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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP40_chr20_38596809_38655653 | 38643145 | CAA | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
a0001a0005a0006others(7): Show | a0001c0001a0001c0002a0001c0004others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(146): Show |
165 | 350 | 0.4714 | -2 | c.136 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38650011 | CAG | C | 3_prime_UTR_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
a0001a0008a0009others(1): Show | a0001c0002a0008c0013a0008c0017others(2): Show | a0001c0002t0008a0008c0013t0008a0008c0017t0008others(2): Show | a0001c0002t0008g0074 a0008c0013t0008g0028 a0008c0013t0008g0303 others(4): Show |
8 | 350 | 0.0229 | -2 | c.*16 others(11): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 164 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100685712 | GAA | G | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(50): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(13): Show | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(50): Show |
53 | 286 | 0.1853 | -2 | c.-19 others(13): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1575 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100694441 | CTT | C | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
a0001a0002 | a0001c0010a0002c0006 | a0001c0010t0001a0002c0006t0008a0002c0006t0011 | a0001c0010t0001g0238 a0002c0006t0008g0240 a0002c0006t0008g0243 others(3): Show |
6 | 286 | 0.0210 | -2 | c.154 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699480 | GTA | G | intron_variant | MODIFIER | HG00408.hp1 HG01192.hp2 HG01261.hp1 others(29): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0032others(7): Show | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 others(29): Show |
32 | 286 | 0.1119 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699506 | ATT | A | intron_variant | MODIFIER | HG00642.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0037a0002c0002t0002a0002c0002t0005others(2): Show | a0001c0001t0037g0041 a0002c0002t0002g0147 a0002c0002t0005g0105 others(3): Show |
6 | 286 | 0.0210 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100702671 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(57): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(16): Show | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0062 others(57): Show |
60 | 286 | 0.2098 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100703977 | GGT | G | intron_variant | MODIFIER | HG00738.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0009 | a0001c0001t0001a0002c0002t0008a0002c0002t0035others(2): Show | a0001c0001t0001g0093 a0001c0001t0001g0095 a0002c0002t0008g0009 others(3): Show |
6 | 286 | 0.0210 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100705032 | AAG | A | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002others(1): Show | a0001c0001t0001a0001c0010t0001a0002c0002t0028others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0010t0001g0238 others(7): Show |
10 | 286 | 0.0350 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100711867 | AAT | A | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0001a0002c0002t0002a0002c0004t0007 | a0002c0002t0001g0012 a0002c0002t0001g0013 a0002c0002t0001g0015 others(3): Show |
6 | 286 | 0.0210 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTG | T | intron_variant | MODIFIER | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(24): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(11): Show | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0117 others(24): Show |
27 | 286 | 0.0944 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100715048 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(37): Show | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(131): Show |
134 | 286 | 0.4685 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100725009 | TAA | T | intron_variant | MODIFIER | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(6): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0002a0001c0003t0006a0002c0002t0002others(3): Show | a0001c0001t0002g0096 a0001c0003t0006g0112 a0002c0002t0002g0067 others(6): Show |
9 | 286 | 0.0315 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGT | C | intron_variant | MODIFIER | HG00673.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0019a0001c0003t0003others(6): Show | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0072 others(13): Show |
16 | 286 | 0.0559 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTA | G | intron_variant | MODIFIER | HG00544.hp1 HG02602.hp1 HG03098.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(1): Show | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0148 others(4): Show |
7 | 286 | 0.0245 | -2 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100735602 | CTT | C | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02970.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0002c0002t0001a0002c0002t0028others(1): Show | a0001c0001t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0013 others(4): Show |
7 | 286 | 0.0245 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100740066 | ATT | A | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02523.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0001others(2): Show | a0001c0001t0001g0281 a0001c0003t0003g0257 a0001c0003t0003g0280 others(7): Show |
10 | 286 | 0.0350 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100745023 | AAG | A | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0004others(2): Show | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0072 others(8): Show |
11 | 286 | 0.0385 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751266 | AGT | A | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(14): Show | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(66): Show |
69 | 286 | 0.2413 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751279 | GTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0037a0001c0003t0014others(12): Show | a0001c0001t0001g0007 a0001c0001t0037g0041 a0001c0003t0014g0234 others(22): Show |
25 | 286 | 0.0874 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751356 | CTG | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0062 others(67): Show |
70 | 286 | 0.2448 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(3): Show | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0276 others(16): Show |
19 | 286 | 0.0664 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100756222 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(50): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0062 others(50): Show |
53 | 286 | 0.1853 | -2 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100772550 | CCA | C | intron_variant | MODIFIER | HG01074.hp2 HG01175.hp1 HG01257.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0020 others(2): Show |
5 | 286 | 0.0175 | -2 | c.250 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100776981 | CAA | C | intron_variant | MODIFIER | HG01109.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
a0001a0002 | a0001c0008a0001c0010a0002c0002others(1): Show | a0001c0008t0001a0001c0010t0001a0002c0002t0001others(6): Show | a0001c0008t0001g0004 a0001c0010t0001g0238 a0002c0002t0001g0013 others(16): Show |
19 | 286 | 0.0664 | -2 | c.250 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100786579 | TTA | T | intron_variant | MODIFIER | HG02723.hp1 HG02895.hp2 HG02922.hp2 others(2): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0011a0002c0005t0010 | a0002c0002t0002g0254 a0002c0002t0011g0207 a0002c0002t0011g0231 others(2): Show |
5 | 286 | 0.0175 | -2 | c.251 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAA | C | intron_variant | MODIFIER | HG00423.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(12): Show | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0070 others(34): Show |
37 | 286 | 0.1294 | -2 | c.251 others(17): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100810068 | TAA | T | intron_variant | MODIFIER | HG02280.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0004others(1): Show | a0001c0001t0001g0002 a0002c0002t0002g0173 a0002c0002t0002g0174 others(2): Show |
5 | 286 | 0.0175 | -2 | c.312 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100814361 | CAA | C | intron_variant | MODIFIER | HG01433.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0002c0002t0001others(1): Show | a0001c0001t0001g0162 a0001c0003t0003g0273 a0002c0002t0001g0012 others(4): Show |
7 | 286 | 0.0245 | -2 | c.312 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100845104 | CAT | C | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(9): Show |
a0002 | a0002c0002a0002c0005a0002c0009 | a0002c0002t0004a0002c0002t0008a0002c0002t0009others(2): Show | a0002c0002t0004g0108 a0002c0002t0004g0109 a0002c0002t0008g0028 others(9): Show |
12 | 286 | 0.0420 | -2 | c.313 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100850873 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(15): Show | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0062 others(77): Show |
80 | 286 | 0.2797 | -2 | c.313 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | GGT | G | intron_variant | MODIFIER | HG00099.hp1 HG03017.hp2 HG03834.hp2 others(1): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0016 | a0001c0001t0002a0002c0002t0002a0002c0002t0004others(1): Show | a0001c0001t0002g0003 a0002c0002t0002g0102 a0002c0002t0004g0077 others(1): Show |
4 | 286 | 0.0140 | -2 | c.313 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100870947 | TAA | T | intron_variant | MODIFIER | HG01070.hp1 HG01433.hp1 HG01981.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0001c0003t0006others(2): Show | a0001c0001t0001g0266 a0001c0003t0003g0119 a0001c0003t0003g0155 others(6): Show |
9 | 286 | 0.0315 | -2 | c.384 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | GTC | G | intron_variant | MODIFIER | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(1): Show |
a0002 | a0002c0002a0002c0005a0002c0009 | a0002c0002t0009a0002c0005t0010a0002c0009t0004 | a0002c0002t0009g0043 a0002c0005t0010g0030 a0002c0005t0010g0044 others(1): Show |
4 | 286 | 0.0140 | -2 | c.384 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTG | C | intron_variant | MODIFIER | HG01123.hp1 HG01261.hp2 HG01358.hp2 others(6): Show |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0002c0002t0004a0002c0002t0009others(3): Show | a0002c0002t0002g0050 a0002c0002t0004g0107 a0002c0002t0009g0035 others(6): Show |
9 | 286 | 0.0315 | -2 | c.384 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100889510 | GTA | G | intron_variant | MODIFIER | HG01081.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0008a0002c0002t0009 | a0002c0002t0008g0028 a0002c0002t0008g0029 a0002c0002t0008g0230 others(1): Show |
4 | 286 | 0.0140 | -2 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100891439 | CTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0008a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(29): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0066 others(147): Show |
150 | 286 | 0.5245 | -2 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100896233 | AGT | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016 a0002c0004t0007g0060 a0002c0004t0007g0074 others(5): Show |
8 | 286 | 0.0280 | -2 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100898692 | CTT | C | intron_variant | MODIFIER | HG00323.hp2 HG01934.hp1 HG01934.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0036 | a0001c0001t0001g0007 a0001c0001t0001g0163 a0001c0001t0036g0090 |
3 | 286 | 0.0105 | -2 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100899732 | TTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
a0002a0003a0005 | a0002c0002a0002c0006a0002c0011others(2): Show | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(13): Show | a0002c0002t0002g0006 a0002c0002t0002g0034 a0002c0002t0002g0045 others(46): Show |
49 | 286 | 0.1713 | -2 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100929680 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(30): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0157 a0001c0003t0001g0158 a0001c0003t0001g0170 others(30): Show |
33 | 286 | 0.1154 | -2 | c.598 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100940843 | CAT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(50): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(261): Show |
264 | 286 | 0.9231 | -2 | c.833 others(17): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100958267 | ATC | A | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
a0001a0002 | a0001c0003a0001c0008a0002c0002others(2): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(9): Show | a0001c0003t0001g0157 a0001c0003t0001g0158 a0001c0003t0001g0170 others(43): Show |
46 | 286 | 0.1608 | -2 | c.116 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100958520 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
a0001a0002a0003others(1): Show | a0001c0003a0001c0008a0002c0002others(5): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(30): Show | a0001c0003t0001g0157 a0001c0003t0001g0158 a0001c0003t0001g0170 others(131): Show |
134 | 286 | 0.4685 | -2 | c.116 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100981426 | CTG | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(13): Show |
a0002 | a0002c0002a0002c0004a0002c0005 | a0002c0002t0025a0002c0004t0007a0002c0005t0010others(1): Show | a0002c0002t0025g0247 a0002c0004t0007g0016 a0002c0004t0007g0060 others(13): Show |
16 | 286 | 0.0559 | -2 | c.245 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12801651 | GTC | G | intron_variant | MODIFIER | HG03225.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0012a0001c0004t0012 | a0001c0001t0012g0095 a0001c0004t0012g0166 |
2 | 230 | 0.0087 | -2 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTA | T | intron_variant | MODIFIER | HG00738.hp2 NA18947.hp1 NA19007.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0002 | a0001c0001t0001g0117 a0001c0001t0002g0118 a0001c0001t0002g0159 others(1): Show |
4 | 230 | 0.0174 | -2 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | TTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(72): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0035 others(72): Show |
75 | 230 | 0.3261 | -2 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12828028 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(71): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0185 others(71): Show |
74 | 230 | 0.3217 | -2 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841585 | GTC | G | intron_variant | MODIFIER | HG02280.hp1 HG02300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0204 a0001c0001t0013g0161 |
2 | 230 | 0.0087 | -2 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |