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 | 11176300 | CATATATA others(23): Show |
C | intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 | 1 | 13 | 0.0769 | -30 | c.162 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590775 | CGAAAAGA others(23): Show |
C | intron_variant | MODIFIER | NA18990.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0120 | 1 | 129 | 0.0078 | -30 | c.588 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(23): Show |
C | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 5 | 0.2000 | -30 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1832793 | CAGAGGCA others(23): Show |
C | intron_variant | MODIFIER | HG00597.hp2 HG01978.hp1 HG01981.hp2 others(11): Show |
a0001a0002a0007 | a0001c0006a0001c0011a0001c0069others(10): Show | a0001c0006t0001a0001c0011t0001a0001c0069t0001others(10): Show | a0001c0006t0001g0009 a0001c0011t0001g0016 a0001c0069t0001g0010 others(11): Show |
14 | 362 | 0.0387 | -30 | c.-48 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1887621 | TTGTGAGG others(23): Show |
T | intron_variant | MODIFIER | HG00597.hp1 HG00673.hp2 HG01496.hp1 others(30): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0003a0001c0001t0038a0001c0002t0001others(23): Show | a0001c0001t0003g0109 a0001c0001t0038g0100 a0001c0002t0001g0053 others(30): Show |
33 | 362 | 0.0912 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888104 | TGAGGAGA others(23): Show |
T | intron_variant | MODIFIER | NA18949.hp1 NA18963.hp2 NA18970.hp1 |
a0002 | a0002c0031a0002c0033 | a0002c0031t0001a0002c0033t0001 | a0002c0031t0001g0182 a0002c0031t0001g0247 a0002c0033t0001g0230 |
3 | 358 | 0.0084 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888124 | TGAGGGTT others(23): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(29): Show |
a0002a0009a0021 | a0002c0017a0002c0022a0002c0024others(19): Show | a0002c0017t0002a0002c0017t0005a0002c0022t0001others(23): Show | a0002c0017t0002g0043 a0002c0017t0002g0044 a0002c0017t0002g0059 others(28): Show |
32 | 239 | 0.1339 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888159 | GTTGCGAG others(23): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG02647.hp1 HG03834.hp2 |
a0001 | a0001c0005a0001c0140a0001c0157 | a0001c0005t0040a0001c0140t0004a0001c0157t0005 | a0001c0005t0040g0356 a0001c0140t0004g0294 a0001c0157t0005g0309 |
3 | 354 | 0.0085 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888183 | TGAGGGTT others(23): Show |
T | intron_variant | MODIFIER | HG02486.hp2 HG03209.hp1 |
a0003a0020 | a0003c0044a0020c0089 | a0003c0044t0010a0020c0089t0041 | a0003c0044t0010g0361 a0020c0089t0041g0343 |
2 | 267 | 0.0075 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888992 | GGTCTACA others(23): Show |
G | intron_variant | MODIFIER | HG01975.hp2 | a0002 | a0002c0025 | a0002c0025t0001 | a0002c0025t0001g0175 | 1 | 362 | 0.0028 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889523 | GGTATTGA others(23): Show |
G | intron_variant | MODIFIER | HG00597.hp2 HG01943.hp1 HG01993.hp2 others(18): Show |
a0001a0006a0007others(1): Show | a0001c0001a0001c0007a0001c0010others(15): Show | a0001c0001t0014a0001c0007t0001a0001c0010t0001others(16): Show | a0001c0001t0014g0185 a0001c0007t0001g0323 a0001c0010t0001g0176 others(18): Show |
21 | 249 | 0.0843 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889845 | AGGTTTGT others(23): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 |
a0012a0019 | a0012c0130a0019c0103 | a0012c0130t0061a0019c0103t0002 | a0012c0130t0061g0342 a0019c0103t0002g0040 |
2 | 361 | 0.0055 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1890130 | GGAGTGGG others(23): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0003others(113): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(173): Show | a0001c0001t0002g0054 a0001c0001t0002g0069 a0001c0001t0002g0249 others(241): Show |
245 | 359 | 0.6825 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157035894 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG03098.hp1 | a0007 | a0007c0014 | a0007c0014t0014 | a0007c0014t0014g0200 | 1 | 359 | 0.0028 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157035950 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG02109.hp2 | a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0028 | 1 | 360 | 0.0028 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157036006 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | 360 | 0.0111 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120351427 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00621.hp2 HG01074.hp1 HG01978.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0152 others(7): Show |
10 | 265 | 0.0377 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351429 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 | 1 | 299 | 0.0033 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351437 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02572.hp2 | a0006 | a0006c0014 | a0006c0014t0019 | a0006c0014t0019g0011 | 1 | 304 | 0.0033 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332379 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 | 1 | 226 | 0.0044 | -30 | c.319 others(51): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(23): Show |
G | intron_variant | MODIFIER | HG02895.hp1 | a0019 | a0019c0041 | a0019c0041t0002 | a0019c0041t0002g0295 | 1 | 88 | 0.0114 | -30 | c.-11 others(49): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362011 | AAGAAGGA others(23): Show |
A | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0142 | 1 | 246 | 0.0041 | -30 | c.-11 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362143 | GAGAAGGA others(23): Show |
G | intron_variant | MODIFIER | HG01496.hp1 HG02040.hp1 NA18998.hp2 others(1): Show |
a0001a0004a0005 | a0001c0002a0004c0015a0005c0008 | a0001c0002t0002a0001c0002t0003a0004c0015t0003others(1): Show | a0001c0002t0002g0158 a0001c0002t0003g0191 a0004c0015t0003g0194 others(1): Show |
4 | 295 | 0.0136 | -30 | c.-11 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385873 | CCCCTCCC others(23): Show |
C | intron_variant | MODIFIER | HG01106.hp2 NA18942.hp1 |
a0001 | a0001c0019a0001c0021 | a0001c0019t0006a0001c0021t0006 | a0001c0019t0006g0139 a0001c0021t0006g0232 |
2 | 286 | 0.0070 | -30 | c.967 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385885 | TCCCTCCC others(23): Show |
T | intron_variant | MODIFIER | HG03834.hp1 NA18973.hp2 |
a0001a0027 | a0001c0019a0027c0053 | a0001c0019t0006a0027c0053t0001 | a0001c0019t0006g0230 a0027c0053t0001g0219 |
2 | 293 | 0.0068 | -30 | c.967 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7419949 | TCACACTC others(23): Show |
T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
a0001a0002a0004others(17): Show | a0001c0001a0001c0002a0001c0013others(32): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(37): Show | a0001c0001t0002g0012 a0001c0001t0002g0055 a0001c0001t0002g0075 others(81): Show |
84 | 296 | 0.2838 | -30 | c.968 others(49): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671694 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp2 HG02257.hp2 others(1): Show |
a0001a0005a0010 | a0001c0001a0001c0023a0005c0008others(1): Show | a0001c0001t0001a0001c0023t0001a0005c0008t0001others(1): Show | a0001c0001t0001g0038 a0001c0023t0001g0034 a0005c0008t0001g0017 others(1): Show |
4 | 170 | 0.0235 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671710 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00280.hp1 NA18962.hp2 |
a0003a0005 | a0003c0005a0005c0008 | a0003c0005t0001a0005c0008t0002 | a0003c0005t0001g0029 a0005c0008t0002g0037 |
2 | 157 | 0.0127 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671712 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02074.hp1 NA18995.hp2 |
a0005a0036 | a0005c0008a0036c0074 | a0005c0008t0002a0036c0074t0001 | a0005c0008t0002g0005 a0036c0074t0001g0174 |
2 | 175 | 0.0114 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671714 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG01517.hp2 others(13): Show |
a0001a0002a0003others(8): Show | a0001c0001a0002c0003a0003c0005others(9): Show | a0001c0001t0002a0002c0003t0001a0002c0003t0002others(10): Show | a0001c0001t0002g0050 a0001c0001t0002g0058 a0001c0001t0002g0062 others(13): Show |
16 | 148 | 0.1081 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671716 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | NA18975.hp1 | a0033 | a0033c0053 | a0033c0053t0001 | a0033c0053t0001g0044 | 1 | 172 | 0.0058 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | CTTCTTTT others(23): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG01069.hp1 others(6): Show |
a0002a0004a0006others(3): Show | a0002c0002a0002c0006a0004c0004others(6): Show | a0002c0002t0002a0002c0006t0004a0004c0004t0001others(6): Show | a0002c0002t0002g0158 a0002c0006t0004g0109 a0004c0004t0001g0170 others(6): Show |
9 | 28 | 0.3214 | -30 | c.34- others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741371 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | 186 | 0.0108 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741379 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG03017.hp1 NA18962.hp1 |
a0029a0032 | a0029c0040a0032c0067 | a0029c0040t0004a0032c0067t0001 | a0029c0040t0004g0116 a0032c0067t0001g0056 |
2 | 177 | 0.0113 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741385 | GTATATAT others(23): Show |
G | intron_variant | MODIFIER | HG01169.hp1 | a0002 | a0002c0006 | a0002c0006t0003 | a0002c0006t0003g0111 | 1 | 128 | 0.0078 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38934557 | CCTCCCGC others(23): Show |
C | intron_variant | MODIFIER | HG01069.hp1 HG01361.hp1 NA19012.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0015 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0015g0173 |
3 | 169 | 0.0178 | -30 | c.506 others(47): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149598348 | TTCTTCTT others(23): Show |
T | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(30): Show |
a0001a0002a0004others(2): Show | a0001c0002a0002c0001a0004c0010others(2): Show | a0001c0002t0005a0001c0002t0006a0001c0002t0008others(10): Show | a0001c0002t0005g0342 a0001c0002t0006g0063 a0001c0002t0006g0086 others(28): Show |
33 | 316 | 0.1044 | -30 | c.186 others(45): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561419 | AGAATGGA others(23): Show |
A | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0013 | a0001c0013t0006 | a0001c0013t0006g0022 | 1 | 166 | 0.0060 | -30 | c.196 others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | GGAATAGA others(23): Show |
G | intron_variant | MODIFIER | HG01516.hp1 HG02145.hp1 |
a0002a0008 | a0002c0003a0008c0017 | a0002c0003t0004a0008c0017t0001 | a0002c0003t0004g0136 a0008c0017t0001g0131 |
2 | 117 | 0.0171 | -30 | c.196 others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833367 | GAAGGAAG others(23): Show |
G | upstream_gene_variant | MODIFIER | HG02615.hp1 | a0017 | a0017c0052 | a0017c0052t0006 | a0017c0052t0006g0069 | 1 | 139 | 0.0072 | -30 | c.-35 others(41): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3546 | chr2 | TogoVar | |||||||
ARHGEF5_chr7_144350402_144385632 | 144354828 | ACAACAAC others(23): Show |
A | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(2): Show |
a0003a0004 | a0003c0012a0004c0003 | a0003c0012t0002a0004c0003t0001 | a0003c0012t0002g0006 a0004c0003t0001g0003 |
5 | 286 | 0.0175 | -30 | c.-68 others(39): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 573 | chr7 | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136726299 | CCATTATC others(23): Show |
C | intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 1 | 245 | 0.0041 | -30 | c.732 others(47): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111133763 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG02015.hp1 HG02132.hp2 HG02280.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(2): Show | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0002g0162 others(9): Show |
12 | 101 | 0.1188 | -30 | c.165 others(49): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221493 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0005 | a0001c0005t0020 | a0001c0005t0020g0112 | 1 | 179 | 0.0056 | -30 | c.670 others(47): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221551 | CTATATAT others(23): Show |
C | intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0005 | a0001c0005t0020 | a0001c0005t0020g0112 | 1 | 270 | 0.0037 | -30 | c.670 others(47): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897215 | GCTGCTTC others(23): Show |
G | intron_variant | MODIFIER | HG02257.hp1 NA19240.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0072 a0001c0002t0001g0071 |
2 | 131 | 0.0153 | -30 | c.198 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156934912 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG01515.hp2 others(15): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0004c0029others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0032 others(15): Show |
18 | 37 | 0.4865 | -30 | c.213 others(47): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156961446 | AGCCTTGG others(23): Show |
A | intron_variant | MODIFIER | HG03195.hp2 | a0002 | a0002c0014 | a0002c0014t0002 | a0002c0014t0002g0024 | 1 | 148 | 0.0068 | -30 | c.224 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157039664 | TCCTTCCT others(23): Show |
T | intron_variant | MODIFIER | HG01496.hp2 HG02717.hp1 HG03195.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0059 a0001c0001t0001g0086 a0001c0002t0003g0058 |
3 | 148 | 0.0203 | -30 | c.224 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | chr6 | TogoVar | |||||||
ARL15_chr5_53878942_54315573 | 53979829 | TTGTGTGT others(23): Show |
T | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 4 | 0.2500 | -30 | c.463 others(49): Show |
ARL15 | ENSG00000185305.12 | transcript | ENST00000504924.6 | protein_coding | 4/4 | chr5 | TogoVar |