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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTG | intron_variant | MODIFIER | HG00741.hp2 HG01069.hp1 HG02145.hp2 others(2): Show |
a0001a0002 | a0001c0008a0002c0002 | a0001c0008t0010a0002c0002t0004a0002c0002t0008others(1): Show | a0001c0008t0010g0254 a0002c0002t0004g0114 a0002c0002t0004g0115 others(2): Show |
5 | 8 | 0.6250 | 4 | c.486 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935656 | T | TCACA | intron_variant | MODIFIER | HG01346.hp1 HG02055.hp2 HG02056.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0002others(1): Show | a0001c0001t0001a0001c0014t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0147 a0001c0014t0001g0135 a0002c0002t0002g0010 others(1): Show |
4 | 160 | 0.0250 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935673 | C | CAGAG | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(11): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0006a0001c0003t0014others(1): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0172 others(11): Show |
14 | 284 | 0.0493 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACAG | intron_variant | MODIFIER | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
a0001a0002 | a0001c0008a0002c0002a0002c0005others(1): Show | a0001c0008t0010a0002c0002t0001a0002c0002t0002others(11): Show | a0001c0008t0010g0254 a0002c0002t0001g0013 a0002c0002t0001g0015 others(48): Show |
51 | 197 | 0.2589 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CAGAG | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(33): Show |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(7): Show | a0002c0002t0002g0024 a0002c0002t0002g0034 a0002c0002t0002g0141 others(33): Show |
36 | 182 | 0.1978 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100972516 | T | TTGGA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
a0001a0002 | a0001c0001a0001c0008a0001c0010others(4): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0024others(11): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0022 others(80): Show |
83 | 229 | 0.3624 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCT | intron_variant | MODIFIER | HG01243.hp1 HG01361.hp1 HG02280.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0024a0001c0001t0032others(1): Show | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0161 others(9): Show |
12 | 35 | 0.3429 | 4 | c.245 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTT | intron_variant | MODIFIER | HG00423.hp1 HG01256.hp1 HG02004.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0003t0001others(2): Show | a0001c0001t0001g0046 a0001c0001t0006g0075 a0001c0003t0001g0172 others(4): Show |
7 | 30 | 0.2333 | 4 | c.245 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | A | AAAAT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(103): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0014others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0024others(19): Show | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0046 others(103): Show |
106 | 135 | 0.7852 | 4 | c.253 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100993327 | C | CATAT | 3_prime_UTR_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0014 a0002c0004t0007g0061 a0002c0004t0007g0076 others(5): Show |
8 | 252 | 0.0317 | 4 | c.*45 others(15): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 24/24 | 4540 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100995655 | G | GAATA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(76): Show |
79 | 97 | 0.8144 | 4 | c.*68 others(15): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12818335 | G | GAAAA | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0033 a0001c0001t0001g0176 a0001c0001t0001g0224 others(14): Show |
17 | 102 | 0.1667 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTG | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | 124 | 0.0403 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12828636 | C | CTTTT | intron_variant | MODIFIER | HG00738.hp2 HG02132.hp2 HG02145.hp2 others(7): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0154 a0001c0001t0001g0164 a0001c0001t0002g0110 others(7): Show |
10 | 103 | 0.0971 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841637 | C | CAAAA | intron_variant | MODIFIER | HG01891.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(2): Show | a0001c0001t0001g0009 a0001c0001t0003g0072 a0001c0001t0003g0090 others(3): Show |
6 | 103 | 0.0583 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGT | intron_variant | MODIFIER | HG01884.hp2 HG01934.hp1 HG02280.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0214 a0001c0001t0001g0226 a0001c0001t0001g0227 others(6): Show |
9 | 112 | 0.0804 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849568 | C | CTTTT | intron_variant | MODIFIER | HG00673.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
a0001 | a0001c0001a0001c0004a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0033 a0001c0001t0001g0113 a0001c0001t0001g0140 others(4): Show |
7 | 189 | 0.0370 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849594 | T | TTTTG | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(2): Show | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0007g0036 others(3): Show |
6 | 119 | 0.0504 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATA | intron_variant | MODIFIER | HG01070.hp1 HG01074.hp1 HG02071.hp2 others(9): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0101 others(9): Show |
12 | 141 | 0.0851 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12870048 | C | CTTTT | intron_variant | MODIFIER | HG00735.hp1 HG01192.hp1 HG01192.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0037 others(19): Show |
22 | 82 | 0.2683 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12894227 | T | TGAGA | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0012 a0001c0001t0001g0187 a0001c0001t0002g0019 others(5): Show |
8 | 223 | 0.0359 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12894241 | A | AGAGT | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG02027.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0111 others(11): Show |
14 | 192 | 0.0729 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12894241 | A | AGTGT | intron_variant | MODIFIER | HG02559.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0005t0005others(2): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
8 | 186 | 0.0430 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12894308 | G | GGAGA | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0012 a0001c0001t0001g0187 a0001c0001t0002g0019 others(6): Show |
9 | 40 | 0.2250 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12898956 | G | GATTT | intron_variant | MODIFIER | HG00642.hp1 HG01192.hp2 HG01258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0033others(3): Show | a0001c0001t0002g0008 a0001c0001t0006g0096 a0001c0001t0033g0029 others(3): Show |
6 | 37 | 0.1622 | 4 | c.198 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | T | TGAGA | intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0187 a0001c0001t0006g0096 |
2 | 205 | 0.0098 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GAGGA | intron_variant | MODIFIER | HG01952.hp2 HG02735.hp2 HG03831.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0101 a0001c0001t0002g0195 a0001c0001t0003g0051 others(1): Show |
4 | 146 | 0.0274 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGTGT | intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0187 a0001c0001t0006g0096 |
2 | 108 | 0.0185 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12910446 | C | CTTTT | intron_variant | MODIFIER | HG00735.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0119 a0001c0001t0001g0147 a0001c0001t0001g0187 others(16): Show |
19 | 36 | 0.5278 | 4 | c.275 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12913968 | C | CAAAA | intron_variant | MODIFIER | HG02027.hp1 HG02129.hp1 HG02602.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0180 others(6): Show |
9 | 49 | 0.1837 | 4 | c.276 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACAC | intron_variant | MODIFIER | HG02559.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0010 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | 46 | 0.1522 | 4 | c.582 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12938582 | T | TTAAA | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01074.hp2 others(44): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0017 a0001c0001t0001g0133 a0001c0001t0001g0139 others(44): Show |
47 | 178 | 0.2640 | 4 | c.583 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12946799 | T | TAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(4): Show | a0001c0001t0001g0026 a0001c0001t0008g0035 a0001c0001t0008g0228 others(5): Show |
8 | 71 | 0.1127 | 4 | c.862 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACAC | intron_variant | MODIFIER | HG00140.hp1 HG01074.hp2 HG01169.hp1 others(21): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0025others(8): Show | a0001c0001t0006g0168 a0001c0001t0010g0032 a0001c0001t0025g0038 others(21): Show |
24 | 66 | 0.3636 | 4 | c.862 others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12956866 | A | AACAC | intron_variant | MODIFIER | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(6): Show | a0001c0001t0001g0030 a0001c0001t0001g0148 a0001c0001t0001g0181 others(14): Show |
17 | 96 | 0.1771 | 4 | c.134 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12962080 | A | AATAT | intron_variant | MODIFIER | HG00673.hp2 HG03942.hp1 NA18942.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0011 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0010 others(5): Show |
8 | 148 | 0.0541 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | C | CAAAA | intron_variant | MODIFIER | HG01074.hp2 HG01169.hp1 HG01192.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(5): Show | a0001c0001t0001g0200 a0001c0001t0010g0186 a0001c0002t0001g0089 others(10): Show |
13 | 108 | 0.1204 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12966155 | C | CAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(7): Show | a0001c0001t0001g0181 a0001c0001t0003g0028 a0001c0001t0003g0074 others(13): Show |
16 | 121 | 0.1322 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12970378 | A | AAAAG | intron_variant | MODIFIER | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(40): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0017 others(40): Show |
43 | 183 | 0.2350 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12975119 | G | GGATT | intron_variant | MODIFIER | HG02698.hp2 HG03704.hp2 HG03942.hp2 |
a0001a0004 | a0001c0001a0004c0017 | a0001c0001t0003a0001c0001t0011a0004c0017t0003 | a0001c0001t0003g0172 a0001c0001t0011g0070 a0004c0017t0003g0050 |
3 | 228 | 0.0132 | 4 | c.176 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0013 | a0001c0001t0001g0187 a0001c0001t0006g0025 a0001c0001t0006g0098 others(4): Show |
7 | 142 | 0.0493 | 4 | c.231 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991576 | T | TTATC | 3_prime_UTR_variant | MODIFIER | HG01884.hp2 HG01934.hp1 HG02280.hp2 others(3): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0008a0001c0005t0032 | a0001c0001t0008g0035 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | 228 | 0.0263 | 4 | c.*14 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 21/21 | 1411 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12991773 | G | GTCTT | downstream_gene_variant | MODIFIER | HG02922.hp1 HG02965.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | 228 | 0.0132 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 131 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12991846 | A | AACTT | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(13): Show |
a0001a0003 | a0001c0001a0001c0003a0003c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0093 others(13): Show |
16 | 227 | 0.0705 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 204 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12991869 | T | TTTAC | downstream_gene_variant | MODIFIER | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0003t0001 | a0001c0001t0001g0009 a0001c0001t0001g0148 a0001c0001t0001g0181 others(2): Show |
5 | 210 | 0.0238 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 227 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12992119 | C | CTGAT | downstream_gene_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02074.hp1 others(12): Show |
a0001a0005 | a0001c0001a0005c0015 | a0001c0001t0004a0001c0001t0011a0001c0001t0024others(2): Show | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0010 others(12): Show |
15 | 228 | 0.0658 | 4 | c.*19 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 477 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12992127 | T | TTTGA | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01192.hp1 HG02602.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0025others(4): Show | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0160 others(9): Show |
12 | 196 | 0.0612 | 4 | c.*19 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 485 | chr17 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1075236 | C | CTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00621.hp1 HG01978.hp2 others(5): Show |
a0001 | a0001c0002a0001c0004a0001c0017 | a0001c0002t0001a0001c0004t0006a0001c0017t0006 | a0001c0002t0001g0240 a0001c0004t0006g0039 a0001c0004t0006g0184 others(4): Show |
8 | 115 | 0.0696 | 4 | c.118 others(21): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1090460 | A | ATTTT | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
a0001a0002a0003others(4): Show | a0001c0004a0002c0001a0002c0019others(6): Show | a0001c0004t0024a0002c0001t0003a0002c0001t0005others(9): Show | a0001c0004t0024g0201 a0002c0001t0003g0003 a0002c0001t0003g0019 others(24): Show |
32 | 240 | 0.1333 | 4 | c.*44 others(15): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3833 | chr19 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32130525 | C | CATTG | intron_variant | MODIFIER | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(8): Show |
a0001a0003a0004others(1): Show | a0001c0002a0001c0018a0003c0003others(2): Show | a0001c0002t0005a0001c0018t0023a0003c0003t0001others(3): Show | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(7): Show |
11 | 177 | 0.0621 | 4 | c.386 others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |