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TCCAAATTAGCTTCAGTTTTCAGTG[A/G]GCTTAAAAAAAAGTGTATATTTATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603046 | ||||||||||||||||||||
Literature Links: |
RNF139 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 |
RNF139 - ring finger protein 139 | ||||||
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There are no transcripts associated with this gene. |
TATDN1 - TatD DNase domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146160.1 | 521 | Missense Mutation | CCA,TCA | P,S 152 | NP_001139632.1 | |
NM_001317889.1 | 521 | Missense Mutation | CCA,TCA | P,S 235 | NP_001304818.1 | |
NM_001317890.1 | 521 | Missense Mutation | CCA,TCA | P,S 145 | NP_001304819.1 | |
NM_001317891.1 | 521 | Missense Mutation | CCA,TCA | P,S 54 | NP_001304820.1 | |
NM_032026.3 | 521 | Missense Mutation | CCA,TCA | P,S 199 | NP_114415.1 | |
XM_006716666.3 | 521 | Intron | XP_006716729.1 | |||
XM_006716667.3 | 521 | Intron | XP_006716730.1 | |||
XM_006716668.3 | 521 | Intron | XP_006716731.1 | |||
XM_006716669.3 | 521 | Intron | XP_006716732.1 | |||
XM_006716670.3 | 521 | Intron | XP_006716733.1 | |||
XM_006716671.3 | 521 | Intron | XP_006716734.1 | |||
XM_011517331.2 | 521 | Intron | XP_011515633.1 | |||
XM_017013895.1 | 521 | Intron | XP_016869384.1 | |||
XM_017013896.1 | 521 | Intron | XP_016869385.1 | |||
XM_017013897.1 | 521 | Intron | XP_016869386.1 | |||
XM_017013898.1 | 521 | Intron | XP_016869387.1 | |||
XM_017013899.1 | 521 | Intron | XP_016869388.1 |