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AAACAGAACAACATTTAGGAATCGA[C/T]GCTCTCTGGTAAGGAAATGCTTATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM122C 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
|
FAM122C - family with sequence similarity 122C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170779.1 | 453 | Missense Mutation | CGC,TGC | R,C 61 | NP_001164250.1 | |
NM_001170780.1 | 453 | Missense Mutation | CGC,TGC | R,C 97 | NP_001164251.1 | |
NM_001170781.1 | 453 | Intron | NP_001164252.1 | |||
NM_001170782.1 | 453 | Missense Mutation | CGC,TGC | R,C 61 | NP_001164253.1 | |
NM_001170783.1 | 453 | Missense Mutation | CGC,TGC | R,C 61 | NP_001164254.1 | |
NM_001170784.1 | 453 | Missense Mutation | CGC,TGC | R,C 61 | NP_001164255.1 | |
NM_138819.3 | 453 | Missense Mutation | CGC,TGC | R,C 61 | NP_620174.1 | |
XM_005262382.1 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_005262439.1 | |
XM_005262383.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_005262440.1 | |
XM_005262384.4 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_005262441.1 | |
XM_005262386.3 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_005262443.1 | |
XM_005262387.3 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_005262444.1 | |
XM_006724734.3 | 453 | Missense Mutation | CGC,TGC | R,C 61 | XP_006724797.1 | |
XM_006724735.1 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_006724798.1 | |
XM_006724736.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_006724799.1 | |
XM_011531295.1 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529597.1 | |
XM_011531296.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529598.1 | |
XM_011531297.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529599.1 | |
XM_011531298.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529600.1 | |
XM_011531299.1 | 453 | Intron | XP_011529601.1 | |||
XM_011531300.2 | 453 | Intron | XP_011529602.1 | |||
XM_011531301.2 | 453 | Intron | XP_011529603.1 | |||
XM_011531302.2 | 453 | Intron | XP_011529604.1 | |||
XM_011531305.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529607.1 | |
XM_011531306.2 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_011529608.1 | |
XM_017029308.1 | 453 | Missense Mutation | CGC,TGC | R,C 97 | XP_016884797.1 | |
XM_017029309.1 | 453 | Intron | XP_016884798.1 | |||
XM_017029310.1 | 453 | Intron | XP_016884799.1 | |||
XM_017029311.1 | 453 | Missense Mutation | CGC,TGC | R,C 61 | XP_016884800.1 |