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TTACGGGCCACGGCTATCCCGACCC[C/T]AACTACCTGCAGAACGTGCTGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613141 | ||||||||||||||||||||
Literature Links: |
DTX2 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 |
DTX2 - deltex E3 ubiquitin ligase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102594.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | NP_001096064.1 | |
NM_001102595.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | NP_001096065.1 | |
NM_001102596.1 | 2353 | Silent Mutation | CCC,CCT | P,P 552 | NP_001096066.1 | |
NM_020892.2 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | NP_065943.2 | |
XM_005250131.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_005250188.1 | |
XM_005250132.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_005250189.1 | |
XM_011515772.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_011514074.1 | |
XM_011515773.2 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_011514075.1 | |
XM_011515774.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_011514076.1 | |
XM_011515775.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_011514077.1 | |
XM_017011723.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_016867212.1 | |
XM_017011724.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_016867213.1 | |
XM_017011725.1 | 2353 | Silent Mutation | CCC,CCT | P,P 599 | XP_016867214.1 | |
XM_017011726.1 | 2353 | Silent Mutation | CCC,CCT | P,P 552 | XP_016867215.1 | |
XM_017011727.1 | 2353 | Silent Mutation | CCC,CCT | P,P 552 | XP_016867216.1 | |
XM_017011728.1 | 2353 | Silent Mutation | CCC,CCT | P,P 545 | XP_016867217.1 | |
XM_017011729.1 | 2353 | Intron | XP_016867218.1 | |||
XM_017011730.1 | 2353 | Intron | XP_016867219.1 |
LOC105375355 - uroplakin-3b | ||||||
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There are no transcripts associated with this gene. |