Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATGACGACCCCCGAGTGAGGACC[A/G]CTACCCAGCCACCAAGAGGTAGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
C10orf35 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
|
C10orf35 - chromosome 10 open reading frame 35 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145306.2 | 772 | Missense Mutation | ACT,GCT | T,A 21 | NP_660349.1 | |
XM_005269606.1 | 772 | Missense Mutation | ACT,GCT | T,A 63 | XP_005269663.1 | |
XM_005269608.3 | 772 | Missense Mutation | ACT,GCT | T,A 21 | XP_005269665.1 | |
XM_011539455.2 | 772 | Missense Mutation | ACT,GCT | T,A 21 | XP_011537757.1 | |
XM_017015836.1 | 772 | Missense Mutation | ACT,GCT | T,A 21 | XP_016871325.1 |