regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(21): Show |
intron_variant | MODIFIER | HG01943.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0009 | 1 | 248 | 0.0040 | 28 | c.122 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(21): Show |
intron_variant | MODIFIER | HG02818.hp2 HG04115.hp2 NA18986.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0018a0003c0004t0001 | a0001c0001t0001g0113a0001c0001t0018g0111a0003c0004t0001g0112 | 3 | 248 | 0.0121 | 28 | c.122 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730221 | G | GTATATAT others(21): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0010 | a0010c0014 | a0010c0014t0001 | a0010c0014t0001g0142 | 1 | 248 | 0.0040 | 28 | c.122 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730236 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0103 | 1 | 248 | 0.0040 | 28 | c.122 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(21): Show |
upstream_gene_variant | MODIFIER | HG01099.hp1 HG01106.hp2 HG02257.hp1 others(19): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0001c0005others(4): Show | a0001c0001t0006a0001c0001t0020a0001c0001t0029others(9): Show | a0001c0001t0006g0065a0001c0001t0006g0066a0001c0001t0020g0010others(19): Show | 22 | 310 | 0.0710 | 28 | c.-12 others(39): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(21): Show |
intron_variant | MODIFIER | HG00408.hp1 HG03130.hp2 HG04184.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0001t0024a0001c0002t0001 | a0001c0001t0020g0056a0001c0001t0024g0221a0001c0002t0001g0171 | 3 | 310 | 0.0097 | 28 | c.683 others(45): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | HG03669.hp1 HG03831.hp2 NA18940.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0033 | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(1): Show | a0001c0001t0002g0100a0001c0001t0002g0103a0001c0001t0002g0132others(11): Show | 14 | 398 | 0.0352 | 28 | c.226 others(47): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193575 | T | TAATATAT others(21): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0188 | 1 | 398 | 0.0025 | 28 | c.-13 others(39): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1251 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46879587 | A | AAAATAAA others(21): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0200 | 1 | 298 | 0.0034 | 28 | c.-18 others(49): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(21): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0250 | 1 | 286 | 0.0035 | 28 | c.313 others(47): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(21): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0011 | a0002c0011t0017 | a0002c0011t0017g0205 | 1 | 286 | 0.0035 | 28 | c.313 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903114 | T | TGCGCGCG others(21): Show |
intron_variant | MODIFIER | HG01891.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
a0002 | a0002c0005 | a0002c0005t0010a0002c0005t0016 | a0002c0005t0010g0044a0002c0005t0010g0056a0002c0005t0010g0255others(3): Show | 6 | 286 | 0.0210 | 28 | c.385 others(47): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(21): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0004 | a0004c0013 | a0004c0013t0038 | a0004c0013t0038g0236 | 1 | 286 | 0.0035 | 28 | c.385 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(21): Show |
intron_variant | MODIFIER | HG02615.hp1 NA19012.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0009 | a0001c0001t0001g0153a0002c0002t0009g0042 | 2 | 286 | 0.0070 | 28 | c.245 others(47): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(21): Show |
intron_variant | MODIFIER | HG02080.hp2 HG04115.hp1 NA18943.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0030a0001c0003t0003 | a0001c0001t0030g0183a0001c0003t0003g0156a0001c0003t0003g0258others(2): Show | 5 | 286 | 0.0175 | 28 | c.245 others(47): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(21): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0178 | 1 | 230 | 0.0044 | 28 | c.53+ others(45): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(21): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02074.hp1 HG02080.hp1 others(6): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0148others(6): Show | 9 | 230 | 0.0391 | 28 | c.862 others(43): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01496.hp1 HG01934.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(3): Show | a0001c0001t0001g0152a0001c0001t0003g0028a0001c0001t0008g0037others(4): Show | 7 | 230 | 0.0304 | 28 | c.176 others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TTAAAAAA others(21): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0119 | 1 | 230 | 0.0044 | 28 | c.176 others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174592 | T | TTTTCTTT others(21): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 144 | 0.0069 | 28 | c.162 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11190473 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 28 | c.821 others(45): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(21): Show |
intron_variant | MODIFIER | HG02647.hp1 NA18906.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0003 | a0001c0001t0002g0129a0002c0002t0003g0010 | 2 | 144 | 0.0139 | 28 | c.589 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11453193 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0128 | 1 | 144 | 0.0069 | 28 | c.589 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 144 | 0.0069 | 28 | c.588 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11567566 | A | AAAAAAAA others(21): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0012 | 1 | 144 | 0.0069 | 28 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAAAGAAA others(21): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 144 | 0.0069 | 28 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 286073 | G | GTCCCTCC others(21): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 94 | 442 | 0.2127 | 28 | c.*32 others(39): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3064 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 286087 | C | CAAACCCC others(21): Show |
downstream_gene_variant | MODIFIER | NA19075.hp2 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0012 | 1 | 442 | 0.0023 | 28 | c.*32 others(39): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3078 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17683200 | G | GGGGTGCT others(21): Show |
intron_variant | MODIFIER | HG02976.hp1 NA18747.hp1 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0071a0001c0001t0001g0154a0001c0001t0003g0131others(1): Show | 4 | 168 | 0.0238 | 28 | c.301 others(47): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17683312 | C | CGGGTGCT others(21): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 168 | 0.0060 | 28 | c.301 others(47): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888189 | T | TTGCGAGG others(21): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0141 | a0001c0141t0007 | a0001c0141t0007g0099 | 1 | 363 | 0.0028 | 28 | c.118 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889220 | G | GGTGAGGG others(21): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(144): Show |
a0001a0003a0004others(10): Show | a0001c0001a0001c0002a0001c0003others(71): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(104): Show | a0001c0001t0002g0053a0001c0001t0002g0066a0001c0001t0004g0354others(144): Show | 147 | 363 | 0.4050 | 28 | c.118 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1951918 | G | GCCACCGT others(21): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0001c0003others(122): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(181): Show | a0001c0001t0002g0224a0001c0001t0002g0239a0001c0001t0004g0141others(259): Show | 263 | 363 | 0.7245 | 28 | c.339 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1951930 | C | CGGGGTCT others(21): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0008others(36): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(53): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(80): Show | 83 | 363 | 0.2287 | 28 | c.339 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATATA others(21): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0316 | 1 | 362 | 0.0028 | 28 | c.463 others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AATATATA others(21): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0002 | a0002c0004 | a0002c0004t0008 | a0002c0004t0008g0194 | 1 | 362 | 0.0028 | 28 | c.463 others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(21): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0004a0003c0003 | a0001c0001t0004a0002c0004t0008a0002c0004t0013others(2): Show | a0001c0001t0004g0171a0002c0004t0008g0198a0002c0004t0013g0185others(6): Show | 9 | 362 | 0.0249 | 28 | c.33- others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACAC others(21): Show |
intron_variant | MODIFIER | NA18951.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0110 | 1 | 362 | 0.0028 | 28 | c.33- others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347179 | C | CCTTTCTT others(21): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0275 | 1 | 308 | 0.0033 | 28 | c.32+ others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(21): Show |
intron_variant | MODIFIER | HG01433.hp2 HG04204.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0210a0001c0001t0011g0286 | 2 | 308 | 0.0065 | 28 | c.32+ others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(21): Show |
intron_variant | MODIFIER | HG01934.hp1 NA18973.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0213a0001c0001t0011g0199 | 2 | 308 | 0.0065 | 28 | c.32+ others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364365 | A | AAAGGAAG others(21): Show |
intron_variant | MODIFIER | NA19067.hp1 | a0008 | a0008c0010 | a0008c0010t0001 | a0008c0010t0001g0285 | 1 | 298 | 0.0034 | 28 | c.15+ others(43): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(21): Show |
intron_variant | MODIFIER | HG00609.hp2 NA18939.hp2 NA19004.hp1 |
a0002a0029 | a0002c0004a0002c0006a0029c0035 | a0002c0004t0002a0002c0006t0003a0029c0035t0001 | a0002c0004t0002g0231a0002c0006t0003g0232a0029c0035t0001g0233 | 3 | 298 | 0.0101 | 28 | c.15+ others(43): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7368019 | G | GAGGGCGG others(21): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0016 | a0001c0016t0014 | a0001c0016t0014g0268 | 1 | 298 | 0.0034 | 28 | c.16- others(43): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385870 | T | TCTCTCTC others(21): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0009 | a0009c0012 | a0009c0012t0010 | a0009c0012t0010g0071 | 1 | 298 | 0.0034 | 28 | c.967 others(45): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7431529 | A | AAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG03834.hp1 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0063 | 1 | 298 | 0.0034 | 28 | c.968 others(45): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | A | AGTGTGTG others(21): Show |
downstream_gene_variant | MODIFIER | HG02451.hp1 HG02809.hp2 HG03139.hp1 others(1): Show |
a0001a0011a0012 | a0001c0001a0011c0025a0012c0028 | a0001c0001t0005a0011c0025t0005a0012c0028t0018 | a0001c0001t0005g0291a0001c0001t0005g0292a0011c0025t0005g0013others(1): Show | 4 | 298 | 0.0134 | 28 | c.*44 others(39): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806422 | A | ACTATATA others(21): Show |
intron_variant | MODIFIER | HG00733.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
a0001a0003a0004others(2): Show | a0001c0077a0003c0005a0004c0017others(2): Show | a0001c0077t0002a0003c0005t0001a0004c0017t0005others(2): Show | a0001c0077t0002g0028a0003c0005t0001g0043a0004c0017t0005g0078others(2): Show | 5 | 188 | 0.0266 | 28 | c.102 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598761 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0004 | a0004c0010 | a0004c0010t0014 | a0004c0010t0014g0326 | 1 | 394 | 0.0025 | 28 | c.186 others(43): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598761 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG01496.hp1 | a0008 | a0008c0009 | a0008c0009t0003 | a0008c0009t0003g0322 | 1 | 394 | 0.0025 | 28 | c.186 others(43): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |