Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTCCCCGGAGACAGCCGTGGCCGG[A/G]GTGGGTCATGAGTTGGGTACCGCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM63B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
FAM63B - family with sequence similarity 63 member B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040450.2 | 556 | Silent Mutation | GGA,GGG | G,G 118 | NP_001035540.1 | |
NM_001040453.2 | 556 | Silent Mutation | GGA,GGG | G,G 118 | NP_001035543.1 | |
XM_011521687.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_011519989.1 | |
XM_011521688.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_011519990.1 | |
XM_011521689.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_011519991.1 | |
XM_011521690.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_011519992.1 | |
XM_017022332.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_016877821.1 | |
XM_017022333.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_016877822.1 | |
XM_017022334.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_016877823.1 | |
XM_017022335.1 | 556 | Silent Mutation | GGA,GGG | G,G 118 | XP_016877824.1 |
LOC101928725 - uncharacterized LOC101928725 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |