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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF9_chrX_63629967_63790214 | 63682133 | CAATA | C | intron_variant | MODIFIER | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | 168 | 0.0893 | -4 | c.583 others(21): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63705357 | ATGTG | A | intron_variant | MODIFIER | HG00735.hp1 HG01943.hp1 HG02896.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0084others(6): Show | 9 | 168 | 0.0536 | -4 | c.402 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63771748 | GTAGA | G | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0072a0001c0001t0003g0073 | 2 | 168 | 0.0119 | -4 | c.30+ others(21): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63774045 | ATATC | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(80): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(78): Show | 83 | 168 | 0.4941 | -4 | c.30+ others(21): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26747851 | AAAAC | A | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(8): Show | 12 | 146 | 0.0822 | -4 | c.192 others(25): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156787631 | TCTAA | T | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(28): Show |
a0001a0002a0008others(12): Show | a0001c0001a0001c0002a0001c0007others(16): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(19): Show | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0115others(28): Show | 31 | 150 | 0.2067 | -4 | c.179 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156804867 | CAAAA | C | intron_variant | MODIFIER | HG02717.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
a0001a0005a0007others(2): Show | a0001c0001a0005c0004a0007c0032others(2): Show | a0001c0001t0001a0005c0004t0008a0007c0032t0015others(2): Show | a0001c0001t0001g0003a0005c0004t0008g0001a0005c0004t0008g0002others(4): Show | 7 | 150 | 0.0467 | -4 | c.179 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156812933 | GGTGT | G | intron_variant | MODIFIER | HG01175.hp1 HG01256.hp1 HG01496.hp1 others(15): Show |
a0001a0002a0014others(1): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(9): Show | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0056others(15): Show | 18 | 150 | 0.1200 | -4 | c.179 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156812974 | GTGTA | G | intron_variant | MODIFIER | HG00642.hp1 HG01071.hp2 |
a0006 | a0006c0006 | a0006c0006t0001 | a0006c0006t0001g0042a0006c0006t0001g0132 | 2 | 150 | 0.0133 | -4 | c.179 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156819481 | TAGTC | T | intron_variant | MODIFIER | HG01891.hp1 HG02622.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0035a0001c0001t0007g0036 | 2 | 150 | 0.0133 | -4 | c.179 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156856698 | TCTCA | T | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0004a0002c0003t0002 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0129others(3): Show | 6 | 150 | 0.0400 | -4 | c.198 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156856700 | TCACA | T | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(12): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0017others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0017t0020others(8): Show | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0106others(12): Show | 15 | 150 | 0.1000 | -4 | c.198 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156865872 | CTTAT | C | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 NA20905.hp2 |
a0003 | a0003c0010a0003c0011a0003c0012 | a0003c0010t0001a0003c0011t0004a0003c0012t0013 | a0003c0010t0001g0099a0003c0011t0004g0103a0003c0012t0013g0022 | 3 | 150 | 0.0200 | -4 | c.198 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156891424 | TAGAC | T | intron_variant | MODIFIER | HG01109.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
a0001a0007a0008others(8): Show | a0001c0001a0007c0032a0008c0005others(8): Show | a0001c0001t0001a0007c0032t0015a0008c0005t0002others(8): Show | a0001c0001t0001g0145a0007c0032t0015g0004a0008c0005t0002g0043others(9): Show | 12 | 150 | 0.0800 | -4 | c.198 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156895735 | TACAC | T | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG02145.hp2 others(2): Show |
a0003a0010a0026 | a0003c0010a0003c0011a0003c0012others(2): Show | a0003c0010t0001a0003c0011t0004a0003c0012t0013others(2): Show | a0003c0010t0001g0099a0003c0011t0004g0103a0003c0012t0013g0022others(2): Show | 5 | 150 | 0.0333 | -4 | c.198 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156906546 | CAAAA | C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(2): Show |
a0001a0021a0024 | a0001c0001a0021c0033a0024c0035 | a0001c0001t0001a0001c0001t0007a0021c0033t0002others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0007g0036others(2): Show | 5 | 150 | 0.0333 | -4 | c.213 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156911338 | GTTTT | G | intron_variant | MODIFIER | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
