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TACATCCCGGACATGAACTCCCGCA[C/T]GGCAGGGCAATACAGCTGCATCTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604530 | ||||||||||||||||||||||||||||||||||||||
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 | 409 | Missense Mutation | ACG,ATG | T,M 92 | NP_001138929.2 | |
NM_001145458.2 | 409 | Missense Mutation | ACG,ATG | T,M 92 | NP_001138930.2 | |
NM_001242356.2 | 409 | Intron | NP_001229285.1 | |||
NM_001242357.2 | 409 | Intron | NP_001229286.1 | |||
NM_004829.6 | 409 | Missense Mutation | ACG,ATG | T,M 92 | NP_004820.2 | |
XM_011527528.2 | 409 | Missense Mutation | ACG,ATG | T,M 92 | XP_011525830.1 | |
XM_011527529.2 | 409 | Missense Mutation | ACG,ATG | T,M 92 | XP_011525831.1 | |
XM_011527530.2 | 409 | Missense Mutation | ACG,ATG | T,M 92 | XP_011525832.1 |