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 | 45407516 | T | TTTTC | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
a0004 | a0004c0004 | a0004c0004t0004a0004c0004t0014 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(8): Show |
19 | 346 | 0.0549 | 4 | c.658 others(21): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730221 | G | GTATA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0012others(5): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(8): Show | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0182 others(66): Show |
69 | 97 | 0.7113 | 4 | c.122 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6739645 | T | TTCTC | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0010others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | a0001c0001t0001g0080 a0001c0001t0001g0175 a0001c0001t0001g0180 others(87): Show |
90 | 215 | 0.4186 | 4 | c.122 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6763081 | G | GTTGT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(6): Show | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0019 others(20): Show |
23 | 245 | 0.0939 | 4 | c.122 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6777754 | A | ATGAG | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(6): Show | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0071 others(39): Show |
42 | 224 | 0.1875 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | A | ATTTT | intron_variant | MODIFIER | HG01993.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0003others(3): Show | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0121 others(14): Show |
17 | 29 | 0.5862 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6796821 | T | TACAC | intron_variant | MODIFIER | HG01346.hp1 HG02922.hp2 HG02976.hp2 |
a0001a0002a0006 | a0001c0003a0002c0002a0006c0008 | a0001c0003t0003a0002c0002t0002a0006c0008t0002 | a0001c0003t0003g0084 a0002c0002t0002g0148 a0006c0008t0002g0146 |
3 | 207 | 0.0145 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841159 | C | CACTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0017a0001c0003t0003others(3): Show | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0072 others(14): Show |
17 | 246 | 0.0691 | 4 | c.543 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6847628 | G | GGTGT | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0020others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0003t0001others(11): Show | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0124 others(47): Show |
50 | 234 | 0.2137 | 4 | c.544 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6847630 | G | GGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0003a0001c0015others(5): Show | a0001c0001t0001a0001c0001t0016a0001c0001t0017others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0034 others(52): Show |
55 | 108 | 0.5093 | 4 | c.544 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6892159 | T | TTTGA | intron_variant | MODIFIER | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
a0003 | a0003c0013a0003c0023 | a0003c0013t0011a0003c0023t0001 | a0003c0013t0011g0062 a0003c0013t0011g0063 a0003c0023t0001g0120 |
3 | 246 | 0.0122 | 4 | c.184 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94166813 | G | GCACA | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
a0001a0004 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | a0001c0001t0001g0233 a0001c0001t0003g0006 a0001c0001t0003g0009 others(57): Show |
66 | 290 | 0.2276 | 4 | c.*70 others(15): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2091 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94172612 | G | GATAT | 3_prime_UTR_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
a0001 | a0001c0001a0001c0002a0001c0011others(1): Show | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(9): Show | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(65): Show |
76 | 95 | 0.8000 | 4 | c.*12 others(15): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94207001 | T | TTTTA | intron_variant | MODIFIER | HG02145.hp1 HG02148.hp2 HG02280.hp2 others(14): Show |
a0001a0005 | a0001c0001a0005c0014 | a0001c0001t0004a0001c0001t0011a0001c0001t0032others(2): Show | a0001c0001t0004g0022 a0001c0001t0004g0032 a0001c0001t0004g0053 others(13): Show |
17 | 321 | 0.0530 | 4 | c.511 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94211287 | C | CAAAA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
a0001 | a0001c0001a0001c0002a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(17): Show | a0001c0001t0001g0233 a0001c0001t0002g0003 a0001c0001t0002g0011 others(69): Show |
83 | 143 | 0.5804 | 4 | c.341 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTC | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(16): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(1): Show | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0103 others(14): Show |
19 | 46 | 0.4130 | 4 | c.537 others(17): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055866 | A | AAAAT | intron_variant | MODIFIER | HG00741.hp2 HG01081.hp1 HG02717.hp2 others(8): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0001 | a0001c0001t0001g0051 a0001c0001t0001g0103 a0001c0001t0001g0104 others(8): Show |
11 | 388 | 0.0284 | 4 | c.345 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055911 | A | AAAAT | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02135.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0164 others(6): Show |
9 | 384 | 0.0234 | 4 | c.345 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064777 | G | GAGAA | intron_variant | MODIFIER | HG02735.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0152 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | 375 | 0.0107 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | A | AAAAG | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG00738.hp2 others(16): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0007t0001others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(14): Show |
19 | 325 | 0.0585 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161065868 | C | CTTAT | intron_variant | MODIFIER | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0001a0002c0002t0001a0002c0003t0001others(5): Show | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(37): Show |
43 | 314 | 0.1369 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161066644 | C | CAAAA | intron_variant | MODIFIER | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(34): Show |
38 | 104 | 0.3654 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161067570 | A | AAAAG | intron_variant | MODIFIER | HG00639.hp1 HG01169.hp2 HG02976.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0002c0002t0001a0002c0003t0001 | a0001c0001t0001g0149 a0002c0002t0001g0334 a0002c0003t0001g0147 others(3): Show |
6 | 251 | 0.0239 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACAC | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(37): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(18): Show | a0001c0001t0007g0203 a0001c0001t0008g0194 a0001c0001t0008g0200 others(36): Show |
40 | 156 | 0.2564 | 4 | c.100 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119300842 | A | AAAAG | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0006g0093 a0001c0001t0007g0295 a0001c0001t0008g0002 others(11): Show |
15 | 192 | 0.0781 | 4 | c.100 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCACA | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(14): Show | a0001c0001t0005g0097 a0001c0001t0005g0112 a0001c0001t0006g0028 others(24): Show |
27 | 172 | 0.1570 | 4 | c.101 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCTCA | intron_variant | MODIFIER | HG01243.hp1 HG03669.hp2 NA18522.hp1 |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0006a0001c0004t0010a0001c0005t0001 | a0001c0001t0006g0103 a0001c0004t0010g0177 a0001c0005t0001g0191 |
3 | 148 | 0.0203 | 4 | c.101 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119354476 | T | TTGTG | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(10): Show | a0001c0001t0005g0169 a0001c0001t0005g0170 a0001c0001t0005g0173 others(14): Show |
17 | 56 | 0.3036 | 4 | c.101 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119361374 | C | CTTTT | intron_variant | MODIFIER | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(5): Show | a0001c0001t0005g0169 a0001c0001t0005g0170 a0001c0001t0005g0173 others(8): Show |
11 | 245 | 0.0449 | 4 | c.101 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119407355 | A | AAAAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
a0001a0003a0004others(9): Show | a0001c0001a0001c0002a0001c0004others(14): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(68): Show | a0001c0001t0005g0023 a0001c0001t0005g0059 a0001c0001t0005g0084 others(252): Show |
258 | 307 | 0.8404 | 4 | c.164 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128982474 | C | CGTGT | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
a0001a0005a0014 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
103 | 229 | 0.4498 | 4 | c.152 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985854 | G | GTATA | intron_variant | MODIFIER | HG03239.hp1 NA18965.hp2 NA19065.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0352 others(1): Show |
4 | 365 | 0.0110 | 4 | c.152 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985856 | G | GTATA | intron_variant | MODIFIER | HG01361.hp2 HG03710.hp1 NA18966.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0023 a0001c0002t0001g0295 a0001c0002t0002g0104 |
3 | 282 | 0.0106 | 4 | c.152 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTATA | intron_variant | MODIFIER | HG01070.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
a0001a0015 | a0001c0002a0001c0003a0015c0017 | a0001c0002t0001a0001c0002t0005a0001c0003t0001others(2): Show | a0001c0002t0001g0230 a0001c0002t0001g0244 a0001c0002t0005g0259 others(6): Show |
9 | 148 | 0.0608 | 4 | c.152 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTA | intron_variant | MODIFIER | HG02135.hp1 HG02809.hp1 NA18956.hp2 others(5): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0003a0001c0003t0012 | a0001c0002t0001g0266 a0001c0002t0001g0304 a0001c0003t0003g0337 others(5): Show |
8 | 147 | 0.0544 | 4 | c.152 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128989515 | T | TACAC | intron_variant | MODIFIER | HG02015.hp1 HG03927.hp1 HG03942.hp1 |
a0001 | a0001c0001a0001c0014 | a0001c0001t0002a0001c0001t0004a0001c0014t0004 | a0001c0001t0002g0169 a0001c0001t0004g0174 a0001c0014t0004g0177 |
3 | 374 | 0.0080 | 4 | c.119 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCACA | intron_variant | MODIFIER | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
a0001a0002a0009others(4): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(14): Show | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0048 others(50): Show |
53 | 183 | 0.2896 | 4 | c.119 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129002805 | A | ATTTT | intron_variant | MODIFIER | HG01261.hp2 HG01346.hp1 HG02074.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0032a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0032t0001others(3): Show | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
14 | 178 | 0.0787 | 4 | c.104 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129029801 | C | CAAAA | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(62): Show |
65 | 120 | 0.5417 | 4 | c.104 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129058188 | T | TACAC | intron_variant | MODIFIER | HG02040.hp1 HG02559.hp1 HG02602.hp2 others(3): Show |
a0001a0005 | a0001c0003a0001c0010a0001c0015others(1): Show | a0001c0003t0003a0001c0010t0008a0001c0015t0036others(1): Show | a0001c0003t0003g0318 a0001c0010t0008g0193 a0001c0010t0008g0194 others(3): Show |
6 | 214 | 0.0280 | 4 | c.963 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129060336 | C | CATAG | intron_variant | MODIFIER | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(57): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(18): Show | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0028 others(57): Show |
60 | 236 | 0.2542 | 4 | c.963 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129079930 | C | CCATG | intron_variant | MODIFIER | HG01891.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
a0003 | a0003c0006a0003c0035 | a0003c0006t0002a0003c0006t0004a0003c0035t0004 | a0003c0006t0002g0091 a0003c0006t0002g0092 a0003c0006t0002g0093 others(2): Show |
5 | 396 | 0.0126 | 4 | c.532 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129191670 | G | GCACA | intron_variant | MODIFIER | HG02965.hp2 HG03139.hp2 HG03239.hp2 others(2): Show |
a0001a0002 | a0001c0003a0002c0007 | a0001c0003t0003a0002c0007t0009 | a0001c0003t0003g0381 a0001c0003t0003g0382 a0001c0003t0003g0383 others(2): Show |
5 | 166 | 0.0301 | 4 | c.116 others(19): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1/22 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTT | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00673.hp2 HG01257.hp2 others(50): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(7): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(20): Show |
53 | 54 | 0.9815 | 4 | c.-36 others(15): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46857107 | A | ATTTT | upstream_gene_variant | MODIFIER | HG00597.hp1 HG01070.hp1 HG02080.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0008a0001c0001t0016others(3): Show | a0001c0001t0004g0123 a0001c0001t0004g0126 a0001c0001t0008g0088 others(6): Show |
9 | 84 | 0.1071 | 4 | c.-42 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3889 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46860909 | C | CGAGG | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(284): Show |
287 | 293 | 0.9795 | 4 | c.-48 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 87 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46869476 | T | TTGTG | intron_variant | MODIFIER | HG00597.hp1 HG00639.hp1 HG01257.hp1 others(27): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0001t0001g0191 others(27): Show |
30 | 163 | 0.1840 | 4 | c.-18 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46879587 | A | AAAAT | intron_variant | MODIFIER | HG02071.hp1 HG03098.hp1 HG03195.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0032a0001c0002t0047 | a0001c0001t0003g0086 a0001c0002t0032g0211 a0001c0002t0047g0127 |
3 | 91 | 0.0330 | 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 | 46888261 | A | AATAT | intron_variant | MODIFIER | HG01257.hp1 HG01261.hp2 HG02056.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0001g0295 others(9): Show |
12 | 44 | 0.2727 | 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 | 46888333 | T | TACAC | intron_variant | MODIFIER | HG00642.hp1 HG01243.hp2 HG02258.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0023a0001c0002t0005a0001c0002t0032others(2): Show | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0002t0005g0207 others(12): Show |
15 | 136 | 0.1103 | 4 | c.-18 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |