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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11628984 | CGT | C | intron_variant | MODIFIER | HG00140.hp1 HG01109.hp1 HG01167.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(4): Show | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0044 others(21): Show |
24 | 144 | 0.1667 | -2 | c.588 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11637762 | ATT | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0022others(8): Show | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0020 others(35): Show |
38 | 144 | 0.2639 | -2 | c.588 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11658076 | TAG | T | intron_variant | MODIFIER | HG03516.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0127 | 1 | 144 | 0.0069 | -2 | c.588 others(19): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAA | C | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0132 | 1 | 144 | 0.0069 | -2 | c.588 others(19): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660885 | GCA | G | intron_variant | MODIFIER | HG02145.hp1 | a0004 | a0004c0008 | a0004c0008t0012 | a0004c0008t0012g0002 | 1 | 144 | 0.0069 | -2 | c.588 others(19): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(35): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(18): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(20): Show | a0001c0001t0001g0370 a0001c0001t0003g0201 a0001c0001t0003g0367 others(35): Show |
38 | 390 | 0.0974 | -2 | c.-72 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44762543 | CTT | C | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0037others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(13): Show | a0001c0001t0001g0343 a0001c0001t0003g0081 a0001c0001t0003g0188 others(25): Show |
28 | 390 | 0.0718 | -2 | c.-72 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44763800 | TTC | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(25): Show | a0001c0001t0001g0343 a0001c0001t0003g0211 a0001c0001t0003g0279 others(40): Show |
43 | 390 | 0.1103 | -2 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | CTT | C | intron_variant | MODIFIER | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(16): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0009a0002c0003others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0009t0001others(12): Show | a0001c0001t0001g0343 a0001c0001t0003g0279 a0001c0009t0001g0271 others(16): Show |
19 | 390 | 0.0487 | -2 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44772223 | CTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(33): Show | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0192 others(97): Show |
100 | 390 | 0.2564 | -2 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44777618 | CTT | C | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(18): Show |
a0001a0002a0003others(6): Show | a0001c0004a0001c0007a0001c0009others(13): Show | a0001c0004t0001a0001c0007t0001a0001c0009t0001others(14): Show | a0001c0004t0001g0007 a0001c0007t0001g0058 a0001c0007t0001g0202 others(18): Show |
21 | 390 | 0.0539 | -2 | c.-71 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44787919 | CTT | C | intron_variant | MODIFIER | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0007a0002c0011others(3): Show | a0001c0001t0001a0001c0001t0009a0001c0007t0001others(4): Show | a0001c0001t0001g0042 a0001c0001t0009g0173 a0001c0001t0009g0321 others(5): Show |
8 | 390 | 0.0205 | -2 | c.79+ others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44792828 | GGT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(177): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0004a0001c0007others(43): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(53): Show | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0134 others(177): Show |
180 | 390 | 0.4615 | -2 | c.79+ others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44796533 | CTG | C | intron_variant | MODIFIER | HG02135.hp1 HG02258.hp2 HG02559.hp1 others(16): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0002c0003others(10): Show | a0001c0001t0003a0001c0001t0010a0001c0007t0001others(11): Show | a0001c0001t0003g0006 a0001c0001t0003g0293 a0001c0001t0010g0198 others(16): Show |
19 | 390 | 0.0487 | -2 | c.80- others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44798001 | CAA | C | intron_variant | MODIFIER | HG02056.hp1 HG02083.hp2 HG02135.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0003others(1): Show | a0001c0001t0003a0001c0001t0011a0001c0007t0001others(2): Show | a0001c0001t0003g0312 a0001c0001t0011g0221 a0001c0007t0001g0170 others(4): Show |
7 | 390 | 0.0180 | -2 | c.80- others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44807426 | GCA | G | intron_variant | MODIFIER | HG00280.hp1 HG01243.hp1 HG01255.hp2 others(41): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0007a0002c0003others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(21): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0003g0006 others(41): Show |
44 | 390 | 0.1128 | -2 | c.168 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44808821 | AAC | A | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(31): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0007a0001c0018others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(15): Show | a0001c0001t0001g0024 a0001c0001t0003g0211 a0001c0001t0003g0260 others(31): Show |
34 | 390 | 0.0872 | -2 | c.299 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44810236 | CTT | C | intron_variant | MODIFIER | HG01069.hp1 HG01106.hp2 HG01168.hp1 others(9): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0021a0002c0003others(4): Show | a0001c0001t0003a0001c0021t0001a0002c0003t0003others(5): Show | a0001c0001t0003g0028 a0001c0001t0003g0109 a0001c0001t0003g0375 others(9): Show |
12 | 390 | 0.0308 | -2 | c.299 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44813736 | TAC | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0004a0001c0007others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(38): Show | a0001c0001t0001g0024 a0001c0001t0001g0134 a0001c0001t0001g0161 others(137): Show |
140 | 390 | 0.3590 | -2 | c.300 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44824634 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0004a0001c0007others(40): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(47): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0134 others(143): Show |
146 | 390 | 0.3744 | -2 | c.486 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44828425 | ATT | A | intron_variant | MODIFIER | HG01167.hp1 HG01243.hp1 HG02145.hp1 others(8): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0021a0002c0011others(4): Show | a0001c0001t0003a0001c0021t0001a0002c0011t0005others(4): Show | a0001c0001t0003g0074 a0001c0001t0003g0201 a0001c0021t0001g0014 others(8): Show |
11 | 390 | 0.0282 | -2 | c.596 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44832222 | ATT | A | intron_variant | MODIFIER | HG00323.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0001c0007others(3): Show | a0001c0001t0003a0001c0004t0003a0001c0007t0001others(3): Show | a0001c0001t0003g0188 a0001c0004t0003g0158 a0001c0007t0001g0202 others(5): Show |
8 | 390 | 0.0205 | -2 | c.596 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44832968 | AAC | A | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(18): Show | a0001c0001t0001g0024 a0001c0001t0003g0080 a0001c0001t0003g0081 others(75): Show |
78 | 390 | 0.2000 | -2 | c.596 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44835231 | CTA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0007others(31): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(38): Show | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0161 others(132): Show |
135 | 390 | 0.3462 | -2 | c.596 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44843824 | CAA | C | intron_variant | MODIFIER | HG00423.hp2 HG02257.hp2 HG02738.hp2 others(11): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0003a0002c0011others(8): Show | a0001c0001t0001a0002c0003t0004a0002c0011t0005others(8): Show | a0001c0001t0001g0097 a0001c0001t0001g0370 a0002c0003t0004g0253 others(11): Show |
14 | 390 | 0.0359 | -2 | c.597 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44848361 | GTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
a0001a0002a0003others(22): Show | a0001c0001a0001c0004a0001c0007others(66): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(82): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0097 others(280): Show |
283 | 390 | 0.7256 | -2 | c.748 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44849411 | GCT | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0008others(10): Show | a0001c0001t0003a0001c0004t0003a0001c0008t0003others(11): Show | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0080 others(68): Show |
71 | 390 | 0.1821 | -2 | c.877 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44850963 | CAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00733.hp1 HG00733.hp2 others(80): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(28): Show | a0001c0001t0001g0017 a0001c0001t0003g0074 a0001c0001t0003g0201 others(80): Show |
83 | 390 | 0.2128 | -2 | c.877 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44852189 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(22): Show | a0001c0001t0001g0134 a0001c0001t0001g0161 a0001c0001t0001g0192 others(87): Show |
90 | 390 | 0.2308 | -2 | c.877 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44853116 | TTA | T | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01070.hp2 others(76): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(28): Show | a0001c0001t0001g0017 a0001c0001t0003g0074 a0001c0001t0003g0201 others(76): Show |
79 | 390 | 0.2026 | -2 | c.877 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAA | C | intron_variant | MODIFIER | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0018a0002c0011others(8): Show | a0001c0001t0003a0001c0018t0001a0002c0011t0005others(8): Show | a0001c0001t0003g0201 a0001c0018t0001g0041 a0001c0018t0001g0108 others(11): Show |
14 | 390 | 0.0359 | -2 | c.877 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44854991 | CAG | C | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(9): Show |
a0004a0017a0023 | a0004c0012a0004c0017a0017c0053others(1): Show | a0004c0012t0002a0004c0012t0015a0004c0017t0002others(2): Show | a0004c0012t0002g0172 a0004c0012t0002g0233 a0004c0012t0002g0244 others(9): Show |
12 | 390 | 0.0308 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00673.hp2 others(35): Show |
a0001a0003a0007 | a0001c0001a0001c0004a0003c0002others(5): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0003others(6): Show | a0001c0001t0001g0042 a0001c0004t0001g0029 a0001c0004t0003g0118 others(35): Show |
38 | 390 | 0.0974 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44857799 | GCT | G | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
a0002a0004a0010others(4): Show | a0002c0003a0002c0006a0002c0016others(12): Show | a0002c0003t0003a0002c0003t0004a0002c0006t0004others(14): Show | a0002c0003t0003g0276 a0002c0003t0004g0002 a0002c0003t0004g0011 others(73): Show |
76 | 390 | 0.1949 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858369 | GTT | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(12): Show | a0001c0001t0001g0042 a0001c0001t0003g0373 a0001c0004t0003g0118 others(77): Show |
80 | 390 | 0.2051 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858498 | GCT | G | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(44): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0004a0002c0003others(19): Show | a0001c0001t0009a0001c0001t0010a0001c0004t0010others(22): Show | a0001c0001t0009g0173 a0001c0001t0009g0321 a0001c0001t0010g0198 others(44): Show |
47 | 390 | 0.1205 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858550 | TTA | T | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
a0002 | a0002c0011a0002c0013a0002c0020others(1): Show | a0002c0011t0005a0002c0013t0005a0002c0020t0005others(1): Show | a0002c0011t0005g0333 a0002c0013t0005g0185 a0002c0020t0005g0047 others(4): Show |
7 | 390 | 0.0180 | -2 | c.878 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44859350 | CCT | C | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(23): Show |
a0002a0004a0008others(3): Show | a0002c0003a0002c0006a0002c0011others(9): Show | a0002c0003t0001a0002c0006t0001a0002c0011t0005others(9): Show | a0002c0003t0001g0106 a0002c0003t0001g0387 a0002c0006t0001g0059 others(23): Show |
26 | 390 | 0.0667 | -2 | c.878 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44859652 | CCT | C | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(93): Show |
a0002a0004a0008others(6): Show | a0002c0003a0002c0006a0002c0011others(25): Show | a0002c0003t0003a0002c0003t0004a0002c0006t0004others(26): Show | a0002c0003t0003g0276 a0002c0003t0004g0002 a0002c0003t0004g0011 others(93): Show |
96 | 390 | 0.2462 | -2 | c.878 others(15): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44860638 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0004a0001c0007others(55): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(66): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0097 others(299): Show |
302 | 390 | 0.7744 | -2 | c.981 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44860662 | CAG | C | intron_variant | MODIFIER | HG00099.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
a0008 | a0008c0014a0008c0033 | a0008c0014t0005a0008c0033t0005 | a0008c0014t0005g0022 a0008c0014t0005g0152 a0008c0014t0005g0264 others(3): Show |
6 | 390 | 0.0154 | -2 | c.981 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44860758 | CAG | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(91): Show |
a0001a0005a0006others(7): Show | a0001c0001a0001c0004a0001c0007others(20): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(21): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(91): Show |
94 | 390 | 0.2410 | -2 | c.981 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44861522 | CTG | C | intron_variant | MODIFIER | HG00099.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
a0001a0022 | a0001c0010a0022c0048 | a0001c0010t0001a0022c0048t0001 | a0001c0010t0001g0204 a0001c0010t0001g0263 a0001c0010t0001g0265 others(3): Show |
6 | 390 | 0.0154 | -2 | c.982 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44862609 | CTG | C | 3_prime_UTR_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(69): Show |
a0001a0002a0010others(2): Show | a0001c0001a0001c0004a0002c0003others(12): Show | a0001c0001t0009a0001c0001t0010a0001c0004t0010others(13): Show | a0001c0001t0009g0173 a0001c0001t0009g0321 a0001c0001t0010g0198 others(69): Show |
72 | 390 | 0.1846 | -2 | c.*16 others(9): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 12/12 | 16 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44863021 | ACT | A | downstream_gene_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01070.hp2 others(36): Show |
a0001a0002a0011others(3): Show | a0001c0001a0001c0004a0001c0007others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(14): Show | a0001c0001t0001g0097 a0001c0001t0001g0370 a0001c0001t0003g0080 others(36): Show |
39 | 390 | 0.1000 | -2 | c.*42 others(11): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 238 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44863830 | TTG | T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
a0001a0002a0003others(26): Show | a0001c0001a0001c0004a0001c0007others(76): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(94): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(380): Show |
383 | 390 | 0.9821 | -2 | c.*12 others(13): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1047 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44864491 | AAG | A | downstream_gene_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(68): Show |
a0001a0002a0010others(2): Show | a0001c0001a0002c0003a0002c0006others(14): Show | a0001c0001t0003a0002c0003t0004a0002c0006t0004others(14): Show | a0001c0001t0003g0113 a0002c0003t0004g0002 a0002c0003t0004g0011 others(68): Show |
71 | 390 | 0.1821 | -2 | c.*18 others(13): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1708 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44866910 | ACT | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(78): Show |
a0001a0003a0005others(7): Show | a0001c0001a0001c0004a0001c0007others(21): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(22): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(78): Show |
81 | 390 | 0.2077 | -2 | c.*43 others(13): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4127 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44866918 | ACC | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(25): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(10): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(10): Show | a0001c0001t0001g0024 a0001c0001t0001g0161 a0001c0001t0001g0192 others(25): Show |
28 | 390 | 0.0718 | -2 | c.*43 others(13): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4135 | chr22 | TogoVar | |||||||
ARHGAP9_chr12_57467269_57484866 | 57482838 | GCT | G | upstream_gene_variant | MODIFIER | HG01256.hp1 HG01496.hp1 HG01891.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 a0001c0001t0001g0075 a0001c0001t0001g0080 others(1): Show |
5 | 406 | 0.0123 | -2 | c.-31 others(13): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 2973 | chr12 | TogoVar |