regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF6_chrX_136660550_136785932 | 136727411 | C | CTCT | intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 247 | 0.0041 | 3 | c.732 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727414 | T | TCTC | intron_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0151 | 1 | 247 | 0.0041 | 3 | c.732 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727418 | T | TCTC | intron_variant | MODIFIER | HG00621.hp1 HG02083.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0145a0001c0001t0007g0190 | 2 | 247 | 0.0081 | 3 | c.732 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136729054 | C | CTCT | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 247 | 0.0041 | 3 | c.732 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136740003 | C | CATT | intron_variant | MODIFIER | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0002a0002c0004t0001a0002c0004t0013 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 3 | 247 | 0.0122 | 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(56): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0033others(56): Show | 59 | 247 | 0.2389 | 3 | c.250 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136758095 | G | GGCT | intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0002 | 1 | 247 | 0.0041 | 3 | c.250 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136766392 | T | TGGG | intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 247 | 0.0041 | 3 | c.249 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136767838 | G | GAGC | intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 247 | 0.0041 | 3 | c.249 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 |
a0001a0005 | a0001c0001a0001c0002a0005c0018 | a0001c0001t0013a0001c0001t0014a0001c0001t0025others(2): Show | a0001c0001t0013g0154a0001c0001t0013g0162a0001c0001t0014g0153others(5): Show | 8 | 274 | 0.0292 | 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 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215others(8): Show | 11 | 274 | 0.0402 | 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 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | 274 | 0.0183 | 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 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | 274 | 0.0256 | 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 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | 274 | 0.0256 | 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 | a0001c0001t0001g0019a0001c0001t0001g0066a0001c0001t0001g0131others(4): Show | 7 | 274 | 0.0256 | 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 | a0001c0001t0001g0084a0001c0001t0005g0062a0001c0001t0006g0032others(30): Show | 33 | 274 | 0.1204 | 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 | a0001c0001t0001g0089a0001c0001t0002g0031a0001c0001t0002g0037others(1): Show | 4 | 168 | 0.0238 | 3 | c.*31 others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 58 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63643360 | C | CTTT | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0018 | 1 | 168 | 0.0060 | 3 | c.139 others(20): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63680866 | A | AAAC | intron_variant | MODIFIER | HG03540.hp1 HG03579.hp1 NA18967.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0107a0001c0001t0002g0075a0001c0001t0002g0100 | 3 | 168 | 0.0179 | 3 | c.583 others(20): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63693611 | C | CAAA | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0018 | 1 | 168 | 0.0060 | 3 | c.582 others(20): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63705402 | T | TGTG | intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0019 | 1 | 168 | 0.0060 | 3 | c.402 others(18): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63712543 | T | TTTG | intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 168 | 0.0060 | 3 | c.211 others(20): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26707200 | A | ATTT | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0130others(4): Show | 7 | 146 | 0.0480 | 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 |
a0001a0002a0003 | a0001c0001a0002c0004a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(2): Show | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0028others(15): Show | 18 | 146 | 0.1233 | 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 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(10): Show | 14 | 146 | 0.0959 | 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 |
a0003 | a0003c0010a0003c0011a0003c0012 | a0003c0010t0001a0003c0011t0004a0003c0012t0013 | a0003c0010t0001g0099a0003c0011t0004g0103a0003c0012t0013g0022 | 3 | 150 | 0.0200 | 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 |
a0007 | a0007c0031a0007c0032 | a0007c0031t0001a0007c0032t0015 | a0007c0031t0001g0005a0007c0032t0015g0004 | 2 | 150 | 0.0133 | 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 |
a0004a0011 | a0004c0009a0004c0029a0011c0030 | a0004c0009t0001a0004c0009t0004a0004c0029t0007others(1): Show | a0004c0009t0001g0094a0004c0009t0004g0076a0004c0029t0007g0095others(1): Show | 4 | 150 | 0.0267 | 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 |
a0020a0029 | a0020c0028a0029c0013 | a0020c0028t0001a0029c0013t0009 | a0020c0028t0001g0081a0029c0013t0009g0044 | 2 | 150 | 0.0133 | 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 |
a0021a0022 | a0021c0033a0022c0034 | a0021c0033t0002a0022c0034t0002 | a0021c0033t0002g0051a0022c0034t0002g0048 | 2 | 150 | 0.0133 | 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 |
a0006 | a0006c0006 | a0006c0006t0001 | a0006c0006t0001g0042a0006c0006t0001g0132 | 2 | 150 | 0.0133 | 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 | 156809713 | G | GAAA | intron_variant | MODIFIER | HG02145.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
a0001a0010 | a0001c0001a0001c0002a0010c0015 | a0001c0001t0001a0001c0002t0001a0010c0015t0002 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0002t0001g0077others(2): Show | 5 | 150 | 0.0333 | 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 | 156818098 | A | ATTT | intron_variant | MODIFIER | HG01261.hp1 HG01346.hp1 HG01515.hp2 others(24): Show |
a0001a0014a0015others(2): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0034others(24): Show | 27 | 150 | 0.1800 | 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(3): Show | a0001c0001a0001c0002a0003c0010others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0003others(7): Show | a0001c0001t0001g0003a0001c0001t0006g0041a0001c0002t0003g0080others(9): Show | 12 | 150 | 0.0800 | 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 |
a0003 | a0003c0010a0003c0011a0003c0012 | a0003c0010t0001a0003c0011t0004a0003c0012t0013 | a0003c0010t0001g0099a0003c0011t0004g0103a0003c0012t0013g0022 | 3 | 150 | 0.0200 | 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(101): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0007others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(101): Show | 104 | 150 | 0.6933 | 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 |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0007others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0083others(44): Show | 47 | 150 | 0.3133 | 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 | a0001c0001t0001g0075a0001c0002t0001g0074a0001c0002t0001g0126others(3): Show | 6 | 150 | 0.0400 | 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 |
a0001a0004a0011 | a0001c0001a0004c0009a0011c0030 | a0001c0001t0001a0001c0001t0006a0004c0009t0001others(2): Show | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0065others(4): Show | 7 | 150 | 0.0467 | 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 | a0001c0002t0001g0024a0001c0002t0001g0125a0001c0002t0001g0146 | 3 | 150 | 0.0200 | 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 | a0001c0001t0003g0082a0001c0002t0001g0088 | 2 | 150 | 0.0133 | 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 |
a0004a0014 | a0004c0029a0014c0024 | a0004c0029t0007a0014c0024t0023 | a0004c0029t0007g0095a0014c0024t0023g0012 | 2 | 150 | 0.0133 | 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 | a0001c0001t0001g0070a0001c0001t0012g0068 | 2 | 150 | 0.0133 | 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 |
a0001a0013a0025 | a0001c0001a0013c0025a0025c0039 | a0001c0001t0001a0001c0001t0006a0013c0025t0005others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0006g0136others(2): Show | 5 | 150 | 0.0333 | 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 |
a0001a0009a0013others(1): Show | a0001c0001a0001c0002a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(6): Show | a0001c0001t0001g0003a0001c0001t0004g0066a0001c0001t0005g0067others(6): Show | 9 | 150 | 0.0600 | 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 | a0001c0001t0001g0070a0001c0001t0003g0134a0001c0001t0004g0057others(3): Show | 6 | 150 | 0.0400 | 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 | a0001c0001t0003g0082a0001c0016t0001g0147 | 2 | 150 | 0.0133 | 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 |
a0001a0002a0005others(5): Show | a0001c0001a0001c0007a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0012a0001c0007t0002others(8): Show | a0001c0001t0001g0020a0001c0001t0001g0122a0001c0001t0012g0068others(11): Show | 14 | 150 | 0.0933 | 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 |
a0001a0005a0010 | a0001c0001a0001c0016a0001c0017others(2): Show | a0001c0001t0003a0001c0016t0001a0001c0017t0020others(2): Show | a0001c0001t0003g0082a0001c0016t0001g0147a0001c0017t0020g0055others(4): Show | 7 | 150 | 0.0467 | 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 |
a0001a0004a0010others(2): Show | a0001c0001a0001c0002a0004c0029others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(6): Show | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0065others(11): Show | 14 | 150 | 0.0933 | 3 | c.224 others(24): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |