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GTTGAGAATCGCTGTCTGGTCTTCC[A/G]GAAGCTGGCGGTGGCACAAGTCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613773 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGSF9B 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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IGSF9B - immunoglobulin superfamily member 9B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277285.1 | 2761 | Missense Mutation | CCG,CTG | P,L 1416 | NP_001264214.1 | |
XM_006718795.3 | 2761 | Missense Mutation | CCG,CTG | P,L 892 | XP_006718858.1 | |
XM_011542691.2 | 2761 | Missense Mutation | CCG,CTG | P,L 1518 | XP_011540993.1 | |
XM_011542692.2 | 2761 | Missense Mutation | CCG,CTG | P,L 1514 | XP_011540994.1 | |
XM_011542694.2 | 2761 | UTR 3 | XP_011540996.1 | |||
XM_011542695.2 | 2761 | Missense Mutation | CCG,CTG | P,L 1420 | XP_011540997.1 | |
XM_017017393.1 | 2761 | Missense Mutation | CCG,CTG | P,L 1487 | XP_016872882.1 | |
XM_017017394.1 | 2761 | Intron | XP_016872883.1 | |||
XM_017017395.1 | 2761 | Intron | XP_016872884.1 | |||
XM_017017396.1 | 2761 | Missense Mutation | CCG,CTG | P,L 1119 | XP_016872885.1 |
MIR4697HG - MIR4697 host gene | ||||||
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There are no transcripts associated with this gene. |