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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609077 MIM: 602438 MIM: 603500 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
B3GNT9 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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B3GNT9 - UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 | ||||||
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There are no transcripts associated with this gene. |
C16orf70 - chromosome 16 open reading frame 70 | ||||||
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There are no transcripts associated with this gene. |
FBXL8 - F-box and leucine rich repeat protein 8 | ||||||
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There are no transcripts associated with this gene. |
HSF4 - heat shock transcription factor 4 | ||||||
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There are no transcripts associated with this gene. |
TRADD - TNFRSF1A associated via death domain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323552.1 | 492 | Missense Mutation | GAG,GAT | E,D 133 | NP_001310481.1 | |
NM_003789.3 | 492 | Missense Mutation | GAG,GAT | E,D 133 | NP_003780.1 | |
XM_005256213.3 | 492 | Missense Mutation | GAG,GAT | E,D 73 | XP_005256270.1 | |
XM_017023815.1 | 492 | Missense Mutation | GAG,GAT | E,D 133 | XP_016879304.1 |