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 | 100850873 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(65): Show |
a0001a0002 | a0001c0001a0001c0012a0001c0014others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0067 others(65): Show |
68 | 91 | 0.7473 | -16 | c.313 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875095 | CTCTCTCT others(9): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG01361.hp1 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0011 | a0001c0001t0001g0111 a0002c0006t0011g0239 |
2 | 284 | 0.0070 | -16 | c.384 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875097 | CTCTCTCT others(9): Show |
C | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(9): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(2): Show | a0001c0001t0001g0279 a0001c0001t0002g0020 a0001c0001t0013g0280 others(9): Show |
12 | 284 | 0.0423 | -16 | c.384 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875099 | CTCTCTCT others(9): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(7): Show | a0001c0001t0001g0139 a0001c0001t0001g0259 a0001c0001t0002g0264 others(26): Show |
29 | 274 | 0.1058 | -16 | c.384 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(9): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG00673.hp1 HG01123.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0023 others(31): Show |
34 | 101 | 0.3366 | -16 | c.385 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG01516.hp1 HG03927.hp2 |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0076 a0002c0004t0007g0145 |
2 | 262 | 0.0076 | -16 | c.487 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02897.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0012 | a0002c0002t0002g0226 a0002c0002t0012g0027 |
2 | 271 | 0.0074 | -16 | c.487 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | AAAATAAA others(9): Show |
A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(6): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0025a0002c0004t0007 | a0002c0002t0025g0250 a0002c0004t0007g0014 a0002c0004t0007g0061 others(6): Show |
9 | 38 | 0.2368 | -16 | c.253 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATAT others(9): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG01081.hp1 HG01192.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0037 a0001c0001t0003g0049 a0001c0001t0003g0079 others(8): Show |
11 | 163 | 0.0675 | -16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTATTTA others(9): Show |
G | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 26 | 0.0385 | -16 | c.54- others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATAT others(9): Show |
T | intron_variant | MODIFIER | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0001g0001 a0001c0001t0007g0023 a0001c0001t0008g0041 others(8): Show |
11 | 110 | 0.1000 | -16 | c.54- others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12873914 | TAAATAAA others(9): Show |
T | intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 228 | 0.0044 | -16 | c.54- others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12873939 | AAATAAAT others(9): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(13): Show | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0001g0181 others(26): Show |
29 | 228 | 0.1272 | -16 | c.54- others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGAGA others(9): Show |
G | intron_variant | MODIFIER | HG01109.hp2 HG02647.hp1 HG02970.hp2 |
a0001 | a0001c0005a0001c0011 | a0001c0005t0001a0001c0011t0001 | a0001c0005t0001g0190 a0001c0005t0001g0223 a0001c0011t0001g0215 |
3 | 186 | 0.0161 | -16 | c.199 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | AGTGTGTG others(9): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0174 others(1): Show |
4 | 110 | 0.0364 | -16 | c.199 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12912385 | GAAAAAAT others(9): Show |
G | intron_variant | MODIFIER | HG00673.hp2 HG00735.hp2 HG01928.hp2 others(21): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0002g0107 others(21): Show |
24 | 228 | 0.1053 | -16 | c.275 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0126 | 1 | 65 | 0.0154 | -16 | c.113 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32110583 | AAATTAGG others(9): Show |
A | intron_variant | MODIFIER | HG02809.hp1 | a0010 | a0010c0017 | a0010c0017t0016 | a0010c0017t0016g0005 | 1 | 184 | 0.0054 | -16 | c.371 others(35): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32148163 | AATCTATC others(9): Show |
A | intron_variant | MODIFIER | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
a0003 | a0003c0003 | a0003c0003t0001a0003c0003t0019 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | 59 | 0.0508 | -16 | c.394 others(35): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0164 | 1 | 23 | 0.0435 | -16 | c.418 others(33): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174518 | TTTCCTTC others(9): Show |
T | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0141 | 1 | 117 | 0.0085 | -16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174565 | CCTTCCTT others(9): Show |
C | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 135 | 0.0074 | -16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174623 | TTTTCTTT others(9): Show |
T | intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 75 | 0.0133 | -16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG01106.hp1 HG03486.hp2 HG06807.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0008 | a0001c0001t0001g0014 a0001c0001t0007g0013 a0001c0001t0008g0030 |
3 | 15 | 0.2000 | -16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | CTGTGTGT others(9): Show |
C | intron_variant | MODIFIER | HG01515.hp1 HG02055.hp1 HG02698.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0013a0001c0003t0001others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0013g0050 others(7): Show |
10 | 17 | 0.5882 | -16 | c.749 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11241531 | CGTGTGTG others(9): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG03516.hp1 |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0009a0003c0007t0012 | a0002c0002t0009g0128 a0003c0007t0012g0002 |
2 | 68 | 0.0294 | -16 | c.748 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11320766 | TACACACA others(9): Show |
T | intron_variant | MODIFIER | HG01074.hp1 HG03579.hp1 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0002g0131 |
3 | 30 | 0.1000 | -16 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11357059 | TCCTTAAT others(9): Show |
T | intron_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 144 | 0.0069 | -16 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11382708 | GTCTGAAA others(9): Show |
G | intron_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 144 | 0.0069 | -16 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG00642.hp1 HG01069.hp1 HG01192.hp1 others(26): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(2): Show | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0048 others(26): Show |
29 | 39 | 0.7436 | -16 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11467984 | GAATGAAT others(9): Show |
G | intron_variant | MODIFIER | HG03098.hp1 NA19240.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0002c0005t0006 | a0001c0001t0001g0024 a0002c0005t0006g0018 |
2 | 143 | 0.0140 | -16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11527011 | AGTGTGTG others(9): Show |
A | intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0126 | 1 | 38 | 0.0263 | -16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG02071.hp1 HG02451.hp1 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0014 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(12): Show |
15 | 49 | 0.3061 | -16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590846 | GAAAAGAA others(9): Show |
G | intron_variant | MODIFIER | NA19067.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0112 a0001c0001t0004g0081 |
2 | 132 | 0.0152 | -16 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG02027.hp1 HG04199.hp1 NA18984.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | 8 | 0.5000 | -16 | c.588 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG00673.hp1 HG02027.hp1 HG02280.hp2 others(1): Show |
a0002a0004 | a0002c0006a0002c0016a0004c0012others(1): Show | a0002c0006t0001a0002c0016t0004a0004c0012t0002others(1): Show | a0002c0006t0001g0203 a0002c0016t0004g0229 a0004c0012t0002g0297 others(1): Show |
4 | 62 | 0.0645 | -16 | c.877 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0008others(10): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(13): Show | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0063 others(66): Show |
69 | 93 | 0.7419 | -16 | c.878 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44861454 | TGGGGGAC others(9): Show |
T | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01070.hp2 others(33): Show |
a0001a0005a0008others(2): Show | a0001c0001a0001c0004a0001c0007others(9): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(9): Show | a0001c0001t0001g0101 a0001c0001t0001g0371 a0001c0004t0001g0136 others(33): Show |
36 | 204 | 0.1765 | -16 | c.982 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17586152 | CCCAAGTA others(9): Show |
C | intron_variant | MODIFIER | HG01074.hp2 HG02280.hp2 |
a0002 | a0002c0003a0002c0007 | a0002c0003t0002a0002c0007t0002 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | 166 | 0.0120 | -16 | c.38- others(31): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17611533 | TATCCATC others(9): Show |
T | intron_variant | MODIFIER | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
a0001a0002a0021 | a0001c0001a0002c0004a0021c0030 | a0001c0001t0001a0002c0004t0002a0021c0030t0002 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0002c0004t0002g0120 others(2): Show |
5 | 106 | 0.0472 | -16 | c.610 others(33): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17655464 | CATCCATC others(9): Show |
C | intron_variant | MODIFIER | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
a0002a0005a0008others(1): Show | a0002c0003a0002c0008a0002c0021others(8): Show | a0002c0003t0002a0002c0008t0002a0002c0021t0002others(8): Show | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | 166 | 0.1386 | -16 | c.248 others(33): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17686074 | TTTTTTTT others(9): Show |
T | intron_variant | MODIFIER | NA18982.hp1 | a0020 | a0020c0049 | a0020c0049t0004 | a0020c0049t0004g0075 | 1 | 165 | 0.0061 | -16 | c.301 others(35): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17689558 | TCTTCCCT others(9): Show |
T | intron_variant | MODIFIER | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
a0001a0002a0005others(2): Show | a0001c0017a0001c0033a0001c0043others(14): Show | a0001c0017t0002a0001c0033t0002a0001c0043t0002others(14): Show | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(34): Show |
37 | 165 | 0.2242 | -16 | c.318 others(35): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832609 | CAGAGACA others(9): Show |
C | intron_variant | MODIFIER | HG01255.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
a0001a0011a0012 | a0001c0002a0001c0003a0001c0009others(4): Show | a0001c0002t0026a0001c0003t0026a0001c0009t0051others(5): Show | a0001c0002t0026g0267 a0001c0003t0026g0268 a0001c0009t0051g0274 others(5): Show |
8 | 362 | 0.0221 | -16 | c.-48 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833339 | CAGAGACA others(9): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02615.hp1 HG02818.hp1 |
a0001a0003 | a0001c0002a0001c0007a0003c0044 | a0001c0002t0001a0001c0007t0008a0003c0044t0002 | a0001c0002t0001g0327 a0001c0007t0008g0362 a0003c0044t0002g0328 |
3 | 362 | 0.0083 | -16 | c.-48 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839323 | GGGGACTG others(9): Show |
G | intron_variant | MODIFIER | HG00738.hp2 HG04184.hp2 NA18941.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0014a0001c0002t0001others(5): Show | a0001c0001t0002g0249 a0001c0001t0014g0185 a0001c0002t0001g0248 others(9): Show |
12 | 362 | 0.0331 | -16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839768 | GACTGTCT others(9): Show |
G | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0007 | a0001c0007t0008 | a0001c0007t0008g0347 | 1 | 361 | 0.0028 | -16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839801 | ACTGTCTT others(9): Show |
A | intron_variant | MODIFIER | HG02074.hp2 | a0002 | a0002c0034 | a0002c0034t0010 | a0002c0034t0010g0135 | 1 | 359 | 0.0028 | -16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839887 | TGGTGTGG others(9): Show |
T | intron_variant | MODIFIER | HG02074.hp1 NA18612.hp1 |
a0001 | a0001c0005a0001c0036 | a0001c0005t0001a0001c0036t0002 | a0001c0005t0001g0080 a0001c0036t0002g0205 |
2 | 362 | 0.0055 | -16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | NA18964.hp2 NA19083.hp2 |
a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0116 a0002c0004t0005g0132 |
2 | 17 | 0.1176 | -16 | c.179 others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar |