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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP35_chr19_46855997_47010077 | 46907478 | T | TTTTG | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0007a0001c0009others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0190 others(114): Show |
117 | 292 | 0.4007 | 4 | c.-18 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46939372 | C | CATTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0005 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(29): Show |
32 | 108 | 0.2963 | 4 | c.382 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46959030 | G | GTTGT | intron_variant | MODIFIER | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(18): Show | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | 296 | 0.2162 | 4 | c.382 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46965466 | T | TTTTG | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(17): Show | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(49): Show |
52 | 170 | 0.3059 | 4 | c.382 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | C | CAAAA | intron_variant | MODIFIER | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(3): Show | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0045 others(16): Show |
19 | 77 | 0.2468 | 4 | c.382 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47003913 | G | GACAC | 3_prime_UTR_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0016a0001c0001t0019others(4): Show | a0001c0001t0010g0097 a0001c0001t0010g0122 a0001c0001t0010g0125 others(9): Show |
12 | 259 | 0.0463 | 4 | c.*32 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47003918 | G | GCACA | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG01099.hp2 HG01192.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136 a0001c0001t0001g0143 a0001c0001t0001g0268 others(2): Show |
5 | 181 | 0.0276 | 4 | c.*32 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3263 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | C | CTTTT | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(24): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0132 others(24): Show |
27 | 52 | 0.5192 | 4 | c.*55 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 47006440 | C | CCTGG | downstream_gene_variant | MODIFIER | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0020a0001c0001t0034 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | 296 | 0.0101 | 4 | c.*57 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1364 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 47007643 | C | CTTTT | downstream_gene_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG01192.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(1): Show | a0001c0001t0003g0081 a0001c0001t0004g0102 a0001c0001t0004g0107 others(9): Show |
12 | 97 | 0.1237 | 4 | c.*69 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2567 | chr19 | TogoVar | |||||||
ARHGAP36_chrX_131053346_131094885 | 131075623 | A | ATGTG | intron_variant | MODIFIER | HG00558.hp2 HG00609.hp1 HG00733.hp1 others(45): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0035 a0001c0001t0001g0112 a0001c0001t0001g0115 others(29): Show |
48 | 57 | 0.8421 | 4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | C | CATAT | intron_variant | MODIFIER | HG00323.hp1 HG01358.hp1 HG02965.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0124 a0001c0001t0003g0045 a0001c0001t0003g0046 others(1): Show |
4 | 8 | 0.5000 | 4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562484 | G | GGACT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0222 others(44): Show |
47 | 243 | 0.1934 | 4 | c.513 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601236 | C | CTGTG | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
a0001a0003a0005 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(5): Show | a0001c0001t0001g0228 a0001c0003t0001g0004 a0001c0003t0001g0011 others(10): Show |
13 | 244 | 0.0533 | 4 | c.80+ others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144614354 | A | ATTTT | intron_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(6): Show |
a0001 | a0001c0001a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0017t0001 | a0001c0001t0001g0157 a0001c0001t0004g0149 a0001c0001t0004g0150 others(6): Show |
9 | 209 | 0.0431 | 4 | c.-81 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144633143 | T | TTTTG | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
a0001a0003 | a0001c0002a0001c0003a0001c0005others(2): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0009others(4): Show | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0003t0001g0004 others(9): Show |
12 | 243 | 0.0494 | 4 | c.-81 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144639338 | A | AAAAG | intron_variant | MODIFIER | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0006 | a0001c0001t0001g0120 a0001c0001t0002g0121 a0001c0004t0006g0064 others(4): Show |
7 | 213 | 0.0329 | 4 | c.-81 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144656807 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(6): Show | a0001c0001t0001g0060 a0001c0001t0001g0098 a0001c0001t0001g0117 others(37): Show |
40 | 111 | 0.3604 | 4 | c.-82 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38603451 | A | ATCTG | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
a0001a0003a0005others(3): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0190 others(56): Show |
65 | 210 | 0.3095 | 4 | c.137 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38616935 | C | CTTTA | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0002a0001c0004others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
174 | 228 | 0.7632 | 4 | c.138 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38627621 | G | GTGTA | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(115): Show |
a0001a0002a0003others(14): Show | a0001c0002a0001c0004a0001c0007others(22): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(41): Show | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(107): Show |
118 | 348 | 0.3391 | 4 | c.558 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38630082 | T | TTTTC | intron_variant | MODIFIER | HG02602.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0022 a0001c0001t0002g0083 a0001c0001t0005g0185 |
4 | 343 | 0.0117 | 4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38630147 | T | TTCCC | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(69): Show |
a0001a0004a0008others(4): Show | a0001c0002a0001c0008a0004c0011others(6): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(15): Show | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(64): Show |
72 | 346 | 0.2081 | 4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38642608 | T | TCCTC | intron_variant | MODIFIER | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
a0001a0005a0011 | a0001c0021a0005c0010a0005c0040others(1): Show | a0001c0021t0002a0005c0010t0010a0005c0010t0012others(2): Show | a0001c0021t0002g0278 a0001c0021t0002g0281 a0005c0010t0010g0224 others(6): Show |
9 | 348 | 0.0259 | 4 | c.136 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38647379 | G | GGTTT | intron_variant | MODIFIER | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0007 | a0001c0001t0003g0229 a0001c0001t0003g0268 a0001c0002t0007g0009 others(1): Show |
5 | 338 | 0.0148 | 4 | c.188 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38654114 | G | GATGA | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
a0001a0007 | a0001c0029a0007c0009 | a0001c0029t0003a0007c0009t0006 | a0001c0029t0003g0136 a0007c0009t0006g0068 a0007c0009t0006g0069 |
3 | 109 | 0.0275 | 4 | c.*42 others(15): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3462 | chr20 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100699506 | A | ATATT | intron_variant | MODIFIER | HG00735.hp1 HG02083.hp2 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0011 | a0001c0001t0001g0193 a0001c0001t0001g0211 a0001c0001t0001g0217 others(4): Show |
7 | 165 | 0.0424 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100705015 | A | ACAAC | intron_variant | MODIFIER | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0003a0002c0002t0002a0002c0002t0011 | a0001c0003t0003g0269 a0002c0002t0002g0006 a0002c0002t0011g0224 others(1): Show |
4 | 283 | 0.0141 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100710538 | G | GTTTT | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp1 HG01346.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0003t0003a0001c0003t0006others(8): Show | a0001c0001t0001g0011 a0001c0001t0001g0267 a0001c0003t0003g0269 others(14): Show |
17 | 96 | 0.1771 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | T | TTGTG | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02970.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0139 a0002c0002t0001g0013 a0002c0002t0001g0015 others(2): Show |
5 | 74 | 0.0676 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100729054 | C | CCACT | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
a0001a0002 | a0001c0010a0002c0006 | a0001c0010t0001a0002c0006t0008a0002c0006t0011 | a0001c0010t0001g0238 a0002c0006t0008g0240 a0002c0006t0008g0243 others(3): Show |
6 | 284 | 0.0211 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100733825 | G | GAAAA | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(7): Show | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0178 others(26): Show |
29 | 103 | 0.2816 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100744557 | T | TGTGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(34): Show | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(157): Show |
160 | 275 | 0.5818 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(36): Show |
39 | 191 | 0.2042 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100764025 | C | CTTCT | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0001a0002c0002t0002a0002c0004t0007 | a0002c0002t0001g0013 a0002c0002t0001g0015 a0002c0002t0001g0016 others(3): Show |
6 | 208 | 0.0288 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100766222 | G | GGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(23): Show |
26 | 211 | 0.1232 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100770918 | G | GTGTT | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01891.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0008others(3): Show | a0001c0001t0001g0002 a0002c0002t0002g0141 a0002c0002t0008g0028 others(5): Show |
8 | 284 | 0.0282 | 4 | c.250 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100779483 | T | TACAC | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0037a0001c0003t0003others(8): Show | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0037g0041 others(12): Show |
15 | 267 | 0.0562 | 4 | c.250 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAAA | intron_variant | MODIFIER | HG03195.hp1 HG04228.hp1 NA19005.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0091 a0001c0001t0001g0212 a0001c0001t0001g0217 others(3): Show |
6 | 19 | 0.3158 | 4 | c.251 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100818756 | T | TTTTG | intron_variant | MODIFIER | HG00738.hp2 HG02818.hp1 HG03017.hp2 |
a0002 | a0002c0002a0002c0006a0002c0009 | a0002c0002t0002a0002c0006t0008a0002c0009t0004 | a0002c0002t0002g0119 a0002c0006t0008g0240 a0002c0009t0004g0237 |
3 | 284 | 0.0106 | 4 | c.312 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837663 | A | ATTAT | intron_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(51): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0024others(13): Show | a0001c0001t0001g0022 a0001c0001t0001g0065 a0001c0001t0001g0067 others(51): Show |
54 | 255 | 0.2118 | 4 | c.313 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100845076 | G | GATAT | intron_variant | MODIFIER | HG02622.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0001t0031a0001c0008t0001others(3): Show | a0001c0001t0001g0046 a0001c0001t0031g0249 a0001c0008t0001g0004 others(4): Show |
7 | 280 | 0.0250 | 4 | c.313 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGT | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp2 HG01346.hp1 others(14): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0004a0002c0002t0008others(4): Show | a0002c0002t0002g0010 a0002c0002t0002g0053 a0002c0002t0002g0226 others(14): Show |
17 | 137 | 0.1241 | 4 | c.313 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | G | GTCTC | intron_variant | MODIFIER | HG01081.hp2 HG01106.hp1 HG01175.hp2 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0019 a0002c0002t0002g0025 a0002c0002t0002g0026 others(3): Show |
6 | 262 | 0.0229 | 4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100881829 | T | TTTTG | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0006 | a0001c0001t0001a0001c0010t0001a0002c0006t0008others(1): Show | a0001c0001t0001g0079 a0001c0010t0001g0238 a0002c0006t0008g0240 others(3): Show |
6 | 197 | 0.0305 | 4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGT | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(15): Show |
a0002 | a0002c0002a0002c0004a0002c0009 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(8): Show | a0002c0002t0002g0034 a0002c0002t0002g0222 a0002c0002t0002g0245 others(15): Show |
18 | 47 | 0.3830 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903114 | T | TGCGC | intron_variant | MODIFIER | HG00408.hp2 HG00639.hp1 HG01261.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0021 a0001c0001t0001g0093 a0001c0001t0001g0095 others(7): Show |
10 | 278 | 0.0360 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACA | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG01928.hp2 others(23): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0011 | a0001c0003t0003a0001c0003t0022a0001c0003t0033others(8): Show | a0001c0003t0003g0107 a0001c0003t0003g0162 a0001c0003t0003g0214 others(23): Show |
26 | 65 | 0.4000 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAA | intron_variant | MODIFIER | HG01243.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0008a0002c0002t0011a0002c0002t0018others(1): Show | a0002c0002t0008g0005 a0002c0002t0011g0231 a0002c0002t0018g0205 others(2): Show |
5 | 266 | 0.0188 | 4 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATAT | intron_variant | MODIFIER | HG00741.hp1 HG01346.hp2 HG01928.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0007 | a0001c0001t0001g0068 a0001c0001t0001g0143 a0001c0001t0001g0148 others(4): Show |
7 | 74 | 0.0946 | 4 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |