Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTTAGGCCAAGTCCTGCTCCGTCT[C/T]GCCCAGGCTGAAGGACCAATTGTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf42 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 |
C11orf42 - chromosome 11 open reading frame 42 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173525.2 | 2994 | Intron | NP_775796.2 | |||
XM_011519926.2 | 2994 | Intron | XP_011518228.1 | |||
XM_011519927.2 | 2994 | Intron | XP_011518229.1 |
FAM160A2 - family with sequence similarity 160 member A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098794.1 | 2994 | Missense Mutation | CAA,CGA | Q,R 886 | NP_001092264.1 | |
NM_032127.3 | 2994 | Missense Mutation | CAA,CGA | Q,R 900 | NP_115503.2 | |
XM_006718343.2 | 2994 | Missense Mutation | CAA,CGA | Q,R 900 | XP_006718406.1 | |
XM_011520397.2 | 2994 | Missense Mutation | CAA,CGA | Q,R 900 | XP_011518699.1 | |
XM_011520398.2 | 2994 | Intron | XP_011518700.1 | |||
XM_011520399.2 | 2994 | Intron | XP_011518701.1 |