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ATGTCCTGGCAGCTAACAACTACCC[C/T]GGCCAGCATCAGCAAGCTGTGGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604462 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM178B 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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FAM178B - family with sequence similarity 178 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122646.2 | 265 | Missense Mutation | AGG,GGG | R,G 605 | NP_001116118.2 | |
NM_001172667.1 | 265 | Missense Mutation | AGG,GGG | R,G 64 | NP_001166138.1 | |
NM_016490.4 | 265 | Missense Mutation | AGG,GGG | R,G 45 | NP_057574.2 | |
XM_011511294.2 | 265 | Missense Mutation | AGG,GGG | R,G 569 | XP_011509596.1 | |
XM_011511297.2 | 265 | Intron | XP_011509599.1 | |||
XM_017004263.1 | 265 | Missense Mutation | AGG,GGG | R,G 648 | XP_016859752.1 | |
XM_017004264.1 | 265 | Missense Mutation | AGG,GGG | R,G 635 | XP_016859753.1 | |
XM_017004265.1 | 265 | Intron | XP_016859754.1 | |||
XM_017004266.1 | 265 | Missense Mutation | AGG,GGG | R,G 71 | XP_016859755.1 | |
XM_017004267.1 | 265 | Missense Mutation | AGG,GGG | R,G 70 | XP_016859756.1 | |
XM_017004268.1 | 265 | Missense Mutation | AGG,GGG | R,G 45 | XP_016859757.1 |
SEMA4C - semaphorin 4C | ||||||
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There are no transcripts associated with this gene. |