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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 148045738 | CAA | C | intron_variant | MODIFIER | HG01993.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0103 others(1): Show |
4 | 106 | 0.0377 | -2 | c.186 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32612829 | CAA | C | upstream_gene_variant | MODIFIER | HG02145.hp2 HG02615.hp2 HG03453.hp1 others(3): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0006t0001 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0184 others(3): Show |
6 | 335 | 0.0179 | -2 | c.-33 others(13): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2674 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32618758 | ACC | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(54): Show |
a0001a0007 | a0001c0001a0007c0009 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(29): Show |
57 | 335 | 0.1702 | -2 | c.130 others(19): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32619162 | CAT | C | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
a0001a0007 | a0001c0002a0007c0009 | a0001c0002t0005a0007c0009t0005 | a0001c0002t0005g0020 a0001c0002t0005g0045 a0001c0002t0005g0046 others(4): Show |
8 | 335 | 0.0239 | -2 | c.130 others(17): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32621183 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(74): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0003g0002 others(50): Show |
77 | 335 | 0.2299 | -2 | c.200 others(19): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | AGT | A | intron_variant | MODIFIER | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(23): Show |
a0001a0004a0008 | a0001c0001a0001c0014a0004c0007others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(3): Show | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0026 others(14): Show |
26 | 335 | 0.0776 | -2 | c.110 others(19): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32632720 | CAG | C | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
a0001a0007 | a0001c0002a0007c0009 | a0001c0002t0005a0007c0009t0005 | a0001c0002t0005g0020 a0001c0002t0005g0045 a0001c0002t0005g0046 others(4): Show |
8 | 335 | 0.0239 | -2 | c.110 others(19): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32640119 | TTC | T | downstream_gene_variant | MODIFIER | HG00597.hp2 HG00673.hp1 HG00741.hp1 others(73): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0053 others(47): Show |
76 | 335 | 0.2269 | -2 | c.*22 others(13): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 179 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32642568 | CAA | C | downstream_gene_variant | MODIFIER | HG01081.hp1 HG01109.hp2 HG01261.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0093 others(15): Show |
19 | 335 | 0.0567 | -2 | c.*47 others(13): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2628 | chr15 | TogoVar | |||||||
ARHGAP11B_chr15_30621128_30643810 | 30635211 | TAC | T | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | 247 | 0.0324 | -2 | c.660 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30637816 | CTT | C | intron_variant | MODIFIER | HG01081.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0052 others(8): Show |
14 | 247 | 0.0567 | -2 | c.*4- others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | AGT | A | downstream_gene_variant | MODIFIER | HG00544.hp1 HG00609.hp2 HG01070.hp1 others(32): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(16): Show |
35 | 247 | 0.1417 | -2 | c.*12 others(13): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31803799 | CCG | C | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00621.hp2 HG00733.hp1 others(55): Show |
a0001a0002a0005 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0096 others(55): Show |
58 | 322 | 0.1801 | -2 | c.*38 others(13): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1598 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | TCA | T | 3_prime_UTR_variant | MODIFIER | HG00597.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0033a0001c0001t0037a0001c0001t0038others(5): Show | a0001c0001t0033g0175 a0001c0001t0037g0035 a0001c0001t0038g0205 others(56): Show |
59 | 322 | 0.1832 | -2 | c.*20 others(13): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2008 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31815120 | CAA | C | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG02257.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0004a0001c0003t0010a0001c0003t0016others(4): Show | a0001c0001t0004g0022 a0001c0003t0010g0005 a0001c0003t0010g0006 others(14): Show |
17 | 322 | 0.0528 | -2 | c.173 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | CGT | C | intron_variant | MODIFIER | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0003g0233 a0001c0001t0003g0234 a0001c0001t0004g0030 others(19): Show |
22 | 322 | 0.0683 | -2 | c.173 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31820712 | TTA | T | intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(74): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0015a0002c0002t0002others(7): Show | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0121 others(74): Show |
77 | 322 | 0.2391 | -2 | c.153 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31835216 | AAG | A | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
a0001 | a0001c0001a0001c0006a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(4): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(40): Show |
43 | 322 | 0.1335 | -2 | c.138 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31838830 | CAA | C | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(17): Show | a0001c0001t0001g0135 a0001c0001t0004g0066 a0001c0001t0005g0063 others(95): Show |
98 | 322 | 0.3044 | -2 | c.138 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31852729 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(189): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0007others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(32): Show | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0096 others(189): Show |
192 | 322 | 0.5963 | -2 | c.109 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31858994 | AGT | A | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
a0001 | a0001c0001a0001c0006a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(7): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(46): Show |
49 | 322 | 0.1522 | -2 | c.948 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31859478 | CAT | C | intron_variant | MODIFIER | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0007others(4): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(24): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(142): Show |
145 | 322 | 0.4503 | -2 | c.948 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862703 | CAG | C | intron_variant | MODIFIER | HG00733.hp1 HG01891.hp1 HG02071.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015a0001c0001t0039 | a0001c0001t0001g0102 a0001c0001t0001g0113 a0001c0001t0001g0115 others(6): Show |
9 | 322 | 0.0280 | -2 | c.685 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | GAC | G | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0001c0010others(3): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(19): Show | a0001c0001t0003g0026 a0001c0001t0003g0176 a0001c0001t0003g0178 others(87): Show |
90 | 322 | 0.2795 | -2 | c.685 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31868361 | TTA | T | intron_variant | MODIFIER | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
a0002a0003 | a0002c0002a0003c0004 | a0002c0002t0007a0003c0004t0007 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(1): Show |
4 | 322 | 0.0124 | -2 | c.685 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | CAA | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01071.hp1 others(10): Show |
a0001 | a0001c0001a0001c0013 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(10): Show |
13 | 322 | 0.0404 | -2 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31876052 | GAC | G | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
a0001 | a0001c0001a0001c0006a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(7): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(46): Show |
49 | 322 | 0.1522 | -2 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31882820 | GAA | G | intron_variant | MODIFIER | HG01106.hp1 HG02145.hp1 HG02257.hp1 others(19): Show |
a0001 | a0001c0001a0001c0007a0001c0010 | a0001c0001t0006a0001c0001t0009a0001c0001t0032others(5): Show | a0001c0001t0006g0150 a0001c0001t0006g0153 a0001c0001t0006g0158 others(19): Show |
22 | 322 | 0.0683 | -2 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31901534 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0128 others(64): Show |
67 | 322 | 0.2081 | -2 | c.684 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31907472 | AAT | A | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(45): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0008others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
48 | 322 | 0.1491 | -2 | c.684 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31915110 | GGC | G | intron_variant | MODIFIER | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0032 a0001c0001t0009g0072 a0001c0001t0009g0073 others(7): Show |
10 | 322 | 0.0311 | -2 | c.-11 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | TCA | T | intron_variant | MODIFIER | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(81): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(18): Show | a0001c0001t0001g0083 a0001c0001t0001g0111 a0001c0001t0001g0124 others(81): Show |
84 | 322 | 0.2609 | -2 | c.-11 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31922180 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0113 others(32): Show |
35 | 322 | 0.1087 | -2 | c.-11 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31926336 | GAA | G | intron_variant | MODIFIER | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0032 a0001c0001t0009g0072 a0001c0001t0009g0073 others(7): Show |
10 | 322 | 0.0311 | -2 | c.-11 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31928174 | GCA | G | intron_variant | MODIFIER | HG01167.hp2 HG01175.hp1 HG01993.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0043 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(4): Show |
7 | 322 | 0.0217 | -2 | c.-11 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | CAT | C | upstream_gene_variant | MODIFIER | HG00544.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0014others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(17): Show | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0124 others(47): Show |
50 | 322 | 0.1553 | -2 | c.-46 others(13): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143127137 | CAA | C | upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | 162 | 0.0309 | -2 | c.-23 others(13): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2281 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143143565 | TTC | T | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
40 | 162 | 0.2469 | -2 | c.-14 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143145839 | GGT | G | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp2 HG01243.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(22): Show |
25 | 162 | 0.1543 | -2 | c.-14 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143148561 | CTG | C | intron_variant | MODIFIER | HG02572.hp1 HG02886.hp1 HG03486.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | 162 | 0.0247 | -2 | c.-14 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143207495 | AAC | A | intron_variant | MODIFIER | HG03704.hp1 NA18991.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0086 a0001c0002t0002g0059 |
2 | 162 | 0.0124 | -2 | c.234 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | CAA | C | intron_variant | MODIFIER | HG00733.hp2 HG02071.hp2 HG02109.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
11 | 162 | 0.0679 | -2 | c.385 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143261325 | CTT | C | intron_variant | MODIFIER | HG02109.hp2 HG02148.hp1 HG02300.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0073 others(5): Show |
8 | 162 | 0.0494 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143265221 | ATT | A | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(52): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(52): Show |
55 | 162 | 0.3395 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143283328 | ACT | A | intron_variant | MODIFIER | HG00642.hp1 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0107 |
2 | 162 | 0.0124 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143286303 | CAG | C | intron_variant | MODIFIER | HG01496.hp1 HG02148.hp1 NA18991.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0145 |
3 | 162 | 0.0185 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143308477 | AAC | A | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(64): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
67 | 162 | 0.4136 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143308935 | CAA | C | intron_variant | MODIFIER | HG01358.hp2 HG02071.hp2 HG02074.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0026 others(8): Show |
11 | 162 | 0.0679 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143309866 | TTG | T | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(17): Show |
20 | 162 | 0.1235 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143326409 | CAG | C | intron_variant | MODIFIER | HG02109.hp2 HG02723.hp1 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0100 |
3 | 162 | 0.0185 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |