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GGGAGGCACTTGAGGTGGTACTGTG[A/G]GCATCAGAATCTGCAATAAAGATTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615027 | ||||||||||||||||||||
Literature Links: |
FAM60A 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 |
FAM60A - family with sequence similarity 60 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135811.1 | 692 | Silent Mutation | GCC,GCT | A,A 122 | NP_001129283.1 | |
NM_001135812.1 | 692 | Intron | NP_001129284.1 | |||
NM_021238.2 | 692 | Silent Mutation | GCC,GCT | A,A 122 | NP_067061.1 | |
XM_011520803.2 | 692 | Intron | XP_011519105.1 | |||
XM_017019758.1 | 692 | Intron | XP_016875247.1 | |||
XM_017019759.1 | 692 | Silent Mutation | GCC,GCT | A,A 122 | XP_016875248.1 | |
XM_017019760.1 | 692 | Intron | XP_016875249.1 | |||
XM_017019761.1 | 692 | Intron | XP_016875250.1 | |||
XM_017019762.1 | 692 | Silent Mutation | GCC,GCT | A,A 122 | XP_016875251.1 |