1 | |||
NM_001242357.2 | 3374 | Intron | NP_001229286.1 | |||
NM_004829.6 | 3374 | Intron | NP_004820.2 | |||
XM_011527528.2 | 3374 | Intron | XP_011525830.1 | |||
XM_011527529.2 | 3374 | Intron | XP_011525831.1 | |||
XM_011527530.2 | 3374 | 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 | 3374 | Silent Mutation | GGA,GGT | G,G 952 | NP_001120727.1 | |
NM_139176.3 | 3374 | Silent Mutation | GGA,GGT | G,G 924 | NP_631915.2 | |
NM_206828.3 | 3374 | Intron | NP_996611.2 | |||
XM_006723075.3 | 3374 | Silent Mutation | GGA,GGT | G,G 952 | XP_006723138.1 | |
XM_006723076.3 | 3374 | Silent Mutation | GGA,GGT | G,G 952 | XP_006723139.1 | |
XM_011526596.2 | 3374 | Silent Mutation | GGA,GGT | G,G 980 | XP_011524898.1 | |
XM_011526599.2 | 3374 | Silent Mutation | GGA,GGT | G,G 952 | XP_011524901.1 | |
XM_011526601.2 | 3374 | Intron | XP_011524903.1 |