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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF18_chr19_7343937_7477478 | 7412035 | GTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0013others(27): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(41): Show | a0001c0001t0001g0056 a0001c0001t0002g0028 a0001c0001t0002g0032 others(150): Show |
153 | 298 | 0.5134 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7412180 | GGC | G | intron_variant | MODIFIER | HG01109.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0008a0003c0003t0023 | a0001c0001t0008g0209 a0001c0001t0008g0215 a0001c0001t0008g0253 others(1): Show |
4 | 298 | 0.0134 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7416530 | CGT | C | intron_variant | MODIFIER | HG01358.hp1 HG01361.hp2 HG01884.hp1 others(19): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0019others(10): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0003others(12): Show | a0001c0001t0002g0144 a0001c0001t0004g0049 a0001c0002t0003g0218 others(19): Show |
22 | 298 | 0.0738 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7419432 | TCC | T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(37): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0018a0002c0004others(12): Show | a0001c0001t0002a0001c0018t0001a0002c0004t0002others(14): Show | a0001c0001t0002g0070 a0001c0001t0002g0144 a0001c0001t0002g0202 others(37): Show |
40 | 298 | 0.1342 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7422716 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0013others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(18): Show | a0001c0001t0001g0056 a0001c0001t0002g0159 a0001c0001t0008g0191 others(52): Show |
55 | 298 | 0.1846 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7424074 | GAC | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0013others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | a0001c0001t0001g0056 a0001c0001t0002g0028 a0001c0001t0002g0032 others(138): Show |
141 | 298 | 0.4732 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7426477 | ACT | A | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG03209.hp2 |
a0011a0024 | a0011c0024a0011c0025a0024c0052 | a0011c0024t0015a0011c0025t0005a0024c0052t0022 | a0011c0024t0015g0009 a0011c0025t0005g0013 a0024c0052t0022g0267 |
3 | 298 | 0.0101 | -2 | c.968 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7431510 | CAA | C | intron_variant | MODIFIER | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
a0001a0002a0009 | a0001c0001a0002c0004a0009c0012 | a0001c0001t0004a0002c0004t0004a0009c0012t0010 | a0001c0001t0004g0004 a0001c0001t0004g0007 a0002c0004t0004g0002 others(4): Show |
7 | 298 | 0.0235 | -2 | c.968 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7437422 | CAA | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
a0001a0002a0004others(18): Show | a0001c0001a0001c0013a0001c0016others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(43): Show | a0001c0001t0001g0056 a0001c0001t0002g0012 a0001c0001t0002g0028 others(123): Show |
126 | 298 | 0.4228 | -2 | c.968 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7438408 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
a0001a0002a0004others(19): Show | a0001c0001a0001c0013a0001c0016others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | a0001c0001t0001g0056 a0001c0001t0002g0012 a0001c0001t0002g0028 others(130): Show |
133 | 298 | 0.4463 | -2 | c.968 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7443055 | ATT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0023a0001c0043others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(29): Show | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0081 others(99): Show |
102 | 298 | 0.3423 | -2 | c.136 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7447484 | ACT | A | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0004a0003c0003others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(20): Show | a0001c0001t0002g0012 a0001c0001t0002g0028 a0001c0001t0002g0032 others(87): Show |
90 | 298 | 0.3020 | -2 | c.173 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7457353 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0004others(9): Show | a0001c0001t0002a0001c0001t0005a0001c0002t0002others(14): Show | a0001c0001t0002g0086 a0001c0001t0002g0112 a0001c0001t0002g0237 others(55): Show |
58 | 298 | 0.1946 | -2 | c.218 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7458296 | TTA | T | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01169.hp2 others(11): Show |
a0001a0002a0015others(2): Show | a0001c0013a0002c0007a0015c0057others(2): Show | a0001c0013t0001a0002c0007t0001a0015c0057t0001others(2): Show | a0001c0013t0001g0010 a0001c0013t0001g0195 a0001c0013t0001g0204 others(11): Show |
14 | 298 | 0.0470 | -2 | c.218 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 18/28 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7458297 | TAA | T | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp1 HG02683.hp1 others(5): Show |
a0001a0002a0011others(1): Show | a0001c0001a0001c0048a0002c0004others(2): Show | a0001c0001t0002a0001c0001t0011a0001c0048t0001others(3): Show | a0001c0001t0002g0052 a0001c0001t0002g0134 a0001c0001t0002g0188 others(5): Show |
8 | 298 | 0.0269 | -2 | c.218 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466381 | CAA | C | intron_variant | MODIFIER | HG01167.hp1 HG01167.hp2 HG01515.hp2 others(6): Show |
