iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs346445913	snp	A/G			intron-variant	UPL6	TAIR10	3:5878968	TACTCCATCATCTTT[A/G]CATTTAGTACGTCTA	820979
rs346445995	snp	G/T			intron-variant	UPL6	TAIR10	3:5876206	ATATATATATATATA[G/T]ATATATATTAACTTG	820979
rs346511334	snp	A/C			intron-variant	UPL6	TAIR10	3:5874695	AAACATTGTGTGAGT[A/C]ATATCCCTTGCACCA	820979
rs346571797	snp	C/T			utr-variant-3-prime	UPL6	TAIR10	3:5881605	AGTGGTAAGAATATC[C/T]TTTTTTTTTTTTTTT	820979
rs346587478	snp	G/T			intron-variant	UPL6	TAIR10	3:5875639	AATATATGTAAAATC[G/T]TTGAGGCTAAATGAT	820979
rs346607868	snp	G/T			intron-variant	UPL6	TAIR10	3:5874101	GGGTAAAGGGAAAAA[G/T]TTTTTCAATCATTTA	820979
rs346633003	snp	C/T			intron-variant	UPL6	TAIR10	3:5878213	TATTGCTGATATTTT[C/T]TCCTTTATCCAGGCC	820979
rs346667694	snp	A/G			intron-variant	UPL6	TAIR10	3:5880491	TATCGCTATGTTGTT[A/G]ACACTTGACAGGGAC	820979
rs346750780	snp	G/T			synonymous-codon	UPL6	TAIR10	3:5875889	CCTACTTGGTAACAC[G/T]TTGGACACTGCAAAC	820979
rs346771049	snp	A/C			missense	UPL6	TAIR10	3:5878840	GGTGGTGGCATTTTC[A/C]AAGACTTCATGGAGA	820979
rs346805622	snp	C/T			intron-variant	UPL6	TAIR10	3:5874808	TTCTCTAGTTTCTTT[C/T]CGAAGATGACTGGGA	820979
rs346807022	snp	A/C			intron-variant	UPL6	TAIR10	3:5874070	CTTCTATTATGTGGA[A/C]AAGTGCATTTGTTGT	820979
rs346815789	snp	C/T			intron-variant	UPL6	TAIR10	3:5874665	ATTATGTTTATCTTA[C/T]GAGCAACAAACTTAA	820979
rs346840202	snp	G/T			intron-variant	UPL6	TAIR10	3:5879329	AAATTATTGAATTTG[G/T]CCTTTTGTCGTTATT	820979
rs346929978	snp	A/G			synonymous-codon	UPL6	TAIR10	3:5876556	GACACTTCCTCCTGT[A/G]AAATCATCAGAAGGA	820979
rs346962592	snp	G/T			synonymous-codon	UPL6	TAIR10	3:5876814	GCAGATAACCAATGC[G/T]ATAGACTCACGCTTT	820979
rs346985172	snp	A/G			intron-variant	UPL6	TAIR10	3:5878315	CAAAATATTCACAGT[A/G]AGTGGCTATTGGGAT	820979
rs346998153	snp	A/T			utr-variant-5-prime	UPL6	TAIR10	3:5873364	ATCATCCAAATTCGT[A/T]ATCATTTTTCACCTT	820979
rs347038372	snp	G/T			intron-variant	UPL6	TAIR10	3:5879212	ACAGAAAGCAAACTA[G/T]AATGCTTACAGTGTA	820979
rs347061468	snp	G/T			intron-variant	UPL6	TAIR10	3:5876702	GATCTTGTGCTGAAA[G/T]AGACATACACTTTTA	820979
rs347066745	snp	A/G			missense, intron-variant	UPL6	TAIR10	3:5876764	ATGTTGATTGACGAT[A/G]TACCAGGATTAGTCT	820979
rs347070920	snp	C/T			synonymous-codon	UPL6	TAIR10	3:5877455	CGACAATGAGGAGTT[C/T]TATGAAAGAGAGAAG	820979
rs347077850	snp	C/T			intron-variant	UPL6	TAIR10	3:5874513	TGCCTGCTTCTTTTG[C/T]TGACACTTTTGTTCA	820979
rs347108731	snp	A/G			missense	UPL6	TAIR10	3:5879033	GAGACCGCTGATCAC[A/G]TGCTTTATCCTAATC	820979
rs347111472	snp	C/G			missense	UPL6	TAIR10	3:5877186	ACGATGCCATGAGAA[C/G]CAGAAGTGGTCATCC	820979
rs347165272	snp	G/T			intron-variant	UPL6	TAIR10	3:5876208	ATATATATATATAGA[G/T]ATATATTAACTTGTG	820979
rs347190684	snp	G/T			missense	UPL6	TAIR10	3:5874202	CATTGAGCGCTCGAA[G/T]GTGCGGCATGATTTC	820979
rs347197742	snp	A/G			intron-variant	UPL6	TAIR10	3:5876380	TCTTTGCCTTTCTGC[A/G]AAAATCATTCATTTG	820979
rs347208711	snp	A/C			intron-variant	UPL6	TAIR10	3:5874709	TCATATCCCTTGCAC[A/C]ACAAATTAAAGTCTC	820979
rs347228847	snp	A/G			intron-variant	UPL6	TAIR10	3:5880477	GTTATATATGATTAT[A/G]TCGCTATGTTGTTGA	820979
rs347344197	snp	G/T			intron-variant	UPL6	TAIR10	3:5880993	TAAGAGACTTGTTTT[G/T]TTGCCAAATAGCTTC	820979
rs347354435	snp	C/T			intron-variant	UPL6	TAIR10	3:5879252	TGATTTTTAATACAC[C/T]ACTCGCAATGTTTTT	820979
rs347379878	snp	C/T			missense	UPL6	TAIR10	3:5877796	CCTAACACTGGGAAA[C/T]CTGTCTCCAATGACC	820979
rs347415312	snp	A/G			intron-variant	UPL6	TAIR10	3:5878460	GTTTACTGATAACTT[A/G]GTTGTGGTTGTATTG	820979
rs347443852	snp	A/T			intron-variant	UPL6	TAIR10	3:5873787	TTTTGCAAGATATGT[A/T]GAACTTTTGAGCTAA	820979
rs347456407	snp	A/G			intron-variant	UPL6	TAIR10	3:5875370	GCAATCTAAACTTTT[A/G]AAGCAATTGTGGTTT	820979
rs347476245	snp	C/T			intron-variant	UPL6	TAIR10	3:5876929	AAGTGCTATACTTCC[C/T]CTGGATCAAGTGATT	820979
rs347478882	snp	G/T			synonymous-codon	UPL6	TAIR10	3:5880334	CATATCTGGTTCAGT[G/T]GATAGTTTGGATATA	820979

Full records

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