Joint Open Genome and Omics Platform (JoGo)

Search by Variant

Regionname

e.g. ALDH2_chr12_111761933_111822532, HBB_chr11_5220464_5232071.

Chr

Chromosome name (e.g., chr11).

Snpeff genename

Exact SnpEff gene name.

Sampleids

Target sampleid (e.g. HG02615).

Snpeff haplotype class

Haplotype-annotation class (e.g., ahapid, ahapid+chapid).

Snpeff annotation impact

Exact impact level (e.g., HIGH, MODERATE, LOW).

Snpeff annotation impact detail

Keyword match in SnpEff annotation.

Hapid

One or more haplotype IDs (comma-separated; e.g., a0001, a01, a0001c0001, a01c02, a1c2, a0001c0001t0005, a0001c0001t0005g0018).

Samplehapid

Sample haplotype IDs to include (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

No_hapid

Haplotype IDs to exclude (comma-separated; e.g., a0001, a0002, a0001c0001, a0001c0001t0005, a1, a01).

No_samplehapid

Sample haplotype IDs to exclude (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

Start

Start position (GRCh38).

End

End position (GRCh38).

Minac

Minimum alternate allele count (≥).

Maxac

Maximum alternate allele count (≤).

Minlen

Minimum variant length (≥).

Maxlen

Maximum variant length (≤).

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⚠️ Results limited to 10,000 hits. Refine your search for more specific results.

regionname	pos	ref	alt	annotation	impact	samples	ahapids	achapids	acthapids	actghapids	ac	an	af	len	hgvs_c	genename	geneid	featuretype	featureid	transcript_biotype	rank	distance	status	chr	external
ARHGAP26_chr5_142765377_143234007	143012552	C C	CATACATA others(25): Show CATACATACATACATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG02922.hp1 HG03453.hp2 HG02922.hp1 HG03453.hp2	a0001 a0001	a0001c0001 a0001c0002 a0001c0001 a0001c0002	a0001c0001t0030 a0001c0002t0012 a0001c0001t0030 a0001c0002t0012	a0001c0001t0030g0102 a0001c0002t0012g0093 a0001c0001t0030g0102 a0001c0002t0012g0093	2	198	0.0101	32	c.110 others(51): Show c.1108-1525_1108-1524insCATACATACATATATATATATATATA TATATA	ARHGAP26	ENSG00000145819.18	transcript	ENST00000645722.2	protein_coding	11/22		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGAP26_chr5_142765377_143234007	143012552	C C	CATACATA others(25): Show CATACATATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	NA19081.hp1 NA19081.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0003 a0001c0001t0003	a0001c0001t0003g0119 a0001c0001t0003g0119	1	198	0.0051	32	c.110 others(51): Show c.1108-1525_1108-1524insCATATATATATATATATATATATATA TATATA	ARHGAP26	ENSG00000145819.18	transcript	ENST00000645722.2	protein_coding	11/22		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGAP26_chr5_142765377_143234007	143012552	C C	CATATATA others(25): Show CATATATATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG02735.hp1 HG02809.hp1 HG02735.hp1 HG02809.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0002 a0001c0001t0006 a0001c0001t0002 a0001c0001t0006	a0001c0001t0002g0142 a0001c0001t0006g0084 a0001c0001t0002g0142 a0001c0001t0006g0084	2	198	0.0101	32	c.110 others(51): Show c.1108-1504_1108-1503insATATATATATATATATATATATATAT ATATAT	ARHGAP26	ENSG00000145819.18	transcript	ENST00000645722.2	protein_coding	11/22		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGAP27_chr17_45388908_45437870	45399591	C C	CAAAGAAA others(25): Show CAAAGAAAAGAAAAGAAAAGAAAAAAGAAAAGA	intron_variant intron_variant	MODIFIER	HG01175.hp1 HG01175.hp1	a0003 a0003	a0003c0003 a0003c0003	a0003c0003t0001 a0003c0003t0001	a0003c0003t0001g0154 a0003c0003t0001g0154	1	347	0.0029	32	c.174 others(51): Show c.1744-1545_1744-1544insTCTTTTCTTTTTTCTTTTCTTTTCTT TTCTTT	ARHGAP27	ENSG00000159314.13	transcript	ENST00000685559.1	protein_coding	12/19			chr17	TogoVar
ARHGAP28_chr18_6724716_6920716	6730219	G G	GTATGTAT others(25): Show GTATGTATATATATATATATATATATATATATA	intron_variant intron_variant	MODIFIER	HG03041.hp1 HG03041.hp1	a0003 a0003	a0003c0023 a0003c0023	a0003c0023t0001 a0003c0023t0001	a0003c0023t0001g0120 a0003c0023t0001g0120	1	248	0.0040	32	c.122 others(47): Show c.122+277_122+278insATGTATATATATATATATATATATATATAT AT	ARHGAP28	ENSG00000088756.13	transcript	ENST00000383472.9	protein_coding	1/17		INFO_REALIGN_3_PRIME	chr18	TogoVar
ARHGAP28_chr18_6724716_6920716	6736780	A A	ATTAAATG others(25): Show ATTAAATGCTGTGTTAAGAGAGTGTAGTTGTTC	intron_variant intron_variant	MODIFIER	HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show HG01243.hp2 HG01346.hp1 HG02280.hp2 HG02615.hp1 HG02818.hp1 HG02922.hp2 HG03098.hp1 HG03139.hp1 HG03471.hp2 HG03540.hp1 NA18906.hp2 NA20300.hp1	a0001 a0002 a0006 others(2): Show a0001 a0002 a0006 a0007 a0008	a0001c0001 a0001c0003 a0002c0002 others(3): Show a0001c0001 a0001c0003 a0002c0002 a0006c0009 a0007c0008 a0008c0011	a0001c0001t0001 a0001c0001t0008 a0001c0003t0003 others(6): Show a0001c0001t0001 a0001c0001t0008 a0001c0003t0003 a0002c0002t0002 a0002c0002t0004 a0006c0009t0005 a0006c0009t0009 a0007c0008t0002 a0008c0011t0005	a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0008g0143 a0001c0003t0003g0145 a0001c0003t0003g0154 a0002c0002t0002g0148 a0002c0002t0004g0147 a0006c0009t0005g0144 a0006c0009t0009g0153 a0007c0008t0002g0146 a0008c0011t0005g0152	12	248	0.0484	32	c.122 others(49): Show c.122+6844_122+6875dupGCTGTGTTAAGAGAGTGTAGTTGTTCTT AAAT	ARHGAP28	ENSG00000088756.13	transcript	ENST00000383472.9	protein_coding	1/17		INFO_REALIGN_3_PRIME	chr18	TogoVar
ARHGAP31_chr3_119289383_119425714	119293703	A A	AGTGTGTG others(25): Show AGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	upstream_gene_variant upstream_gene_variant	MODIFIER	HG00438.hp1 HG01975.hp2 HG02015.hp2 others(6): Show HG00438.hp1 HG01975.hp2 HG02015.hp2 HG02615.hp1 HG03516.hp2 HG03579.hp1 HG03834.hp2 NA18994.hp2 NA19086.hp2	a0001 a0007 a0001 a0007	a0001c0001 a0001c0004 a0001c0005 others(1): Show a0001c0001 a0001c0004 a0001c0005 a0007c0012	a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 others(6): Show a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 a0001c0001t0052 a0001c0004t0003 a0001c0005t0012 a0001c0005t0027 a0001c0005t0047 a0007c0012t0001	a0001c0001t0005g0022 a0001c0001t0017g0303 a0001c0001t0018g0207 others(6): Show a0001c0001t0005g0022 a0001c0001t0017g0303 a0001c0001t0018g0207 a0001c0001t0052g0283 a0001c0004t0003g0021 a0001c0005t0012g0287 a0001c0005t0027g0044 a0001c0005t0047g0239 a0007c0012t0001g0050	9	310	0.0290	32	c.-12 others(43): Show c.-1202_-1201insGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	ARHGAP31	ENSG00000031081.11	transcript	ENST00000264245.9	protein_coding		679		chr3	TogoVar
ARHGAP32_chr11_128960060_129197325	129143072	C C	CATATATA others(25): Show CATATATATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG02922.hp1 HG02970.hp1 HG03927.hp1 others(4): Show HG02922.hp1 HG02970.hp1 HG03927.hp1 HG03942.hp1 NA18950.hp2 NA18971.hp2 NA19078.hp1	a0001 a0001	a0001c0001 a0001c0014 a0001c0001 a0001c0014	a0001c0001t0002 a0001c0001t0004 a0001c0014t0004 a0001c0001t0002 a0001c0001t0004 a0001c0014t0004	a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0004g0173 others(4): Show a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0014t0004g0177	7	398	0.0176	32	c.226 others(51): Show c.226-18179_226-18178insATATATATATATATATATATATATAT ATATAT	ARHGAP32	ENSG00000134909.19	transcript	ENST00000682385.1	protein_coding	2/22			chr11	TogoVar
ARHGAP42_chr11_100682288_100998941	100980559	C C	CTTTTTTT others(25): Show CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	intron_variant intron_variant	MODIFIER	HG02602.hp2 HG02602.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0068 a0001c0001t0001g0068	1	286	0.0035	32	c.245 others(51): Show c.2456+1540_2456+1541insTTTTTTTTTTTTTTTTTTTTTTTTTT TTTTTT	ARHGAP42	ENSG00000165895.19	transcript	ENST00000298815.13	protein_coding	22/23		INFO_REALIGN_3_PRIME	chr11	TogoVar
ARHGAP44_chr17_12784498_12996643	12948723	T T	TACACACA others(25): Show TACACACACACACACACACACACACACACACAC	intron_variant intron_variant	MODIFIER	HG00099.hp1 HG01109.hp2 HG01243.hp1 others(15): Show HG00099.hp1 HG01109.hp2 HG01243.hp1 HG01928.hp2 HG02071.hp1 HG02071.hp2 HG02145.hp1 HG02257.hp1 HG02698.hp1 HG03017.hp1 HG03239.hp1 HG03486.hp1 HG03516.hp2 NA18982.hp2 NA18984.hp1 NA19007.hp1 NA19054.hp2 NA19083.hp1	a0001 a0001	a0001c0001 a0001c0005 a0001c0006 others(1): Show a0001c0001 a0001c0005 a0001c0006 a0001c0008	a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(6): Show a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 a0001c0001t0017 a0001c0001t0021 a0001c0005t0001 a0001c0006t0003 a0001c0008t0020	a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0117 others(15): Show a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0005g0050 a0001c0001t0005g0057 a0001c0001t0005g0061 a0001c0001t0005g0072 a0001c0001t0006g0024 a0001c0001t0006g0129 a0001c0001t0013g0098 a0001c0001t0017g0040 a0001c0001t0021g0195 a0001c0005t0001g0224 a0001c0006t0003g0091 a0001c0008t0020g0181	18	230	0.0783	32	c.862 others(47): Show c.862-389_862-388insACACACACACACACACACACACACACACAC AC	ARHGAP44	ENSG00000006740.18	transcript	ENST00000379672.10	protein_coding	10/20		INFO_REALIGN_3_PRIME	chr17	TogoVar
ARHGAP44_chr17_12784498_12996643	12978035	T T	TAAAAAAA others(25): Show TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	intron_variant intron_variant	MODIFIER	NA18984.hp2 NA18984.hp2	a0001 a0001	a0001c0002 a0001c0002	a0001c0002t0001 a0001c0002t0001	a0001c0002t0001g0104 a0001c0002t0001g0104	1	230	0.0044	32	c.176 others(51): Show c.1764-2023_1764-2022insAAAAAAAAAAAAAAAAAAAAAAAAAA AAAAAA	ARHGAP44	ENSG00000006740.18	transcript	ENST00000379672.10	protein_coding	18/20			chr17	TogoVar
ARHGAP6_chrX_11132544_11670920	11346719	A A	AAAAGAAA others(25): Show AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAG	intron_variant intron_variant	MODIFIER	HG06807.hp1 NA19240.hp1 NA20905.hp1 HG06807.hp1 NA19240.hp1 NA20905.hp1	a0001 a0002 a0001 a0002	a0001c0001 a0002c0002 a0002c0005 a0001c0001 a0002c0002 a0002c0005	a0001c0001t0001 a0002c0002t0003 a0002c0005t0006 a0001c0001t0001 a0002c0002t0003 a0002c0005t0006	a0001c0001t0001g0045 a0002c0002t0003g0006 a0002c0005t0006g0018 a0001c0001t0001g0045 a0002c0002t0003g0006 a0002c0005t0006g0018	3	144	0.0208	32	c.589 others(51): Show c.589-92044_589-92013dupCTTTCTTTCTTTCTTTCTTTCTTTCT TTCTTT	ARHGAP6	ENSG00000047648.23	transcript	ENST00000337414.9	protein_coding	1/12			chrX	TogoVar
ARHGAP6_chrX_11132544_11670920	11567566	A A	AAAAAAAA others(25): Show AAAAAAAATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG03098.hp1 NA20129.hp2 HG03098.hp1 NA20129.hp2	a0001 a0002 a0001 a0002	a0001c0001 a0002c0002 a0001c0001 a0002c0002	a0001c0001t0001 a0002c0002t0006 a0001c0001t0001 a0002c0002t0006	a0001c0001t0001g0024 a0002c0002t0006g0031 a0001c0001t0001g0024 a0002c0002t0006g0031	2	144	0.0139	32	c.588 others(51): Show c.588+96674_588+96675insATATATATATATATATATATATATAT TTTTTT	ARHGAP6	ENSG00000047648.23	transcript	ENST00000337414.9	protein_coding	1/12			chrX	TogoVar
ARHGAP8_chr22_44747575_44867784	44800566	C C	CCTCCCCA others(25): Show CCTCCCCACAGCTGTCCGTGTGTGGGGGCACCT	intron_variant intron_variant	MODIFIER	HG01891.hp2 HG01891.hp2	a0002 a0002	a0002c0003 a0002c0003	a0002c0003t0001 a0002c0003t0001	a0002c0003t0001g0387 a0002c0003t0001g0387	1	390	0.0026	32	c.80- others(47): Show c.80-1505_80-1504insACAGCTGTCCGTGTGTGGGGGCACCTCTCC CC	ARHGAP8	ENSG00000241484.10	transcript	ENST00000356099.11	protein_coding	2/11		INFO_REALIGN_3_PRIME	chr22	TogoVar
ARHGAP8_chr22_44747575_44867784	44800566	C C	CCTCCCCG others(25): Show CCTCCCCGCAGCTGTCCGTGTGTGGGGGCACCT	intron_variant intron_variant	MODIFIER	HG02738.hp2 HG02922.hp1 HG02970.hp2 others(2): Show HG02738.hp2 HG02922.hp1 HG02970.hp2 HG03704.hp2 NA19043.hp2	a0001 a0002 a0001 a0002	a0001c0001 a0002c0003 a0002c0020 others(2): Show a0001c0001 a0002c0003 a0002c0020 a0002c0055 a0002c0076	a0001c0001t0001 a0002c0003t0004 a0002c0020t0005 others(2): Show a0001c0001t0001 a0002c0003t0004 a0002c0020t0005 a0002c0055t0005 a0002c0076t0004	a0001c0001t0001g0042 a0002c0003t0004g0177 a0002c0020t0005g0073 others(2): Show a0001c0001t0001g0042 a0002c0003t0004g0177 a0002c0020t0005g0073 a0002c0055t0005g0062 a0002c0076t0004g0143	5	390	0.0128	32	c.80- others(47): Show c.80-1495_80-1494insGTGTGTGGGGGCACCTCTCCCCGCAGCTGT CC	ARHGAP8	ENSG00000241484.10	transcript	ENST00000356099.11	protein_coding	2/11		INFO_REALIGN_3_PRIME	chr22	TogoVar
ARHGAP8_chr22_44747575_44867784	44800688	G G	GGGGGGCG others(25): Show GGGGGGCGCCCCTCCCCGCAGCTGTCCGTGTGT	intron_variant intron_variant	MODIFIER	HG00639.hp2 HG01346.hp1 HG01928.hp1 others(5): Show HG00639.hp2 HG01346.hp1 HG01928.hp1 HG02273.hp1 HG02273.hp2 HG03654.hp1 NA18971.hp1 NA19009.hp1	a0001 a0002 a0003 a0001 a0002 a0003	a0001c0001 a0001c0050 a0002c0051 others(2): Show a0001c0001 a0001c0050 a0002c0051 a0003c0005 a0003c0080	a0001c0001t0003 a0001c0050t0003 a0002c0051t0004 others(2): Show a0001c0001t0003 a0001c0050t0003 a0002c0051t0004 a0003c0005t0002 a0003c0080t0002	a0001c0001t0003g0376 a0001c0050t0003g0217 a0002c0051t0004g0216 others(5): Show a0001c0001t0003g0376 a0001c0050t0003g0217 a0002c0051t0004g0216 a0003c0005t0002g0083 a0003c0005t0002g0121 a0003c0005t0002g0372 a0003c0005t0002g0377 a0003c0080t0002g0147	8	390	0.0205	32	c.80- others(47): Show c.80-1358_80-1357insTGGGGGCGCCCCTCCCCGCAGCTGTCCGTG TG	ARHGAP8	ENSG00000241484.10	transcript	ENST00000356099.11	protein_coding	2/11		INFO_REALIGN_3_PRIME	chr22	TogoVar
ARHGEF10_chr8_1818926_1963641	1839883	T T	AGTCTGGT others(25): Show AGTCTGGTGTGGGGACTGTCTGGTGTGGAAGTT	intron_variant intron_variant	MODIFIER	NA18980.hp2 NA18980.hp2	a0006 a0006	a0006c0113 a0006c0113	a0006c0113t0070 a0006c0113t0070	a0006c0113t0070g0304 a0006c0113t0070g0304	1	363	0.0028	32	c.-47 others(49): Show c.-47-3471_-47-3470insAGTCTGGTGTGGGGACTGTCTGGTGTGG AAGT	ARHGEF10	ENSG00000104728.16	transcript	ENST00000349830.8	protein_coding	1/28			chr8	TogoVar
ARHGEF10_chr8_1818926_1963641	1840185	A A	ACTGTCTG others(25): Show ACTGTCTGGTGTGGGGACCGTCTGGTGTGGAAG	intron_variant intron_variant	MODIFIER	HG03834.hp2 NA21309.hp2 HG03834.hp2 NA21309.hp2	a0001 a0001	a0001c0052 a0001c0140 a0001c0052 a0001c0140	a0001c0052t0052 a0001c0140t0005 a0001c0052t0052 a0001c0140t0005	a0001c0052t0052g0336 a0001c0140t0005g0297 a0001c0052t0052g0336 a0001c0140t0005g0297	2	363	0.0055	32	c.-47 others(49): Show c.-47-3155_-47-3154insGGACCGTCTGGTGTGGAAGCTGTCTGGT GTGG	ARHGEF10	ENSG00000104728.16	transcript	ENST00000349830.8	protein_coding	1/28		INFO_REALIGN_3_PRIME	chr8	TogoVar
ARHGEF10_chr8_1818926_1963641	1860264	C C	CCGTAGAG others(25): Show CCGTAGAGTCCGGGCCTGACCTTCCCCCCTCCT	intron_variant intron_variant	MODIFIER	NA18957.hp1 NA18957.hp1	a0001 a0001	a0001c0009 a0001c0009	a0001c0009t0006 a0001c0009t0006	a0001c0009t0006g0120 a0001c0009t0006g0120	1	363	0.0028	32	c.481 others(45): Show c.481+81_481+82insGTAGAGTCCGGGCCTGACCTTCCCCCCTCCTC	ARHGEF10	ENSG00000104728.16	transcript	ENST00000349830.8	protein_coding	4/28		INFO_REALIGN_3_PRIME	chr8	TogoVar
ARHGEF11_chr1_156929840_157050742	156936495	A A	AATATATA others(25): Show AATATATATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG02647.hp2 HG02647.hp2	a0002 a0002	a0002c0004 a0002c0004	a0002c0004t0008 a0002c0004t0008	a0002c0004t0008g0200 a0002c0004t0008g0200	1	362	0.0028	32	c.463 others(49): Show c.4630+320_4630+321insATATATATATATATATATATATATATAT ATAT	ARHGEF11	ENSG00000132694.19	transcript	ENST00000368194.8	protein_coding	40/40			chr1	TogoVar
ARHGEF11_chr1_156929840_157050742	156936497	A A	AAAATATA others(25): Show AAAATATATATATATATATATATATATATATAT	intron_variant intron_variant	MODIFIER	HG02145.hp2 HG03195.hp1 HG02145.hp2 HG03195.hp1	a0002 a0002	a0002c0004 a0002c0004	a0002c0004t0013 a0002c0004t0013	a0002c0004t0013g0186 a0002c0004t0013g0190 a0002c0004t0013g0186 a0002c0004t0013g0190	2	362	0.0055	32	c.463 others(49): Show c.4630+318_4630+319insATATATATATATATATATATATATATAT ATTT	ARHGEF11	ENSG00000132694.19	transcript	ENST00000368194.8	protein_coding	40/40			chr1	TogoVar
ARHGEF11_chr1_156929840_157050742	157013259	T T	TCACACAC others(25): Show TCACACACACACACACACACACACACACACACA	intron_variant intron_variant	MODIFIER	NA19005.hp2 NA19010.hp1 NA19005.hp2 NA19010.hp1	a0003 a0003	a0003c0003 a0003c0003	a0003c0003t0003 a0003c0003t0003	a0003c0003t0003g0239 a0003c0003t0003g0259 a0003c0003t0003g0239 a0003c0003t0003g0259	2	362	0.0055	32	c.33- others(49): Show c.33-27087_33-27086insTGTGTGTGTGTGTGTGTGTGTGTGTGTG TGTG	ARHGEF11	ENSG00000132694.19	transcript	ENST00000368194.8	protein_coding	1/40			chr1	TogoVar
ARHGEF12_chr11_120331413_120494937	120347179	C C	CCTTGCTT others(25): Show CCTTGCTTCCTTCCTTCCTTCCTTTCTTTCTTT	intron_variant intron_variant	MODIFIER	NA19030.hp1 NA19030.hp1	a0006 a0006	a0006c0013 a0006c0013	a0006c0013t0001 a0006c0013t0001	a0006c0013t0001g0293 a0006c0013t0001g0293	1	308	0.0033	32	c.32+ others(47): Show c.32+9907_32+9908insGCTTCCTTCCTTCCTTCCTTTCTTTCTTTC TT	ARHGEF12	ENSG00000196914.9	transcript	ENST00000397843.7	protein_coding	1/40		INFO_REALIGN_3_PRIME	chr11	TogoVar
ARHGEF12_chr11_120331413_120494937	120347183	C C	CCTTCCTT others(25): Show CCTTCCTTCCTTCCTTCCTTTCTTTCTTTCTTT	intron_variant intron_variant	MODIFIER	HG01243.hp1 HG01243.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0026 a0001c0001t0026	a0001c0001t0026g0230 a0001c0001t0026g0230	1	308	0.0033	32	c.32+ others(47): Show c.32+9911_32+9912insCCTTCCTTCCTTCCTTTCTTTCTTTCTTTC TT	ARHGEF12	ENSG00000196914.9	transcript	ENST00000397843.7	protein_coding	1/40		INFO_REALIGN_3_PRIME	chr11	TogoVar
ARHGEF12_chr11_120331413_120494937	120347183	C C	CCTTCCTT others(25): Show CCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT	intron_variant intron_variant	MODIFIER	HG02257.hp1 NA18906.hp2 HG02257.hp1 NA18906.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0211 a0001c0001t0001g0232 a0001c0001t0001g0211 a0001c0001t0001g0232	2	308	0.0065	32	c.32+ others(47): Show c.32+9911_32+9912insCCTTCCTTTCTTTCTTTCTTTCTTTCTTTC TT	ARHGEF12	ENSG00000196914.9	transcript	ENST00000397843.7	protein_coding	1/40		INFO_REALIGN_3_PRIME	chr11	TogoVar
ARHGEF12_chr11_120331413_120494937	120347183	C C	CCTTTCTT others(25): Show CCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT	intron_variant intron_variant	MODIFIER	NA19079.hp2 homoSapiens_chm13v2.hp1 NA19079.hp2 homoSapiens_chm13v2.hp1	a0001 a0001	a0001c0001 a0001c0018 a0001c0001 a0001c0018	a0001c0001t0001 a0001c0018t0004 a0001c0001t0001 a0001c0018t0004	a0001c0001t0001g0240 a0001c0018t0004g0239 a0001c0001t0001g0240 a0001c0018t0004g0239	2	308	0.0065	32	c.32+ others(47): Show c.32+9930_32+9931insTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT CT	ARHGEF12	ENSG00000196914.9	transcript	ENST00000397843.7	protein_coding	1/40		INFO_REALIGN_3_PRIME	chr11	TogoVar
ARHGEF33_chr2_38884875_38980454	38934578	T T	TCCCCCCC others(25): Show TCCCCCCCTCTCTCCCGCTTCTCTCCCTCCCTC	intron_variant intron_variant	MODIFIER	HG02145.hp1 HG02145.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0003 a0001c0001t0003	a0001c0001t0003g0246 a0001c0001t0003g0246	1	278	0.0036	32	c.506 others(49): Show c.506-1191_506-1190insCTCTCTCCCGCTTCTCTCCCTCCCTCCC CCCC	ARHGEF33	ENSG00000214694.13	transcript	ENST00000409978.7	protein_coding	7/17		INFO_REALIGN_3_PRIME	chr2	TogoVar
ARHGEF37_chr5_149576498_149639968	149598761	T T	TATATATA others(25): Show TATATATATATATATATATATATAGATAGATAG	intron_variant intron_variant	MODIFIER	HG02622.hp1 HG02622.hp1	a0005 a0005	a0005c0011 a0005c0011	a0005c0011t0003 a0005c0011t0003	a0005c0011t0003g0324 a0005c0011t0003g0324	1	394	0.0025	32	c.186 others(47): Show c.186+809_186+810insTATATATATATATATATATAGATAGATAGA TA	ARHGEF37	ENSG00000183111.12	transcript	ENST00000333677.7	protein_coding	2/12		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGEF37_chr5_149576498_149639968	149599434	C C	CTTACTTA others(25): Show CTTACTTATTTATTTATTTATTTATTTATTTAT	intron_variant intron_variant	MODIFIER	NA20129.hp1 NA20129.hp1	a0004 a0004	a0004c0010 a0004c0010	a0004c0010t0014 a0004c0010t0014	a0004c0010t0014g0328 a0004c0010t0014g0328	1	394	0.0025	32	c.186 others(49): Show c.186+1482_186+1483insCTTATTTATTTATTTATTTATTTATTTA TTTA	ARHGEF37	ENSG00000183111.12	transcript	ENST00000333677.7	protein_coding	2/12		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGEF37_chr5_149576498_149639968	149599434	C C	CTTATTTA others(25): Show CTTATTTATTTATTTATTTATTTATTTATTTAT	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00408.hp1 HG00438.hp2 others(37): Show HG00099.hp2 HG00408.hp1 HG00438.hp2 HG00621.hp2 HG01069.hp1 HG01081.hp2 HG01257.hp1 HG01361.hp2 HG01952.hp1 HG01975.hp1 HG01978.hp1 HG02129.hp2 HG02647.hp2 HG02683.hp2 NA18612.hp1 NA18948.hp1 NA18949.hp2 NA18951.hp1 NA18951.hp2 NA18956.hp1 NA18957.hp2 NA18965.hp1 NA18966.hp1 NA18969.hp1 NA18973.hp2 NA18975.hp2 NA18989.hp2 NA18991.hp2 NA18995.hp2 NA19001.hp1 NA19007.hp2 NA19009.hp1 NA19060.hp2 NA19062.hp1 NA19067.hp2 NA19080.hp2 NA19085.hp1 NA19085.hp2 NA19088.hp2 NA19090.hp2	a0001 a0003 a0005 others(1): Show a0001 a0003 a0005 a0014	a0001c0002 a0003c0003 a0003c0029 others(2): Show a0001c0002 a0003c0003 a0003c0029 a0005c0027 a0014c0022	a0001c0002t0005 a0001c0002t0011 a0003c0003t0002 others(4): Show a0001c0002t0005 a0001c0002t0011 a0003c0003t0002 a0003c0003t0016 a0003c0029t0002 a0005c0027t0003 a0014c0022t0004	a0001c0002t0005g0374 a0001c0002t0011g0365 a0003c0003t0002g0012 others(36): Show a0001c0002t0005g0374 a0001c0002t0011g0365 a0003c0003t0002g0012 a0003c0003t0002g0248 a0003c0003t0002g0270 a0003c0003t0002g0274 a0003c0003t0002g0277 a0003c0003t0002g0278 a0003c0003t0002g0279 a0003c0003t0002g0280 a0003c0003t0002g0281 a0003c0003t0002g0282 a0003c0003t0002g0293 a0003c0003t0002g0294 a0003c0003t0002g0298 a0003c0003t0002g0299 a0003c0003t0002g0300 a0003c0003t0002g0301 a0003c0003t0002g0302 a0003c0003t0002g0304 a0003c0003t0002g0305 a0003c0003t0002g0308 a0003c0003t0002g0309 a0003c0003t0002g0310 a0003c0003t0002g0311 a0003c0003t0002g0313 a0003c0003t0002g0315 a0003c0003t0002g0316 a0003c0003t0002g0330 a0003c0003t0002g0331 a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0346 a0003c0003t0002g0377 a0003c0003t0016g0290 a0003c0003t0016g0312 a0003c0029t0002g0273 a0005c0027t0003g0237 a0014c0022t0004g0366	40	394	0.1015	32	c.186 others(49): Show c.186+1502_186+1503insTTTATTTATTTATTTATTTATTTATTTA TTTA	ARHGEF37	ENSG00000183111.12	transcript	ENST00000333677.7	protein_coding	2/12		INFO_REALIGN_3_PRIME	chr5	TogoVar
ARHGEF38_chr4_105547620_105685914	105561400	T T	TAGAATAG others(25): Show TAGAATAGAATAGAATAGAATGGAATAGAATAG	intron_variant intron_variant	MODIFIER	HG03516.hp1 HG03516.hp1	a0005 a0005	a0005c0008 a0005c0008	a0005c0008t0001 a0005c0008t0001	a0005c0008t0001g0151 a0005c0008t0001g0151	1	186	0.0054	32	c.196 others(49): Show c.196+8440_196+8441insGAATAGAATAGAATAGAATGGAATAGAA TAGA	ARHGEF38	ENSG00000236699.9	transcript	ENST00000420470.3	protein_coding	1/13		INFO_REALIGN_3_PRIME	chr4	TogoVar
ARHGEF38_chr4_105547620_105685914	105561400	T T	TAGAATAG others(25): Show TAGAATAGAATAGAATGGAATAGAATAGAATAG	intron_variant intron_variant	MODIFIER	HG01256.hp1 HG01256.hp1	a0001 a0001	a0001c0002 a0001c0002	a0001c0002t0002 a0001c0002t0002	a0001c0002t0002g0001 a0001c0002t0002g0001	1	186	0.0054	32	c.196 others(49): Show c.196+8440_196+8441insGAATAGAATAGAATGGAATAGAATAGAA TAGA	ARHGEF38	ENSG00000236699.9	transcript	ENST00000420470.3	protein_coding	1/13		INFO_REALIGN_3_PRIME	chr4	TogoVar
ARHGEF4_chr2_130831914_131052253	130926048	C C	CTTTCTTT others(25): Show CTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTT	intron_variant intron_variant	MODIFIER	HG01109.hp2 HG02895.hp1 HG01109.hp2 HG02895.hp1	a0003 a0007 a0003 a0007	a0003c0003 a0007c0017 a0003c0003 a0007c0017	a0003c0003t0001 a0007c0017t0001 a0003c0003t0001 a0007c0017t0001	a0003c0003t0001g0030 a0007c0017t0001g0108 a0003c0003t0001g0030 a0007c0017t0001g0108	2	144	0.0139	32	c.355 others(51): Show c.3553-4903_3553-4902insTTCTTTCTCTTTCTTTCTTTCTTTCT TTCTTT	ARHGEF4	ENSG00000136002.21	transcript	ENST00000409359.7	protein_coding	2/13		INFO_REALIGN_3_PRIME	chr2	TogoVar
ARHGEF4_chr2_130831914_131052253	130926048	C C	CTTTCTTT others(25): Show CTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTT	intron_variant intron_variant	MODIFIER	HG03516.hp1 NA18971.hp2 NA18990.hp1 others(1): Show HG03516.hp1 NA18971.hp2 NA18990.hp1 NA20129.hp1	a0003 a0009 a0012 a0003 a0009 a0012	a0003c0003 a0009c0047 a0012c0019 a0003c0003 a0009c0047 a0012c0019	a0003c0003t0001 a0009c0047t0001 a0012c0019t0001 a0003c0003t0001 a0009c0047t0001 a0012c0019t0001	a0003c0003t0001g0081 a0009c0047t0001g0110 a0012c0019t0001g0127 others(1): Show a0003c0003t0001g0081 a0009c0047t0001g0110 a0012c0019t0001g0127 a0012c0019t0001g0129	4	144	0.0278	32	c.355 others(51): Show c.3553-4903_3553-4902insTTCTTTCTTTCTCTTTCTTTCTTTCT TTCTTT	ARHGEF4	ENSG00000136002.21	transcript	ENST00000409359.7	protein_coding	2/13		INFO_REALIGN_3_PRIME	chr2	TogoVar
ARHGEF4_chr2_130831914_131052253	130926048	C C	CTTTCTTT others(25): Show CTTTCTTTCTTTCTTTCTCTTTCTTTCTTTCTT	intron_variant intron_variant	MODIFIER	HG04115.hp2 NA18970.hp2 HG04115.hp2 NA18970.hp2	a0004 a0004	a0004c0004 a0004c0020 a0004c0004 a0004c0020	a0004c0004t0007 a0004c0020t0001 a0004c0004t0007 a0004c0020t0001	a0004c0004t0007g0006 a0004c0020t0001g0016 a0004c0004t0007g0006 a0004c0020t0001g0016	2	144	0.0139	32	c.355 others(51): Show c.3553-4903_3553-4902insTTCTTTCTTTCTTTCTCTTTCTTTCT TTCTTT	ARHGEF4	ENSG00000136002.21	transcript	ENST00000409359.7	protein_coding	2/13		INFO_REALIGN_3_PRIME	chr2	TogoVar
ARID1A_chr1_26691015_26787104	26710494	T T	TACACACA others(25): Show TACACACACACACACACACACACACACACACAC	intron_variant intron_variant	MODIFIER	HG01928.hp1 HG01928.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0106 a0001c0001t0001g0106	1	146	0.0069	32	c.113 others(53): Show c.1137+12957_1137+12988dupACACACACACACACACACACACAC ACACACAC	ARID1A	ENSG00000117713.21	transcript	ENST00000324856.13	protein_coding	1/19		INFO_REALIGN_3_PRIME	chr1	TogoVar
ARID1B_chr6_156772378_157215779	157147439	T T	TCCCTCAC others(25): Show TCCCTCACCCCCGCCTCCGGCCCTGCCCGCCAG	intron_variant intron_variant	MODIFIER	HG02895.hp1 HG02895.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0070 a0001c0001t0001g0070	1	150	0.0067	32	c.276 others(51): Show c.2762-1161_2762-1160insCCCGCCAGCCCTCACCCCCGCCTCCG GCCCTG	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157147448	C C	CCCGCCTC others(25): Show CCCGCCTCCGACCCTGCCATCCGTCCCTCACCT	intron_variant intron_variant	MODIFIER	HG02895.hp1 HG02895.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0070 a0001c0001t0001g0070	1	150	0.0067	32	c.276 others(51): Show c.2762-1167_2762-1166insACCCTGCCATCCGTCCCTCACCTCCG CCTCCG	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157147554	A A	ACCCTGCC others(25): Show ACCCTGCCCTCCGTCCCTCACCTCCGCCTCCGG	intron_variant intron_variant	MODIFIER	NA18906.hp1 NA18906.hp1	a0001 a0001	a0001c0017 a0001c0017	a0001c0017t0020 a0001c0017t0020	a0001c0017t0020g0055 a0001c0017t0020g0055	1	150	0.0067	32	c.276 others(51): Show c.2762-1061_2762-1030dupTCCGTCCCTCACCTCCGCCTCCGGCC CTGCCC	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157147642	A A	AGCCTCCG others(25): Show AGCCTCCGACCCTGCCCGCCAGCCCTCACCCCC	intron_variant intron_variant	MODIFIER	HG01884.hp1 HG02109.hp1 HG02145.hp1 others(6): Show HG01884.hp1 HG02109.hp1 HG02145.hp1 HG03471.hp1 HG03486.hp1 HG03540.hp2 HG03579.hp1 NA18964.hp2 NA20905.hp2	a0001 a0003 a0004 others(4): Show a0001 a0003 a0004 a0011 a0015 a0019 a0025	a0001c0002 a0001c0008 a0001c0021 others(6): Show a0001c0002 a0001c0008 a0001c0021 a0003c0010 a0004c0029 a0011c0030 a0015c0023 a0019c0027 a0025c0039	a0001c0002t0001 a0001c0008t0010 a0001c0021t0007 others(6): Show a0001c0002t0001 a0001c0008t0010 a0001c0021t0007 a0003c0010t0001 a0004c0029t0007 a0011c0030t0001 a0015c0023t0002 a0019c0027t0001 a0025c0039t0021	a0001c0002t0001g0032 a0001c0008t0010g0135 a0001c0021t0007g0124 others(6): Show a0001c0002t0001g0032 a0001c0008t0010g0135 a0001c0021t0007g0124 a0003c0010t0001g0099 a0004c0029t0007g0095 a0011c0030t0001g0096 a0015c0023t0002g0014 a0019c0027t0001g0112 a0025c0039t0021g0047	9	150	0.0600	32	c.276 others(49): Show c.2762-965_2762-934dupGCCAGCCCTCACCCCCGCCTCCGACCCT GCCC	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157147688	C C	CCCTCCGT others(25): Show CCCTCCGTCCCTCACCTCCGCCTCCGACCCTGA	intron_variant intron_variant	MODIFIER	HG01891.hp1 HG02109.hp2 HG02258.hp1 others(10): Show HG01891.hp1 HG02109.hp2 HG02258.hp1 HG02559.hp2 HG02717.hp2 HG02809.hp2 HG02818.hp2 HG02965.hp2 HG03041.hp2 HG03130.hp2 HG03139.hp1 HG03195.hp2 NA19030.hp1	a0001 a0002 a0007 others(6): Show a0001 a0002 a0007 a0014 a0020 a0022 a0023 a0026 a0028	a0001c0001 a0001c0007 a0001c0016 others(9): Show a0001c0001 a0001c0007 a0001c0016 a0002c0003 a0002c0014 a0007c0032 a0014c0024 a0020c0028 a0022c0034 a0023c0036 a0026c0038 a0028c0040	a0001c0001t0007 a0001c0007t0001 a0001c0007t0002 others(10): Show a0001c0001t0007 a0001c0007t0001 a0001c0007t0002 a0001c0016t0001 a0002c0003t0018 a0002c0014t0002 a0007c0032t0015 a0014c0024t0023 a0020c0028t0001 a0022c0034t0002 a0023c0036t0017 a0026c0038t0002 a0028c0040t0002	a0001c0001t0007g0036 a0001c0007t0001g0139 a0001c0007t0002g0011 others(10): Show a0001c0001t0007g0036 a0001c0007t0001g0139 a0001c0007t0002g0011 a0001c0016t0001g0147 a0002c0003t0018g0028 a0002c0014t0002g0029 a0007c0032t0015g0004 a0014c0024t0023g0012 a0020c0028t0001g0081 a0022c0034t0002g0048 a0023c0036t0017g0006 a0026c0038t0002g0045 a0028c0040t0002g0050	13	150	0.0867	32	c.276 others(49): Show c.2762-921_2762-920insTCCGCCTCCGACCCTGACCTCCGTCCCT CACC	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157147732	C C	CACCTCCG others(25): Show CACCTCCGCCTCCGACCCTGCCCTCCGTCCCTT	intron_variant intron_variant	MODIFIER	HG01884.hp2 HG02280.hp2 HG03453.hp1 others(2): Show HG01884.hp2 HG02280.hp2 HG03453.hp1 HG03471.hp2 NA19043.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0004 a0001c0001t0006 a0001c0001t0004 a0001c0001t0006	a0001c0001t0004g0057 a0001c0001t0004g0066 a0001c0001t0004g0150 others(2): Show a0001c0001t0004g0057 a0001c0001t0004g0066 a0001c0001t0004g0150 a0001c0001t0006g0089 a0001c0001t0006g0136	5	150	0.0333	32	c.276 others(49): Show c.2762-861_2762-860insTACCTCCGCCTCCGACCCTGCCCTCCGT CCCT	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	7/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID1B_chr6_156772378_157215779	157161431	G G	GTGTGTGT others(25): Show GTGTGTGTGTGTGTGTGTATATATATATATATA	intron_variant intron_variant	MODIFIER	HG03471.hp2 HG03471.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0006 a0001c0001t0006	a0001c0001t0006g0136 a0001c0001t0006g0136	1	150	0.0067	32	c.309 others(51): Show c.3090-5608_3090-5607insGTGTGTGTGTGTGTGTATATATATAT ATATAT	ARID1B	ENSG00000049618.25	transcript	ENST00000636930.2	protein_coding	8/19		INFO_REALIGN_3_PRIME	chr6	TogoVar
ARID3A_chr19_921035_980939	973104	A A	ATTTTTTT others(25): Show ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	HG03669.hp2 HG03669.hp2	a0001 a0001	a0001c0003 a0001c0003	a0001c0003t0221 a0001c0003t0221	a0001c0003t0221g0036 a0001c0003t0221g0036	1	364	0.0028	32	c.10 others(43): Show c.1060_*1061insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ARID3A	ENSG00000116017.11	transcript	ENST00000263620.8	protein_coding	9/9	1061	INFO_REALIGN_3_PRIME	chr19	TogoVar
ARID4A_chr14_58293555_58378876	58337242	T T	TTATATAT others(25): Show TTATATATATATATATATATATATATATATATA	intron_variant intron_variant	MODIFIER	HG02080.hp1 HG02559.hp2 HG02080.hp1 HG02559.hp2	a0001 a0001	a0001c0001 a0001c0003 a0001c0001 a0001c0003	a0001c0001t0001 a0001c0003t0002 a0001c0001t0001 a0001c0003t0002	a0001c0001t0001g0087 a0001c0003t0002g0137 a0001c0001t0001g0087 a0001c0003t0002g0137	2	294	0.0068	32	c.906 others(49): Show c.906+7076_906+7077insATATATATATATATATATATATATATAT ATAT	ARID4A	ENSG00000032219.19	transcript	ENST00000355431.8	protein_coding	11/23		INFO_REALIGN_3_PRIME	chr14	TogoVar
ARID4A_chr14_58293555_58378876	58337246	T T	TTATATAT others(25): Show TTATATATATATATATATATATATATATATATA	intron_variant intron_variant	MODIFIER	HG00544.hp2 HG01891.hp1 HG02970.hp1 others(5): Show HG00544.hp2 HG01891.hp1 HG02970.hp1 NA18962.hp2 NA18994.hp1 NA19005.hp1 NA19077.hp2 NA19087.hp2	a0001 a0002 a0011 a0001 a0002 a0011	a0001c0001 a0001c0003 a0002c0016 others(1): Show a0001c0001 a0001c0003 a0002c0016 a0011c0014	a0001c0001t0001 a0001c0003t0002 a0002c0016t0001 others(1): Show a0001c0001t0001 a0001c0003t0002 a0002c0016t0001 a0011c0014t0001	a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0043 others(5): Show a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0099 a0001c0003t0002g0163 a0002c0016t0001g0166 a0011c0014t0001g0059	8	294	0.0272	32	c.906 others(49): Show c.906+7099_906+7100insTATATATATATATATATATATATATATA TATA	ARID4A	ENSG00000032219.19	transcript	ENST00000355431.8	protein_coding	11/23		INFO_REALIGN_3_PRIME	chr14	TogoVar
ARID4B_chr1_235161902_235333179	235236831	A A	AATATATA others(25): Show AATATATATATATATATATATATATATATGTGT	intron_variant intron_variant	MODIFIER	HG02735.hp2 HG02735.hp2	a0001 a0001	a0001c0002 a0001c0002	a0001c0002t0001 a0001c0002t0001	a0001c0002t0001g0043 a0001c0002t0001g0043	1	272	0.0037	32	c.586 others(49): Show c.586-2340_586-2339insACACATATATATATATATATATATATAT ATAT	ARID4B	ENSG00000054267.22	transcript	ENST00000264183.9	protein_coding	8/23			chr1	TogoVar
ARID4B_chr1_235161902_235333179	235236862	A A	ATATATAT others(25): Show ATATATATATATATATATATATATATATATTTT	intron_variant intron_variant	MODIFIER	HG02886.hp1 HG02886.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0260 a0001c0001t0001g0260	1	272	0.0037	32	c.586 others(49): Show c.586-2371_586-2370insAAAATATATATATATATATATATATATA TATA	ARID4B	ENSG00000054267.22	transcript	ENST00000264183.9	protein_coding	8/23			chr1	TogoVar
ARID4B_chr1_235161902_235333179	235255265	A A	AGATAGAT others(25): Show AGATAGATAGATCTATCTATCTATCTATCTATC	intron_variant intron_variant	MODIFIER	HG00438.hp2 HG03017.hp1 HG04199.hp2 HG00438.hp2 HG03017.hp1 HG04199.hp2	a0001 a0005 a0001 a0005	a0001c0002 a0005c0013 a0001c0002 a0005c0013	a0001c0002t0001 a0005c0013t0001 a0001c0002t0001 a0005c0013t0001	a0001c0002t0001g0015 a0001c0002t0001g0078 a0005c0013t0001g0054 a0001c0002t0001g0015 a0001c0002t0001g0078 a0005c0013t0001g0054	3	272	0.0110	32	c.274 others(47): Show c.274+394_274+395insGATAGATAGATAGATAGATAGATCTATCTA TC	ARID4B	ENSG00000054267.22	transcript	ENST00000264183.9	protein_coding	5/23			chr1	TogoVar
ARID5B_chr10_61896699_62101944	62099312	C C	CAAAAAAA others(25): Show CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	downstream_gene_variant downstream_gene_variant	MODIFIER	HG01243.hp1 HG01884.hp1 NA19085.hp1 HG01243.hp1 HG01884.hp1 NA19085.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0002 a0001c0001t0001 a0001c0001t0002	a0001c0001t0001g0010 a0001c0001t0001g0128 a0001c0001t0002g0095 a0001c0001t0001g0010 a0001c0001t0001g0128 a0001c0001t0002g0095	3	242	0.0124	32	c.62 others(43): Show c.6282_*6283insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ARID5B	ENSG00000150347.17	transcript	ENST00000279873.12	protein_coding		2369		chr10	TogoVar

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