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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARGFX_chr3_121562949_121595622 | 121577259 | A | ATATT | intron_variant | MODIFIER | HG01243.hp1 HG02083.hp1 HG02148.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0236 a0001c0001t0002g0074 a0001c0001t0003g0111 others(3): Show |
6 | 193 | 0.0311 | 4 | c.220 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580567 | A | AGTGT | intron_variant | MODIFIER | HG01255.hp1 HG01261.hp2 HG02074.hp1 others(7): Show |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0007 | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(5): Show | a0001c0001t0002g0149 a0001c0001t0004g0286 a0001c0001t0004g0304 others(7): Show |
10 | 242 | 0.0413 | 4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580594 | G | GTGTA | intron_variant | MODIFIER | HG01169.hp1 HG02027.hp1 HG02818.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0001a0002c0002t0011others(1): Show | a0001c0001t0004g0312 a0002c0002t0001g0187 a0002c0002t0001g0191 others(4): Show |
7 | 299 | 0.0234 | 4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580604 | A | ATTTT | intron_variant | MODIFIER | HG02071.hp1 NA18978.hp1 NA19057.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0054 a0001c0001t0002g0084 a0001c0001t0002g0208 |
3 | 403 | 0.0074 | 4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580606 | A | ATTTT | intron_variant | MODIFIER | HG00438.hp1 HG00741.hp1 HG01256.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0034 | a0001c0001t0002g0055 a0001c0001t0002g0140 a0001c0001t0003g0046 others(9): Show |
12 | 254 | 0.0472 | 4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121584204 | G | GAGGA | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0026 a0001c0001t0001g0224 a0001c0001t0001g0270 others(53): Show |
60 | 166 | 0.3614 | 4 | c.221 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121584207 | G | GAAGC | intron_variant | MODIFIER | HG01192.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
a0002a0009 | a0002c0002a0009c0008 | a0002c0002t0001a0002c0002t0006a0009c0008t0001 | a0002c0002t0001g0020 a0002c0002t0001g0159 a0002c0002t0001g0187 others(3): Show |
6 | 407 | 0.0147 | 4 | c.221 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106540792 | C | CTAGA | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02886.hp2 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042 a0001c0001t0001g0137 |
3 | 20 | 0.1500 | 4 | c.*32 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 880 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106540792 | C | CTGGA | downstream_gene_variant | MODIFIER | HG02080.hp1 HG02630.hp2 HG02970.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0012 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0002g0031 others(1): Show |
10 | 27 | 0.3704 | 4 | c.*32 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 880 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106544394 | T | TTAAG | intron_variant | MODIFIER | HG01243.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0019 | a0001c0001t0008g0069 a0001c0001t0008g0070 a0001c0001t0008g0071 others(2): Show |
5 | 374 | 0.0134 | 4 | c.658 others(19): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 3/3 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106561424 | T | TACAC | intron_variant | MODIFIER | HG01243.hp2 HG02630.hp1 HG02970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0011 | a0001c0001t0001g0202 a0001c0001t0008g0069 a0001c0001t0008g0070 others(2): Show |
5 | 72 | 0.0694 | 4 | c.348 others(21): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106567322 | C | CTTAT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(157): Show |
289 | 374 | 0.7727 | 4 | c.347 others(19): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147736120 | C | CTGTG | intron_variant | MODIFIER | HG00558.hp2 HG01261.hp1 HG02055.hp1 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(19): Show |
22 | 54 | 0.4074 | 4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147736150 | G | GTGTC | intron_variant | MODIFIER | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0002t0001a0001c0005t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(3): Show |
6 | 102 | 0.0588 | 4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147741786 | A | ACACG | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0097 a0002c0003t0001g0096 |
2 | 96 | 0.0208 | 4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147741792 | G | GCGCA | intron_variant | MODIFIER | HG03098.hp1 HG03471.hp1 |
a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0059 a0001c0008t0001g0060 |
2 | 85 | 0.0235 | 4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147741798 | A | ACACG | intron_variant | MODIFIER | HG02976.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | 103 | 0.0194 | 4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147745483 | G | GTGTT | intron_variant | MODIFIER | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0001 | a0001c0001t0001g0077 a0001c0008t0001g0059 a0001c0008t0001g0060 |
3 | 104 | 0.0288 | 4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147762499 | C | CTTAT | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | 21 | 0.7143 | 4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147765323 | G | GGTGT | intron_variant | MODIFIER | HG02056.hp1 HG02056.hp2 HG03710.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0093 others(1): Show |
4 | 99 | 0.0404 | 4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147765337 | T | TGTGG | intron_variant | MODIFIER | HG01243.hp1 HG02738.hp1 HG02738.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0002t0001a0001c0008t0001 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0053 others(10): Show |
13 | 52 | 0.2500 | 4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147766799 | C | CATAT | intron_variant | MODIFIER | HG02818.hp1 HG02886.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0080 a0001c0001t0003g0087 |
2 | 45 | 0.0444 | 4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783764 | T | TTGTG | intron_variant | MODIFIER | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0036 others(18): Show |
21 | 104 | 0.2019 | 4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784719 | A | AAAAT | intron_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0001a0001c0005t0001a0002c0003t0001 | a0001c0001t0001g0097 a0001c0005t0001g0098 a0002c0003t0001g0096 |
3 | 104 | 0.0288 | 4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147785083 | T | TAAAA | intron_variant | MODIFIER | HG01071.hp2 HG01169.hp2 HG02056.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0027 others(3): Show |
6 | 43 | 0.1395 | 4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147830512 | C | CTTTT | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0017 others(27): Show |
30 | 48 | 0.6250 | 4 | c.312 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839092 | G | GTATC | intron_variant | MODIFIER | HG02886.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0002t0001g0032 others(2): Show |
5 | 61 | 0.0820 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839114 | A | ATCTG | intron_variant | MODIFIER | HG01884.hp2 HG03098.hp2 NA18906.hp2 |
a0001 | a0001c0002a0001c0004a0001c0006 | a0001c0002t0001a0001c0004t0001a0001c0006t0001 | a0001c0002t0001g0090 a0001c0004t0001g0102 a0001c0006t0001g0071 |
3 | 104 | 0.0288 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839138 | A | ATCTG | intron_variant | MODIFIER | HG02109.hp2 NA18906.hp1 NA19064.hp2 |
a0001a0004 | a0001c0001a0001c0002a0004c0010 | a0001c0001t0001a0001c0002t0001a0004c0010t0001 | a0001c0001t0001g0046 a0001c0002t0001g0028 a0004c0010t0001g0048 |
3 | 89 | 0.0337 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839142 | A | ATCTG | intron_variant | MODIFIER | HG00558.hp2 HG01169.hp2 HG02080.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0008t0001others(2): Show | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0029 others(11): Show |
14 | 66 | 0.2121 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147869996 | G | GTTTT | intron_variant | MODIFIER | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0083 others(7): Show |
10 | 71 | 0.1408 | 4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | T | TTTTG | intron_variant | MODIFIER | HG02615.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0080 others(1): Show |
4 | 67 | 0.0597 | 4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | C | CTGTG | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0051 others(10): Show |
13 | 25 | 0.5200 | 4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | A | AACAC | intron_variant | MODIFIER | HG02896.hp2 HG03209.hp2 NA19043.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0062 others(1): Show |
4 | 23 | 0.1739 | 4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911992 | C | CATAT | intron_variant | MODIFIER | HG02080.hp2 HG02895.hp1 HG03098.hp2 others(5): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0001a0001c0004t0001a0001c0005t0001 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0035 others(5): Show |
8 | 97 | 0.0825 | 4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147917839 | G | GTCTT | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(40): Show |
43 | 104 | 0.4135 | 4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147969345 | T | TTTTG | intron_variant | MODIFIER | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0049 others(5): Show |
8 | 75 | 0.1067 | 4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147982546 | C | CTTTT | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0021 others(15): Show |
18 | 62 | 0.2903 | 4 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATA | intron_variant | MODIFIER | HG02056.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0006t0001 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0044 others(9): Show |
12 | 65 | 0.1846 | 4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148036066 | C | CTGTG | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01071.hp1 others(30): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0005others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0024 others(30): Show |
33 | 73 | 0.4521 | 4 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATAT | intron_variant | MODIFIER | HG02145.hp1 HG02896.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0097 others(1): Show |
4 | 13 | 0.3077 | 4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043746 | G | GTATA | intron_variant | MODIFIER | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0011others(2): Show | a0001c0001t0001a0001c0006t0001a0001c0011t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0025 others(25): Show |
28 | 102 | 0.2745 | 4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148049795 | G | GTTTT | intron_variant | MODIFIER | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0036 a0001c0002t0001g0018 a0001c0002t0001g0020 others(6): Show |
9 | 103 | 0.0874 | 4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148059973 | T | TGAGA | intron_variant | MODIFIER | HG02080.hp1 NA18983.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0056 a0001c0002t0001g0012 |
2 | 69 | 0.0290 | 4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAAA | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(31): Show |
34 | 64 | 0.5313 | 4 | c.227 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32610719 | C | CAAAT | upstream_gene_variant | MODIFIER | HG00738.hp2 HG01099.hp1 HG01433.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0014 a0001c0001t0001g0104 a0001c0001t0002g0003 others(5): Show |
10 | 97 | 0.1031 | 4 | c.-54 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4784 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32613813 | C | CAAAA | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(107): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(58): Show |
110 | 243 | 0.4527 | 4 | c.-23 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1690 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGT | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(52): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0015others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(29): Show |
55 | 175 | 0.3143 | 4 | c.110 others(21): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30621327 | C | CAAAT | upstream_gene_variant | MODIFIER | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
4 | 246 | 0.0163 | 4 | c.-54 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4800 | chr15 | TogoVar | |||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | A | AGTGT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(31): Show |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0001a0001c0001t0005a0005c0004t0001 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(16): Show |
34 | 100 | 0.3400 | 4 | c.*12 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar |