Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGTGCCATGTGCAGCATGAGGGGC[A/T]GCCGGAGCCCCTCATGCTGAGATGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142871 | ||||||||||||||||||||
Literature Links: |
HLA-G 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 |
HLA-G - major histocompatibility complex, class I, G | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002127.5 | 602 | Missense Mutation | CAG,CTG | Q,L 290 | NP_002118.1 | |
XM_017010816.1 | 602 | Missense Mutation | CAG,CTG | Q,L 295 | XP_016866305.1 | |
XM_017010817.1 | 602 | Missense Mutation | CAG,CTG | Q,L 198 | XP_016866306.1 | |
XM_017010818.1 | 602 | Missense Mutation | CAG,CTG | Q,L 198 | XP_016866307.1 |