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CGTTGCCGGCAGCGCTGTGGCCCCG[C/T]CGTCGTAGACCGCCAGCACGCACAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607403 MIM: 612807 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFNL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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IFNL1 - interferon lambda 1 | ||||||
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There are no transcripts associated with this gene. |
LRFN1 - leucine rich repeat and fibronectin type III domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020862.1 | 1496 | Missense Mutation | GAC,GGC | D,G 499 | NP_065913.1 | |
XM_005259102.4 | 1496 | Missense Mutation | GAC,GGC | D,G 499 | XP_005259159.1 | |
XM_017027033.1 | 1496 | Missense Mutation | GAC,GGC | D,G 499 | XP_016882522.1 |