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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP19_chr10_97217179_97297637 | 97231059 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | NA18951.hp1 NA18984.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0002 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0003t0002g0076 | 3 | 242 | 0.0124 | -15 | c.128 others(34): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97246994 | GGGTGTGG others(8): Show |
G | intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0236 | 1 | 242 | 0.0041 | -15 | c.928 others(30): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110625017 | TTTATTTT others(8): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(29): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(28): Show | 32 | 226 | 0.1416 | -15 | c.354 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580572 | ACAACAGA others(8): Show |
A | downstream_gene_variant | MODIFIER | HG00733.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0130 | 1 | 352 | 0.0028 | -15 | c.*38 others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3041 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG02818.hp2 HG03486.hp2 HG04228.hp1 others(4): Show |
a0001a0007a0011others(2): Show | a0001c0001a0007c0007a0011c0011others(2): Show | a0001c0001t0001a0007c0007t0006a0007c0007t0015others(3): Show | a0001c0001t0001g0244a0007c0007t0006g0292a0007c0007t0015g0288others(4): Show | 7 | 352 | 0.0199 | -15 | c.64- others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01255.hp2 HG01993.hp1 NA19043.hp2 |
a0001a0015 | a0001c0007a0001c0010a0015c0039 | a0001c0007t0013a0001c0010t0001a0015c0039t0001 | a0001c0007t0013g0146a0001c0010t0001g0168a0015c0039t0001g0186 | 3 | 309 | 0.0097 | -15 | c.344 others(34): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | GTTTTTTT others(8): Show |
G | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG03486.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0004t0003others(1): Show | a0001c0001t0001g0032a0001c0002t0002g0068a0001c0004t0003g0061others(1): Show | 4 | 108 | 0.0370 | -15 | c.180 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01433.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0010 | a0001c0001t0001a0001c0003t0011a0004c0010t0001 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | 108 | 0.0556 | -15 | c.268 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85827502 | GTGTGTGT others(8): Show |
G | intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 108 | 0.0093 | -15 | c.269 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85885540 | CTGAAAGT others(8): Show |
C | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0100 | 1 | 108 | 0.0093 | -15 | c.269 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(11): Show | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0135others(23): Show | 26 | 198 | 0.1313 | -15 | c.198 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45406169 | GGGGTTTA others(8): Show |
G | intron_variant | MODIFIER | HG03579.hp2 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0183a0002c0002t0001g0049 | 2 | 347 | 0.0058 | -15 | c.658 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | NA18939.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0192 | 1 | 347 | 0.0029 | -15 | c.658 others(32): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6736993 | TCATTCCA others(8): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0016a0001c0003t0001others(13): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | 248 | 0.2581 | -15 | c.122 others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841144 | GTCTCTCT others(8): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG02080.hp2 NA19070.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0186a0003c0004t0001g0058a0003c0004t0001g0219 | 3 | 248 | 0.0121 | -15 | c.543 others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841197 | CTCTCTCC others(8): Show |
C | intron_variant | MODIFIER | HG02155.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0125 | 1 | 248 | 0.0040 | -15 | c.543 others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161051967 | TCACCACC others(8): Show |
T | intron_variant | MODIFIER | HG00558.hp1 HG00738.hp1 HG01074.hp2 others(63): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0030others(60): Show | 66 | 390 | 0.1692 | -15 | c.101 others(32): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 9/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055871 | AAAATAAA others(8): Show |
A | intron_variant | MODIFIER | HG03669.hp2 HG03831.hp2 NA18951.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0072a0001c0001t0003g0145a0001c0001t0003g0146others(1): Show | 4 | 390 | 0.0103 | -15 | c.345 others(30): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055886 | TAAATAAA others(8): Show |
T | intron_variant | MODIFIER | HG02523.hp1 NA20905.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090a0001c0001t0001g0130 | 2 | 390 | 0.0051 | -15 | c.345 others(30): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119304894 | CAAAATAA others(8): Show |
C | intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0096 | 1 | 310 | 0.0032 | -15 | c.100 others(32): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119408027 | CAAGCAAC others(8): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0004a0003c0006others(6): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(26): Show | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(103): Show | 107 | 310 | 0.3452 | -15 | c.164 others(34): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129044024 | ATGTTTTA others(8): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0005others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 217 | 398 | 0.5452 | -15 | c.964 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(8): Show |
C | downstream_gene_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0011 | a0001c0011t0002 | a0001c0011t0002g0274 | 1 | 298 | 0.0034 | -15 | c.*55 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144604518 | TAGGCATC others(8): Show |
T | intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0007 | a0001c0007t0017 | a0001c0007t0017g0019 | 1 | 246 | 0.0041 | -15 | c.80+ others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144606620 | AGGAGGAG others(8): Show |
A | intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0041 | 1 | 246 | 0.0041 | -15 | c.-81 others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699496 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG01515.hp2 NA19012.hp1 |
a0001 | a0001c0003a0001c0015 | a0001c0003t0003a0001c0015t0001 | a0001c0003t0003g0258a0001c0015t0001g0277 | 2 | 286 | 0.0070 | -15 | c.154 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699498 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG00597.hp2 HG00673.hp2 HG02080.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0002c0002t0004 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0275others(13): Show | 16 | 286 | 0.0559 | -15 | c.154 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699500 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG03130.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0025a0002c0002t0002g0034 | 2 | 286 | 0.0070 | -15 | c.154 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699502 | ATATATTT others(8): Show |
A | intron_variant | MODIFIER | HG01346.hp1 HG02280.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0013a0002c0002t0002g0010 | 2 | 286 | 0.0070 | -15 | c.154 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0255 | 1 | 286 | 0.0035 | -15 | c.155 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0004a0002c0002t0029 | a0002c0002t0002g0226a0002c0002t0002g0228a0002c0002t0004g0172others(1): Show | 4 | 286 | 0.0140 | -15 | c.487 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921237 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG01069.hp2 HG03453.hp2 |
a0001a0002 | a0001c0008a0002c0002 | a0001c0008t0010a0002c0002t0005 | a0001c0008t0010g0253a0002c0002t0005g0055 | 2 | 286 | 0.0070 | -15 | c.487 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(8): Show |
A | intron_variant | MODIFIER | NA19054.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0264 | 1 | 286 | 0.0035 | -15 | c.487 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0041 | 1 | 286 | 0.0035 | -15 | c.245 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12788461 | CTTTTTTT others(8): Show |
C | upstream_gene_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 1 | 230 | 0.0044 | -15 | c.-13 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1036 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802946 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | 230 | 0.0087 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802948 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG00741.hp2 HG01109.hp2 HG01978.hp2 others(8): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0003g0069others(8): Show | 11 | 230 | 0.0478 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802950 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG02071.hp1 HG02129.hp2 HG02257.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(4): Show | a0001c0001t0003g0047a0001c0001t0003g0059a0001c0001t0003g0086others(7): Show | 10 | 230 | 0.0435 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802952 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG02074.hp2 HG02132.hp2 HG03453.hp2 |
a0001a0002 | a0001c0001a0001c0004a0002c0007 | a0001c0001t0010a0001c0004t0005a0002c0007t0003 | a0001c0001t0010g0034a0001c0004t0005g0051a0002c0007t0003g0052 | 3 | 230 | 0.0130 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802954 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 | 1 | 230 | 0.0044 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802955 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG03491.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0002g0015 | 2 | 230 | 0.0087 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802957 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0012 | 1 | 230 | 0.0044 | -15 | c.53+ others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp2 HG01109.hp2 others(66): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0094others(66): Show | 69 | 230 | 0.3000 | -15 | c.113 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986691 | AAAAAAAA others(8): Show |
A | intron_variant | MODIFIER | HG03831.hp1 | a0005 | a0005c0013 | a0005c0013t0003 | a0005c0013t0003g0055 | 1 | 230 | 0.0044 | -15 | c.231 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0022 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 3 | 186 | 0.0161 | -15 | c.418 others(32): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11174632 | TTTCTTTC others(8): Show |
T | intron_variant | MODIFIER | NA18965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 144 | 0.0069 | -15 | c.162 others(34): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11185891 | TGTATAAA others(8): Show |
T | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0132 | 1 | 144 | 0.0069 | -15 | c.127 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 5/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | AGAGGAGG others(8): Show |
A | intron_variant | MODIFIER | HG01258.hp1 HG01433.hp1 HG01934.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0091others(1): Show | 4 | 144 | 0.0278 | -15 | c.589 others(36): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG02895.hp1 HG02965.hp1 HG03209.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0005others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(3): Show | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0052others(5): Show | 8 | 144 | 0.0556 | -15 | c.588 others(36): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590775 | CGAAAAGA others(8): Show |
C | intron_variant | MODIFIER | NA18966.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 | 1 | 144 | 0.0069 | -15 | c.588 others(34): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |