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AGTTATCAAGTTCACTGTCTTCATC[A/G]GAAAAAACTCTGTCACAAAGGTCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300478 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM9B 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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FAM9B - family with sequence similarity 9 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_205849.3 | 1472 | Silent Mutation | TCC,TCT | S,S 178 | NP_995321.1 | |
XM_011545464.2 | 1472 | Silent Mutation | TCC,TCT | S,S 178 | XP_011543766.1 | |
XM_011545465.2 | 1472 | Intron | XP_011543767.1 |