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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02647.hp2 HG02717.hp2 HG03471.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0004 | a0001c0001t0002g0045a0001c0001t0004g0111a0001c0002t0004g0100 | 3 | 198 | 0.0152 | -17 | c.198 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0042 | 1 | 198 | 0.0051 | -17 | c.198 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143177987 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0037 | 1 | 198 | 0.0051 | -17 | c.198 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG03540.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0045 | 1 | 347 | 0.0029 | -17 | c.658 others(34): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6772720 | GTTTTATT others(10): Show |
G | intron_variant | MODIFIER | HG01106.hp1 NA19043.hp1 |
a0001a0010 | a0001c0003a0010c0014 | a0001c0003t0003a0010c0014t0001 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | 248 | 0.0081 | -17 | c.122 others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6834230 | AAATAATA others(10): Show |
A | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 248 | 0.0040 | -17 | c.326 others(34): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841165 | CTCCTCTC others(10): Show |
C | intron_variant | MODIFIER | NA18747.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0215 | 1 | 248 | 0.0040 | -17 | c.543 others(34): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055865 | TAAAATAA others(10): Show |
T | intron_variant | MODIFIER | HG03516.hp2 NA19083.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218a0001c0001t0001g0254 | 2 | 390 | 0.0051 | -17 | c.345 others(32): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144689426 | CTTTTTTT others(10): Show |
C | upstream_gene_variant | MODIFIER | HG02258.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | 246 | 0.0081 | -17 | c.-38 others(28): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3581 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38627628 | TGTTGGGG others(10): Show |
T | intron_variant | MODIFIER | HG03540.hp2 | a0019 | a0019c0039 | a0019c0039t0013 | a0019c0039t0013g0284 | 1 | 350 | 0.0029 | -17 | c.558 others(32): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699498 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG00738.hp2 NA19054.hp1 |
a0001a0002 | a0001c0003a0002c0009 | a0001c0003t0003a0002c0009t0004 | a0001c0003t0003g0264a0002c0009t0004g0237 | 2 | 286 | 0.0070 | -17 | c.154 others(36): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699500 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0022a0002c0002t0002g0018a0002c0002t0002g0019others(2): Show | 5 | 286 | 0.0175 | -17 | c.154 others(36): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100745082 | GGAATGAG others(10): Show |
G | intron_variant | MODIFIER | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
a0002 | a0002c0006 | a0002c0006t0008a0002c0006t0011 | a0002c0006t0008g0240a0002c0006t0008g0243a0002c0006t0011g0241others(1): Show | 4 | 286 | 0.0140 | -17 | c.155 others(36): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(3): Show | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0002g0003others(11): Show | 14 | 286 | 0.0490 | -17 | c.155 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0002 | a0002c0002t0040 | a0002c0002t0040g0101 | 1 | 286 | 0.0035 | -17 | c.251 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG03490.hp2 HG03492.hp1 |
a0002 | a0002c0002 | a0002c0002t0012 | a0002c0002t0012g0052a0002c0002t0012g0053 | 2 | 286 | 0.0070 | -17 | c.487 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG01975.hp1 HG03540.hp1 |
a0002 | a0002c0004a0002c0006 | a0002c0004t0007a0002c0006t0008 | a0002c0004t0007g0201a0002c0006t0008g0243 | 2 | 286 | 0.0070 | -17 | c.487 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | NA18522.hp1 NA18992.hp1 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0003a0002c0002t0008 | a0001c0003t0003g0273a0002c0002t0008g0175 | 2 | 286 | 0.0070 | -17 | c.487 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(10): Show |
A | intron_variant | MODIFIER | NA19012.hp1 NA19057.hp2 |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0258a0001c0003t0003g0269 | 2 | 286 | 0.0070 | -17 | c.487 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(10): Show |
A | intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0270 | 1 | 286 | 0.0035 | -17 | c.487 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100960001 | AAAACTCT others(10): Show |
A | intron_variant | MODIFIER | HG01123.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 | 1 | 286 | 0.0035 | -17 | c.122 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12873926 | TAAACAAA others(10): Show |
T | intron_variant | MODIFIER | HG01192.hp1 HG02809.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009a0001c0001t0025 | a0001c0001t0001g0035a0001c0001t0009g0191a0001c0001t0025g0036 | 3 | 230 | 0.0130 | -17 | c.54- others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12926405 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG01934.hp2 HG01978.hp1 HG02027.hp1 others(6): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0009t0002 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0154others(6): Show | 9 | 230 | 0.0391 | -17 | c.465 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12926488 | GTATAATA others(10): Show |
G | intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0125 | 1 | 230 | 0.0044 | -17 | c.465 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0150a0001c0001t0002g0043 | 2 | 186 | 0.0108 | -17 | c.418 others(34): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0128 | 1 | 144 | 0.0069 | -17 | c.588 others(38): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590836 | GAAAAGAA others(10): Show |
G | intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 144 | 0.0069 | -17 | c.588 others(36): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG01433.hp1 HG03654.hp1 NA18612.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | 144 | 0.0208 | -17 | c.588 others(34): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG02970.hp1 others(7): Show |
a0004a0017a0023 | a0004c0012a0004c0017a0017c0053others(1): Show | a0004c0012t0002a0004c0012t0015a0004c0017t0002others(2): Show | a0004c0012t0002g0172a0004c0012t0002g0233a0004c0012t0002g0244others(7): Show | 10 | 390 | 0.0256 | -17 | c.877 others(34): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG02559.hp2 HG02922.hp2 HG03195.hp1 others(3): Show |
a0001a0002a0003 | a0001c0007a0002c0019a0002c0020others(1): Show | a0001c0007t0001a0002c0019t0008a0002c0020t0005others(1): Show | a0001c0007t0001g0128a0001c0007t0001g0238a0002c0019t0008g0046others(3): Show | 6 | 390 | 0.0154 | -17 | c.878 others(34): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIG_chr16_275591_288010 | 276164 | TGGGCCGG others(10): Show |
T | upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(38): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(22): Show | 41 | 442 | 0.0928 | -17 | c.-45 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4426 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285908 | CCCCAACC others(10): Show |
C | downstream_gene_variant | MODIFIER | HG03041.hp2 NA18944.hp2 NA18946.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007 | a0001c0001t0002g0001a0001c0001t0007g0004 | 6 | 442 | 0.0136 | -17 | c.*30 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2899 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285949 | CCCCAACC others(10): Show |
C | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
a0001a0006a0007 | a0001c0001a0001c0003a0006c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(8): Show | 38 | 442 | 0.0860 | -17 | c.*31 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2940 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 287738 | GCCTGGGC others(10): Show |
G | downstream_gene_variant | MODIFIER | HG02735.hp2 HG03834.hp2 HG03942.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0027 | a0001c0001t0002g0001a0001c0001t0027g0002 | 3 | 442 | 0.0068 | -17 | c.*49 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4729 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17552571 | GTTTTTTT others(10): Show |
G | intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0020 | a0001c0020t0001 | a0001c0020t0001g0016 | 1 | 168 | 0.0060 | -17 | c.-44 others(36): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17640631 | GAGGTGAT others(10): Show |
G | intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 1 | 168 | 0.0060 | -17 | c.227 others(34): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1843802 | AGCTCGCC others(10): Show |
A | intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0008 | a0001c0008t0002 | a0001c0008t0002g0152 | 1 | 363 | 0.0028 | -17 | c.37+ others(30): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02572.hp1 HG03139.hp2 |
a0002 | a0002c0004 | a0002c0004t0021 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | 362 | 0.0055 | -17 | c.179 others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351430 | TATATATA others(10): Show |
T | intron_variant | MODIFIER | HG02040.hp1 HG02155.hp1 |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | 308 | 0.0065 | -17 | c.32+ others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351434 | TATATATA others(10): Show |
T | intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0048 | 1 | 308 | 0.0033 | -17 | c.32+ others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351436 | TATATATA others(10): Show |
T | intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0002 | a0001c0002t0019 | a0001c0002t0019g0012 | 1 | 308 | 0.0033 | -17 | c.32+ others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3464245 | ACTGCATG others(10): Show |
A | intron_variant | MODIFIER | HG02083.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0021 | 1 | 334 | 0.0030 | -17 | c.588 others(32): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73304363 | GATATAGT others(10): Show |
G | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(39): Show |
a0002a0004a0017 | a0002c0002a0002c0004a0002c0008others(4): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0008others(8): Show | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(37): Show | 42 | 228 | 0.1842 | -17 | c.-42 others(28): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3912 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329354 | TATATATA others(10): Show |
T | intron_variant | MODIFIER | HG01074.hp2 HG01168.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104a0001c0001t0001g0118 | 2 | 228 | 0.0088 | -17 | c.319 others(38): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329356 | TATATATA others(10): Show |
T | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
a0001 | a0001c0001a0001c0020 | a0001c0001t0001a0001c0020t0001 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0084others(6): Show | 9 | 228 | 0.0395 | -17 | c.319 others(38): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329357 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 228 | 0.0044 | -17 | c.319 others(38): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7354370 | CTGATTTG others(10): Show |
C | intron_variant | MODIFIER | NA18942.hp1 NA19000.hp2 |
a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0057a0001c0019t0006g0078 | 2 | 298 | 0.0067 | -17 | c.-11 others(36): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154161099 | TTTGTGTG others(10): Show |
T | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0007a0001c0001t0015a0001c0001t0030others(16): Show | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(70): Show | 73 | 283 | 0.2580 | -17 | c.148 others(36): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154235336 | TGTGGGTT others(10): Show |
T | intron_variant | MODIFIER | NA18947.hp2 NA18960.hp2 NA18983.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | 283 | 0.0106 | -17 | c.209 others(36): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149609999 | AGTAACTG others(10): Show |
A | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0173 | 1 | 394 | 0.0025 | -17 | c.458 others(32): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | TogoVar |