a0001a0004a0007others(3): Show | a0001c0007a0004c0029a0007c0032others(3): Show | a0001c0007t0001a0004c0029t0007a0007c0032t0015others(3): Show | a0001c0007t0001g0139a0004c0029t0007g0095a0007c0032t0015g0004others(4): Show | 7 | 150 | 0.0467 | -4 | c.213 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156921438 | AACAC | A | intron_variant | MODIFIER | HG01891.hp1 HG01934.hp1 HG01934.hp2 others(16): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0016others(5): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(8): Show | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0058others(16): Show | 19 | 150 | 0.1267 | -4 | c.213 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156927041 | TTAAA | T | intron_variant | MODIFIER | HG01175.hp2 HG01261.hp1 HG01496.hp2 others(39): Show |
a0001a0004a0011others(4): Show | a0001c0001a0001c0002a0001c0007others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | 150 | 0.2800 | -4 | c.213 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156931190 | CAAAA | C | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
a0001a0002a0004others(9): Show | a0001c0001a0001c0007a0001c0008others(12): Show | a0001c0001t0001a0001c0007t0002a0001c0008t0014others(12): Show | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0083others(16): Show | 19 | 150 | 0.1267 | -4 | c.213 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156934912 | TTATA | T | intron_variant | MODIFIER | HG00621.hp2 HG01175.hp1 HG02109.hp2 others(7): Show |
a0001a0002a0010others(2): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(5): Show | a0001c0001t0001g0142a0001c0001t0005g0067a0001c0002t0001g0009others(7): Show | 10 | 150 | 0.0667 | -4 | c.213 others(21): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156939795 | AAAAT | A | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG01515.hp2 others(9): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0002a0001c0008others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0008t0014others(7): Show | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | 150 | 0.0800 | -4 | c.224 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156943718 | CACTT | C | intron_variant | MODIFIER | HG00621.hp2 HG01515.hp1 HG01517.hp1 others(11): Show |
a0001a0002a0013 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0142others(11): Show | 14 | 150 | 0.0933 | -4 | c.224 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156945233 | CTTTT | C | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp1 HG02055.hp1 others(12): Show |
a0001a0004a0018others(1): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0007t0001others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0070others(12): Show | 15 | 150 | 0.1000 | -4 | c.224 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156963694 | AGTTT | A | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp2 |
a0001 | a0001c0001a0001c0016 | a0001c0001t0003a0001c0016t0001 | a0001c0001t0003g0082a0001c0016t0001g0147 | 2 | 150 | 0.0133 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156967528 | GGAGA | G | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG02258.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0010a0003c0011others(1): Show | a0001c0001t0006a0003c0010t0001a0003c0011t0004others(1): Show | a0001c0001t0006g0143a0003c0010t0001g0099a0003c0011t0004g0103others(1): Show | 4 | 150 | 0.0267 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156969892 | CTTTT | C | intron_variant | MODIFIER | HG00621.hp1 HG01109.hp2 HG01175.hp2 others(29): Show |
a0001a0004a0005others(7): Show | a0001c0001a0001c0002a0001c0007others(9): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(11): Show | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0056others(29): Show | 32 | 150 | 0.2133 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156972471 | ATATT | A | intron_variant | MODIFIER | HG02630.hp1 NA21309.hp1 |
a0001a0013 | a0001c0001a0013c0025 | a0001c0001t0001a0013c0025t0005 | a0001c0001t0001g0003a0013c0025t0005g0133 | 2 | 150 | 0.0133 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156977163 | TTTTC | T | intron_variant | MODIFIER | HG00280.hp2 HG03453.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0073a0001c0002t0001g0113 | 2 | 150 | 0.0133 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156987159 | CAGAG | C | intron_variant | MODIFIER | HG02080.hp1 HG02083.hp2 HG02622.hp1 others(5): Show |
a0001a0005a0023others(1): Show | a0001c0001a0005c0004a0023c0036others(1): Show | a0001c0001t0001a0005c0004t0008a0023c0036t0017others(1): Show | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0106others(5): Show | 8 | 150 | 0.0533 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157010276 | CTGTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(26): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0002a0003c0010others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(11): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0065others(26): Show | 29 | 150 | 0.1933 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157010278 | GTTTT | G | intron_variant | MODIFIER | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
a0001a0002a0010 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0003others(2): Show | a0001c0001t0001g0035a0001c0001t0001g0056a0001c0001t0001g0069others(4): Show | 7 | 150 | 0.0467 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039646 | TTTCC | T | intron_variant | MODIFIER | HG01071.hp2 HG01346.hp1 HG02080.hp2 others(7): Show |
a0001a0006a0007 | a0001c0001a0001c0002a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(3): Show | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0101others(7): Show | 10 | 150 | 0.0667 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039743 | CCCTT | C | intron_variant | MODIFIER | HG00280.hp2 HG01109.hp1 HG01261.hp2 |
a0001a0003 | a0001c0002a0003c0011a0003c0012 | a0001c0002t0001a0003c0011t0004a0003c0012t0013 | a0001c0002t0001g0113a0003c0011t0004g0103a0003c0012t0013g0022 | 3 | 150 | 0.0200 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039755 | TCCTA | T | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0003a0002c0003t0002others(1): Show | a0001c0001t0001g0145a0001c0001t0003g0134a0002c0003t0002g0054others(2): Show | 5 | 150 | 0.0333 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039763 | TCCTA | T | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(33): Show |
a0001a0002a0006others(6): Show | a0001c0001a0001c0002a0001c0021others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(13): Show | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | 150 | 0.2400 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039775 | ACCTT | A | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
a0001a0008a0009others(3): Show | a0001c0001a0001c0007a0001c0016others(5): Show | a0001c0001t0003a0001c0001t0007a0001c0007t0001others(7): Show | a0001c0001t0003g0082a0001c0001t0007g0036a0001c0007t0001g0139others(7): Show | 10 | 150 | 0.0667 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039826 | TTCTC | T | intron_variant | MODIFIER | HG02717.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
a0005a0023a0029 | a0005c0004a0023c0036a0029c0013 | a0005c0004t0008a0023c0036t0017a0029c0013t0009 | a0005c0004t0008g0001a0005c0004t0008g0002a0005c0004t0008g0007others(2): Show | 5 | 150 | 0.0333 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039882 | TCTTC | T | intron_variant | MODIFIER | HG00280.hp1 HG03041.hp1 HG06807.hp2 |
a0001a0009 | a0001c0002a0001c0008a0009c0041 | a0001c0002t0001a0001c0008t0014a0009c0041t0005 | a0001c0002t0001g0107a0001c0008t0014g0102a0009c0041t0005g0008 | 3 | 150 | 0.0200 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157060339 | GATTA | G | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp2 |
a0001 | a0001c0001a0001c0016 | a0001c0001t0003a0001c0016t0001 | a0001c0001t0003g0082a0001c0016t0001g0147 | 2 | 150 | 0.0133 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157064515 | ATTTG | A | intron_variant | MODIFIER | HG02055.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
a0001a0005a0023others(1): Show | a0001c0001a0005c0004a0023c0036others(1): Show | a0001c0001t0001a0005c0004t0008a0023c0036t0017others(1): Show | a0001c0001t0001g0141a0001c0001t0001g0145a0005c0004t0008g0001others(4): Show | 7 | 150 | 0.0467 | -4 | c.224 others(25): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157085517 | GTTAT | G | intron_variant | MODIFIER | HG02622.hp1 HG02922.hp2 NA21309.hp1 |
a0001a0007 | a0001c0001a0007c0031 | a0001c0001t0001a0007c0031t0001 | a0001c0001t0001g0003a0001c0001t0001g0035a0007c0031t0001g0005 | 3 | 150 | 0.0200 | -4 | c.249 others(21): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157115419 | CTTTG | C | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG01175.hp2 others(3): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0006 | a0001c0001t0001a0001c0002t0001a0006c0006t0001 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0097others(3): Show | 6 | 150 | 0.0400 | -4 | c.258 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157138200 | TTTGG | T | intron_variant | MODIFIER | HG00735.hp1 HG01884.hp2 HG02257.hp2 others(9): Show |
a0001a0014a0023 | a0001c0001a0001c0017a0014c0024others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0114others(9): Show | 12 | 150 | 0.0800 | -4 | c.276 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157161421 | TTGTG | T | intron_variant | MODIFIER | HG01346.hp1 HG01433.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075a0001c0001t0001g0109 | 2 | 150 | 0.0133 | -4 | c.309 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157202825 | CACAG | C | intron_variant | MODIFIER | HG03041.hp2 NA19043.hp1 |
a0001a0007 | a0001c0001a0007c0032 | a0001c0001t0006a0007c0032t0015 | a0001c0001t0006g0089a0007c0032t0015g0004 | 2 | 150 | 0.0133 | -4 | c.526 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45735418 | CGTGT | C | intron_variant | MODIFIER | NA18612.hp2 NA18957.hp2 NA18986.hp2 others(1): Show |
a0001a0006 | a0001c0001a0006c0007 | a0001c0001t0001a0006c0007t0001 | a0001c0001t0001g0011a0001c0001t0001g0013a0006c0007t0001g0010others(1): Show | 4 | 318 | 0.0126 | -4 | c.284 others(21): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45749412 | TACAG | T | intron_variant | MODIFIER | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0111a0004c0005t0001g0147a0004c0005t0001g0169 | 3 | 318 | 0.0094 | -4 | c.284 others(23): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45790341 | TTGTA | T | intron_variant | MODIFIER | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
a0002 | a0002c0003a0002c0020 | a0002c0003t0001a0002c0020t0001 | a0002c0003t0001g0210a0002c0003t0001g0248a0002c0003t0001g0249others(6): Show | 9 | 318 | 0.0283 | -4 | c.285 others(23): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45791204 | CTGTG | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(16): Show |
a0001a0009a0011 | a0001c0001a0001c0002a0009c0014others(1): Show | a0001c0001t0003a0001c0001t0009a0001c0002t0002others(2): Show | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(16): Show | 19 | 318 | 0.0598 | -4 | c.285 others(23): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |