Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAAATTCTGAGTCAGATAAGGAG[T/C]TATGTGATTCCAGACAGCTGGAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 107470 | ||||||||||||||||||||
Literature Links: |
IFNGR1 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 |
IFNGR1 - interferon gamma receptor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000416.2 | 1442 | Missense Mutation | AAC,AGC | N,S 423 | NP_000407.1 | |
XM_006715470.2 | 1442 | Missense Mutation | AAC,AGC | N,S 413 | XP_006715533.1 | |
XM_006715471.2 | 1442 | Missense Mutation | AAC,AGC | N,S 382 | XP_006715534.1 | |
XM_011535793.2 | 1442 | Missense Mutation | AAC,AGC | N,S 413 | XP_011534095.1 | |
XM_011535794.1 | 1442 | Missense Mutation | AAC,AGC | N,S 413 | XP_011534096.1 | |
XM_017010827.1 | 1442 | Missense Mutation | AAC,AGC | N,S 413 | XP_016866316.1 |