regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 68 | 286 | 0.2378 | -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 | a0001c0001t0001g0123a0002c0006t0011g0239 | 2 | 286 | 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 | a0001c0001t0001g0279a0001c0001t0002g0025a0001c0001t0013g0283others(9): Show | 12 | 286 | 0.0420 | -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 | a0001c0001t0001g0135a0001c0001t0001g0266a0001c0001t0002g0265others(26): Show | 29 | 286 | 0.1014 | -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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | 286 | 0.1189 | -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 | a0002c0004t0007g0082a0002c0004t0007g0146 | 2 | 286 | 0.0070 | -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 | a0002c0002t0002g0225a0002c0002t0012g0024 | 2 | 286 | 0.0070 | -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 | a0002c0002t0025g0247a0002c0004t0007g0016a0002c0004t0007g0060others(6): Show | 9 | 286 | 0.0315 | -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 | a0001c0001t0001g0035a0001c0001t0003g0049a0001c0001t0003g0056others(8): Show | 11 | 230 | 0.0478 | -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 | a0001c0001t0001g0027 | 1 | 230 | 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 | 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 | a0001c0001t0001g0001a0001c0001t0007g0026a0001c0001t0008g0043others(8): Show | 11 | 230 | 0.0478 | -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 | a0001c0001t0001g0013 | 1 | 230 | 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 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0189others(26): Show | 29 | 230 | 0.1261 | -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 | a0001c0005t0001g0200a0001c0005t0001g0224a0001c0011t0001g0215 | 3 | 230 | 0.0130 | -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 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0174others(1): Show | 4 | 230 | 0.0174 | -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 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0002g0105others(21): Show | 24 | 230 | 0.1044 | -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 | a0001c0002t0001g0145 | 1 | 230 | 0.0044 | -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 | a0013 | a0013c0017 | a0013c0017t0016 | a0013c0017t0016g0005 | 1 | 186 | 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 |
a0002 | a0002c0003 | a0002c0003t0001a0002c0003t0019 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 3 | 186 | 0.0161 | -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 | 186 | 0.0054 | -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 | 144 | 0.0069 | -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 | 144 | 0.0069 | -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 | a0001c0001t0001g0075 | 1 | 144 | 0.0069 | -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 | a0001c0001t0001g0014a0001c0001t0007g0013a0001c0001t0008g0030 | 3 | 144 | 0.0208 | -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 | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0015g0050others(7): Show | 10 | 144 | 0.0694 | -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 |
a0002a0004 | a0002c0002a0004c0008 | a0002c0002t0009a0004c0008t0012 | a0002c0002t0009g0127a0004c0008t0012g0002 | 2 | 144 | 0.0139 | -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 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0002g0136 | 3 | 144 | 0.0208 | -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 | a0001c0001t0013 | a0001c0001t0013g0066 | 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 |
a0001a0002a0005 | a0001c0001a0001c0009a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(3): Show | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0055others(26): Show | 29 | 144 | 0.2014 | -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 | a0001c0001t0001g0024a0002c0005t0006g0018 | 2 | 144 | 0.0139 | -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 | 144 | 0.0069 | -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 | a0001c0001t0001a0002c0002t0003a0002c0002t0016 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(12): Show | 15 | 144 | 0.1042 | -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 | a0001c0001t0001a0001c0001t0014 | a0001c0001t0001g0107a0001c0001t0014g0083 | 2 | 144 | 0.0139 | -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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | 144 | 0.0278 | -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 | a0002c0006t0001g0203a0002c0016t0004g0229a0004c0012t0002g0297others(1): Show | 4 | 390 | 0.0103 | -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(67): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0008others(10): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(13): Show | a0001c0001t0003g0006a0001c0001t0003g0028a0001c0001t0003g0063others(67): Show | 70 | 390 | 0.1795 | -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 |
a0001a0005a0006others(2): Show | a0001c0001a0001c0004a0001c0007others(9): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(10): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0136others(33): Show | 36 | 390 | 0.0923 | -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 | a0002c0003t0002g0122a0002c0007t0002g0058 | 2 | 168 | 0.0119 | -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 |
a0001a0002a0009 | a0001c0001a0002c0004a0009c0030 | a0001c0001t0001a0002c0004t0002a0009c0030t0002 | a0001c0001t0001g0021a0001c0001t0001g0118a0002c0004t0002g0119others(2): Show | 5 | 168 | 0.0298 | -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 | a0002c0003t0002g0025a0002c0003t0002g0037a0002c0003t0002g0055others(20): Show | 23 | 168 | 0.1369 | -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 | a0018 | a0018c0049 | a0018c0049t0004 | a0018c0049t0004g0075 | 1 | 168 | 0.0060 | -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 | a0001c0017t0002g0113a0001c0017t0002g0148a0001c0033t0002g0110others(34): Show | 37 | 168 | 0.2202 | -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 |
a0001a0009a0012 | a0001c0002a0001c0003a0001c0009others(4): Show | a0001c0002t0026a0001c0003t0026a0001c0009t0058others(5): Show | a0001c0002t0026g0192a0001c0003t0026g0190a0001c0009t0058g0200others(5): Show | 8 | 363 | 0.0220 | -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 |
a0001a0004 | a0001c0002a0001c0007a0004c0044 | a0001c0002t0001a0001c0007t0003a0004c0044t0002 | a0001c0002t0001g0327a0001c0007t0003g0360a0004c0044t0002g0328 | 3 | 363 | 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 | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(5): Show | a0001c0001t0002g0271a0001c0001t0012g0207a0001c0002t0001g0270others(9): Show | 12 | 363 | 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 | a0001c0007t0003 | a0001c0007t0003g0346 | 1 | 363 | 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 | a0002c0034t0004 | a0002c0034t0004g0148 | 1 | 363 | 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 | a0001c0005t0001g0078a0001c0036t0002g0229 | 2 | 363 | 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 | a0002c0004t0005g0113a0002c0004t0005g0129 | 2 | 362 | 0.0055 | -16 | c.179 others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar |