Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGGCACCAGCTCATTGCTGTCCC[A/G]AGGCCGATAGCTGGGTGGGGATAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 608515 MIM: 610964 | ||||||||||||||||||||
Literature Links: |
NCF2 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 |
NCF2 - neutrophil cytosolic factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000433.3 | 1464 | Missense Mutation | CGG,TGG | R,W 397 | NP_000424.2 | |
NM_001127651.2 | 1464 | Missense Mutation | CGG,TGG | R,W 397 | NP_001121123.1 | |
NM_001190789.1 | 1464 | Missense Mutation | CGG,TGG | R,W 316 | NP_001177718.1 | |
NM_001190794.1 | 1464 | Missense Mutation | CGG,TGG | R,W 352 | NP_001177723.1 | |
XM_005245207.1 | 1464 | Missense Mutation | CGG,TGG | R,W 361 | XP_005245264.1 | |
XM_011509580.1 | 1464 | Missense Mutation | CGG,TGG | R,W 397 | XP_011507882.1 | |
XM_011509581.1 | 1464 | Missense Mutation | CGG,TGG | R,W 397 | XP_011507883.1 |
SMG7 - SMG7, nonsense mediated mRNA decay factor | ||||||
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There are no transcripts associated with this gene. |