Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGTTCTCGGGGAGTTGCTGGAGGAT[C/T]GGTTGACTTGCAGTAGTGGGGGAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605327 | ||||||||||||||||||||
Literature Links: |
NFIL3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
NFIL3 - nuclear factor, interleukin 3 regulated | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289999.1 | 1330 | Missense Mutation | CAA,CGA | Q,R 266 | NP_001276928.1 | |
NM_001290000.1 | 1330 | Missense Mutation | CAA,CGA | Q,R 266 | NP_001276929.1 | |
NM_005384.2 | 1330 | Missense Mutation | CAA,CGA | Q,R 266 | NP_005375.2 | |
XM_017014743.1 | 1330 | Missense Mutation | CAA,CGA | Q,R 266 | XP_016870232.1 | |
XM_017014744.1 | 1330 | Missense Mutation | CAA,CGA | Q,R 266 | XP_016870233.1 |