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 | 46983054 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0014 | 1 | 59 | 0.0169 | -12 | c.382 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(5): Show |
C | downstream_gene_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0020a0001c0001t0034others(1): Show | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0020g0032 others(3): Show |
6 | 31 | 0.1935 | -12 | c.*55 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG02129.hp1 HG02155.hp2 NA18939.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008 | a0001c0001t0001g0019 a0001c0001t0001g0083 a0001c0001t0002g0013 others(6): Show |
13 | 17 | 0.7647 | -12 | c.-14 others(31): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144579201 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0057 | 1 | 163 | 0.0061 | -12 | c.512 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144608156 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0090 | 1 | 125 | 0.0080 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144609683 | TGAGCCAC others(5): Show |
T | intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 244 | 0.0041 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144611516 | ATAGCTCT others(5): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | 244 | 0.0164 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38601410 | GTCCTGCT others(5): Show |
G | upstream_gene_variant | MODIFIER | HG03130.hp2 | a0009 | a0009c0035 | a0009c0035t0011 | a0009c0035t0011g0123 | 1 | 348 | 0.0029 | -12 | c.-53 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 398 | chr20 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38603407 | GTCTATCT others(5): Show |
G | intron_variant | MODIFIER | HG01167.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
a0001a0006a0008others(3): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0002a0001c0002t0002a0001c0004t0007others(6): Show | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(16): Show |
22 | 240 | 0.0917 | -12 | c.137 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38603517 | CCATCTAT others(5): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
a0004a0006a0008 | a0004c0011a0006c0013a0008c0006 | a0004c0011t0007a0006c0013t0008a0008c0006t0002 | a0004c0011t0007g0288 a0006c0013t0008g0027 a0006c0013t0008g0299 others(1): Show |
6 | 348 | 0.0172 | -12 | c.137 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38644613 | GTCACCCA others(5): Show |
G | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
a0001a0004a0023 | a0001c0002a0001c0004a0001c0008others(3): Show | a0001c0002t0004a0001c0004t0004a0001c0008t0004others(4): Show | a0001c0002t0004g0072 a0001c0004t0004g0044 a0001c0008t0004g0025 others(7): Show |
12 | 348 | 0.0345 | -12 | c.156 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG02698.hp1 HG04228.hp2 |
a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0261 a0002c0002t0004g0278 |
2 | 71 | 0.0282 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(5): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG01358.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(2): Show | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0074 others(5): Show |
8 | 138 | 0.0580 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | NA19077.hp2 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0166 | 1 | 164 | 0.0061 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG03017.hp2 NA20905.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0096 a0002c0002t0002g0119 |
2 | 11 | 0.1818 | -12 | c.155 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100789531 | GGGCATGA others(5): Show |
G | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(9): Show | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(34): Show |
37 | 284 | 0.1303 | -12 | c.251 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 34 | 0.0294 | -12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100841396 | GATTTCAC others(5): Show |
G | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0008 | a0001c0008t0010 | a0001c0008t0010g0254 | 1 | 284 | 0.0035 | -12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | GTCTCTCT others(5): Show |
G | intron_variant | MODIFIER | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
a0001a0002a0005 | a0001c0010a0002c0002a0002c0006others(1): Show | a0001c0010t0001a0002c0002t0002a0002c0006t0008others(2): Show | a0001c0010t0001g0238 a0002c0002t0002g0119 a0002c0006t0008g0240 others(4): Show |
7 | 263 | 0.0266 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875099 | CTCTCTCT others(5): Show |
C | intron_variant | MODIFIER | HG01515.hp2 HG03669.hp2 NA18968.hp1 |
a0001 | a0001c0001a0001c0015 | a0001c0001t0001a0001c0001t0032a0001c0015t0001 | a0001c0001t0001g0131 a0001c0001t0032g0008 a0001c0015t0001g0272 |
3 | 248 | 0.0121 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875101 | CTCTCTCT others(5): Show |
C | intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0270 | 1 | 203 | 0.0049 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTGT others(5): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0037a0002c0002t0002a0002c0002t0021others(1): Show | a0001c0001t0037g0041 a0002c0002t0002g0141 a0002c0002t0002g0227 others(3): Show |
6 | 272 | 0.0221 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875105 | CTCTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG02897.hp1 NA19088.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0220 a0002c0002t0002g0226 |
2 | 272 | 0.0074 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp1 HG01361.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0005 | a0002c0002t0002g0006 a0002c0002t0005g0116 a0002c0002t0005g0117 others(1): Show |
4 | 202 | 0.0198 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00738.hp2 HG03225.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0009 | a0001c0001t0001a0001c0001t0019a0001c0001t0037others(2): Show | a0001c0001t0001g0128 a0001c0001t0001g0220 a0001c0001t0019g0078 others(3): Show |
6 | 73 | 0.0822 | -12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG00408.hp2 HG00639.hp1 HG01123.hp2 others(41): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0023 others(41): Show |
44 | 47 | 0.9362 | -12 | c.486 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG01074.hp1 HG01516.hp2 HG01884.hp2 |
a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0146 |
3 | 268 | 0.0112 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(5): Show |
A | intron_variant | MODIFIER | HG01106.hp2 HG01175.hp1 HG01981.hp1 |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0003c0007t0005 | a0002c0002t0002g0024 a0002c0002t0002g0150 a0003c0007t0005g0059 |
3 | 276 | 0.0109 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(5): Show |
A | intron_variant | MODIFIER | HG01261.hp2 HG02257.hp1 |
a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0058 a0003c0007t0005g0060 |
2 | 279 | 0.0072 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921245 | ATTTTTTT others(5): Show |
A | intron_variant | MODIFIER | HG04204.hp2 NA20905.hp2 |
a0001 | a0001c0003 | a0001c0003t0014 | a0001c0003t0014g0234 a0001c0003t0014g0235 |
2 | 266 | 0.0075 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01496.hp2 NA21309.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0041a0002c0002t0025 | a0001c0001t0041g0127 a0002c0002t0025g0250 |
2 | 25 | 0.0800 | -12 | c.245 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | AAAATAAA others(5): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(22): Show |
a0001a0002 | a0001c0003a0001c0008a0002c0005 | a0001c0003t0003a0001c0003t0022a0001c0008t0010others(2): Show | a0001c0003t0003g0107 a0001c0003t0003g0138 a0001c0003t0003g0153 others(22): Show |
25 | 54 | 0.4630 | -12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATAT others(5): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG03486.hp2 NA19084.hp1 |
a0001a0002 | a0001c0003a0001c0005a0002c0007 | a0001c0003t0001a0001c0005t0001a0002c0007t0001 | a0001c0003t0001g0179 a0001c0005t0001g0216 a0002c0007t0001g0011 |
3 | 155 | 0.0194 | -12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802959 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG00642.hp1 HG01192.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0002t0001 | a0001c0001t0006g0096 a0001c0002t0001g0097 |
2 | 220 | 0.0091 | -12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTATTTA others(5): Show |
G | intron_variant | MODIFIER | HG02809.hp2 HG02886.hp2 HG03239.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(1): Show | a0001c0001t0001g0212 a0001c0001t0013g0100 a0001c0001t0014g0178 others(1): Show |
4 | 29 | 0.1379 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12860856 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(122): Show |
125 | 176 | 0.7102 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868557 | CAAAAAGT others(5): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0033 a0001c0001t0001g0193 a0001c0001t0001g0214 others(5): Show |
8 | 228 | 0.0351 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATAT others(5): Show |
T | intron_variant | MODIFIER | HG01169.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0007 a0001c0001t0001g0133 a0001c0001t0001g0164 others(19): Show |
22 | 121 | 0.1818 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | TTATATAT others(5): Show |
T | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0215 | 1 | 130 | 0.0077 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12873918 | TAAATAAA others(5): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(5): Show | a0001c0001t0001g0187 a0001c0001t0003g0028 a0001c0001t0010g0186 others(6): Show |
9 | 228 | 0.0395 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12873943 | AAATAAAT others(5): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG03209.hp2 HG03688.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0002t0001g0131 |
3 | 228 | 0.0132 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | TGAGAGAG others(5): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0160 a0001c0001t0002g0149 a0001c0001t0002g0167 others(4): Show |
7 | 210 | 0.0333 | -12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0116 others(6): Show |
9 | 73 | 0.1233 | -12 | c.113 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991861 | TTACTTAC others(5): Show |
T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0013 | a0001c0001t0006g0025 a0001c0001t0006g0096 a0001c0001t0006g0098 others(7): Show |
10 | 228 | 0.0439 | -12 | c.*16 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 219 | chr17 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1073365 | TGGGTTTT others(5): Show |
T | intron_variant | MODIFIER | HG02257.hp2 | a0003 | a0003c0040 | a0003c0040t0028 | a0003c0040t0028g0125 | 1 | 416 | 0.0024 | -12 | c.565 others(25): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3/22 | chr19 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG01070.hp1 HG02293.hp2 others(12): Show |
a0002a0004a0005others(2): Show | a0002c0001a0004c0005a0005c0008others(2): Show | a0002c0001t0005a0002c0001t0016a0002c0001t0025others(4): Show | a0002c0001t0005g0046 a0002c0001t0005g0241 a0002c0001t0005g0242 others(10): Show |
15 | 137 | 0.1095 | -12 | c.118 others(31): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153906778 | TTCCTGGG others(5): Show |
T | downstream_gene_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 306 | 0.0033 | -12 | c.*93 others(21): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 599 | chrX | TogoVar | |||||||
ARHGAP4_chrX_153902378_153931264 | 153928810 | GTATATGT others(5): Show |
G | upstream_gene_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 306 | 0.0033 | -12 | c.-26 others(23): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2547 | chrX | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0018 | a0001c0018t0023 | a0001c0018t0023g0181 | 1 | 23 | 0.0435 | -12 | c.418 others(29): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32159387 | TATTTTAG others(5): Show |
T | 3_prime_UTR_variant | MODIFIER | HG00609.hp2 | a0004 | a0004c0014 | a0004c0014t0015 | a0004c0014t0015g0159 | 1 | 184 | 0.0054 | -12 | c.*44 others(23): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4444 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |