Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603028 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF175 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
RNF175 - ring finger protein 175 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173662.2 | 1402 | Missense Mutation | ATA,ATG | I,M 315 | NP_775933.1 | |
XM_005262938.3 | 1402 | Missense Mutation | ATA,ATG | I,M 281 | XP_005262995.1 | |
XM_005262939.3 | 1402 | Missense Mutation | ATA,ATG | I,M 235 | XP_005262996.1 | |
XM_005262940.4 | 1402 | Missense Mutation | ATA,ATG | I,M 234 | XP_005262997.1 | |
XM_011531879.2 | 1402 | Missense Mutation | ATA,ATG | I,M 283 | XP_011530181.1 | |
XM_011531881.2 | 1402 | Missense Mutation | ATA,ATG | I,M 275 | XP_011530183.1 | |
XM_011531882.2 | 1402 | Intron | XP_011530184.1 | |||
XM_011531883.2 | 1402 | Missense Mutation | ATA,ATG | I,M 243 | XP_011530185.1 | |
XM_017008047.1 | 1402 | Missense Mutation | ATA,ATG | I,M 216 | XP_016863536.1 |
TLR2 - toll like receptor 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318787.1 | 1402 | Intron | NP_001305716.1 | |||
NM_001318789.1 | 1402 | Intron | NP_001305718.1 | |||
NM_001318790.1 | 1402 | Intron | NP_001305719.1 | |||
NM_001318791.1 | 1402 | Intron | NP_001305720.1 | |||
NM_001318793.1 | 1402 | Intron | NP_001305722.1 | |||
NM_001318795.1 | 1402 | Intron | NP_001305724.1 | |||
NM_001318796.1 | 1402 | Intron | NP_001305725.1 | |||
NM_003264.4 | 1402 | Intron | NP_003255.2 | |||
XM_011532215.2 | 1402 | UTR 3 | XP_011530517.1 | |||
XM_011532216.2 | 1402 | UTR 3 | XP_011530518.1 | |||
XM_017008573.1 | 1402 | UTR 3 | XP_016864062.1 | |||
XM_017008574.1 | 1402 | UTR 3 | XP_016864063.1 | |||
XM_017008575.1 | 1402 | UTR 3 | XP_016864064.1 | |||
XM_017008576.1 | 1402 | UTR 3 | XP_016864065.1 |
Set Membership: |
HapMap |