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ATATGGGAGTAAAGACCTTGGCATG[A/G]TACATACCCCTCATGCAAGAACTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM104B 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 |
FAM104B - family with sequence similarity 104 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166699.1 | 298 | Intron | NP_001160171.1 | |||
NM_001166700.1 | 298 | Missense Mutation | CCA,TCA | P,S 88 | NP_001160172.1 | |
NM_001166701.1 | 298 | Missense Mutation | CCA,TCA | P,S 87 | NP_001160173.1 | |
NM_001166702.1 | 298 | Missense Mutation | CCA,TCA | P,S 84 | NP_001160174.1 | |
NM_001166703.1 | 298 | Missense Mutation | CCA,TCA | P,S 86 | NP_001160175.1 | |
NM_001166704.1 | 298 | UTR 3 | NP_001160176.1 | |||
NM_138362.3 | 298 | Intron | NP_612371.2 | |||
XM_017029951.1 | 298 | Missense Mutation | CCA,TCA | P,S 103 | XP_016885440.1 | |
XM_017029952.1 | 298 | Missense Mutation | CCA,TCA | P,S 96 | XP_016885441.1 | |
XM_017029953.1 | 298 | Intron | XP_016885442.1 |