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Search Thermo Fisher Scientific
CTCAGCTTCCCAGAACCTACCGGGC[C/T]ATCTGCAGGGGCACACATGCCCGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM186B 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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FAM186B - family with sequence similarity 186 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032130.2 | 2691 | Missense Mutation | ATA,ATG | I,M 843 | NP_115506.1 | |
XM_006719625.2 | 2691 | Missense Mutation | ATA,ATG | I,M 843 | XP_006719688.1 | |
XM_006719626.2 | 2691 | Missense Mutation | ATA,ATG | I,M 843 | XP_006719689.1 | |
XM_006719627.3 | 2691 | Missense Mutation | ATA,ATG | I,M 843 | XP_006719690.1 | |
XM_011538796.2 | 2691 | Missense Mutation | ATA,ATG | I,M 843 | XP_011537098.1 | |
XM_011538797.2 | 2691 | Intron | XP_011537099.1 | |||
XM_017020008.1 | 2691 | Missense Mutation | ATA,ATG | I,M 753 | XP_016875497.1 |
LOC100422296 - Parkinsonism associated deglycase pseudogene | ||||||
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There are no transcripts associated with this gene. |