a0001a0019 | a0001c0001a0001c0018a0019c0045 | a0001c0001t0002a0001c0018t0001a0019c0045t0002 | a0001c0001t0002g0032 a0001c0001t0002g0042 a0001c0001t0002g0114 others(6): Show |
9 | 298 | 0.0302 | -2 | c.290 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7473808 | CAA | C | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0001c0016others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(25): Show | a0001c0001t0001g0109 a0001c0001t0002g0028 a0001c0001t0002g0032 others(86): Show |
89 | 298 | 0.2987 | -2 | c.*35 others(13): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1331 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7476344 | CAT | C | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(65): Show |
a0001a0002a0004others(12): Show | a0001c0001a0001c0002a0001c0013others(23): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(29): Show | a0001c0001t0001g0053 a0001c0001t0001g0216 a0001c0001t0004g0048 others(65): Show |
68 | 298 | 0.2282 | -2 | c.*60 others(13): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3867 | chr19 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16194459 | CAA | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0006a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
151 | 362 | 0.4171 | -2 | c.*41 others(13): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 3394 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16195129 | CAA | C | downstream_gene_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
a0001a0002a0011 | a0001c0001a0002c0002a0011c0012 | a0001c0001t0001a0002c0002t0002a0011c0012t0005 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0093 others(2): Show |
6 | 362 | 0.0166 | -2 | c.*34 others(13): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 2724 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16195146 | AAG | A | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0006a0002c0002t0002 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0056 others(2): Show |
19 | 362 | 0.0525 | -2 | c.*34 others(13): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 2707 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16196938 | TTC | T | downstream_gene_variant | MODIFIER | HG01106.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0009 a0001c0001t0004g0087 |
6 | 362 | 0.0166 | -2 | c.*16 others(13): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 915 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16203222 | ACT | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(6): Show |
a0003a0010 | a0003c0003a0010c0015 | a0003c0003t0001a0010c0015t0001 | a0003c0003t0001g0012 a0003c0003t0001g0032 a0003c0003t0001g0033 others(1): Show |
9 | 362 | 0.0249 | -2 | c.190 others(19): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 12/15 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16204284 | CAG | C | intron_variant | MODIFIER | HG00544.hp2 HG00741.hp1 HG01069.hp1 others(83): Show |
a0002a0004 | a0002c0002a0002c0009a0004c0004 | a0002c0002t0001a0002c0002t0002a0002c0002t0010others(3): Show | a0002c0002t0001g0010 a0002c0002t0001g0076 a0002c0002t0002g0002 others(12): Show |
86 | 362 | 0.2376 | -2 | c.190 others(19): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 12/15 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16211286 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
a0001a0003a0008others(1): Show | a0001c0001a0003c0003a0008c0010others(1): Show | a0001c0001t0001a0001c0001t0006a0003c0003t0001others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(15): Show |
85 | 362 | 0.2348 | -2 | c.-30 others(19): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1/15 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16212047 | GCC | G | intron_variant | MODIFIER | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0090 a0001c0001t0003g0019 a0001c0001t0003g0089 others(3): Show |
15 | 362 | 0.0414 | -2 | c.-30 others(17): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1/15 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16215189 | AAG | A | upstream_gene_variant | MODIFIER | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
a0001a0012 | a0001c0001a0012c0013 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0003g0008 others(4): Show |
20 | 362 | 0.0553 | -2 | c.-27 others(13): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 2538 | chr1 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41880391 | AAG | A | upstream_gene_variant | MODIFIER | HG02559.hp1 HG03453.hp1 NA18961.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | 234 | 0.0342 | -2 | c.-29 others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2792 | chr19 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41881941 | CTT | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
a0001a0003a0008 | a0001c0001a0001c0006a0003c0012others(1): Show | a0001c0001t0001a0001c0006t0001a0003c0012t0001others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(34): Show |
47 | 234 | 0.2009 | -2 | c.-13 others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1242 | chr19 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41896862 | TAC | T | intron_variant | MODIFIER | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0117 a0001c0001t0001g0118 |
5 | 234 | 0.0214 | -2 | c.112 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41899505 | CTT | C | intron_variant | MODIFIER | HG00738.hp1 HG02897.hp2 HG04204.hp2 others(4): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0010 a0001c0002t0001g0066 a0001c0002t0001g0071 others(3): Show |
7 | 234 | 0.0299 | -2 | c.126 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41900786 | GTT | G | intron_variant | MODIFIER | HG00438.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0045 others(10): Show |
13 | 234 | 0.0556 | -2 | c.126 others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41903093 | GTT | G | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0010 | a0001c0001t0001a0001c0003t0001a0004c0010t0001 | a0001c0001t0001g0122 a0001c0003t0001g0022 a0001c0003t0001g0023 others(5): Show |
8 | 234 | 0.0342 | -2 | c.173 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41905391 | ATG | A | intron_variant | MODIFIER | NA19001.hp2 NA19088.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 a0001c0001t0001g0176 |
2 | 234 | 0.0086 | -2 | c.233 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41905440 | GTA | G | intron_variant | MODIFIER | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0026 others(1): Show |
4 | 234 | 0.0171 | -2 | c.233 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41905480 | GGT | G | intron_variant | MODIFIER | HG00423.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0010 | a0001c0001t0001a0001c0003t0001a0004c0010t0001 | a0001c0001t0001g0098 a0001c0001t0001g0122 a0001c0003t0001g0022 others(6): Show |
9 | 234 | 0.0385 | -2 | c.233 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41911878 | CAT | C | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0122 a0001c0003t0001g0022 a0001c0003t0001g0023 others(4): Show |
7 | 234 | 0.0299 | -2 | c.*47 others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4427 | chr19 | TogoVar | |||||||
ARHGEF25_chr12_57606435_57622245 | 57610491 | TGA | T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0001 a0002c0002t0001g0002 |
9 | 424 | 0.0212 | -2 | c.-14 others(13): Show |
ARHGEF25 | ENSG00000240771.8 | transcript | ENST00000286494.9 | protein_coding | 943 | chr12 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154127600 | ATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0009a0001c0015others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(154): Show |
160 | 283 | 0.5654 | -2 | c.112 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154127794 | CAT | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
a0002a0006a0010others(1): Show | a0002c0002a0002c0003a0002c0007others(5): Show | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(29): Show | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0024 others(105): Show |
109 | 283 | 0.3852 | -2 | c.112 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154150058 | TTG | T | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
a0001a0002a0006others(3): Show | a0001c0001a0002c0002a0002c0003others(7): Show | a0001c0001t0007a0001c0001t0015a0001c0001t0030others(30): Show | a0001c0001t0007g0144 a0001c0001t0007g0175 a0001c0001t0015g0124 others(107): Show |
111 | 283 | 0.3922 | -2 | c.132 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154186136 | GAC | G | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG02818.hp2 others(1): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0001c0001t0023a0001c0001t0043others(1): Show | a0001c0001t0001g0130 a0001c0001t0023g0131 a0001c0001t0043g0134 others(1): Show |
4 | 283 | 0.0141 | -2 | c.148 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154193546 | CAT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(41): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0169 others(41): Show |
44 | 283 | 0.1555 | -2 | c.177 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154211867 | ATG | A | intron_variant | MODIFIER | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
a0001a0002a0005 | a0001c0001a0002c0003a0005c0008 | a0001c0001t0015a0001c0001t0021a0001c0001t0030others(2): Show | a0001c0001t0015g0124 a0001c0001t0015g0126 a0001c0001t0015g0127 others(4): Show |
7 | 283 | 0.0247 | -2 | c.184 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154216507 | TTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(120): Show |
126 | 283 | 0.4452 | -2 | c.184 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | TAC | T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(19): Show |
a0001a0002a0007 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0157 others(19): Show |
22 | 283 | 0.0777 | -2 | c.209 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154227292 | ATT | A | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG00738.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0015others(5): Show | a0001c0001t0001g0146 a0001c0001t0001g0185 a0001c0001t0001g0194 others(12): Show |
15 | 283 | 0.0530 | -2 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154231876 | CAT | C | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0041a0001c0009t0022 | a0001c0001t0041g0165 a0001c0009t0022g0163 a0001c0009t0022g0164 |
3 | 283 | 0.0106 | -2 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154237538 | TCA | T | intron_variant | MODIFIER | HG01175.hp2 HG02886.hp1 HG03239.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(1): Show | a0001c0001t0001g0188 a0001c0001t0002g0152 a0001c0001t0014g0276 others(1): Show |
4 | 283 | 0.0141 | -2 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239249 | CGA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0015a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(32): Show | a0001c0001t0001g0130 a0001c0001t0001g0150 a0001c0001t0001g0153 others(136): Show |
143 | 283 | 0.5053 | -2 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |