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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP27_chr17_45388908_45437870 | 45414537 | AAGCAATC others(6): Show |
A | intron_variant | MODIFIER | NA18992.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0288 | 1 | 346 | 0.0029 | -13 | c.658 others(30): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45432378 | TGGGGAAG others(6): Show |
T | intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0168 | 1 | 346 | 0.0029 | -13 | c.-28 others(28): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841157 | TTCTCTCT others(6): Show |
T | intron_variant | MODIFIER | HG02922.hp1 HG03579.hp2 |
a0001a0002 | a0001c0003a0002c0017 | a0001c0003t0003a0002c0017t0002 | a0001c0003t0003g0119 a0002c0017t0002g0086 |
2 | 225 | 0.0089 | -13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841197 | CTCTCTCC others(6): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG01346.hp2 HG01943.hp2 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0003a0002c0002a0003c0004others(1): Show | a0001c0003t0003a0002c0002t0002a0003c0004t0001others(1): Show | a0001c0003t0003g0013 a0001c0003t0003g0202 a0002c0002t0002g0083 others(5): Show |
8 | 244 | 0.0328 | -13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064842 | AAAGAAAG others(6): Show |
A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(10): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0004 | a0002c0002t0001g0262 a0002c0002t0001g0265 a0002c0002t0001g0270 others(10): Show |
13 | 388 | 0.0335 | -13 | c.97+ others(28): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161066644 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 67 | 0.0149 | -13 | c.97+ others(28): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161073084 | AGCAGAGA others(6): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG01071.hp2 others(25): Show |
a0001a0002a0007 | a0001c0001a0001c0014a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0095 others(24): Show |
28 | 388 | 0.0722 | -13 | c.-34 others(24): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3194 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119303788 | TGTTGTTG others(6): Show |
T | intron_variant | MODIFIER | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0011a0001c0001t0017a0001c0001t0045others(4): Show | a0001c0001t0011g0299 a0001c0001t0011g0300 a0001c0001t0017g0176 others(7): Show |
10 | 215 | 0.0465 | -13 | c.100 others(30): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119350784 | AGCTGGGG others(6): Show |
A | intron_variant | MODIFIER | NA19060.hp1 | a0001 | a0001c0001 | a0001c0001t0045 | a0001c0001t0045g0306 | 1 | 308 | 0.0032 | -13 | c.101 others(32): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129002957 | CGCCACTA others(6): Show |
C | intron_variant | MODIFIER | HG01123.hp1 HG06807.hp1 |
a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0188 a0001c0003t0005g0189 |
2 | 396 | 0.0051 | -13 | c.104 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129038810 | CCTGGAGT others(6): Show |
C | intron_variant | MODIFIER | NA18955.hp2 NA19002.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0183 a0001c0001t0004g0184 |
2 | 396 | 0.0051 | -13 | c.104 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129051953 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0271 | 1 | 72 | 0.0139 | -13 | c.963 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTTT others(6): Show |
C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0005others(9): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(9): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(30): Show |
120 | 201 | 0.5970 | -13 | c.-16 others(24): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46862908 | ATTACGAT others(6): Show |
A | intron_variant | MODIFIER | NA19062.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264 | 1 | 296 | 0.0034 | -13 | c.-18 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0012 | a0001c0001t0007a0004c0012t0007 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | 63 | 0.0794 | -13 | c.382 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG02071.hp2 NA18943.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0041 | a0001c0001t0002g0042 a0001c0001t0041g0043 |
2 | 27 | 0.0741 | -13 | c.*55 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 47007643 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0024a0001c0001t0036 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | 89 | 0.0449 | -13 | c.*69 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2567 | chr19 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100699506 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 159 | 0.0063 | -13 | c.154 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG03834.hp2 | a0005 | a0005c0016 | a0005c0016t0012 | a0005c0016t0012g0120 | 1 | 10 | 0.1000 | -13 | c.155 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921237 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG00642.hp1 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0108 | 1 | 268 | 0.0037 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG03669.hp1 NA20752.hp1 |
a0002 | a0002c0002 | a0002c0002t0004a0002c0002t0006 | a0002c0002t0004g0113 a0002c0002t0006g0057 |
2 | 267 | 0.0075 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(6): Show |
A | intron_variant | MODIFIER | HG01358.hp2 HG02922.hp1 HG02976.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0020 | a0002c0002t0002g0245 a0002c0002t0002g0246 a0002c0002t0020g0106 |
3 | 276 | 0.0109 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802946 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0062 | 1 | 222 | 0.0045 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802948 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG02258.hp2 HG02886.hp2 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014 | a0001c0001t0003g0028 a0001c0001t0003g0060 a0001c0001t0014g0178 |
3 | 214 | 0.0140 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802950 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0029 | 1 | 215 | 0.0047 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802952 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA19007.hp2 NA19054.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0061 a0001c0002t0003g0064 |
2 | 225 | 0.0089 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802954 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG02559.hp2 HG02630.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0033 a0001c0003t0001g0031 |
2 | 226 | 0.0088 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802956 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0010 | 1 | 225 | 0.0044 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802957 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | NA18947.hp2 NA18963.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0012 a0001c0001t0004g0014 |
2 | 227 | 0.0088 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12860085 | AAAGGCAT others(6): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0127 others(35): Show |
38 | 228 | 0.1667 | -13 | c.54- others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0005 | a0001c0005t0007 | a0001c0005t0007g0039 | 1 | 65 | 0.0154 | -13 | c.113 others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12964466 | TGGAGAAG others(6): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(18): Show |
21 | 228 | 0.0921 | -13 | c.152 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12967249 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(19): Show |
22 | 104 | 0.2115 | -13 | c.152 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12975795 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 | 1 | 79 | 0.0127 | -13 | c.176 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02602.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0017 | a0001c0001t0001a0001c0001t0003a0004c0017t0003 | a0001c0001t0001g0017 a0001c0001t0001g0160 a0001c0001t0003g0172 others(1): Show |
4 | 139 | 0.0288 | -13 | c.231 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991856 | CTTACTTA others(6): Show |
C | downstream_gene_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 228 | 0.0044 | -13 | c.*16 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 214 | chr17 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02809.hp1 | a0010 | a0010c0017 | a0010c0017t0016 | a0010c0017t0016g0005 | 1 | 23 | 0.0435 | -13 | c.418 others(30): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11163599 | ACACTAAA others(6): Show |
A | intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 144 | 0.0069 | -13 | c.180 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 9/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174612 | CTTTCTCT others(6): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0013a0001c0003t0001 | a0001c0001t0013g0050 a0001c0003t0001g0125 |
2 | 142 | 0.0141 | -13 | c.162 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44809069 | CCTCAGCC others(6): Show |
C | intron_variant | MODIFIER | HG02165.hp2 HG02965.hp1 HG03098.hp1 |
a0001a0002a0008 | a0001c0008a0002c0046a0008c0030 | a0001c0008t0001a0002c0046t0007a0008c0030t0001 | a0001c0008t0001g0057 a0002c0046t0007g0231 a0008c0030t0001g0105 |
3 | 388 | 0.0077 | -13 | c.299 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG06807.hp2 NA18906.hp1 |
a0001 | a0001c0001a0001c0024 | a0001c0001t0003a0001c0024t0003 | a0001c0001t0003g0063 a0001c0024t0003g0064 |
2 | 60 | 0.0333 | -13 | c.877 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02129.hp1 HG03704.hp1 HG03831.hp1 others(4): Show |
a0002 | a0002c0003a0002c0006a0002c0016others(1): Show | a0002c0003t0004a0002c0006t0004a0002c0016t0004others(1): Show | a0002c0003t0004g0055 a0002c0003t0004g0180 a0002c0003t0004g0351 others(4): Show |
7 | 31 | 0.2258 | -13 | c.878 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858692 | AGGCTATG others(6): Show |
A | intron_variant | MODIFIER | NA18961.hp2 | a0003 | a0003c0002 | a0003c0002t0002 | a0003c0002t0002g0026 | 1 | 388 | 0.0026 | -13 | c.878 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17693079 | CCTTGTTT others(6): Show |
C | intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0018 | a0002c0018t0002 | a0002c0018t0002g0155 | 1 | 166 | 0.0060 | -13 | c.318 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1825177 | CCTGTCCC others(6): Show |
C | intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0009 | a0001c0009t0004 | a0001c0009t0004g0303 | 1 | 362 | 0.0028 | -13 | c.-48 others(30): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156962878 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02132.hp1 HG02135.hp1 |
a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0249 a0003c0003t0003g0250 |
2 | 155 | 0.0129 | -13 | c.114 others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157035818 | AGGAATAT others(6): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0002c0004others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(21): Show | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(163): Show |
170 | 360 | 0.4722 | -13 | c.32+ others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120344265 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02922.hp2 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0280 a0001c0001t0018g0281 |
2 | 65 | 0.0308 | -13 | c.32+ others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351438 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0002 | a0001c0002t0034 | a0001c0002t0034g0013 | 1 | 306 | 0.0033 | -13 | c.32+ others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0133 | 1 | 72 | 0.0139 | -13 | c.33- others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |