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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP28_chr18_6724716_6920716 | 6805479 | CTTTTTTT | C | intron_variant | MODIFIER | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0010others(1): Show | a0001c0001t0001a0001c0003t0003a0001c0010t0003others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0003t0003g0119 others(4): Show |
7 | 175 | 0.0400 | -7 | c.123 others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94194959 | CAAAAGTA | C | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
a0001a0005 | a0001c0001a0005c0014 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(2): Show | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(36): Show |
46 | 354 | 0.1299 | -7 | c.128 others(26): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161065545 | CTTTTTCT | C | intron_variant | MODIFIER | HG02602.hp1 HG02735.hp1 HG03209.hp2 others(6): Show |
a0001a0009 | a0001c0001a0009c0010 | a0001c0001t0001a0001c0001t0002a0009c0010t0001 | a0001c0001t0001g0013 a0001c0001t0001g0152 a0001c0001t0001g0160 others(5): Show |
9 | 388 | 0.0232 | -7 | c.97+ others(22): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119393316 | ATCAAGCT | A | intron_variant | MODIFIER | HG01884.hp1 HG02895.hp1 HG02970.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0020a0004c0007t0015a0004c0007t0043others(1): Show | a0001c0001t0020g0011 a0004c0007t0015g0017 a0004c0007t0043g0197 others(1): Show |
4 | 308 | 0.0130 | -7 | c.882 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129016254 | CACATAAT | C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02895.hp1 others(2): Show |
a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0201 a0001c0003t0006g0202 a0001c0003t0006g0203 others(2): Show |
5 | 396 | 0.0126 | -7 | c.104 others(28): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46861077 | GGCCCCCC | G | 5_prime_UTR_variant | MODIFIER | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0013a0001c0001t0048others(2): Show | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(9): Show |
12 | 296 | 0.0405 | -7 | c.-31 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/7 | 57589 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888837 | CAAAAAAA | C | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(2): Show | a0001c0001t0002g0054 a0001c0001t0011g0029 a0001c0001t0015g0040 others(3): Show |
6 | 200 | 0.0300 | -7 | c.-18 others(28): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47007528 | GGGTTTCA | G | downstream_gene_variant | MODIFIER | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0002a0001c0001t0043a0002c0004t0002 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(8): Show |
11 | 296 | 0.0372 | -7 | c.*68 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2452 | chr19 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531235 | AAGGGCAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0052 others(74): Show |
77 | 232 | 0.3319 | -7 | c.298 others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531294 | AAGGGCAC | A | intron_variant | MODIFIER | HG01168.hp2 HG01192.hp1 HG01952.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0022others(3): Show | a0001c0001t0001g0141 a0001c0002t0001g0078 a0001c0002t0001g0087 others(7): Show |
10 | 234 | 0.0427 | -7 | c.298 others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531353 | AAGGGCAC | A | intron_variant | MODIFIER | HG00323.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0155 a0001c0001t0002g0234 a0001c0001t0002g0235 others(3): Show |
6 | 238 | 0.0252 | -7 | c.298 others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531412 | AAGGGCAC | A | intron_variant | MODIFIER | HG02486.hp1 HG03041.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | 244 | 0.0082 | -7 | c.298 others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531471 | AAGGGCAC | A | intron_variant | MODIFIER | HG02132.hp2 HG03225.hp2 NA18980.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 a0001c0002t0001g0037 a0001c0002t0001g0124 |
3 | 244 | 0.0123 | -7 | c.298 others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38640189 | TTTTCTTC | T | intron_variant | MODIFIER | HG00558.hp2 HG00741.hp2 HG02015.hp1 others(28): Show |
a0001a0004a0020others(2): Show | a0001c0001a0001c0004a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0004others(7): Show | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0140 others(27): Show |
31 | 348 | 0.0891 | -7 | c.127 others(24): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699502 | ATATATTT | A | intron_variant | MODIFIER | HG00423.hp2 HG01175.hp2 HG01256.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0019a0001c0001t0031others(3): Show | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0077 others(5): Show |
8 | 256 | 0.0313 | -7 | c.154 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699504 | ATATTTTT | A | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(10): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0006a0002c0002t0004others(4): Show | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0091 others(10): Show |
13 | 248 | 0.0524 | -7 | c.154 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751279 | GTTTTTTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(26): Show |
29 | 200 | 0.1450 | -7 | c.155 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100756501 | GATAAGAA | G | intron_variant | MODIFIER | HG02486.hp2 HG03098.hp1 HG03130.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0034 a0002c0002t0002g0247 a0002c0002t0002g0248 |
3 | 284 | 0.0106 | -7 | c.155 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0140 a0001c0001t0001g0259 a0001c0001t0001g0265 others(19): Show |
22 | 35 | 0.6286 | -7 | c.251 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100836177 | GTTAGTTA | G | intron_variant | MODIFIER | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(5): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0002a0002c0002t0018a0002c0011t0017 | a0002c0002t0002g0034 a0002c0002t0002g0222 a0002c0002t0002g0245 others(5): Show |
8 | 284 | 0.0282 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837663 | ATCCTTTT | A | intron_variant | MODIFIER | HG01346.hp1 HG02145.hp2 HG02723.hp1 others(6): Show |
a0001a0002 | a0001c0008a0002c0002a0002c0004others(1): Show | a0001c0008t0001a0002c0002t0002a0002c0002t0011others(4): Show | a0001c0008t0001g0004 a0002c0002t0002g0010 a0002c0002t0002g0253 others(6): Show |
9 | 210 | 0.0429 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0001c0003t0006others(3): Show | a0001c0001t0001g0139 a0001c0003t0001g0163 a0001c0003t0001g0172 others(8): Show |
11 | 44 | 0.2500 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100849220 | TATCACTC | T | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0037a0001c0003t0014a0001c0008t0001others(13): Show | a0001c0001t0037g0041 a0001c0003t0014g0234 a0001c0003t0014g0235 others(26): Show |
29 | 284 | 0.1021 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903710 | ATATATAT | A | intron_variant | MODIFIER | HG01106.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
a0001a0002a0003 | a0001c0008a0002c0002a0003c0007 | a0001c0008t0001a0002c0002t0002a0002c0002t0009others(1): Show | a0001c0008t0001g0004 a0002c0002t0002g0252 a0002c0002t0009g0035 others(4): Show |
7 | 259 | 0.0270 | -7 | c.385 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802753 | CTTTTTTT | C | intron_variant | MODIFIER | HG01109.hp1 HG01517.hp1 HG02109.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0018others(4): Show | a0001c0001t0001g0212 a0001c0001t0009g0151 a0001c0001t0009g0183 others(5): Show |
8 | 191 | 0.0419 | -7 | c.53+ others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802962 | TATATATA | T | intron_variant | MODIFIER | HG01074.hp1 HG02074.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0198 a0001c0001t0004g0106 |
2 | 228 | 0.0088 | -7 | c.53+ others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTATTTA | G | intron_variant | MODIFIER | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(11): Show | a0001c0001t0001g0181 a0001c0001t0003g0060 a0001c0001t0003g0078 others(17): Show |
20 | 45 | 0.4444 | -7 | c.54- others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868584 | ATGCATTT | A | intron_variant | MODIFIER | HG02622.hp1 HG03041.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0008a0001c0006t0001 | a0001c0001t0008g0228 a0001c0006t0001g0194 |
2 | 222 | 0.0090 | -7 | c.54- others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGAGA | G | intron_variant | MODIFIER | HG01934.hp2 HG02300.hp2 HG02559.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | 199 | 0.0804 | -7 | c.199 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903114 | GAGAGAGA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0113 a0001c0001t0003g0084 a0001c0001t0004g0217 others(6): Show |
9 | 214 | 0.0421 | -7 | c.199 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | CAAAAAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(30): Show |
a0001a0003 | a0001c0001a0003c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(30): Show |
33 | 128 | 0.2578 | -7 | c.152 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | CAAAAAAA | C | intron_variant | MODIFIER | HG02559.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | 17 | 0.2941 | -7 | c.176 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978678 | CTTTTCTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(36): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0002g0008 others(36): Show |
39 | 228 | 0.1711 | -7 | c.176 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12992357 | TAGCAGCA | T | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(129): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
132 | 228 | 0.5789 | -7 | c.*21 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 715 | chr17 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174616 | CTCTTTCT | C | intron_variant | MODIFIER | NA18944.hp1 NA19005.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0037 |
2 | 128 | 0.0156 | -7 | c.162 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11287074 | AATTATGT | A | intron_variant | MODIFIER | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0046 others(3): Show |
6 | 144 | 0.0417 | -7 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590841 | GAAAAGAA | G | intron_variant | MODIFIER | NA18986.hp1 NA19000.hp1 NA19004.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0022 a0001c0001t0001g0108 a0001c0001t0007g0078 |
3 | 138 | 0.0217 | -7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590846 | GAAAAGAA | G | intron_variant | MODIFIER | HG02015.hp1 HG02129.hp1 HG03490.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(2): Show |
5 | 135 | 0.0370 | -7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44782145 | GCCAATGT | G | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
a0001a0002a0008others(1): Show | a0001c0007a0002c0011a0008c0027others(2): Show | a0001c0007t0001a0002c0011t0005a0008c0027t0001others(2): Show | a0001c0007t0001g0058 a0001c0007t0001g0202 a0002c0011t0005g0061 others(4): Show |
7 | 388 | 0.0180 | -7 | c.-71 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44817318 | CCAAAGAG | C | intron_variant | MODIFIER | HG01243.hp1 HG02630.hp1 HG02809.hp1 others(10): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0003a0002c0011others(7): Show | a0001c0001t0001a0002c0003t0004a0002c0011t0005others(7): Show | a0001c0001t0001g0101 a0001c0001t0001g0371 a0002c0003t0004g0253 others(10): Show |
13 | 388 | 0.0335 | -7 | c.386 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44821205 | GCGGATCA | G | intron_variant | MODIFIER | HG01168.hp1 HG01517.hp1 HG02602.hp2 others(1): Show |
a0001a0002 | a0001c0004a0002c0003 | a0001c0004t0001a0001c0004t0003a0002c0003t0004 | a0001c0004t0001g0164 a0001c0004t0001g0165 a0001c0004t0003g0037 others(1): Show |
4 | 388 | 0.0103 | -7 | c.387 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT | C | intron_variant | MODIFIER | HG00438.hp2 HG01071.hp2 HG01261.hp1 others(3): Show |
a0001a0003 | a0001c0009a0001c0021a0003c0002 | a0001c0009t0001a0001c0021t0001a0003c0002t0002 | a0001c0009t0001g0077 a0001c0009t0001g0205 a0001c0021t0001g0014 others(3): Show |
6 | 30 | 0.2000 | -7 | c.878 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858450 | CTCTGTCT | C | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(23): Show |
a0002a0004a0006others(3): Show | a0002c0003a0002c0006a0002c0011others(9): Show | a0002c0003t0001a0002c0006t0001a0002c0011t0005others(9): Show | a0002c0003t0001g0106 a0002c0003t0001g0387 a0002c0006t0001g0059 others(23): Show |
26 | 388 | 0.0670 | -7 | c.878 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGDIA_chr17_81862721_81876337 | 81876006 | CAAAAAAA | C | upstream_gene_variant | MODIFIER | HG01261.hp2 HG02055.hp2 HG02559.hp1 others(9): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0004a0001c0006t0012 | a0001c0001t0001g0005 a0001c0001t0004g0013 a0001c0001t0004g0041 others(1): Show |
12 | 264 | 0.0455 | -7 | c.-47 others(18): Show |
ARHGDIA | ENSG00000141522.12 | transcript | ENST00000269321.12 | protein_coding | 4670 | chr17 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17538282 | CCTGTCTG | C | upstream_gene_variant | MODIFIER | HG01106.hp2 HG01884.hp2 HG02622.hp2 |
a0001 | a0001c0001a0001c0044 | a0001c0001t0001a0001c0001t0005a0001c0044t0004 | a0001c0001t0001g0163 a0001c0001t0005g0162 a0001c0044t0004g0161 |
3 | 166 | 0.0181 | -7 | c.-17 others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1415 | chr1 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1870233 | ATTTTTTT | A | intron_variant | MODIFIER | HG00642.hp1 HG01346.hp1 HG01884.hp1 others(13): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0005others(9): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(11): Show | a0001c0001t0002g0069 a0001c0001t0019g0245 a0001c0002t0001g0068 others(13): Show |
16 | 140 | 0.1143 | -7 | c.679 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351448 | TATATATA | T | intron_variant | MODIFIER | HG01517.hp2 NA19012.hp1 NA19084.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 a0001c0001t0001g0241 a0001c0001t0001g0251 |
3 | 306 | 0.0098 | -7 | c.32+ others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7347395 | CAAAAAAA | C | upstream_gene_variant | MODIFIER | HG02602.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0012 | a0001c0001t0002a0001c0001t0030a0001c0002t0003others(1): Show | a0001c0001t0002g0055 a0001c0001t0030g0010 a0001c0002t0003g0143 others(3): Show |
6 | 67 | 0.0896 | -7 | c.-19 others(18): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1541 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7350762 | GGGTGGGT | G | intron_variant | MODIFIER | HG01952.hp1 HG03688.hp2 HG03704.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0097 a0001c0002t0003g0167 a0001c0002t0003g0180 |
3 | 293 | 0.0102 | -7 | c.-11 others(26): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7375354 | AAAGGAAG | A | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
a0001a0009 | a0001c0001a0001c0047a0009c0012 | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(1): Show | a0001c0001t0002g0055 a0001c0001t0004g0003 a0001c0001t0004g0006 others(4): Show |
7 | 240 | 0.0292 | -7 | c.276 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | chr19 | TogoVar |