view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP31_chr3_119289383_119425714 | 119372280 | CTTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(31): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(10): Show | a0001c0001t0006g0132 a0001c0001t0007g0233 a0001c0001t0007g0248 others(30): Show |
34 | 234 | 0.1453 | -3 | c.348 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119376758 | CAAA | C | intron_variant | MODIFIER | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
a0001a0003a0004others(1): Show | a0001c0002a0001c0005a0003c0006others(2): Show | a0001c0002t0012a0001c0005t0001a0001c0005t0056others(5): Show | a0001c0002t0012g0175 a0001c0005t0001g0030 a0001c0005t0001g0032 others(11): Show |
14 | 179 | 0.0782 | -3 | c.349 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119390456 | CATT | C | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(22): Show | a0001c0001t0005g0120 a0001c0001t0005g0129 a0001c0001t0006g0026 others(58): Show |
62 | 308 | 0.2013 | -3 | c.683 others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119412402 | AAAG | A | intron_variant | MODIFIER | HG00323.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0001t0008a0001c0004t0058 | a0001c0001t0006g0028 a0001c0001t0006g0101 a0001c0001t0006g0149 others(2): Show |
6 | 308 | 0.0195 | -3 | c.192 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119424496 | TTTC | T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(37): Show |
a0001a0013 | a0001c0001a0013c0019 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(3): Show | a0001c0001t0005g0023 a0001c0001t0005g0059 a0001c0001t0005g0084 others(36): Show |
40 | 308 | 0.1299 | -3 | c.*82 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3783 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119424505 | CTTT | C | downstream_gene_variant | MODIFIER | HG00609.hp2 HG02129.hp1 NA18940.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0007a0001c0001t0011 | a0001c0001t0005g0129 a0001c0001t0005g0170 a0001c0001t0007g0227 others(3): Show |
6 | 240 | 0.0250 | -3 | c.*82 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3792 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119424672 | ATTT | A | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(31): Show |
a0001a0007 | a0001c0002a0001c0004a0007c0014 | a0001c0002t0003a0001c0004t0003a0001c0004t0010others(5): Show | a0001c0002t0003g0144 a0001c0002t0003g0145 a0001c0004t0003g0010 others(30): Show |
34 | 100 | 0.3400 | -3 | c.*84 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3959 | chr3 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | TTTA | T | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(56): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0027 others(56): Show |
59 | 143 | 0.4126 | -3 | c.212 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128979881 | GTTA | G | intron_variant | MODIFIER | HG02809.hp2 HG03209.hp1 HG03540.hp1 |
a0005 | a0005c0011 | a0005c0011t0008a0005c0011t0021 | a0005c0011t0008g0072 a0005c0011t0008g0073 a0005c0011t0021g0071 |
3 | 396 | 0.0076 | -3 | c.197 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 18/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128987987 | TAAG | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
a0001a0003a0005others(3): Show | a0001c0001a0001c0010a0001c0014others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(17): Show | a0001c0001t0002g0002 a0001c0001t0002g0041 a0001c0001t0002g0094 others(105): Show |
109 | 396 | 0.2753 | -3 | c.129 others(18): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 13/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129028744 | AGAG | A | intron_variant | MODIFIER | HG02280.hp1 HG03139.hp1 HG03831.hp2 others(1): Show |
a0001 | a0001c0001a0001c0010 | a0001c0001t0016a0001c0001t0033a0001c0010t0014 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0033g0301 others(1): Show |
4 | 396 | 0.0101 | -3 | c.104 others(24): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129051953 | CAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(38): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(14): Show | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0002g0109 others(38): Show |
41 | 112 | 0.3661 | -3 | c.963 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129067618 | GCAA | G | intron_variant | MODIFIER | HG01496.hp2 HG02451.hp1 HG02451.hp2 others(7): Show |
a0001a0004a0005others(1): Show | a0001c0010a0001c0015a0001c0016others(3): Show | a0001c0010t0008a0001c0015t0035a0001c0016t0002others(5): Show | a0001c0010t0008g0193 a0001c0010t0008g0194 a0001c0015t0035g0095 others(7): Show |
10 | 392 | 0.0255 | -3 | c.532 others(18): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129073782 | CAAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(31): Show |
a0001a0002a0011others(1): Show | a0001c0001a0001c0014a0002c0008others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(4): Show | a0001c0001t0002g0156 a0001c0001t0002g0158 a0001c0001t0002g0166 others(31): Show |
34 | 392 | 0.0867 | -3 | c.532 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129086820 | CAAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(31): Show |
a0001a0002a0011others(1): Show | a0001c0001a0001c0014a0002c0007others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(5): Show | a0001c0001t0002g0156 a0001c0001t0002g0158 a0001c0001t0002g0166 others(31): Show |
34 | 351 | 0.0969 | -3 | c.531 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129088995 | CAAA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(49): Show | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0352 others(208): Show |
211 | 347 | 0.6081 | -3 | c.531 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129127769 | TAAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0034others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(4): Show | a0001c0001t0002g0002 a0001c0001t0002g0094 a0001c0001t0002g0096 others(58): Show |
62 | 396 | 0.1566 | -3 | c.226 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129138313 | AAAG | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(97): Show |
a0001a0002a0011others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(16): Show | a0001c0001t0002g0002 a0001c0001t0002g0094 a0001c0001t0002g0098 others(96): Show |
100 | 396 | 0.2525 | -3 | c.226 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193308 | TGGG | T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(4): Show | a0001c0001t0002g0107 a0001c0001t0002g0114 a0001c0001t0002g0122 others(24): Show |
27 | 158 | 0.1709 | -3 | c.-11 others(14): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 984 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | CTTT | C | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(67): Show |
a0001 | a0001c0003a0001c0007a0001c0012others(2): Show | a0001c0003t0001a0001c0007t0001a0001c0012t0001others(2): Show | a0001c0003t0001g0006 a0001c0003t0001g0009 a0001c0003t0001g0011 others(16): Show |
70 | 71 | 0.9859 | -3 | c.-36 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTT | C | upstream_gene_variant | MODIFIER | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
a0001 | a0001c0002a0001c0004a0001c0006others(2): Show | a0001c0002t0001a0001c0004t0001a0001c0006t0001others(2): Show | a0001c0002t0001g0018 a0001c0004t0001g0008 a0001c0004t0001g0010 others(6): Show |
18 | 99 | 0.1818 | -3 | c.-16 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46886781 | CTTA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(79): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0022 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(79): Show |
82 | 296 | 0.2770 | -3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46899628 | AGGT | A | intron_variant | MODIFIER | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | 296 | 0.0135 | -3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46908482 | TTTG | T | intron_variant | MODIFIER | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0005a0001c0002t0032a0001c0005t0005others(1): Show | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | 296 | 0.0473 | -3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46914446 | AAAT | A | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0011a0001c0001t0019a0006c0008t0011 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(2): Show |
5 | 284 | 0.0176 | -3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46978607 | TGTG | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(46): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0001t0022others(2): Show | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0172 others(46): Show |
49 | 295 | 0.1661 | -3 | c.382 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTT | C | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00558.hp1 NA18951.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0035 | a0001c0001t0003g0022 a0001c0001t0003g0072 a0001c0001t0003g0237 others(5): Show |
8 | 33 | 0.2424 | -3 | c.*55 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144525287 | TCTC | T | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0149 a0001c0001t0004g0151 a0001c0001t0004g0152 others(4): Show |
7 | 244 | 0.0287 | -3 | c.*51 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3891 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144528689 | GCCC | G | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0016others(4): Show | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0219 others(18): Show |
21 | 61 | 0.3443 | -3 | c.*17 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 489 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144535795 | TGAA | T | intron_variant | MODIFIER | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
a0001 | a0001c0001a0001c0007a0001c0018 | a0001c0001t0001a0001c0007t0001a0001c0018t0001 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(8): Show |
11 | 244 | 0.0451 | -3 | c.261 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | CAAA | C | intron_variant | MODIFIER | HG00558.hp2 HG00639.hp1 HG01168.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0008 | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(2): Show | a0001c0001t0001g0117 a0001c0001t0005g0190 a0001c0001t0020g0075 others(2): Show |
5 | 85 | 0.0588 | -3 | c.513 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144576332 | CAAA | C | intron_variant | MODIFIER | HG02572.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0003g0020 others(9): Show |
12 | 124 | 0.0968 | -3 | c.512 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144600975 | TGGA | T | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0007others(1): Show | a0001c0001t0007a0001c0004t0006a0001c0007t0001others(1): Show | a0001c0001t0007g0017 a0001c0004t0006g0064 a0001c0004t0006g0065 others(5): Show |
8 | 244 | 0.0328 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601583 | TGGA | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(4): Show | a0001c0001t0001g0117 a0001c0003t0001g0004 a0001c0003t0001g0011 others(9): Show |
12 | 244 | 0.0492 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144602240 | TGGA | T | intron_variant | MODIFIER | HG00639.hp2 NA18941.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0002t0001a0001c0017t0001 | a0001c0001t0001g0181 a0001c0002t0001g0080 a0001c0017t0001g0059 |
3 | 244 | 0.0123 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144602703 | TGGA | T | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0003a0001c0001t0018a0001c0001t0021others(1): Show | a0001c0001t0003g0020 a0001c0001t0018g0019 a0001c0001t0021g0057 others(1): Show |
4 | 244 | 0.0164 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144682548 | CAAA | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
33 | 193 | 0.1710 | -3 | c.-82 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38635366 | ATAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
a0001a0004a0020others(1): Show | a0001c0002a0001c0008a0004c0011others(3): Show | a0001c0002t0004a0001c0008t0004a0004c0011t0004others(4): Show | a0001c0002t0004g0072 a0001c0008t0004g0025 a0001c0008t0004g0305 others(7): Show |
12 | 348 | 0.0345 | -3 | c.949 others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38640101 | TTCC | T | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
a0001a0005a0006others(2): Show | a0001c0002a0001c0007a0005c0040others(4): Show | a0001c0002t0008a0001c0002t0010a0001c0007t0001others(6): Show | a0001c0002t0008g0073 a0001c0002t0010g0081 a0001c0007t0001g0187 others(12): Show |
16 | 348 | 0.0460 | -3 | c.127 others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38648505 | ATGC | A | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
a0006a0020 | a0006c0013a0006c0017a0020c0023 | a0006c0013t0008a0006c0017t0008a0020c0023t0011 | a0006c0013t0008g0027 a0006c0013t0008g0299 a0006c0017t0008g0045 others(2): Show |
6 | 348 | 0.0172 | -3 | c.188 others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38653148 | GATA | G | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(29): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0002t0004a0001c0004t0004others(10): Show | a0001c0001t0005g0185 a0001c0001t0005g0251 a0001c0002t0004g0072 others(25): Show |
32 | 348 | 0.0920 | -3 | c.*33 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2496 | chr20 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38653151 | AATG | A | downstream_gene_variant | MODIFIER | HG01109.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
a0001a0005 | a0001c0002a0005c0010 | a0001c0002t0008a0001c0002t0010a0005c0010t0010others(1): Show | a0001c0002t0008g0073 a0001c0002t0010g0081 a0005c0010t0010g0224 others(3): Show |
6 | 316 | 0.0190 | -3 | c.*33 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2499 | chr20 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38653371 | ATGG | A | downstream_gene_variant | MODIFIER | HG01192.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0169 a0001c0001t0002g0060 a0001c0001t0002g0108 others(1): Show |
4 | 348 | 0.0115 | -3 | c.*35 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2719 | chr20 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100690262 | GTTA | G | intron_variant | MODIFIER | HG00597.hp2 HG00673.hp2 HG01070.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(27): Show |
30 | 284 | 0.1056 | -3 | c.154 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100700406 | CTCT | C | intron_variant | MODIFIER | HG00597.hp2 HG00673.hp2 HG01070.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(27): Show |
30 | 284 | 0.1056 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100702952 | GTAA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(43): Show | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(183): Show |
186 | 284 | 0.6549 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100715048 | CAAA | C | intron_variant | MODIFIER | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(41): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(11): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0077 others(41): Show |
44 | 122 | 0.3607 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100735002 | AAAC | A | intron_variant | MODIFIER | HG01081.hp1 HG02055.hp2 HG02630.hp1 others(1): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0008a0002c0005t0010 | a0002c0002t0002g0141 a0002c0002t0008g0028 a0002c0002t0008g0029 others(1): Show |
4 | 274 | 0.0146 | -3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | CTTT | C | intron_variant | MODIFIER | HG00673.hp2 HG01109.hp2 HG01515.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0010others(2): Show | a0001c0001t0001a0001c0003t0003a0001c0010t0001others(3): Show | a0001c0001t0001g0279 a0001c0003t0003g0262 a0001c0003t0003g0268 others(8): Show |
11 | 163 | 0.0675 | -3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100764005 | CTCT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0066 others(54): Show |
57 | 280 | 0.2036 | -3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |