Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTCTCCTGAGATTGCCTTTCACC[C/T]TCACAAACTCGGGGGCATTTTCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM107B 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 |
FAM107B - family with sequence similarity 107 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282695.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269624.1 | |
NM_001282696.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269625.1 | |
NM_001282697.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269626.1 | |
NM_001282698.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269627.1 | |
NM_001282699.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269628.1 | |
NM_001282700.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269629.1 | |
NM_001282701.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269630.1 | |
NM_001282702.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269631.1 | |
NM_001282703.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001269632.1 | |
NM_001320735.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307664.1 | |
NM_001320736.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307665.1 | |
NM_001320737.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307666.1 | |
NM_001320738.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307667.1 | |
NM_001320739.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307668.1 | |
NM_001320740.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | NP_001307669.1 | |
NM_001320741.1 | 494 | Missense Mutation | AAG,AGG | K,R 152 | NP_001307670.1 | |
NM_031453.3 | 494 | Missense Mutation | AAG,AGG | K,R 288 | NP_113641.2 | |
XM_005252616.3 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_005252673.1 | |
XM_011519735.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_011518037.1 | |
XM_017016746.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_016872235.1 | |
XM_017016747.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_016872236.1 | |
XM_017016748.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_016872237.1 | |
XM_017016749.1 | 494 | Missense Mutation | AAG,AGG | K,R 113 | XP_016872238.1 |