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GCCTTTATACGCCACCACGGAAGCT[C/T]GGTAGATAGCGCTCCCCCACCCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611947 | ||||||||||||||||||||
Literature Links: |
NLRX1 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 |
NLRX1 - NLR family member X1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282143.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | NP_001269072.1 | |
NM_001282144.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | NP_001269073.1 | |
NM_001282358.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | NP_001269287.1 | |
NM_024618.3 | 648 | Missense Mutation | TCG,TTG | S,L 56 | NP_078894.2 | |
XM_005271669.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | XP_005271726.1 | |
XM_005271670.1 | 648 | UTR 5 | XP_005271727.1 | |||
XM_005271671.1 | 648 | UTR 5 | XP_005271728.1 | |||
XM_005271672.1 | 648 | UTR 5 | XP_005271729.1 | |||
XM_006718904.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | XP_006718967.1 | |
XM_011542980.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | XP_011541282.1 | |
XM_017018294.1 | 648 | Missense Mutation | TCG,TTG | S,L 56 | XP_016873783.1 |