Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATGTCCTTGAGATCCTGGGCCATG[C/T]GCTTGAGCTGTGCATCGATGTTCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609742 MIM: 605815 | ||||||||||||||||||||
Literature Links: |
IL4I1 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 |
IL4I1 - interleukin 4 induced 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258017.1 | 1540 | Intron | NP_001244946.1 | |||
NM_001258018.1 | 1540 | Intron | NP_001244947.1 | |||
NM_152899.1 | 1540 | Intron | NP_690863.1 | |||
NM_172374.2 | 1540 | Intron | NP_758962.1 |
NUP62 - nucleoporin 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193357.1 | 1540 | Missense Mutation | CAC,CGC | H,R 446 | NP_001180286.1 | |
NM_012346.4 | 1540 | Missense Mutation | CAC,CGC | H,R 446 | NP_036478.2 | |
NM_016553.4 | 1540 | Missense Mutation | CAC,CGC | H,R 446 | NP_057637.2 | |
NM_153718.3 | 1540 | Missense Mutation | CAC,CGC | H,R 446 | NP_714940.1 | |
NM_153719.3 | 1540 | Missense Mutation | CAC,CGC | H,R 446 | NP_714941.1 |