SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8161986 | snp | C/T | | | utr-variant-3-prime, intron-variant | Usp29, LOC103690204 | Rn_Celera | 1:69990325 | TCTGTACTATTTTTT[C/T]ATGTTTGAAACACTG | 361495 |
rs8172846 | snp | G/T | | | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70037101 | TTCAGCCAGTACTAT[G/T]TTCTCCTCATATTAT | 361495 |
rs105105126 | snp | A/C | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:69997387 | ACCACATGTTGGCTC[A/C]CAACCATCTGTAATG | 361495 |
rs105254466 | snp | C/T | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70009183 | GGGCCCAGTGCAGAC[C/T]CATGGAGGCTGCTCG | 361495 |
rs105418100 | snp | A/G | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:69999855 | AAAAATAAATAAAAC[A/G]TTGCGTTTTTCTGCC | 361495 |
rs105482345 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70042454 | CTCTCTCTCTCTCTC[A/T]CACATGTGCTTGCAT | 361495 |
rs105547807 | snp | C/T | 0 | 0 | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70027166 | TCCTGAAGAGCGCTC[C/T]CTCTCTCTCTCTCTC | 361495 |
rs105572547 | snp | C/T | 0.5 | 0 | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70033051 | ACCAGGCAGGAGTCA[C/T]GACTTGAAATTTATT | 361495 |
rs105597351 | snp | G/T | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70009242 | GTGAGCCTTGCTTAG[G/T]TGATTCTTAAAAACA | 361495 |
rs105605465 | snp | C/G | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70009356 | GGGTCTCCGTGTGTA[C/G]CCCTGGAAGTCACTA | 361495 |
rs105648308 | snp | A/T | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:69996025 | CAAATAAATATAATT[A/T]AAAAAAACTGCACAG | 361495 |
rs105871375 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70042138 | GCTCCCGGCATCTAC[A/C]TGGCGGCTCACAACC | 361495 |
rs106303102 | snp | A/T | 0.5 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70002960 | TACATCTATGAAATG[A/T]CATAACGAACCCCAT | 361495 |
rs106354570 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70044001 | TGATACCTCAGGTTT[C/T]TCTCAGACCTCCACA | 361495 |
rs106449305 | snp | C/T | 0 | 0 | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70027046 | ATTGCAAGTACAGAC[C/T]CCCAGGTTGTTCTCC | 361495 |
rs106528490 | snp | G/T | 0.5 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70002928 | AAATTGGGCAAAAAT[G/T]ATGGAGTTCGTTTAT | 361495 |
rs106618397 | snp | A/G | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70009168 | TAACATAGACGCAGA[A/G]GGCCCAGTGCAGACC | 361495 |
rs106725862 | snp | G/T | 0.5 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70008263 | GTGTTGTGCCTCCTT[G/T]TCTGTGAACCATTCC | 361495 |
rs106772130 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Usp29, LOC102547903 | Rn_Celera | 1:70017423 | CTCTTGGCATGGCAC[A/G]AATTTATAAGAAGAT | 361495 |
rs106810045 | snp | C/T | 0 | 0 | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70021060 | AATGCACATGTATAA[C/T]GAAAGACAAATACAC | 361495 |
rs106886065 | snp | G/T | 0.5 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70000609 | GTTTTTGTTTGTTTG[G/T]TTGGTTGGTTGGTTT | 361495 |
rs106973312 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70042452 | CTCTCTCTCTCTCTC[A/T]CTCACATGTGCTTGC | 361495 |
rs107212849 | snp | C/T | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:70007528 | TGACTTGTTAACCAG[C/T]CAGCAAAAAGACAGA | 361495 |
rs107271120 | snp | A/C | 0 | 0 | intron-variant | Usp29 | Rn_Celera | 1:69997607 | TGCTATCGCCAGTGA[A/C]TGTCCAATGGGCCAC | 361495 |
rs107465212 | snp | A/T | 0.5 | 0 | intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70020795 | AAACACTTCCTTCAT[A/T]GACCAGGCTGACCTT | 361495 |
rs107508887 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | Usp29 | Rn_Celera | 1:69994960 | AAGGGTGTGGCACTA[C/T]TCCCTGGTCTAGTGT | 361495 |
rs107541053 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Usp29, LOC102547903 | Rn_Celera | 1:70042217 | GTACCAGGCATGAAT[A/G]TGGTACATAGACATG | 361495 |