view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF7_chr13_111110310_111310732 | 111142939 | CTT | C | intron_variant | MODIFIER | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0002t0002 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | 274 | 0.0292 | -2 | c.166 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111156211 | AAG | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | 274 | 0.7336 | -2 | c.252 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111159883 | CCT | C | intron_variant | MODIFIER | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0019 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | 274 | 0.0146 | -2 | c.252 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111174840 | ACT | A | intron_variant | MODIFIER | HG01192.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
a0001 | a0001c0001a0001c0014a0001c0016 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(8): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0068others(12): Show | 15 | 274 | 0.0547 | -2 | c.252 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111185961 | CGT | C | intron_variant | MODIFIER | HG00140.hp1 HG01099.hp1 HG01516.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(3): Show | a0001c0001t0003g0087a0001c0001t0003g0178a0001c0001t0003g0213others(14): Show | 17 | 274 | 0.0620 | -2 | c.253 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221311 | CTA | C | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(99): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(99): Show | 102 | 274 | 0.3723 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221353 | CTA | C | intron_variant | MODIFIER | HG01891.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0003g0025others(1): Show | 4 | 274 | 0.0146 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221377 | CTA | C | intron_variant | MODIFIER | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0013a0001c0001t0014 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(10): Show | 13 | 274 | 0.0475 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221386 | TAG | T | intron_variant | MODIFIER | NA18941.hp2 NA19000.hp1 NA19005.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0029 | a0001c0001t0009g0171a0001c0001t0009g0214a0001c0001t0009g0258others(3): Show | 6 | 274 | 0.0219 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221389 | ATG | A | intron_variant | MODIFIER | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(8): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(8): Show | 11 | 274 | 0.0402 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221401 | CTA | C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(2): Show | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(10): Show | 13 | 274 | 0.0475 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221432 | TAG | T | intron_variant | MODIFIER | HG02451.hp1 HG02559.hp2 HG03540.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0003a0001c0003t0019 | a0001c0001t0002g0099a0001c0003t0003g0021a0001c0003t0019g0022 | 3 | 274 | 0.0110 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221469 | CTA | C | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02258.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0011 | a0001c0001t0005g0062a0001c0001t0011g0006a0001c0001t0011g0007 | 3 | 274 | 0.0110 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221478 | TAG | T | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG01081.hp2 others(41): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0001others(8): Show | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272others(41): Show | 44 | 274 | 0.1606 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221480 | GAT | G | intron_variant | MODIFIER | HG00099.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
a0001a0003 | a0001c0001a0001c0016a0003c0011 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0123a0001c0001t0001g0219a0001c0001t0003g0128others(14): Show | 17 | 274 | 0.0620 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221492 | CAT | C | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp1 HG01081.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0006a0003c0011 | a0001c0001t0003a0001c0001t0005a0001c0006t0012others(1): Show | a0001c0001t0003g0128a0001c0001t0005g0062a0001c0001t0005g0063others(12): Show | 15 | 274 | 0.0547 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221549 | ATC | A | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0009others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0015others(9): Show | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(47): Show | 50 | 274 | 0.1825 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221559 | CTA | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(23): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(5): Show | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(23): Show | 26 | 274 | 0.0949 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111221643 | TTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
a0001a0004a0005 | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | 274 | 0.3759 | -2 | c.670 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111243422 | CTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0075 | 3 | 274 | 0.0110 | -2 | c.760 others(17): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111248499 | TAC | T | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011a0001c0001t0017others(1): Show | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | 274 | 0.0365 | -2 | c.950 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111262413 | CAT | C | intron_variant | MODIFIER | HG01243.hp1 HG02300.hp2 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0006a0001c0005t0020 | a0001c0001t0006g0042a0001c0005t0020g0117a0001c0005t0020g0118 | 3 | 274 | 0.0110 | -2 | c.951 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | TogoVar | |||||||
ARHGEF7_chr13_111110310_111310732 | 111274360 | ACT | A | intron_variant | MODIFIER | HG00558.hp2 NA18939.hp1 NA18950.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0032a0001c0001t0006g0083a0001c0001t0006g0218others(1): Show | 4 | 274 | 0.0146 | -2 | c.121 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111281181 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0014others(10): Show | a0001c0001t0003g0024a0001c0001t0003g0178a0001c0001t0003g0216others(49): Show | 52 | 274 | 0.1898 | -2 | c.172 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111293436 | TAA | T | intron_variant | MODIFIER | HG00558.hp1 HG01169.hp2 HG01243.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(2): Show | a0001c0001t0002g0099a0001c0001t0005g0103a0001c0001t0006g0083others(4): Show | 7 | 274 | 0.0256 | -2 | c.231 others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63634908 | AAC | A | downstream_gene_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113 | 1 | 168 | 0.0060 | -2 | c.*31 others(13): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 58 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63637840 | ATC | A | 3_prime_UTR_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0029 | 1 | 168 | 0.0060 | -2 | c.*18 others(11): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 186 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63637846 | CTG | C | 3_prime_UTR_variant | MODIFIER | HG00735.hp1 HG01167.hp1 HG01255.hp1 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(3): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0023others(33): Show | 36 | 168 | 0.2143 | -2 | c.*18 others(11): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 180 | chrX | TogoVar | ||||||
ARHGEF9_chrX_63629967_63790214 | 63644146 | CAT | C | intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 168 | 0.0060 | -2 | c.132 others(18): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63644762 | ATT | A | intron_variant | MODIFIER | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0016 | a0001c0001t0002g0026a0001c0001t0002g0030a0001c0001t0002g0032others(4): Show | 7 | 168 | 0.0417 | -2 | c.132 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63661755 | CTT | C | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0013 | 1 | 168 | 0.0060 | -2 | c.107 others(21): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63666402 | TTA | T | intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 168 | 0.0060 | -2 | c.946 others(17): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63666453 | TAC | T | intron_variant | MODIFIER | HG02280.hp1 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | 168 | 0.0119 | -2 | c.946 others(17): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63674168 | CTG | C | splice_acceptor_variant others(2): Show |
HIGH | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0052 | 1 | 168 | 0.0060 | -2 | c.816 others(13): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63705357 | ATG | A | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(111): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(108): Show | 114 | 168 | 0.6786 | -2 | c.402 others(17): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63713701 | TAC | T | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0020 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | 168 | 0.0357 | -2 | c.211 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63715385 | GCT | G | intron_variant | MODIFIER | NA18953.hp1 NA18955.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0143 | 3 | 168 | 0.0179 | -2 | c.211 others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | TogoVar | |||||||
ARHGEF9_chrX_63629967_63790214 | 63740283 | CTT | C | intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0003 | 1 | 168 | 0.0060 | -2 | c.31- others(19): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | TogoVar | |||||||
ARID1A_chr1_26691015_26787104 | 26702172 | TGA | T | intron_variant | MODIFIER | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | 146 | 0.0411 | -2 | c.113 others(21): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26704397 | CAA | C | intron_variant | MODIFIER | HG02109.hp1 HG02818.hp1 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0007t0001 | a0001c0001t0001g0118a0001c0007t0001g0117 | 2 | 146 | 0.0137 | -2 | c.113 others(21): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | chr1 | TogoVar | |||||||
ARID1A_chr1_26691015_26787104 | 26736628 | CAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01069.hp2 others(13): Show |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0055a0001c0001t0001g0118a0001c0001t0002g0126others(12): Show | 16 | 146 | 0.1096 | -2 | c.192 others(21): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26762514 | CTT | C | intron_variant | MODIFIER | HG02055.hp2 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110a0001c0001t0001g0114 | 2 | 146 | 0.0137 | -2 | c.241 others(19): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26778068 | CAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(12): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0118a0001c0001t0002g0126a0001c0001t0002g0127others(11): Show | 15 | 146 | 0.1027 | -2 | c.512 others(19): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26780906 | TTC | T | 3_prime_UTR_variant | MODIFIER | HG01261.hp1 HG01261.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0016a0001c0001t0005g0088 | 2 | 146 | 0.0137 | -2 | c.*15 others(11): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 20/20 | 157 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156781975 | CTT | C | intron_variant | MODIFIER | HG01496.hp2 HG01884.hp2 HG01934.hp2 others(12): Show |
a0001a0018 | a0001c0001a0001c0002a0018c0026 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0065others(12): Show | 15 | 150 | 0.1000 | -2 | c.179 others(21): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156794570 | CTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(72): Show |
a0001a0002a0004others(15): Show | a0001c0001a0001c0002a0001c0016others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(30): Show | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0034others(72): Show | 75 | 150 | 0.5000 | -2 | 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 | 156805007 | CAA | C | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | 150 | 0.0133 | -2 | c.179 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | chr6 | TogoVar | |||||||
ARID1B_chr6_156772378_157215779 | 156812933 | GGT | G | intron_variant | MODIFIER | HG00280.hp1 HG01109.hp1 HG01261.hp2 others(16): Show |
a0001a0003a0007others(2): Show | a0001c0001a0001c0002a0003c0010others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(7): Show | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0039others(16): Show | 19 | 150 | 0.1267 | -2 | 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 | 156813031 | CAT | C | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(7): Show |
a0001a0019 | a0001c0001a0001c0002a0001c0017others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0017t0020others(1): Show | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | 150 | 0.0667 | -2 | 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 | 156813095 | TAC | T | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(24): Show |
a0001a0005a0008others(11): Show | a0001c0001a0001c0002a0001c0017others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(14): Show | a0001c0001t0001g0003a0001c0001t0001g0109a0001c0001t0001g0114others(24): Show | 27 | 150 | 0.1800 | -2 | c.179 others(23): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |