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
rs346503553	snp	A/C			intron-variant	BT2	TAIR10	3:17910266	ATTTTAGCTAAAAAC[A/C]AAACCAGAAAAATGT	823994
rs346516634	snp	A/G			utr-variant-5-prime	BT2	TAIR10	3:17910494	TTGTAGAGAAGAAGA[A/G]GAAGAGAGATTTCTG	823994
rs346559617	snp	C/T			intron-variant	BT2	TAIR10	3:17910024	AAAATTGTGTAGTAC[C/T]GGAAATAACCATCGG	823994
rs346585866	snp	C/G			utr-variant-3-prime	BT2	TAIR10	3:17908325	GACCTACTTATACAG[C/G]CAATTTAAAAGGGTT	823994
rs346633062	snp	A/T			synonymous-codon	BT2	TAIR10	3:17909744	GTCGCAGAGCCGAGC[A/T]AGCTGGAGGACGTCG	823994
rs346699107	snp	A/C			intron-variant	BT2	TAIR10	3:17909528	AACAAAATGTGTTAT[A/C]GAAGGTACTAAGAAA	823994
rs346702904	snp	A/G			synonymous-codon	BT2	TAIR10	3:17909756	AGCTAGCTGGAGGAC[A/G]TCGACTACGTTCTCT	823994
rs346756346	snp	A/C			synonymous-codon	BT2	TAIR10	3:17908533	TGACTGACACAACGA[A/C]GTCATAGCTTTTGCA	823994
rs346767888	snp	C/G			synonymous-codon	BT2	TAIR10	3:17909819	CCGTTGCTTCAGCTG[C/G]GTGACCATGTAGACG	823994
rs346786814	snp	A/T			missense	BT2	TAIR10	3:17910381	CGTCCGACGTCGGCG[A/T]TAGATTATATGAAAG	823994
rs346813723	snp	A/T			intron-variant	BT2	TAIR10	3:17908777	TTCTAAAGGTGGGTC[A/T]ACACAAAAAGATAAA	823994
rs346830240	snp	A/G			missense	BT2	TAIR10	3:17909164	TCTGACTTTTCCGCA[A/G]TCATTGACTTTTTGT	823994
rs346896564	snp	A/G			synonymous-codon	BT2	TAIR10	3:17909241	GCATATGTGCTCTAT[A/G]CACTCCATTGCCTCG	823994
rs346910902	snp	C/T			utr-variant-3-prime	BT2	TAIR10	3:17908320	AATATGACCTACTTA[C/T]ACAGCCAATTTAAAA	823994
rs346939993	snp	A/T			intron-variant	BT2	TAIR10	3:17910045	TAACCATCGGTTTGA[A/T]GTTTCTACATTTGGA	823994
rs347036305	snp	A/T			synonymous-codon	BT2	TAIR10	3:17910185	TCCACAGCCTCTGTA[A/T]CGTCTCATCGGTTTC	823994
rs347060569	snp	A/C			intron-variant	BT2	TAIR10	3:17909905	TAAAACAGAGACGCA[A/C]AAGGGTAGTTTAGTC	823994
rs347076866	snp	G/T			intron-variant	BT2	TAIR10	3:17908906	TAATTAAGCGTAAAT[G/T]GATTCGCTCATACTT	823994
rs347078168	snp	G/T			missense	BT2	TAIR10	3:17910112	AAGAGTAGAGGAATT[G/T]GATAAAAACCGAAAC	823994
rs347086134	snp	C/G			intron-variant	BT2	TAIR10	3:17910020	CGGGAAAATTGTGTA[C/G]TACCGGAAATAACCA	823994
rs347120036	snp	A/C			utr-variant-5-prime	BT2	TAIR10	3:17910476	ACAGCTTCCATTGAA[A/C]TTTTGTAGAGAAGAA	823994
rs347166052	snp	A/C			intron-variant	BT2	TAIR10	3:17910265	AATTTTAGCTAAAAA[A/C]CAAACCAGAAAAATG	823994
rs347175108	snp	A/C			missense	BT2	TAIR10	3:17909593	AGTTTACCGATTCGG[A/C]GTCATCGATGAACTG	823994
rs347186492	snp	G/T			intron-variant	BT2	TAIR10	3:17910075	AAAATTCAAGAAGAA[G/T]AACCGAACCAAACCA	823994
rs347187797	snp	A/G			synonymous-codon	BT2	TAIR10	3:17909698	ACTGCGAATGGATCA[A/G]ACGCATAGATCGAAG	823994
rs347477226	snp	C/T			synonymous-codon	BT2	TAIR10	3:17909175	CGCAGTCATTGACTT[C/T]TTGTTGTTATCTACT	823994

Full records

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