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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11226139 | T | TCCCTCCC | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 7 | c.748 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11280745 | C | CAAAAAAA | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 144 | 0.0069 | 7 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11500663 | C | CAAAAAAA | intron_variant | MODIFIER | HG02451.hp2 HG03130.hp1 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0007t0001 | a0001c0001t0001g0020a0001c0007t0001g0021 | 2 | 144 | 0.0139 | 7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | T | TATATATA | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0021 | 1 | 144 | 0.0069 | 7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590857 | A | AAGGAAAG | intron_variant | MODIFIER | HG00673.hp1 HG02074.hp1 NA19070.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0085a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | 144 | 0.0208 | 7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAGGAAAG | intron_variant | MODIFIER | HG01069.hp1 HG03130.hp1 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0007t0001 | a0001c0001t0001g0102a0001c0007t0001g0021 | 2 | 144 | 0.0139 | 7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590915 | A | AAAGAAAG | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0129 | 1 | 144 | 0.0069 | 7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11646738 | A | AAATAAAC | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | 7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAAAAAA | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 144 | 0.0069 | 7 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00558.hp1 HG01106.hp2 others(28): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0010others(15): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(18): Show | a0001c0001t0001g0370a0001c0001t0003g0155a0001c0001t0003g0156others(28): Show | 31 | 390 | 0.0795 | 7 | c.-72 others(26): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787029 | C | CAAAAAAA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(40): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(24): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0003others(27): Show | a0001c0001t0001g0017a0001c0001t0010g0198a0001c0004t0003g0371others(40): Show | 43 | 390 | 0.1103 | 7 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787031 | A | AAAAAAAC | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(15): Show |
a0001a0002a0003others(3): Show | a0001c0004a0001c0009a0001c0039others(7): Show | a0001c0004t0001a0001c0004t0003a0001c0009t0001others(9): Show | a0001c0004t0001g0007a0001c0004t0003g0283a0001c0009t0001g0076others(15): Show | 18 | 390 | 0.0462 | 7 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787047 | A | AAAAAAAC | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0008others(21): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(24): Show | a0001c0001t0001g0024a0001c0001t0001g0134a0001c0001t0001g0343others(63): Show | 66 | 390 | 0.1692 | 7 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44816803 | C | CAAAAAAA | intron_variant | MODIFIER | HG02280.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
a0001a0002a0005others(1): Show | a0001c0008a0002c0003a0002c0023others(4): Show | a0001c0008t0001a0002c0003t0004a0002c0023t0005others(4): Show | a0001c0008t0001g0038a0002c0003t0004g0351a0002c0023t0005g0071others(7): Show | 10 | 390 | 0.0256 | 7 | c.386 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTTTT | intron_variant | MODIFIER | HG01257.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0008a0001c0009others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0008t0001others(6): Show | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0134others(8): Show | 11 | 390 | 0.0282 | 7 | c.596 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(57): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0004a0001c0006others(29): Show | a0001c0003t0068a0001c0004t0002a0001c0004t0004others(41): Show | a0001c0003t0068g0338a0001c0004t0002g0072a0001c0004t0002g0230others(57): Show | 60 | 363 | 0.1653 | 7 | c.679 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1953625 | A | ATTTAATT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
a0001a0002a0003others(21): Show | a0001c0001a0001c0002a0001c0003others(146): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(229): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(341): Show | 345 | 363 | 0.9504 | 7 | c.352 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1953630 | A | ATTTTTAG | intron_variant | MODIFIER | NA18949.hp1 NA18960.hp2 NA18963.hp2 others(1): Show |
a0002 | a0002c0022a0002c0031a0002c0082 | a0002c0022t0001a0002c0031t0001a0002c0082t0001 | a0002c0022t0001g0258a0002c0031t0001g0188a0002c0031t0001g0273others(1): Show | 4 | 363 | 0.0110 | 7 | c.352 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | ATATATAT | intron_variant | MODIFIER | HG01070.hp2 HG01346.hp1 HG01928.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0028others(2): Show | a0001c0001t0001g0278a0001c0001t0001g0311a0001c0001t0004g0135others(10): Show | 13 | 362 | 0.0359 | 7 | c.463 others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATATAT | intron_variant | MODIFIER | HG01099.hp2 HG01175.hp2 HG01884.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0030others(2): Show | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0004g0151others(8): Show | 11 | 362 | 0.0304 | 7 | c.463 others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156943065 | C | CTTTTTTT | intron_variant | MODIFIER | HG01070.hp1 HG01433.hp2 HG01891.hp1 others(29): Show |
a0002a0005 | a0002c0002a0002c0004a0005c0006 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(6): Show | a0002c0002t0002g0028a0002c0002t0002g0040a0002c0002t0002g0073others(29): Show | 32 | 362 | 0.0884 | 7 | c.323 others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156991710 | A | ATTTTTTT | intron_variant | MODIFIER | HG00408.hp2 HG01346.hp2 HG03704.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0006a0002c0004t0005a0002c0004t0009others(1): Show | a0001c0001t0006g0110a0002c0004t0005g0113a0002c0004t0005g0119others(7): Show | 10 | 362 | 0.0276 | 7 | c.33- others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347151 | C | CTTTCTTT | intron_variant | MODIFIER | HG00438.hp2 HG01884.hp1 HG02027.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0009a0001c0001t0029others(3): Show | a0001c0001t0006g0138a0001c0001t0009g0003a0001c0001t0009g0004others(8): Show | 11 | 308 | 0.0357 | 7 | c.32+ others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAAA | intron_variant | MODIFIER | HG00639.hp1 HG01358.hp2 HG02083.hp2 others(11): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0007others(4): Show | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0114others(11): Show | 14 | 308 | 0.0455 | 7 | c.33- others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120492723 | G | GTTTTTTT | downstream_gene_variant | MODIFIER | HG00597.hp1 HG00621.hp2 HG02071.hp2 others(6): Show |
a0001a0007 | a0001c0001a0001c0004a0007c0011 | a0001c0001t0001a0001c0001t0009a0001c0004t0005others(1): Show | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0154others(6): Show | 9 | 308 | 0.0292 | 7 | c.*76 others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2787 | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7352832 | C | CTTTTTTT | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02723.hp2 others(4): Show |
a0001a0009a0011 | a0001c0001a0001c0047a0009c0012others(1): Show | a0001c0001t0004a0001c0001t0011a0001c0047t0002others(2): Show | a0001c0001t0004g0007a0001c0001t0011g0223a0001c0001t0011g0224others(4): Show | 7 | 298 | 0.0235 | 7 | c.-11 others(26): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7398704 | A | AAATAAAG | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
a0001a0009 | a0001c0001a0001c0042a0001c0047others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0042t0025others(2): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(5): Show | 8 | 298 | 0.0269 | 7 | c.967 others(26): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7457353 | C | CTTTTTTT | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
a0002a0030a0033 | a0002c0007a0030c0037a0033c0030 | a0002c0007t0001a0030c0037t0001a0033c0030t0006 | a0002c0007t0001g0016a0002c0007t0001g0017a0002c0007t0001g0021others(5): Show | 8 | 298 | 0.0269 | 7 | c.218 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7466804 | C | CAAAAAAA | intron_variant | MODIFIER | HG01099.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
a0001a0002a0030 | a0001c0013a0002c0007a0030c0037 | a0001c0013t0001a0002c0007t0001a0030c0037t0001 | a0001c0013t0001g0204a0002c0007t0001g0011a0002c0007t0001g0016others(3): Show | 6 | 298 | 0.0201 | 7 | c.290 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154130147 | A | ATTTTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
a0001a0004a0005others(4): Show | a0001c0001a0001c0009a0001c0015others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(28): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(139): Show | 145 | 283 | 0.5124 | 7 | c.126 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73806463 | T | TATATACG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806491 | T | TATATACG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806519 | T | TATATACG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806547 | T | TATATACG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806575 | T | TATATACG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02145.hp1 others(5): Show |
a0002a0007a0013others(3): Show | a0002c0002a0002c0006a0007c0009others(4): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(5): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(5): Show | 8 | 188 | 0.0426 | 7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149636995 | G | GCTCTTCC | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
a0001a0002a0003others(16): Show | a0001c0002a0001c0005a0001c0030others(25): Show | a0001c0002t0004a0001c0002t0005a0001c0002t0006others(57): Show | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(273): Show | 290 | 394 | 0.7360 | 7 | c.*48 others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2028 | chr5 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561400 | T | TAGAATAG | intron_variant | MODIFIER | HG01978.hp1 HG02004.hp1 HG02027.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0002a0002c0001a0003c0005others(2): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(4): Show | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0002g0146others(6): Show | 9 | 186 | 0.0484 | 7 | c.196 others(24): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105585726 | C | CTTTTTTT | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0003a0001c0009others(5): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(11): Show | a0001c0002t0001g0080a0001c0002t0001g0163a0001c0002t0001g0167others(35): Show | 38 | 186 | 0.2043 | 7 | c.197 others(24): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF3_chr3_56722420_56806949 | 56723352 | G | GTTTTTTT | downstream_gene_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG01981.hp2 others(35): Show |
a0001a0005 | a0001c0002a0001c0006a0005c0015 | a0001c0002t0002a0001c0002t0006a0001c0006t0002others(1): Show | a0001c0002t0002g0002a0001c0002t0002g0019a0001c0002t0002g0026others(35): Show | 38 | 358 | 0.1062 | 7 | c.*59 others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4067 | chr3 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56729853 | C | CTCTCAGA | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
a0001a0004a0005 | a0001c0002a0001c0006a0001c0009others(2): Show | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(8): Show | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | 358 | 0.2989 | 7 | c.122 others(24): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | TogoVar | ||||||
ARHGEF40_chr14_21065304_21095248 | 21094726 | T | TGGGGGGG | downstream_gene_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01081.hp1 others(47): Show |
a0001a0003a0008others(2): Show | a0001c0001a0001c0003a0001c0011others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0018others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(33): Show | 50 | 386 | 0.1295 | 7 | c.*57 others(18): Show |
ARHGEF40 | ENSG00000165801.10 | transcript | ENST00000298694.9 | protein_coding | 4479 | chr14 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130902915 | G | GTCCTTAA | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(92): Show |
a0001a0002a0004others(15): Show | a0001c0001a0001c0002a0001c0014others(37): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(45): Show | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(92): Show | 95 | 144 | 0.6597 | 7 | c.40- others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926810 | A | ATTTTTTT | intron_variant | MODIFIER | HG02155.hp2 HG02818.hp2 HG03130.hp2 others(10): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0046others(10): Show | 13 | 144 | 0.0903 | 7 | c.355 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 131023074 | C | CAAAAAAA | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01081.hp1 others(42): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0014others(22): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(24): Show | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0040others(42): Show | 45 | 144 | 0.3125 | 7 | c.398 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF6_chrX_136660550_136785932 | 136663411 | A | ATATATAT | downstream_gene_variant | MODIFIER | HG02976.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0180 | 1 | 247 | 0.0041 | 7 | c.*46 others(18): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2138 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727326 | T | TCTTTCTC | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0113 | 1 | 247 | 0.0041 | 7 | c.732 others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136758031 | C | CTTTTTTT | intron_variant | MODIFIER | HG01243.hp1 HG02074.hp1 HG02559.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0002 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0078others(4): Show | 7 | 247 | 0.0283 | 7 | c.250 others(26): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156893045 | C | CTTTTTTT | intron_variant | MODIFIER | HG01109.hp2 HG01433.hp1 HG01884.hp1 others(12): Show |
a0001a0007a0008others(8): Show | a0001c0001a0001c0017a0007c0032others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0017t0020others(10): Show | a0001c0001t0001g0109a0001c0001t0001g0145a0001c0001t0003g0060others(12): Show | 15 | 150 | 0.1000 | 7 | c.198 others(26): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157000696 | C | CTTTTTTT | intron_variant | MODIFIER | HG01109.hp2 HG01934.hp2 HG02109.hp1 others(4): Show |
a0001a0015a0021others(1): Show | a0001c0001a0001c0002a0015c0023others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(3): Show | a0001c0001t0001g0058a0001c0001t0001g0093a0001c0001t0003g0062others(4): Show | 7 | 150 | 0.0467 | 7 | c.224 others(28): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157082590 | A | AGTGCAGT | intron_variant | MODIFIER | HG01496.hp2 HG03579.hp1 |
a0001 | a0001c0002a0001c0021 | a0001c0002t0003a0001c0021t0007 | a0001c0002t0003g0064a0001c0021t0007g0124 | 2 | 150 | 0.0133 | 7 | c.224 others(26): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |