Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTAATAGTATTGTTATATAGTGTA[C/T]TGGCTAATTCCAGTGGATCCTCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603046 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF139 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
|
RNF139 - ring finger protein 139 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007218.3 | 774 | Intron | NP_009149.2 | |||
XM_017013002.1 | 774 | Intron | XP_016868491.1 |
TATDN1 - TatD DNase domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146160.1 | 774 | Missense Mutation | AAT,AGT | N,S 236 | NP_001139632.1 | |
NM_001317889.1 | 774 | Missense Mutation | AAT,AGT | N,S 319 | NP_001304818.1 | |
NM_001317890.1 | 774 | Missense Mutation | AAT,AGT | N,S 229 | NP_001304819.1 | |
NM_001317891.1 | 774 | Missense Mutation | AAT,AGT | N,S 138 | NP_001304820.1 | |
NM_032026.3 | 774 | Missense Mutation | AAT,AGT | N,S 283 | NP_114415.1 | |
XM_006716666.3 | 774 | Intron | XP_006716729.1 | |||
XM_006716667.3 | 774 | Intron | XP_006716730.1 | |||
XM_006716668.3 | 774 | Intron | XP_006716731.1 | |||
XM_006716669.3 | 774 | Intron | XP_006716732.1 | |||
XM_006716670.3 | 774 | Intron | XP_006716733.1 | |||
XM_006716671.3 | 774 | Intron | XP_006716734.1 | |||
XM_011517331.2 | 774 | Intron | XP_011515633.1 | |||
XM_017013895.1 | 774 | Intron | XP_016869384.1 | |||
XM_017013896.1 | 774 | Intron | XP_016869385.1 | |||
XM_017013897.1 | 774 | Intron | XP_016869386.1 | |||
XM_017013898.1 | 774 | Intron | XP_016869387.1 | |||
XM_017013899.1 | 774 | Intron | XP_016869388.1 |