Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGTGAGCCTACAGCAGACTCTTC[C/T]CTGGCTCCGAAGCACCCACAGCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
C11orf42 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
|
C11orf42 - chromosome 11 open reading frame 42 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173525.2 | 500 | Missense Mutation | CCC,CTC | P,L 151 | NP_775796.2 | |
XM_011519926.2 | 500 | Missense Mutation | CCC,CTC | P,L 151 | XP_011518228.1 | |
XM_011519927.2 | 500 | Missense Mutation | CCC,CTC | P,L 151 | XP_011518229.1 |
FAM160A2 - family with sequence similarity 160 member A2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |