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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143700685 | T | TATGA | intron_variant | MODIFIER | NA18991.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 a0001c0001t0001g0083 |
2 | 160 | 0.0125 | 4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143724051 | A | ATGTG | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
37 | 104 | 0.3558 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143730945 | T | TTTAA | intron_variant | MODIFIER | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | 104 | 0.1346 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143737726 | T | TTTTA | intron_variant | MODIFIER | HG03209.hp1 HG03710.hp2 NA18966.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0068 |
3 | 49 | 0.0612 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143765080 | T | TTATC | intron_variant | MODIFIER | NA19043.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0122 |
2 | 160 | 0.0125 | 4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | A | ATGTG | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp2 HG02109.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0096 others(4): Show |
7 | 32 | 0.2188 | 4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | C | CTTTT | downstream_gene_variant | MODIFIER | HG01358.hp2 HG02040.hp1 HG02055.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 a0001c0001t0001g0088 a0001c0001t0001g0116 others(6): Show |
9 | 54 | 0.1667 | 4 | c.*37 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | T | TACAC | downstream_gene_variant | MODIFIER | HG02486.hp2 HG02572.hp2 HG02922.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0002a0001c0004t0008 | a0001c0001t0001g0121 a0001c0001t0001g0196 a0001c0004t0002g0103 others(3): Show |
6 | 125 | 0.0480 | 4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916784 | G | GTATA | downstream_gene_variant | MODIFIER | HG03098.hp1 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | 148 | 0.0135 | 4 | c.*33 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2604 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24958237 | A | AAAAC | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(139): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): Show |
142 | 238 | 0.5966 | 4 | c.724 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961972 | G | GTTTT | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0003t0003others(3): Show | a0001c0001t0001g0029 a0001c0001t0001g0107 a0001c0001t0001g0227 others(21): Show |
25 | 132 | 0.1894 | 4 | c.574 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24999399 | T | TTTTA | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(51): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
54 | 234 | 0.2308 | 4 | c.53+ others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25003038 | C | CAAAA | intron_variant | MODIFIER | HG01243.hp2 HG01256.hp1 HG01516.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0084 others(17): Show |
20 | 138 | 0.1449 | 4 | c.53+ others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020117 | A | AAAAG | upstream_gene_variant | MODIFIER | HG00323.hp1 HG01884.hp1 HG01934.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0025 others(11): Show |
15 | 238 | 0.0630 | 4 | c.-48 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4749 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020176 | A | AACGG | upstream_gene_variant | MODIFIER | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0116 others(9): Show |
12 | 235 | 0.0511 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4808 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020190 | C | CGGAA | upstream_gene_variant | MODIFIER | HG02895.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0146 a0001c0001t0001g0231 a0001c0001t0002g0031 others(1): Show |
4 | 98 | 0.0408 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4822 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | G | GAAGA | upstream_gene_variant | MODIFIER | HG06807.hp1 NA18747.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0099 |
3 | 74 | 0.0405 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129602987 | T | TTATA | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(19): Show |
22 | 131 | 0.1679 | 4 | c.136 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129608064 | G | GAAAA | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | 138 | 0.0725 | 4 | c.112 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129619979 | A | AGAAG | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0002c0002t0001others(1): Show | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(12): Show |
15 | 236 | 0.0636 | 4 | c.787 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625357 | T | TGATA | intron_variant | MODIFIER | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0002c0002t0005 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | 234 | 0.0128 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625551 | T | TTATA | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | 236 | 0.2161 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625732 | T | TAATA | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | 226 | 0.0088 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625732 | T | TTATA | intron_variant | MODIFIER | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0011t0001others(1): Show | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | 230 | 0.0261 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129626065 | T | TACAC | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(26): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0002c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(3): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0071 others(26): Show |
29 | 93 | 0.3118 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129631941 | G | GAATT | intron_variant | MODIFIER | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0011a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
67 | 236 | 0.2839 | 4 | c.616 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129661512 | G | GAAAA | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
10 | 103 | 0.0971 | 4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129667469 | A | ATGTG | intron_variant | MODIFIER | HG01169.hp1 HG01169.hp2 HG01175.hp2 others(2): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(2): Show | a0001c0001t0001g0188 a0001c0001t0002g0081 a0001c0001t0013g0119 others(2): Show |
5 | 180 | 0.0278 | 4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129667503 | G | GTGTA | intron_variant | MODIFIER | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(11): Show |
14 | 108 | 0.1296 | 4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129668362 | T | TCACA | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(27): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0099 others(27): Show |
30 | 123 | 0.2439 | 4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129685602 | G | GGTTA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(41): Show |
a0001a0003 | a0001c0001a0001c0009a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(41): Show |
44 | 236 | 0.1864 | 4 | c.113 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129690124 | C | CGTGT | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
a0001a0002a0008 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0135 a0001c0001t0001g0201 a0001c0001t0001g0206 others(31): Show |
34 | 212 | 0.1604 | 4 | c.113 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218631 | T | TTGTG | downstream_gene_variant | MODIFIER | HG06807.hp1 NA21309.hp2 |
a0001 | a0001c0003 | a0001c0003t0004a0001c0003t0015 | a0001c0003t0004g0062 a0001c0003t0015g0061 |
2 | 17 | 0.1176 | 4 | c.*74 others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3547 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218631 | T | TTTTG | downstream_gene_variant | MODIFIER | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
a0001a0005 | a0001c0001a0001c0002a0005c0007 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(8): Show | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(63): Show |
66 | 81 | 0.8148 | 4 | c.*74 others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3547 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218895 | A | ATGTG | downstream_gene_variant | MODIFIER | HG00639.hp2 HG01255.hp1 |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0001a0004c0006t0001 | a0001c0001t0001g0230 a0004c0006t0001g0195 |
2 | 209 | 0.0096 | 4 | c.*72 others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3283 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97233353 | A | AAAAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0002a0003c0005others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(19): Show | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | 240 | 0.7708 | 4 | c.128 others(23): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97248816 | T | TTTTG | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0002a0001c0001t0006a0001c0001t0014others(1): Show | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | 240 | 0.0292 | 4 | c.928 others(21): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97251072 | T | TAAGG | intron_variant | MODIFIER | HG02486.hp1 HG02895.hp2 HG02897.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0018 |
3 | 240 | 0.0125 | 4 | c.928 others(21): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97251506 | A | AAAGG | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0002a0001c0001t0006a0001c0001t0014others(1): Show | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | 240 | 0.0292 | 4 | c.927 others(21): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97279495 | T | TTTTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(191): Show |
194 | 240 | 0.8083 | 4 | c.56+ others(21): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | TogoVar | |||||||
ARHGAP1_chr11_46672080_46705619 | 46676471 | G | GTCTC | downstream_gene_variant | MODIFIER | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0007a0001c0002t0016others(2): Show | a0001c0002t0003g0006 a0001c0002t0003g0079 a0001c0002t0003g0080 others(7): Show |
18 | 342 | 0.0526 | 4 | c.*25 others(15): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 608 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110578507 | G | GTCTT | 3_prime_UTR_variant | MODIFIER | HG00639.hp1 HG00735.hp1 HG03239.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0004 a0001c0001t0009g0118 |
3 | 224 | 0.0134 | 4 | c.*85 others(13): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 862 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110584965 | A | ATATG | intron_variant | MODIFIER | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
a0002a0010 | a0002c0003a0010c0020 | a0002c0003t0007a0010c0020t0020 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | 224 | 0.0223 | 4 | c.141 others(23): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110587086 | C | CACAA | intron_variant | MODIFIER | HG03491.hp1 HG03688.hp1 NA19067.hp1 |
a0003a0012 | a0003c0004a0012c0017 | a0003c0004t0002a0012c0017t0002 | a0003c0004t0002g0142 a0003c0004t0002g0160 a0012c0017t0002g0139 |
3 | 224 | 0.0134 | 4 | c.130 others(21): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110610310 | C | CAATT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0005others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0039 a0001c0001t0001g0130 a0001c0001t0001g0161 others(126): Show |
134 | 224 | 0.5982 | 4 | c.708 others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110614466 | A | AGCCT | intron_variant | MODIFIER | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0002c0003t0007 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | 224 | 0.0268 | 4 | c.630 others(17): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110644997 | T | TTCTC | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0005others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(74): Show |
78 | 213 | 0.3662 | 4 | c.189 others(23): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110657920 | G | GAGGA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0058 others(15): Show |
18 | 81 | 0.2222 | 4 | c.189 others(23): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATAT | intron_variant | MODIFIER | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0190 |
4 | 129 | 0.0310 | 4 | c.188 others(21): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110687083 | T | TAGAC | intron_variant | MODIFIER | HG00639.hp2 HG01981.hp1 HG02165.hp1 others(5): Show |
a0001a0004 | a0001c0001a0004c0010 | a0001c0001t0001a0001c0001t0021a0004c0010t0001 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | 220 | 0.0364 | 4 | c.188 others(21): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar |