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 | 121577226 | CAT | C | intron_variant | MODIFIER | HG01358.hp2 HG03540.hp1 HG04199.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0007a0001c0001t0029 | a0001c0001t0004g0337 a0001c0001t0007g0020 a0001c0001t0029g0243 |
3 | 410 | 0.0073 | -2 | c.220 others(17): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121578120 | CTT | C | intron_variant | MODIFIER | HG03942.hp2 NA18944.hp2 NA18961.hp2 others(3): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0004c0004t0002 | a0001c0001t0002g0038 a0001c0001t0002g0060 a0001c0001t0002g0108 others(3): Show |
6 | 410 | 0.0146 | -2 | 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 | 121587964 | AAT | A | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(36): Show | a0001c0001t0002g0006 a0001c0001t0002g0029 a0001c0001t0002g0035 others(211): Show |
217 | 410 | 0.5293 | -2 | c.*13 others(13): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 5/5 | 1378 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121594235 | CTG | C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0008 | a0001c0001t0001a0002c0002t0001a0002c0002t0006others(6): Show | a0001c0001t0001g0189 a0002c0002t0001g0002 a0002c0002t0001g0007 others(49): Show |
54 | 410 | 0.1317 | -2 | c.*76 others(13): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3614 | chr3 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106538587 | CAA | C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(245): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
248 | 376 | 0.6596 | -2 | c.*54 others(13): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 3085 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106561424 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(76): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(43): Show |
79 | 376 | 0.2101 | -2 | c.348 others(19): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106563007 | AAC | A | intron_variant | MODIFIER | HG00639.hp1 HG01433.hp1 HG01891.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(1): Show | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0048 others(13): Show |
19 | 376 | 0.0505 | -2 | c.348 others(19): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147741790 | ACG | A | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02165.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0011others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0011t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0088 others(5): Show |
8 | 106 | 0.0755 | -2 | c.154 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147759580 | GCC | G | intron_variant | MODIFIER | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
21 | 106 | 0.1981 | -2 | 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 | 147766838 | ATT | A | intron_variant | MODIFIER | HG02895.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(2): Show | a0001c0001t0001g0006 a0001c0002t0001g0005 a0001c0004t0001g0045 others(3): Show |
6 | 106 | 0.0566 | -2 | 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 | 147783553 | AAC | A | intron_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0001a0001c0005t0001a0002c0003t0001 | a0001c0001t0001g0097 a0001c0005t0001g0098 a0002c0003t0001g0096 |
3 | 106 | 0.0283 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783811 | AAC | A | intron_variant | MODIFIER | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0002t0001g0029 others(1): Show |
4 | 106 | 0.0377 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783843 | AAC | A | intron_variant | MODIFIER | HG00558.hp1 HG01261.hp2 HG01993.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0037 others(4): Show |
7 | 106 | 0.0660 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783875 | AAC | A | intron_variant | MODIFIER | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | 106 | 0.0755 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783907 | AAC | A | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(24): Show |
27 | 106 | 0.2547 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784025 | AAC | A | intron_variant | MODIFIER | HG02738.hp2 HG03492.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072 a0001c0002t0001g0078 |
2 | 106 | 0.0189 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784476 | TTA | T | intron_variant | MODIFIER | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0002t0001g0005 others(1): Show |
4 | 106 | 0.0377 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784533 | CAT | C | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(68): Show |
71 | 106 | 0.6698 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784946 | CAT | C | intron_variant | MODIFIER | HG02896.hp2 HG03471.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0047 a0001c0004t0001g0045 |
2 | 106 | 0.0189 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147791521 | CGT | C | intron_variant | MODIFIER | HG00558.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0001 | a0001c0001t0001g0077 a0001c0008t0001g0060 |
2 | 106 | 0.0189 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147793305 | CAT | C | intron_variant | MODIFIER | HG02896.hp2 HG03471.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0047 a0001c0004t0001g0045 |
2 | 106 | 0.0189 | -2 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147820580 | GTT | G | intron_variant | MODIFIER | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(12): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(2): Show | a0001c0001t0001a0001c0005t0001a0001c0006t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0035 others(12): Show |
15 | 106 | 0.1415 | -2 | c.155 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147821230 | GCA | G | intron_variant | MODIFIER | HG02258.hp1 HG02622.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 a0001c0001t0001g0076 a0001c0001t0001g0093 |
3 | 106 | 0.0283 | -2 | c.155 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147825187 | CCT | C | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
105 | 106 | 0.9906 | -2 | c.312 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147849236 | CTT | C | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(13): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(3): Show | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0038 others(13): Show |
16 | 106 | 0.1509 | -2 | c.384 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147852729 | TTA | T | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(48): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | 106 | 0.4811 | -2 | c.385 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147855190 | CAG | C | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0067 others(4): Show |
7 | 106 | 0.0660 | -2 | c.385 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147855415 | CTA | C | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0063 others(4): Show |
7 | 106 | 0.0660 | -2 | c.385 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147864062 | ATT | A | intron_variant | MODIFIER | HG02572.hp2 HG03471.hp2 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0045 a0001c0004t0001g0105 |
2 | 106 | 0.0189 | -2 | c.487 others(17): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147865589 | CTG | C | intron_variant | MODIFIER | HG02572.hp2 HG03471.hp2 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0045 a0001c0004t0001g0105 |
2 | 106 | 0.0189 | -2 | c.597 others(17): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147867863 | CAA | C | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(32): Show |
35 | 106 | 0.3302 | -2 | c.702 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147867926 | CTT | C | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
66 | 106 | 0.6226 | -2 | c.702 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | TTG | T | intron_variant | MODIFIER | HG01070.hp1 HG02896.hp1 HG04184.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0002g0023 |
3 | 106 | 0.0283 | -2 | c.702 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | CTG | C | intron_variant | MODIFIER | HG01993.hp2 HG02165.hp1 HG02165.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0080 others(2): Show |
5 | 106 | 0.0472 | -2 | c.703 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147872099 | CAA | C | intron_variant | MODIFIER | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0038 others(4): Show |
7 | 106 | 0.0660 | -2 | c.703 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | AAC | A | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp1 HG01993.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0008t0001others(1): Show | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0037 others(10): Show |
13 | 106 | 0.1226 | -2 | c.703 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147910348 | CAA | C | intron_variant | MODIFIER | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
a0001 | a0001c0001a0001c0006a0001c0009others(1): Show | a0001c0001t0001a0001c0006t0001a0001c0009t0001others(1): Show | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0006t0001g0040 others(4): Show |
7 | 106 | 0.0660 | -2 | c.116 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911994 | CGT | C | intron_variant | MODIFIER | HG02145.hp1 NA19064.hp1 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0097 |
3 | 106 | 0.0283 | -2 | c.116 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AAT | A | intron_variant | MODIFIER | HG02055.hp2 NA18995.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 a0001c0001t0001g0095 |
2 | 106 | 0.0189 | -2 | c.116 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147914389 | ACT | A | intron_variant | MODIFIER | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
a0001 | a0001c0008a0001c0009 | a0001c0008t0001a0001c0009t0001 | a0001c0008t0001g0059 a0001c0008t0001g0060 a0001c0009t0001g0008 |
3 | 106 | 0.0283 | -2 | c.122 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147914556 | TCC | T | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(50): Show |
53 | 106 | 0.5000 | -2 | c.122 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147933423 | CTG | C | intron_variant | MODIFIER | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002a0001c0011 | a0001c0001t0001a0001c0002t0001a0001c0011t0001 | a0001c0001t0001g0093 a0001c0002t0001g0090 a0001c0011t0001g0092 |
3 | 106 | 0.0283 | -2 | c.122 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147947227 | CTT | C | intron_variant | MODIFIER | HG01070.hp2 HG02895.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0065 others(2): Show |
5 | 106 | 0.0472 | -2 | c.139 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147969324 | CTT | C | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(5): Show | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0052 others(15): Show |
18 | 106 | 0.1698 | -2 | c.171 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147971093 | CAA | C | intron_variant | MODIFIER | HG01993.hp2 HG02056.hp2 HG02896.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0034 others(4): Show |
7 | 106 | 0.0660 | -2 | c.171 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147988167 | CGT | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(21): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(5): Show | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0036 others(21): Show |
24 | 106 | 0.2264 | -2 | 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 | 148013858 | ACT | A | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0083 others(2): Show |
5 | 106 | 0.0472 | -2 | c.171 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148032327 | TCC | T | intron_variant | MODIFIER | HG01071.hp1 HG01071.hp2 HG01993.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0003 | a0001c0001t0001a0001c0004t0001a0002c0003t0001 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0075 others(5): Show |
8 | 106 | 0.0755 | -2 | c.186 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148036066 | CTG | C | intron_variant | MODIFIER | HG02109.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0065 others(4): Show |
7 | 106 | 0.0660 | -2 | 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 | 148043614 | AAT | A | intron_variant | MODIFIER | HG00558.hp1 HG01993.hp2 HG02165.hp1 others(3): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0010 | a0001c0001t0001a0002c0003t0001a0004c0010t0001 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0104 others(3): Show |
6 | 106 | 0.0566 | -2 | c.186 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |