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 | 11174592 | T | TCTTTC | intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0010 | 1 | 144 | 0.0069 | 5 | c.162 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176264 | T | TATATA | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | 5 | c.162 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11196135 | A | AAAAAC | intron_variant | MODIFIER | HG00738.hp1 HG01074.hp1 HG01515.hp1 others(21): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(21): Show | 24 | 144 | 0.1667 | 5 | c.820 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11280745 | C | CAAAAA | intron_variant | MODIFIER | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0003t0001others(3): Show | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0024others(10): Show | 13 | 144 | 0.0903 | 5 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11411223 | A | ATATAT | intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 144 | 0.0069 | 5 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11493835 | C | CTTTTT | intron_variant | MODIFIER | NA18955.hp1 NA19068.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113a0001c0001t0001g0122 | 2 | 144 | 0.0139 | 5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11500663 | C | CAAAAA | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(11): Show | 14 | 144 | 0.0972 | 5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | C | CAAAAA | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0010 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0008g0030others(1): Show | 4 | 144 | 0.0278 | 5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590857 | A | AAGAAG | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | 5 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAAAA | intron_variant | MODIFIER | HG00609.hp1 HG01255.hp1 HG02129.hp1 others(3): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(1): Show | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | 144 | 0.0417 | 5 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTTT | intron_variant | MODIFIER | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(41): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0007others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(15): Show | a0001c0001t0001g0097a0001c0001t0001g0134a0001c0001t0003g0113others(41): Show | 44 | 390 | 0.1128 | 5 | c.-72 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44779564 | A | ATTTTT | intron_variant | MODIFIER | HG00438.hp1 HG02080.hp1 HG02615.hp2 others(5): Show |
a0001a0003a0004 | a0001c0001a0001c0007a0001c0010others(4): Show | a0001c0001t0003a0001c0007t0001a0001c0010t0001others(4): Show | a0001c0001t0003g0081a0001c0007t0001g0058a0001c0010t0001g0243others(5): Show | 8 | 390 | 0.0205 | 5 | c.-71 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787321 | C | CTTTGT | intron_variant | MODIFIER | HG01496.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
a0001a0002a0005others(2): Show | a0001c0004a0001c0007a0002c0006others(5): Show | a0001c0004t0001a0001c0007t0001a0002c0006t0001others(5): Show | a0001c0004t0001g0165a0001c0007t0001g0304a0002c0006t0001g0386others(5): Show | 8 | 390 | 0.0205 | 5 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44805558 | G | GTAAGA | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0007a0001c0018others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(16): Show | a0001c0001t0001g0024a0001c0001t0003g0211a0001c0001t0003g0260others(33): Show | 36 | 390 | 0.0923 | 5 | c.168 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTT | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(42): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(19): Show | a0001c0001t0001g0343a0001c0001t0003g0023a0001c0001t0003g0074others(42): Show | 45 | 390 | 0.1154 | 5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | C | CAAAAA | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
a0002a0008a0028 | a0002c0003a0002c0006a0002c0068others(2): Show | a0002c0003t0001a0002c0006t0001a0002c0068t0008others(2): Show | a0002c0003t0001g0106a0002c0003t0001g0387a0002c0006t0001g0203others(3): Show | 6 | 390 | 0.0154 | 5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44833076 | T | TTTTTC | intron_variant | MODIFIER | HG00280.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
a0001a0012 | a0001c0007a0001c0008a0012c0038others(1): Show | a0001c0007t0001a0001c0008t0001a0012c0038t0005others(1): Show | a0001c0007t0001g0058a0001c0007t0001g0140a0001c0008t0001g0380others(2): Show | 5 | 390 | 0.0128 | 5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858369 | G | GTTTTC | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(22): Show |
