view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP12_chr10_31800398_31933831 | 31804673 | C | CTTTT | downstream_gene_variant | MODIFIER | HG00673.hp2 HG01106.hp1 HG01175.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(1): Show | a0001c0001t0001g0108 a0001c0001t0001g0212 a0001c0001t0001g0227 others(11): Show |
14 | 55 | 0.2545 | 4 | c.*29 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 724 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACA | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(6): Show | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(76): Show |
79 | 108 | 0.7315 | 4 | c.*20 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGT | intron_variant | MODIFIER | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(26): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0144 others(26): Show |
29 | 70 | 0.4143 | 4 | c.173 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | G | GACAC | intron_variant | MODIFIER | HG01934.hp1 HG02273.hp2 HG02735.hp1 others(6): Show |
a0001a0005 | a0001c0001a0005c0012 | a0001c0001t0003a0001c0001t0022a0005c0012t0003 | a0001c0001t0003g0168 a0001c0001t0003g0169 a0001c0001t0003g0187 others(6): Show |
9 | 138 | 0.0652 | 4 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | C | CAAAA | intron_variant | MODIFIER | HG00673.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
a0001a0002a0003 | a0001c0007a0002c0002a0003c0004 | a0001c0007t0028a0002c0002t0002a0002c0002t0007others(5): Show | a0001c0007t0028g0239 a0002c0002t0002g0254 a0002c0002t0002g0260 others(26): Show |
29 | 77 | 0.3766 | 4 | c.685 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31901768 | C | CTCTT | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(13): Show |
16 | 320 | 0.0500 | 4 | c.684 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | T | TCACA | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01258.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0111 a0001c0001t0001g0141 a0001c0001t0001g0225 others(16): Show |
19 | 78 | 0.2436 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAAA | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG01978.hp2 others(10): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0001c0010others(2): Show | a0001c0001t0004a0001c0007t0028a0001c0010t0053others(3): Show | a0001c0001t0004g0042 a0001c0007t0028g0238 a0001c0007t0028g0239 others(10): Show |
13 | 150 | 0.0867 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAAA | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(82): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0007others(2): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(12): Show | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(81): Show |
85 | 223 | 0.3812 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31923152 | A | AAAAC | intron_variant | MODIFIER | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0076 others(6): Show |
9 | 319 | 0.0282 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31931872 | C | CAAAT | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(20): Show |
24 | 296 | 0.0811 | 4 | c.-33 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3042 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | C | CATAT | upstream_gene_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01515.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(5): Show | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0108 others(13): Show |
16 | 110 | 0.1455 | 4 | c.-46 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATC | upstream_gene_variant | MODIFIER | HG02717.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0017 | a0001c0001t0011g0056 a0001c0001t0011g0057 a0001c0001t0017g0048 others(2): Show |
5 | 277 | 0.0181 | 4 | c.-46 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143134104 | A | AATCT | intron_variant | MODIFIER | HG00741.hp1 NA18612.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0002t0001g0093 |
3 | 79 | 0.0380 | 4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165948 | A | AAGAG | intron_variant | MODIFIER | HG01261.hp1 HG02109.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0096 others(1): Show |
4 | 160 | 0.0250 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165960 | G | GAGAA | intron_variant | MODIFIER | HG01496.hp2 HG02698.hp1 HG03490.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014 a0001c0001t0001g0058 a0001c0001t0001g0076 others(3): Show |
6 | 31 | 0.1935 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165997 | A | AGAAG | intron_variant | MODIFIER | HG00609.hp2 HG01255.hp1 HG02145.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0053 others(3): Show |
6 | 124 | 0.0484 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143166041 | A | AAAAG | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01069.hp2 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
51 | 127 | 0.4016 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143179891 | C | CAAAA | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(39): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(39): Show |
42 | 125 | 0.3360 | 4 | c.166 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143194709 | C | CTGTT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(136): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
139 | 160 | 0.8688 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143197967 | T | TACAC | intron_variant | MODIFIER | HG00609.hp2 HG00741.hp1 HG01261.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(18): Show |
21 | 119 | 0.1765 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143200425 | G | GATCT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
32 | 160 | 0.2000 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143209557 | T | TAAAA | intron_variant | MODIFIER | HG02109.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0062 others(2): Show |
5 | 131 | 0.0382 | 4 | c.235 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143215279 | C | CTTGT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(31): Show |
34 | 160 | 0.2125 | 4 | c.235 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAAA | intron_variant | MODIFIER | HG02074.hp2 HG03195.hp2 NA18953.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0072 others(2): Show |
5 | 21 | 0.2381 | 4 | c.385 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143258252 | C | CATAT | intron_variant | MODIFIER | HG00733.hp2 HG01361.hp1 HG01517.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0092 others(8): Show |
11 | 114 | 0.0965 | 4 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | C | CTTTT | intron_variant | MODIFIER | HG01243.hp1 HG02071.hp1 HG02976.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0091 others(3): Show |
6 | 26 | 0.2308 | 4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143309866 | T | TTGTG | intron_variant | MODIFIER | HG02523.hp1 HG02602.hp1 HG03490.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
10 | 105 | 0.0952 | 4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346220 | T | TCTCA | intron_variant | MODIFIER | HG00642.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0074 others(7): Show |
10 | 158 | 0.0633 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346236 | T | TCACA | intron_variant | MODIFIER | HG02145.hp1 HG02559.hp1 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0099 a0001c0001t0001g0121 |
3 | 73 | 0.0411 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143365012 | A | AAAAT | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp1 HG01081.hp2 others(28): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
31 | 158 | 0.1962 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143372011 | G | GAAAT | intron_variant | MODIFIER | HG00609.hp1 HG01261.hp2 HG02886.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(3): Show |
6 | 50 | 0.1200 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143373063 | G | GAGAA | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(98): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
101 | 160 | 0.6313 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379480 | C | CATAT | intron_variant | MODIFIER | HG01261.hp1 HG02109.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0119 others(1): Show |
4 | 148 | 0.0270 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01069.hp1 others(23): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0019 others(23): Show |
26 | 75 | 0.3467 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01071.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(19): Show |
22 | 89 | 0.2472 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407985 | G | GTGTA | intron_variant | MODIFIER | HG00738.hp2 HG01256.hp2 HG01261.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0080 others(3): Show |
6 | 160 | 0.0375 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTGTA | intron_variant | MODIFIER | HG00642.hp1 HG01071.hp2 HG02129.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0048 others(12): Show |
15 | 71 | 0.2113 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143411244 | C | CATTA | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(139): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
142 | 160 | 0.8875 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143412372 | G | GATAA | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(145): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
148 | 160 | 0.9250 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143461281 | C | CAAAA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0019 others(21): Show |
24 | 29 | 0.8276 | 4 | c.703 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143462773 | A | AGATG | intron_variant | MODIFIER | HG00733.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 a0001c0001t0001g0141 |
2 | 155 | 0.0129 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143468659 | A | AGTGT | intron_variant | MODIFIER | HG03491.hp1 HG04199.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 a0001c0001t0001g0151 |
2 | 154 | 0.0130 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143468661 | A | AGTGT | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(37): Show |
40 | 79 | 0.5063 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143468663 | A | AGTGT | intron_variant | MODIFIER | HG03710.hp2 HG04228.hp1 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0153 |
3 | 11 | 0.2727 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143511568 | T | TTTTG | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(83): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
86 | 159 | 0.5409 | 4 | c.827 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143590942 | G | GCTCT | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02109.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004 a0001c0001t0001g0096 a0001c0002t0001g0065 others(2): Show |
5 | 89 | 0.0562 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAA | intron_variant | MODIFIER | HG01071.hp2 HG02071.hp1 HG02615.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | 98 | 0.0918 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143610719 | G | GTATT | intron_variant | MODIFIER | HG01361.hp2 HG01515.hp1 HG01517.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(7): Show |
10 | 98 | 0.1020 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143684073 | T | TTATC | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(47): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0029 others(47): Show |
50 | 160 | 0.3125 | 4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |