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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAA | intron_variant | MODIFIER | HG00621.hp1 HG00741.hp1 HG01256.hp2 others(25): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(15): Show | a0001c0001t0005g0277 a0001c0001t0007g0224 a0001c0001t0007g0225 others(25): Show |
28 | 35 | 0.8000 | 6 | c.100 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332604 | T | TTCTCTC | intron_variant | MODIFIER | HG02451.hp2 HG02886.hp2 HG03098.hp2 |
a0001 | a0001c0004a0001c0005 | a0001c0004t0003a0001c0005t0014 | a0001c0004t0003g0040 a0001c0004t0003g0041 a0001c0005t0014g0029 |
3 | 287 | 0.0105 | 6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCACACA | intron_variant | MODIFIER | HG00323.hp1 HG01261.hp1 HG01358.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(6): Show | a0001c0001t0006g0149 a0001c0001t0008g0002 a0001c0001t0008g0194 others(7): Show |
10 | 155 | 0.0645 | 6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCTCACA | intron_variant | MODIFIER | HG01261.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
a0001a0002 | a0001c0002a0001c0004a0002c0003 | a0001c0002t0004a0001c0004t0065a0002c0003t0009 | a0001c0002t0004g0234 a0001c0004t0065g0216 a0002c0003t0009g0296 others(1): Show |
4 | 149 | 0.0268 | 6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(19): Show |
a0001a0002a0006 | a0001c0001a0001c0004a0002c0003others(1): Show | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(9): Show | a0001c0001t0005g0023 a0001c0001t0005g0112 a0001c0001t0007g0292 others(18): Show |
22 | 120 | 0.1833 | 6 | c.683 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | T | TTTATTA | intron_variant | MODIFIER | HG01515.hp2 HG02004.hp1 HG02451.hp2 others(3): Show |
a0001a0004 | a0001c0003a0001c0014a0004c0009 | a0001c0003t0001a0001c0003t0003a0001c0014t0004others(1): Show | a0001c0003t0001g0370 a0001c0003t0003g0341 a0001c0014t0004g0182 others(3): Show |
6 | 90 | 0.0667 | 6 | c.212 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128982474 | C | CGTGTGT | intron_variant | MODIFIER | HG00423.hp1 HG01358.hp2 HG01934.hp1 others(21): Show |
a0001 | a0001c0001a0001c0003a0001c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(20): Show |
24 | 150 | 0.1600 | 6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985852 | G | GTATATA | intron_variant | MODIFIER | HG02683.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
a0001a0005 | a0001c0010a0005c0011 | a0001c0010t0008a0005c0011t0008a0005c0011t0021 | a0001c0010t0008g0194 a0005c0011t0008g0072 a0005c0011t0008g0073 others(1): Show |
4 | 388 | 0.0103 | 6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTATATA | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(24): Show |
a0001a0009a0012others(1): Show | a0001c0002a0009c0025a0012c0023others(1): Show | a0001c0002t0001a0001c0002t0005a0001c0002t0006others(5): Show | a0001c0002t0001g0234 a0001c0002t0001g0235 a0001c0002t0001g0237 others(24): Show |
27 | 166 | 0.1627 | 6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTATA | intron_variant | MODIFIER | HG02027.hp1 HG02083.hp1 HG02735.hp2 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0024 | a0001c0002t0001a0001c0002t0006a0001c0003t0003others(2): Show | a0001c0002t0001g0262 a0001c0002t0006g0302 a0001c0003t0003g0322 others(3): Show |
6 | 145 | 0.0414 | 6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCACACA | intron_variant | MODIFIER | HG00408.hp1 HG00642.hp2 HG01123.hp2 others(20): Show |
a0001a0002a0014 | a0001c0001a0001c0002a0001c0022others(2): Show | a0001c0001t0002a0001c0001t0007a0001c0002t0001others(6): Show | a0001c0001t0002g0100 a0001c0001t0002g0105 a0001c0001t0002g0112 others(20): Show |
23 | 153 | 0.1503 | 6 | c.119 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129029801 | C | CAAAAAA | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp1 HG02965.hp2 others(3): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0002c0007others(1): Show | a0001c0001t0002a0001c0003t0005a0002c0007t0009others(1): Show | a0001c0001t0002g0190 a0001c0003t0005g0189 a0002c0007t0009g0320 others(3): Show |
6 | 61 | 0.0984 | 6 | c.104 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46869476 | T | TTGTGTG | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(3): Show | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0020 others(7): Show |
10 | 143 | 0.0699 | 6 | c.-18 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | A | AATATAT | intron_variant | MODIFIER | HG01192.hp2 HG01496.hp1 HG02027.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(1): Show | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0096 others(3): Show |
6 | 38 | 0.1579 | 6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888333 | T | TACACAC | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0014 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 others(1): Show |
4 | 125 | 0.0320 | 6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46898775 | A | AGCTGCT | intron_variant | MODIFIER | HG02004.hp1 HG02155.hp1 NA19000.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0173 a0001c0001t0002g0012 a0001c0001t0003g0233 others(1): Show |
4 | 237 | 0.0169 | 6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46938342 | A | ATTTTAT | intron_variant | MODIFIER | HG00733.hp1 HG03471.hp1 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0169 a0001c0001t0001g0278 a0001c0001t0002g0253 |
3 | 296 | 0.0101 | 6 | c.382 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47003913 | G | GACACAC | 3_prime_UTR_variant | MODIFIER | HG01099.hp1 HG02135.hp2 HG04228.hp1 |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0028 | a0001c0001t0017g0109 a0001c0001t0017g0254 a0001c0001t0028g0104 |
3 | 250 | 0.0120 | 6 | c.*32 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | C | CTTTTTT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(25): Show |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(4): Show | a0001c0001t0001g0141 a0001c0001t0001g0149 a0001c0001t0001g0154 others(25): Show |
28 | 53 | 0.5283 | 6 | c.*55 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP36_chrX_131053346_131094885 | 131075623 | A | ATGTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(60): Show |
98 | 107 | 0.9159 | 6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | C | CATATAT | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0003g0077 others(4): Show |
7 | 11 | 0.6364 | 6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144574181 | A | AGACGAG | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(22): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(11): Show | a0001c0001t0001g0157 a0001c0001t0004g0149 a0001c0001t0004g0150 others(22): Show |
25 | 229 | 0.1092 | 6 | c.512 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38640104 | C | CTCTTCT | intron_variant | MODIFIER | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(32): Show |
a0001a0002a0004others(5): Show | a0001c0002a0001c0004a0001c0008others(9): Show | a0001c0002t0004a0001c0004t0004a0001c0004t0016others(13): Show | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0004t0016g0228 others(28): Show |
35 | 152 | 0.2303 | 6 | c.127 others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38640145 | T | TTCTTCC | intron_variant | MODIFIER | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(67): Show |
a0001a0002a0003others(13): Show | a0001c0002a0001c0004a0001c0007others(22): Show | a0001c0002t0010a0001c0004t0004a0001c0004t0007others(31): Show | a0001c0002t0010g0081 a0001c0004t0004g0044 a0001c0004t0007g0112 others(61): Show |
70 | 174 | 0.4023 | 6 | c.127 others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100725934 | C | CAAAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(24): Show |
27 | 117 | 0.2308 | 6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100766222 | G | GGTGTGT | intron_variant | MODIFIER | HG01256.hp1 HG01258.hp2 HG03927.hp1 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0006a0002c0002t0004 | a0001c0003t0006g0271 a0001c0003t0006g0274 a0002c0002t0004g0260 |
3 | 188 | 0.0160 | 6 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100779483 | T | TACACAC | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0002c0002t0005a0002c0002t0006others(3): Show | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0151 others(11): Show |
14 | 266 | 0.0526 | 6 | c.250 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100779485 | T | TACACAC | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(27): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(12): Show | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0068 others(27): Show |
30 | 161 | 0.1863 | 6 | c.250 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGTGT | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(23): Show |
a0001a0002 | a0001c0001a0001c0015a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(9): Show | a0001c0001t0001g0071 a0001c0001t0001g0098 a0001c0001t0001g0101 others(23): Show |
26 | 146 | 0.1781 | 6 | c.313 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGT | intron_variant | MODIFIER | HG01515.hp2 HG03579.hp1 NA19072.hp2 others(2): Show |
a0001 | a0001c0001a0001c0008a0001c0015 | a0001c0001t0001a0001c0001t0002a0001c0001t0024others(2): Show | a0001c0001t0001g0021 a0001c0001t0002g0003 a0001c0001t0024g0173 others(2): Show |
5 | 34 | 0.1471 | 6 | c.385 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACA | intron_variant | MODIFIER | HG00408.hp1 HG00733.hp2 HG01081.hp1 others(17): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0006others(1): Show | a0001c0003t0003a0002c0002t0002a0002c0002t0005others(4): Show | a0001c0003t0003g0138 a0001c0003t0003g0153 a0001c0003t0003g0258 others(17): Show |
20 | 59 | 0.3390 | 6 | c.385 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCA | intron_variant | MODIFIER | HG01123.hp2 HG02071.hp2 HG02074.hp2 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(1): Show | a0001c0001t0001g0023 a0001c0001t0001g0046 a0001c0001t0001g0062 others(27): Show |
30 | 69 | 0.4348 | 6 | c.385 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATAT | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp1 HG01515.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0015a0002c0004 | a0001c0001t0001a0001c0015t0001a0002c0004t0007 | a0001c0001t0001g0007 a0001c0001t0001g0088 a0001c0001t0001g0098 others(10): Show |
13 | 80 | 0.1625 | 6 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTGTG | intron_variant | MODIFIER | HG00741.hp1 HG01516.hp1 HG01975.hp1 others(2): Show |
a0002 | a0002c0004a0002c0009 | a0002c0004t0007a0002c0009t0027 | a0002c0004t0007g0061 a0002c0004t0007g0076 a0002c0004t0007g0122 others(2): Show |
5 | 8 | 0.6250 | 6 | c.486 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935675 | C | CAGAGAG | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(15): Show |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0022a0001c0003t0033 | a0001c0003t0003g0107 a0001c0003t0003g0138 a0001c0003t0003g0153 others(15): Show |
18 | 268 | 0.0672 | 6 | c.703 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACACAG | intron_variant | MODIFIER | HG02630.hp2 HG02723.hp2 HG03239.hp2 |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0004t0007 | a0002c0002t0002g0006 a0002c0002t0002g0043 a0002c0004t0007g0085 |
3 | 149 | 0.0201 | 6 | c.703 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100993327 | C | CATATAT | 3_prime_UTR_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(15): Show |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0022a0001c0003t0033 | a0001c0003t0003g0107 a0001c0003t0003g0138 a0001c0003t0003g0153 others(15): Show |
18 | 262 | 0.0687 | 6 | c.*45 others(17): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 24/24 | 4540 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTGTG | intron_variant | MODIFIER | HG02559.hp2 HG02630.hp1 HG02886.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(2): Show | a0001c0001t0001g0033 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | 126 | 0.0556 | 6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841579 | C | CTGTCTG | intron_variant | MODIFIER | HG01109.hp2 HG02258.hp1 HG03579.hp1 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0009a0001c0001t0022a0001c0005t0001others(1): Show | a0001c0001t0009g0151 a0001c0001t0022g0128 a0001c0005t0001g0223 others(1): Show |
4 | 228 | 0.0175 | 6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841637 | C | CACACAA | intron_variant | MODIFIER | NA18989.hp1 NA19009.hp2 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0002a0001c0009t0002 | a0001c0001t0002g0165 a0001c0009t0002g0104 |
2 | 99 | 0.0202 | 6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12845517 | A | AAAAAAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(67): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0037 others(67): Show |
70 | 207 | 0.3382 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGTGT | intron_variant | MODIFIER | HG00738.hp2 HG02132.hp2 HG02630.hp2 others(17): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
20 | 123 | 0.1626 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849594 | T | TTTTTTG | intron_variant | MODIFIER | HG00423.hp2 HG03491.hp1 HG03516.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(4): Show |
7 | 120 | 0.0583 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12852548 | G | GTTTTTT | intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG02071.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0015 a0001c0001t0002g0016 a0001c0001t0004g0013 others(2): Show |
5 | 179 | 0.0279 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | T | TTATATA | intron_variant | MODIFIER | HG02451.hp1 HG03139.hp1 HG03831.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0002g0019 others(2): Show |
5 | 104 | 0.0481 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATATA | intron_variant | MODIFIER | HG00642.hp1 HG01167.hp1 HG02602.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0002g0199 a0001c0001t0003g0051 a0001c0001t0004g0004 others(7): Show |
10 | 139 | 0.0719 | 6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12894241 | A | AGTGTGT | intron_variant | MODIFIER | HG01109.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
a0001 | a0001c0005a0001c0006a0001c0011 | a0001c0005t0001a0001c0006t0003a0001c0011t0001 | a0001c0005t0001g0190 a0001c0005t0001g0223 a0001c0006t0003g0091 others(1): Show |
4 | 182 | 0.0220 | 6 | c.54- others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GAGAGGA | intron_variant | MODIFIER | HG01106.hp2 HG01255.hp1 HG01884.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0002g0158 others(2): Show |
5 | 147 | 0.0340 | 6 | c.199 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GAGGAGA | intron_variant | MODIFIER | HG03098.hp2 NA20905.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 a0001c0001t0001g0214 |
2 | 144 | 0.0139 | 6 | c.199 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GGAGAGA | intron_variant | MODIFIER | HG00673.hp2 HG00735.hp2 HG02572.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0127 a0001c0001t0002g0115 a0001c0001t0003g0063 others(7): Show |
10 | 152 | 0.0658 | 6 | c.199 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |