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CTCCCTAGTGGCTAGGATTACAGGC[A/C]TGCTGTTTCAATTTTTAGTCTGTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
18 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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
NCF2 - neutrophil cytosolic factor 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000433.3 | Intron | NP_000424.2 | ||||
NM_001127651.2 | Intron | NP_001121123.1 | ||||
NM_001190789.1 | Intron | NP_001177718.1 | ||||
NM_001190794.1 | Intron | NP_001177723.1 | ||||
XM_005245207.1 | Intron | XP_005245264.1 | ||||
XM_011509580.1 | Intron | XP_011507882.1 | ||||
XM_011509581.1 | Intron | XP_011507883.1 |
SMG7 - SMG7, nonsense mediated mRNA decay factor | ||||||
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There are no transcripts associated with this gene. |