a0002a0004a0008others(3): Show | a0002c0011a0002c0013a0002c0019others(9): Show | a0002c0011t0005a0002c0013t0005a0002c0019t0008others(9): Show | a0002c0011t0005g0016a0002c0011t0005g0086a0002c0011t0005g0284others(22): Show | 25 | 390 | 0.0641 | 5 | c.878 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTTTT | intron_variant | MODIFIER | HG01099.hp1 HG01346.hp1 HG01516.hp2 others(29): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0003a0002c0006others(11): Show | a0001c0001t0003a0002c0003t0004a0002c0006t0004others(12): Show | a0001c0001t0003g0006a0002c0003t0004g0011a0002c0003t0004g0180others(29): Show | 32 | 390 | 0.0821 | 5 | c.878 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44860550 | C | CAACTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0004a0001c0007others(60): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(70): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0042others(327): Show | 330 | 390 | 0.8462 | 5 | c.981 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIG_chr16_275591_288010 | 275640 | C | CGCGGG | upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(10): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(23): Show | 43 | 442 | 0.0973 | 5 | c.-50 others(16): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4950 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888287 | G | GGCACT | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01243.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(15): Show | a0001c0001t0002g0271a0001c0001t0004g0165a0001c0002t0001g0270others(17): Show | 20 | 363 | 0.0551 | 5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888375 | T | TGAGGA | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0059a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0033t0002g0006others(4): Show | 7 | 363 | 0.0193 | 5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | ATATAT | intron_variant | MODIFIER | HG00323.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0001g0274a0001c0001t0001g0306a0001c0001t0001g0310others(9): Show | 12 | 362 | 0.0332 | 5 | c.463 others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATAT | intron_variant | MODIFIER | HG01243.hp2 HG02818.hp2 HG03486.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0002a0002c0002t0017 | a0001c0001t0004g0168a0002c0002t0002g0033a0002c0002t0002g0038others(3): Show | 6 | 362 | 0.0166 | 5 | c.463 others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | C | CAAAAA | intron_variant | MODIFIER | HG00741.hp2 HG01433.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0004t0005others(1): Show | a0001c0001t0001g0348a0002c0002t0002g0049a0002c0002t0002g0067others(6): Show | 9 | 362 | 0.0249 | 5 | c.33- others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120393258 | A | ATAATT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | 308 | 0.4675 | 5 | 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 | 120399321 | C | CAAAAA | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0003 | a0001c0001t0002a0001c0001t0006a0001c0006t0002others(1): Show | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0113others(9): Show | 12 | 308 | 0.0390 | 5 | c.33- others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120411581 | C | CTTTTT | intron_variant | MODIFIER | HG00597.hp2 HG02602.hp2 HG02698.hp2 others(9): Show |
a0001 | a0001c0004 | a0001c0004t0005a0001c0004t0012 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(9): Show | 12 | 308 | 0.0390 | 5 | c.199 others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120428030 | T | TTTCCC | intron_variant | MODIFIER | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | 308 | 0.0162 | 5 | c.407 others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120436983 | T | TAAATA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0009a0001c0001t0029a0001c0002t0002others(8): Show | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(56): Show | 60 | 308 | 0.1948 | 5 | c.925 others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120477177 | T | TTGTTG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(24): Show | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | 308 | 0.4675 | 5 | c.336 others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120480722 | A | AAGTCT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0016 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | 308 | 0.0909 | 5 | c.423 others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7352832 | C | CTTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0013others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(30): Show | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0081others(91): Show | 94 | 298 | 0.3154 | 5 | c.-11 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7367870 | T | TATATA | intron_variant | MODIFIER | HG02622.hp2 HG02886.hp1 NA18943.hp2 |
a0002a0003 | a0002c0005a0003c0003 | a0002c0005t0001a0003c0003t0026 | a0002c0005t0001g0259a0002c0005t0001g0260a0003c0003t0026g0208 | 3 | 298 | 0.0101 | 5 | c.16- others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7373463 | G | GTTTGT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
a0001a0002a0005others(18): Show | a0001c0001a0001c0019a0001c0021others(30): Show | a0001c0001t0002a0001c0001t0004a0001c0019t0006others(40): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(94): Show | 97 | 298 | 0.3255 | 5 | c.275 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7395531 | C | CAGGAG | intron_variant | MODIFIER | HG02165.hp2 NA18967.hp1 NA18990.hp2 others(3): Show |
a0006a0008 | a0006c0008a0008c0010 | a0006c0008t0002a0008c0010t0001a0008c0010t0033 | a0006c0008t0002g0287a0008c0010t0001g0285a0008c0010t0001g0288others(3): Show | 6 | 298 | 0.0201 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7410809 | C | CAAAAA | intron_variant | MODIFIER | HG00438.hp1 HG02165.hp2 HG02647.hp2 others(3): Show |
a0002a0005a0008 | a0002c0005a0005c0039a0008c0010 | a0002c0005t0013a0005c0039t0001a0008c0010t0001others(1): Show | a0002c0005t0013g0037a0005c0039t0001g0062a0008c0010t0001g0288others(3): Show | 6 | 298 | 0.0201 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7411285 | T | TCCCTC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0013others(25): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | a0001c0001t0001g0056a0001c0001t0002g0028a0001c0001t0002g0032others(143): Show | 146 | 298 | 0.4899 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7416578 | T | TGTGTG | intron_variant | MODIFIER | HG00738.hp2 NA19066.hp1 NA20752.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0143a0001c0002t0003g0079a0001c0002t0003g0131 | 3 | 298 | 0.0101 | 5 | c.968 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7431510 | C | CAAAAA | intron_variant | MODIFIER | HG01099.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
a0001a0002a0030 | a0001c0013a0002c0004a0002c0007others(1): Show | a0001c0013t0001a0002c0004t0004a0002c0007t0001others(1): Show | a0001c0013t0001g0297a0002c0004t0004g0065a0002c0007t0001g0011others(4): Show | 7 | 298 | 0.0235 | 5 | c.968 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7459212 | A | ATTTTG | intron_variant | MODIFIER | HG03139.hp2 NA18942.hp1 NA20300.hp1 |
a0001a0002 | a0001c0001a0001c0019a0002c0004 | a0001c0001t0002a0001c0019t0006a0002c0004t0002 | a0001c0001t0002g0070a0001c0019t0006g0078a0002c0004t0002g0050 | 3 | 298 | 0.0101 | 5 | c.236 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7466381 | C | CAAAAA | intron_variant | MODIFIER | HG01109.hp1 HG01952.hp2 HG02818.hp2 others(5): Show |
a0001a0002a0005others(1): Show | a0001c0002a0002c0006a0005c0009others(1): Show | a0001c0002t0003a0002c0006t0007a0005c0009t0009others(1): Show | a0001c0002t0003g0154a0001c0002t0003g0162a0002c0006t0007g0275others(5): Show | 8 | 298 | 0.0269 | 5 | c.290 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7466804 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
a0001a0002a0027 | a0001c0002a0002c0005a0002c0006others(1): Show | a0001c0002t0003a0002c0005t0001a0002c0006t0007others(1): Show | a0001c0002t0003g0280a0002c0005t0001g0238a0002c0006t0007g0270others(6): Show | 9 | 298 | 0.0302 | 5 | c.290 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF19_chr1_16192854_16217652 | 16213711 | A | AATTTT | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(5): Show |
a0003a0010 | a0003c0003a0010c0015 | a0003c0003t0001a0010c0015t0001 | a0003c0003t0001g0012a0003c0003t0001g0032a0003c0003t0001g0033others(1): Show | 8 | 362 | 0.0221 | 5 | c.-12 others(16): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1060 | chr1 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41880441 | A | AGGAAG | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00741.hp1 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(19): Show | 23 | 234 | 0.0983 | 5 | c.-28 others(16): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2742 | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154186886 | C | CTTTTT | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp1 HG02071.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0001c0001t0007a0002c0003t0025 | a0001c0001t0002g0217a0001c0001t0002g0226a0001c0001t0002g0237others(5): Show | 8 | 283 | 0.0283 | 5 | c.148 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73643814 | C | CAAAAA | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
a0001a0003a0005others(4): Show | a0001c0021a0003c0058a0005c0061others(4): Show | a0001c0021t0008a0003c0058t0001a0005c0061t0002others(6): Show | a0001c0021t0008g0102a0003c0058t0001g0139a0005c0061t0002g0001others(6): Show | 9 | 188 | 0.0479 | 5 | c.-12 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73690065 | A | ATTATT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
a0001a0002a0003others(34): Show | a0001c0001a0001c0021a0001c0023others(60): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(89): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(131): Show | 134 | 188 | 0.7128 | 5 | c.33+ others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73731011 | T | TAAAAA | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(13): Show |
a0003a0004a0005others(9): Show | a0003c0005a0003c0048a0004c0004others(12): Show | a0003c0005t0001a0003c0048t0006a0004c0004t0001others(13): Show | a0003c0005t0001g0043a0003c0048t0006g0176a0004c0004t0001g0170others(13): Show | 16 | 188 | 0.0851 | 5 | c.34- others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |