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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF4_chr2_130831914_131052253 | 130984688 | T | TAAA | intron_variant | MODIFIER | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(22): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0010a0002c0011others(9): Show | a0001c0001t0001a0002c0010t0001a0002c0011t0001others(10): Show | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0043 others(22): Show |
25 | 53 | 0.4717 | 3 | c.398 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 131001302 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0007others(10): Show | a0001c0001t0001a0001c0002t0001a0001c0007t0004others(12): Show | a0001c0001t0001g0086 a0001c0002t0001g0031 a0001c0002t0001g0083 others(15): Show |
18 | 72 | 0.2500 | 3 | c.398 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 131029551 | C | CTTT | intron_variant | MODIFIER | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(8): Show |
a0001a0002a0004others(2): Show | a0001c0015a0001c0018a0002c0011others(5): Show | a0001c0015t0001a0001c0018t0005a0002c0011t0001others(5): Show | a0001c0015t0001g0078 a0001c0015t0001g0079 a0001c0018t0005g0106 others(8): Show |
11 | 48 | 0.2292 | 3 | c.412 others(22): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136668512 | T | TTTC | intron_variant | MODIFIER | HG00323.hp2 HG01243.hp1 HG02056.hp1 others(42): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(41): Show |
45 | 213 | 0.2113 | 3 | c.219 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136668533 | C | CTTA | intron_variant | MODIFIER | HG02055.hp1 HG03225.hp1 HG03492.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0070 others(5): Show |
8 | 153 | 0.0523 | 3 | c.219 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136740003 | C | CATT | intron_variant | MODIFIER | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0002a0002c0004t0001a0002c0004t0009 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | 237 | 0.0127 | 3 | c.661 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136758031 | C | CTTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0033 others(55): Show |
58 | 71 | 0.8169 | 3 | c.250 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111115434 | A | AGGC | 5_prime_UTR_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(5): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0018 | a0001c0001t0013a0001c0001t0014a0001c0001t0025others(2): Show | a0001c0001t0013g0148 a0001c0001t0013g0154 a0001c0001t0014g0147 others(5): Show |
8 | 272 | 0.0294 | 3 | c.-75 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 72 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111147690 | C | CTTT | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0009a0001c0002t0002 | a0001c0001t0003g0101 a0001c0001t0003g0130 a0001c0001t0003g0209 others(8): Show |
11 | 146 | 0.0753 | 3 | c.166 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111223858 | A | ATTT | intron_variant | MODIFIER | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001a0001c0003t0003others(1): Show | a0001c0001t0002g0094 a0001c0003t0001g0136 a0001c0003t0003g0072 others(2): Show |
5 | 208 | 0.0240 | 3 | c.670 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111258689 | C | CCTT | intron_variant | MODIFIER | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0007a0001c0001t0008a0001c0016t0008 | a0001c0001t0007g0089 a0001c0001t0008g0003 a0001c0001t0008g0009 others(4): Show |
7 | 272 | 0.0257 | 3 | c.951 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111266569 | T | TGTC | intron_variant | MODIFIER | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0007a0001c0001t0008a0001c0016t0008 | a0001c0001t0007g0089 a0001c0001t0008g0003 a0001c0001t0008g0009 others(4): Show |
7 | 272 | 0.0257 | 3 | c.951 others(18): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111281181 | C | CTTT | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02055.hp1 others(4): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(1): Show | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0127 others(4): Show |
7 | 52 | 0.1346 | 3 | c.172 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111310205 | T | TCTC | downstream_gene_variant | MODIFIER | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0001g0079 a0001c0001t0005g0036 a0001c0001t0006g0015 others(30): Show |
33 | 272 | 0.1213 | 3 | c.*70 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4474 | chr13 | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63634908 | A | ACAC | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02886.hp2 HG04199.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0086 a0001c0001t0002g0030 a0001c0001t0002g0034 others(1): Show |
4 | 97 | 0.0412 | 3 | c.*31 others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 58 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63680866 | A | AAAC | intron_variant | MODIFIER | HG03540.hp1 HG03579.hp1 NA18967.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0104 a0001c0001t0002g0072 a0001c0001t0002g0098 |
3 | 166 | 0.0181 | 3 | c.583 others(20): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | TogoVar | |||||||
ARID1A_chr1_26691015_26787104 | 26707200 | A | ATTT | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(4): Show |
7 | 105 | 0.0667 | 3 | c.113 others(22): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26708266 | C | CTTT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(15): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(2): Show | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
18 | 32 | 0.5625 | 3 | c.113 others(24): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26749168 | A | AAAT | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01069.hp2 others(11): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(1): Show | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(10): Show |
14 | 144 | 0.0972 | 3 | c.192 others(24): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156777692 | G | GGCA | disruptive_inframe_insertion | MODERATE | HG01109.hp1 HG01261.hp2 NA20905.hp2 |
a0005 | a0005c0010a0005c0011a0005c0012 | a0005c0010t0001a0005c0011t0004a0005c0012t0013 | a0005c0010t0001g0096 a0005c0011t0004g0100 a0005c0012t0013g0017 |
3 | 148 | 0.0203 | 3 | c.18_ others(8): Show |
p.Ala others(4): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 324/10310 | 21/7119 | 7/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156778268 | C | CCAG | disruptive_inframe_insertion | MODERATE | HG02922.hp2 HG03041.hp2 |
a0010 | a0010c0031a0010c0032 | a0010c0031t0001a0010c0032t0015 | a0010c0031t0001g0092 a0010c0032t0015g0091 |
2 | 135 | 0.0148 | 3 | c.609 others(10): Show |
p.Gln others(6): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 915/10310 | 612/7119 | 204/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156778847 | G | GGGC | disruptive_inframe_insertion | MODERATE | HG02559.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
a0004 | a0004c0009a0004c0029a0004c0030 | a0004c0009t0001a0004c0009t0004a0004c0029t0007others(1): Show | a0004c0009t0001g0088 a0004c0009t0004g0070 a0004c0029t0007g0087 others(1): Show |
4 | 148 | 0.0270 | 3 | c.119 others(12): Show |
p.Gly others(6): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 1497/10310 | 1194/7119 | 398/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156778889 | C | CGGA | disruptive_inframe_insertion | MODERATE | HG03130.hp2 HG03579.hp2 |
a0019a0020 | a0019c0028a0020c0013 | a0019c0028t0001a0020c0013t0009 | a0019c0028t0001g0075 a0020c0013t0009g0038 |
2 | 148 | 0.0135 | 3 | c.123 others(12): Show |
p.Gly others(6): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 1538/10310 | 1235/7119 | 412/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156778982 | A | AGGC | conservative_inframe_insertion | MODERATE | HG01109.hp2 HG02559.hp2 |
a0008 | a0008c0033a0008c0034 | a0008c0033t0002a0008c0034t0002 | a0008c0033t0002g0045 a0008c0034t0002g0042 |
2 | 148 | 0.0135 | 3 | c.131 others(12): Show |
p.Gly others(6): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 1624/10310 | 1321/7119 | 441/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156779262 | G | GCGC | conservative_inframe_insertion | MODERATE | HG00642.hp1 HG01071.hp2 |
a0007 | a0007c0006 | a0007c0006t0001 | a0007c0006t0001g0036 a0007c0006t0001g0130 |
2 | 148 | 0.0135 | 3 | c.159 others(12): Show |
p.Pro others(6): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/20 | 1903/10310 | 1600/7119 | 534/2372 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||
ARID1B_chr6_156772378_157215779 | 156818098 | A | ATTT | intron_variant | MODIFIER | HG01261.hp1 HG01346.hp1 HG01515.hp2 others(23): Show |
a0001a0003a0013others(2): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0028 others(23): Show |
26 | 86 | 0.3023 | 3 | c.179 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156823688 | G | GTTT | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG02717.hp2 others(9): Show |
a0001a0003a0005others(2): Show | a0001c0001a0001c0002a0003c0004others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0003others(7): Show | a0001c0001t0001g0003 a0001c0001t0006g0035 a0001c0002t0003g0074 others(9): Show |
12 | 72 | 0.1667 | 3 | c.179 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156832917 | T | TTTA | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 NA20905.hp2 |
a0005 | a0005c0010a0005c0011a0005c0012 | a0005c0010t0001a0005c0011t0004a0005c0012t0013 | a0005c0010t0001g0096 a0005c0011t0004g0100 a0005c0012t0013g0017 |
3 | 148 | 0.0203 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | chr6 | TogoVar | |||||||
ARID1B_chr6_156772378_157215779 | 156835931 | C | CGAG | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(100): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0002a0001c0007others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
103 | 147 | 0.7007 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156840776 | G | GATT | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(44): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0002a0001c0007others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0077 others(44): Show |
47 | 148 | 0.3176 | 3 | c.198 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | chr6 | TogoVar | |||||||
ARID1B_chr6_156772378_157215779 | 156896576 | C | CAAA | intron_variant | MODIFIER | HG01346.hp1 HG01928.hp2 HG02145.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0007t0001others(2): Show | a0001c0001t0001g0067 a0001c0002t0001g0066 a0001c0002t0001g0124 others(3): Show |
6 | 71 | 0.0845 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897191 | A | ACTG | intron_variant | MODIFIER | HG01516.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
a0001a0004 | a0001c0001a0004c0009a0004c0030 | a0001c0001t0001a0001c0001t0006a0004c0009t0001others(2): Show | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0059 others(4): Show |
7 | 139 | 0.0504 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897218 | G | GCTT | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp1 HG02738.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0019 a0001c0002t0001g0123 a0001c0002t0001g0144 |
3 | 95 | 0.0316 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897258 | C | CTTA | intron_variant | MODIFIER | HG02630.hp2 HG03704.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0076 a0001c0002t0001g0082 |
2 | 117 | 0.0171 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897261 | C | CTTA | intron_variant | MODIFIER | HG02818.hp2 HG03540.hp2 |
a0004a0017 | a0004c0029a0017c0024 | a0004c0029t0007a0017c0024t0023 | a0004c0029t0007g0087 a0017c0024t0023g0007 |
2 | 106 | 0.0189 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897264 | C | CTTA | intron_variant | MODIFIER | HG01975.hp2 HG02895.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0064 a0001c0001t0012g0062 |
2 | 37 | 0.0541 | 3 | c.198 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156909123 | C | CTTT | intron_variant | MODIFIER | HG02630.hp1 HG03195.hp1 HG03471.hp2 others(2): Show |
a0001a0006a0015 | a0001c0001a0006c0039a0015c0025 | a0001c0001t0001a0001c0001t0006a0006c0039t0021others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0006g0134 others(2): Show |
5 | 70 | 0.0714 | 3 | c.213 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156917498 | A | ATGT | intron_variant | MODIFIER | HG01884.hp2 HG02630.hp1 HG02717.hp2 others(6): Show |
a0001a0003a0015others(1): Show | a0001c0001a0001c0002a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(6): Show | a0001c0001t0001g0003 a0001c0001t0004g0060 a0001c0001t0005g0061 others(6): Show |
9 | 148 | 0.0608 | 3 | c.213 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156936342 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0064 a0001c0001t0003g0132 a0001c0001t0004g0051 others(3): Show |
6 | 83 | 0.0723 | 3 | c.224 others(20): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156945097 | G | GTTT | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp2 |
a0001 | a0001c0001a0001c0016 | a0001c0001t0003a0001c0016t0001 | a0001c0001t0003g0076 a0001c0016t0001g0145 |
2 | 148 | 0.0135 | 3 | c.224 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156945233 | C | CTTT | intron_variant | MODIFIER | HG00735.hp2 HG01975.hp2 HG02109.hp2 others(11): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0012a0001c0007t0002others(8): Show | a0001c0001t0001g0015 a0001c0001t0001g0120 a0001c0001t0012g0062 others(11): Show |
14 | 34 | 0.4118 | 3 | c.224 others(22): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156946203 | G | GAAA | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp1 HG02630.hp2 others(4): Show |
a0001a0003a0014 | a0001c0001a0001c0016a0001c0017others(2): Show | a0001c0001t0003a0001c0016t0001a0001c0017t0020others(2): Show | a0001c0001t0003g0076 a0001c0016t0001g0145 a0001c0017t0020g0049 others(4): Show |
7 | 76 | 0.0921 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156959925 | C | CTTT | intron_variant | MODIFIER | HG01496.hp2 HG02080.hp2 HG02145.hp2 others(11): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0003c0035others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(6): Show | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0059 others(11): Show |
14 | 104 | 0.1346 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156960687 | T | TCTA | intron_variant | MODIFIER | HG01884.hp2 HG02280.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0060 a0001c0001t0004g0149 |
2 | 148 | 0.0135 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156975613 | C | CTTT | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(2): Show |
a0001a0008a0013 | a0001c0001a0001c0007a0008c0033others(2): Show | a0001c0001t0006a0001c0007t0002a0008c0033t0002others(2): Show | a0001c0001t0006g0083 a0001c0007t0002g0006 a0008c0033t0002g0045 others(2): Show |
5 | 88 | 0.0568 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157005132 | T | TTTG | intron_variant | MODIFIER | HG01891.hp1 HG01934.hp1 HG03130.hp2 others(3): Show |
a0001a0019 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0007a0001c0002t0001a0001c0007t0001others(3): Show | a0001c0001t0007g0030 a0001c0002t0001g0125 a0001c0007t0001g0137 others(3): Show |
6 | 84 | 0.0714 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157017963 | C | CAAA | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
a0001a0004a0005others(4): Show | a0001c0001a0001c0002a0001c0021others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(13): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0031 others(45): Show |
48 | 102 | 0.4706 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157018212 | C | CTTT | intron_variant | MODIFIER | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0077 others(4): Show |
7 | 31 | 0.2258 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157022760 | C | CTTG | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(84): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0007others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(31): Show | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(84): Show |
87 | 148 | 0.5878 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157060630 | C | CTTT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(27): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(20): Show | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0140 others(27): Show |
30 | 32 | 0.9375 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |