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
rs346440255	snp	C/T			utr-variant-5-prime	APC6	TAIR10	1:29617138	CGTCCCTTAACTTTT[C/T]TGTACTATGTCAATG	844213
rs346535330	snp	G/T			utr-variant-5-prime	APC6	TAIR10	1:29617399	AGATTTCGTCTGGAA[G/T]AATTCGATAGGCGAG	844213
rs346630342	snp	A/G			utr-variant-5-prime	APC6	TAIR10	1:29617416	ATTCGATAGGCGAGG[A/G]AATTATGAGGGAAGA	844213
rs346633422	snp	A/T			synonymous-codon	APC6	TAIR10	1:29619922	CAAAGCTACGGGTAT[A/T]GATGGCTCATTCTCA	844213
rs346714528	snp	C/T			intron-variant	APC6	TAIR10	1:29618707	TATAGTTTATGCATT[C/T]TTGTTGCTTTTTATT	844213
rs346730101	snp	A/T			intron-variant	APC6	TAIR10	1:29618043	TGGTTGACTACTACT[A/T]GGTTAGGATAGTAGC	844213
rs346781133	snp	A/T			intron-variant	APC6	TAIR10	1:29618767	GTTTACATGACTAGA[A/T]GGTTACTGAGACTTC	844213
rs346809560	snp	A/C			intron-variant	APC6	TAIR10	1:29618602	TGTAGATATCAGAAA[A/C]CTGACATGGACGTGA	844213
rs346818924	snp	C/T			missense	APC6	TAIR10	1:29619149	ACACTGATCTGTTGG[C/T]CTGTAAAGCTGAGTA	844213
rs346827266	snp	C/T			intron-variant	APC6	TAIR10	1:29620537	GAGAAGATAACTATC[C/T]AGTAAACTGAGTCAA	844213
rs346840049	snp	C/T			utr-variant-5-prime	APC6	TAIR10	1:29617046	ATAGAATAACCGACT[C/T]GTGTCATTAGTCAAA	844213
rs346853746	snp	A/T			intron-variant	APC6	TAIR10	1:29619894	CTTCATTTCTTTTAA[A/T]ATGGTCTTGCAGCAA	844213
rs346854325	snp	C/G			intron-variant	APC6	TAIR10	1:29619858	ATCTAGTAGGTAGGT[C/G]CATATGTGTCTGACC	844213
rs346898469	snp	C/G			utr-variant-5-prime	APC6	TAIR10	1:29617044	CAATAGAATAACCGA[C/G]TTGTGTCATTAGTCA	844213
rs346911650	snp	C/T			synonymous-codon	APC6	TAIR10	1:29619357	CATCTGAAGTGTACG[C/T]TGGTACATTTGGCCG	844213
rs346929748	snp	A/G			intron-variant	APC6	TAIR10	1:29619841	TATGCTGTCTTGATC[A/G]AATCTAGTAGGTAGG	844213
rs346932595	snp	A/G			intron-variant	APC6	TAIR10	1:29619864	TAGGTAGGTGCATAT[A/G]TGTCTGACCTGGAGC	844213
rs347010626	snp	A/G			synonymous-codon	APC6	TAIR10	1:29619976	TTCCTTTGCCGCCCA[A/G]GAGGAGGGTGACCAA	844213
rs347022922	snp	A/C			utr-variant-5-prime	APC6	TAIR10	1:29617329	ACTAGAGAAATCGGA[A/C]GAACAAAAATTTCCC	844213
rs347035973	snp	C/T			intron-variant	APC6	TAIR10	1:29619825	AACTATGCTGTGGCA[C/T]TATGCTGTCTTGATC	844213
rs347065384	snp	A/C/G			synonymous-codon	APC6	TAIR10	1:29619210	TTTTGAACTAACCGC[A/C/G]GCGTAAGAAACTTGA	844213
rs347098405	snp	A/G			synonymous-codon	APC6	TAIR10	1:29619410	AAATGAGCTCTATCT[A/G]ATGGCGTGCAATTTG	844213
rs347106638	snp	A/G			intron-variant	APC6	TAIR10	1:29618968	GCTTGCTGATTCTCT[A/G]TTCTGTCGATTTCCT	844213
rs347185632	snp	A/G			intron-variant	APC6	TAIR10	1:29620704	ATATTGGCGCACACA[A/G]AACTACCATGATCTT	844213
rs347215161	snp	G/T			missense	APC6	TAIR10	1:29621253	CAGAACGGGGTTGAT[G/T]CAAAGGTTGAGCTCT	844213
rs347254461	snp	A/G			intron-variant	APC6	TAIR10	1:29621107	CTTCTCTATCAGATG[A/G]TGAGCTATACATTTT	844213
rs347279474	snp	A/G			intron-variant	APC6	TAIR10	1:29619291	TGAATGATTCTAGCA[A/G]TGTGGTCTCTTTTGG	844213
rs347316826	snp	A/C			intron-variant	APC6	TAIR10	1:29620910	AAACACCAGTCATTT[A/C]TTCGAAACAATACTA	844213
rs347326309	snp	C/T			intron-variant	APC6	TAIR10	1:29619818	TTTAGGTAACTATGC[C/T]GTGGCATTATGCTGT	844213
rs347353366	snp	G/T			intron-variant	APC6	TAIR10	1:29619661	TGAAAATGTTTCAAA[G/T]TTTTGTGTTTGAGAC	844213
rs347370505	snp	C/T			intron-variant	APC6	TAIR10	1:29620181	GAATCTTGATATTAT[C/T]TTGTTCCAGGTGTCA	844213
rs347385820	snp	G/T			utr-variant-5-prime	APC6	TAIR10	1:29617155	GTACTATGTCAATGG[G/T]CTGAAAGCCCACAAC	844213
rs347464633	snp	C/T			synonymous-codon	APC6	TAIR10	1:29620849	CTTAAGCACTTATTC[C/T]GGCTTGGCTTACACT	844213

Full records

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