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GAAGGAGTGGCTTACCGATTTAGCC[A/C]GGATGAGCGCGTCGCTCATGAGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603801 MIM: 606116 | ||||||||||||||||||||
Literature Links: |
NMT2 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 |
NMT2 - N-myristoyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308295.1 | 1387 | Missense Mutation | CGG,CTG | R,L 430 | NP_001295224.1 | |
NM_004808.2 | 1387 | Missense Mutation | CGG,CTG | R,L 443 | NP_004799.1 | |
XM_005252642.4 | 1387 | Missense Mutation | CGG,CTG | R,L 443 | XP_005252699.1 | |
XM_006717539.3 | 1387 | Missense Mutation | CGG,CTG | R,L 386 | XP_006717602.1 | |
XM_017016947.1 | 1387 | Intron | XP_016872436.1 | |||
XM_017016948.1 | 1387 | Missense Mutation | CGG,CTG | R,L 430 | XP_016872437.1 | |
XM_017016949.1 | 1387 | Missense Mutation | CGG,CTG | R,L 430 | XP_016872438.1 | |
XM_017016950.1 | 1387 | Missense Mutation | CGG,CTG | R,L 386 | XP_016872439.1 | |
XM_017016951.1 | 1387 | Missense Mutation | CGG,CTG | R,L 373 | XP_016872440.1 | |
XM_017016952.1 | 1387 | Missense Mutation | CGG,CTG | R,L 356 | XP_016872441.1 | |
XM_017016953.1 | 1387 | Missense Mutation | CGG,CTG | R,L 356 | XP_016872442.1 |
RPP38 - ribonuclease P/MRP subunit p38 | ||||||
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There are no transcripts associated with this gene. |