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 | 130854846 | T | TTTTATTT others(5): Show |
intron_variant | MODIFIER | HG01258.hp2 NA18962.hp1 NA18999.hp2 others(1): Show |
a0001a0015 | a0001c0001a0001c0002a0001c0033others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0033t0001others(1): Show | a0001c0001t0001g0046 a0001c0002t0001g0024 a0001c0033t0001g0111 others(1): Show |
4 | 12 | 0.3333 | 12 | c.39+ others(29): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130865704 | T | TTTTGTTT others(5): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0002 | a0002c0010 | a0002c0010t0001 | a0002c0010t0001g0051 | 1 | 90 | 0.0111 | 12 | c.39+ others(29): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926008 | T | TTTTCTTT others(5): Show |
intron_variant | MODIFIER | HG01515.hp1 HG01515.hp2 HG01884.hp1 others(10): Show |
a0001a0011a0023 | a0001c0001a0001c0002a0011c0021others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(2): Show | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0035 others(10): Show |
13 | 110 | 0.1182 | 12 | c.355 others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926014 | C | CTCTTCCT others(5): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0006 | a0006c0005 | a0006c0005t0003 | a0006c0005t0003g0140 | 1 | 41 | 0.0244 | 12 | c.355 others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926014 | C | CTCTTTCT others(5): Show |
intron_variant | MODIFIER | HG02818.hp1 HG03041.hp1 NA19030.hp2 |
a0001a0006 | a0001c0033a0006c0005 | a0001c0033t0001a0006c0005t0001a0006c0005t0005 | a0001c0033t0001g0111 a0006c0005t0001g0104 a0006c0005t0005g0119 |
3 | 43 | 0.0698 | 12 | c.355 others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926048 | C | CTCTTTCT others(5): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02622.hp1 |
a0001a0016 | a0001c0007a0016c0032 | a0001c0007t0004a0016c0032t0001 | a0001c0007t0004g0093 a0016c0032t0001g0021 |
2 | 70 | 0.0286 | 12 | c.355 others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926810 | A | ATTTTTTT others(5): Show |
intron_variant | MODIFIER | HG01175.hp2 HG03453.hp2 |
a0001a0007 | a0001c0012a0007c0014 | a0001c0012t0001a0007c0014t0002 | a0001c0012t0001g0036 a0007c0014t0002g0095 |
2 | 6 | 0.3333 | 12 | c.355 others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130988899 | T | TAGAGAGA others(5): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0007 | a0007c0017 | a0007c0017t0001 | a0007c0017t0001g0108 | 1 | 105 | 0.0095 | 12 | c.398 others(33): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130988901 | T | TAGAGAGA others(5): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0113 | 1 | 81 | 0.0123 | 12 | c.398 others(33): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF5_chr7_144350402_144385632 | 144354226 | T | TACACACA others(5): Show |
upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01884.hp1 |
a0012a0017 | a0012c0013a0017c0025 | a0012c0013t0002a0017c0025t0001 | a0012c0013t0002g0120 a0017c0025t0001g0009 |
3 | 34 | 0.0882 | 12 | c.-12 others(23): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1175 | chr7 | TogoVar | |||||||
ARHGEF5_chr7_144350402_144385632 | 144354226 | T | TATACACA others(5): Show |
upstream_gene_variant | MODIFIER | NA21309.hp1 | a0048 | a0048c0049 | a0048c0049t0002 | a0048c0049t0002g0023 | 1 | 32 | 0.0313 | 12 | c.-12 others(23): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1175 | chr7 | TogoVar | |||||||
ARHGEF5_chr7_144350402_144385632 | 144358758 | A | AGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0003 | a0003c0004 | a0003c0004t0002 | a0003c0004t0002g0069 | 1 | 87 | 0.0115 | 12 | c.-13 others(29): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136668512 | T | TTTCTTCT others(5): Show |
intron_variant | MODIFIER | HG00423.hp1 HG01167.hp1 HG01981.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0087 a0001c0001t0001g0224 a0001c0001t0003g0143 others(1): Show |
4 | 172 | 0.0233 | 12 | c.219 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136710330 | C | CATATATA others(5): Show |
intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0171 | 1 | 80 | 0.0125 | 12 | c.828 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136727325 | T | TTCTTTTT others(5): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
a0001a0005a0006 | a0001c0001a0005c0005a0006c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(15): Show |
18 | 194 | 0.0928 | 12 | c.732 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136727395 | T | TTCTCTCT others(5): Show |
intron_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 | 1 | 138 | 0.0072 | 12 | c.732 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136736618 | G | GATGTGTG others(5): Show |
intron_variant | MODIFIER | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0063 a0001c0001t0001g0244 a0001c0001t0002g0211 others(1): Show |
4 | 105 | 0.0381 | 12 | c.662 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | TogoVar | |||||||
ARHGEF6_chrX_136660550_136785932 | 136777761 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
a0001a0004a0005 | a0001c0001a0004c0008a0005c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(2): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0049 others(45): Show |
48 | 184 | 0.2609 | 12 | c.249 others(29): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111133812 | T | TATATAAA others(5): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 9 | 0.1111 | 12 | c.165 others(31): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111133812 | T | TATATATA others(5): Show |
intron_variant | MODIFIER | NA19060.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0176 | 1 | 9 | 0.1111 | 12 | c.165 others(31): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111170224 | A | AGTAGCTG others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(58): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0048 others(58): Show |
61 | 272 | 0.2243 | 12 | c.252 others(31): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111185961 | C | CGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01071.hp1 HG01081.hp1 HG01123.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0182 a0001c0001t0005g0108 a0001c0001t0005g0224 |
3 | 42 | 0.0714 | 12 | c.253 others(31): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221356 | T | TATATCTA others(5): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 148 | 0.0068 | 12 | c.670 others(29): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221358 | T | TATATCTA others(5): Show |
intron_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0057 | 1 | 272 | 0.0037 | 12 | c.670 others(29): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221381 | A | AGACATAT others(5): Show |
intron_variant | MODIFIER | NA18979.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0151 | 1 | 271 | 0.0037 | 12 | c.670 others(29): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111221401 | C | CTATATAT others(5): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0133 | 1 | 222 | 0.0045 | 12 | c.670 others(29): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111281181 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG01071.hp1 HG01496.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0133 a0001c0001t0005g0224 |
2 | 47 | 0.0426 | 12 | c.172 others(29): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63666453 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG03490.hp1 HG04115.hp1 NA18612.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0013 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0116 others(2): Show |
5 | 9 | 0.5556 | 12 | c.946 others(27): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63713701 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0002 | 2 | 105 | 0.0190 | 12 | c.211 others(29): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | TogoVar | |||||||
ARID1A_chr1_26691015_26787104 | 26708266 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02818.hp2 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | 16 | 0.1250 | 12 | c.113 others(33): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26710494 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG00642.hp2 HG00673.hp1 HG01081.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0012a0002c0003 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
23 | 37 | 0.6216 | 12 | c.113 others(33): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156838709 | T | TATAATAA others(5): Show |
intron_variant | MODIFIER | HG01433.hp2 HG02922.hp2 HG03579.hp1 |
a0001a0010 | a0001c0002a0001c0021a0010c0031 | a0001c0002t0001a0001c0021t0007a0010c0031t0001 | a0001c0002t0001g0073 a0001c0021t0007g0122 a0010c0031t0001g0092 |
3 | 48 | 0.0625 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156856672 | C | CCTCTCTC others(5): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0108 | 1 | 120 | 0.0083 | 12 | c.198 others(33): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156893045 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0056 | 1 | 68 | 0.0147 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156896576 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0022 | 1 | 66 | 0.0152 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897218 | G | GCTGCTGC others(5): Show |
intron_variant | MODIFIER | HG01928.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0124 | 1 | 93 | 0.0108 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897218 | G | GCTGCTGC others(5): Show |
intron_variant | MODIFIER | HG03540.hp1 NA20752.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0056 a0001c0002t0001g0108 |
2 | 94 | 0.0213 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897218 | G | GCTTCTTC others(5): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0018 | a0001c0018t0001 | a0001c0018t0001g0129 | 1 | 93 | 0.0108 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897252 | C | CTTATTAT others(5): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0142 | 1 | 140 | 0.0071 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897255 | C | CTTATTAT others(5): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0126 | 1 | 131 | 0.0076 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897258 | C | CTTATTAT others(5): Show |
intron_variant | MODIFIER | HG01175.hp1 HG02280.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0001 | a0001c0001t0004g0149 a0001c0002t0001g0004 |
2 | 117 | 0.0171 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897261 | C | CTTATTAT others(5): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0048 | 1 | 105 | 0.0095 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897264 | C | CTTATTAT others(5): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01891.hp1 HG01928.hp2 others(2): Show |
a0001a0015 | a0001c0001a0001c0002a0015c0025 | a0001c0001t0007a0001c0002t0001a0015c0025t0005 | a0001c0001t0007g0030 a0001c0002t0001g0108 a0001c0002t0001g0124 others(2): Show |
5 | 40 | 0.1250 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897264 | C | CTTCTTAT others(5): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01256.hp1 HG01496.hp1 others(1): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0037 | a0001c0001t0001a0001c0002t0001a0006c0037t0019 | a0001c0001t0001g0140 a0001c0002t0001g0101 a0001c0002t0001g0135 others(1): Show |
4 | 39 | 0.1026 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156897264 | C | CTTCTTCT others(5): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0007 | a0007c0006 | a0007c0006t0001 | a0007c0006t0001g0036 | 1 | 36 | 0.0278 | 12 | c.198 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156905250 | G | GCACACAC others(5): Show |
intron_variant | MODIFIER | HG01261.hp1 HG01346.hp1 HG01433.hp2 others(17): Show |
a0001a0019 | a0001c0001a0001c0002a0001c0016others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(4): Show | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0028 others(17): Show |
20 | 65 | 0.3077 | 12 | c.213 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156905250 | G | GCACGCAC others(5): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0066 | 1 | 46 | 0.0217 | 12 | c.213 others(31): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156934961 | T | TATATATA others(5): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0137 | 1 | 122 | 0.0082 | 12 | c.213 others(29): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156936342 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02083.hp2 NA18964.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0103 a0001c0002t0001g0026 |
2 | 79 | 0.0253 | 12 | c.224 others(29): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157018212 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02145.hp2 HG02257.hp1 |
a0001a0014 | a0001c0001a0001c0002a0014c0015 | a0001c0001t0001a0001c0002t0001a0014c0015t0002 | a0001c0001t0001g0139 a0001c0002t0001g0071 a0014c0015t0002g0010 |
3 | 27 | 0.1111 | 12 | c.224 others(33): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |