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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BCL11A_chr2_60452194_60558654 | 60538719 | GTC | G | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0001g0025a0001c0001t0003g0181a0001c0001t0005g0233others(7): Show | 10 | 262 | 0.0382 | -2 | c.385 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | TogoVar | ||||||
BCL11A_chr2_60452194_60558654 | 60538739 | CTG | C | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0002g0090others(19): Show | 22 | 262 | 0.0840 | -2 | c.385 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | TogoVar | ||||||
BCL11A_chr2_60452194_60558654 | 60540946 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0046others(49): Show | 52 | 262 | 0.1985 | -2 | c.385 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | TogoVar | ||||||
BCL11A_chr2_60452194_60558654 | 60546552 | AAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(130): Show | 135 | 262 | 0.5153 | -2 | c.56- others(15): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99179473 | TAA | T | intron_variant | MODIFIER | HG01069.hp2 HG01099.hp1 HG02615.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(9): Show | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0218others(16): Show | 19 | 350 | 0.0543 | -2 | c.641 others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99185446 | GAA | G | intron_variant | MODIFIER | HG02615.hp1 HG02809.hp1 HG02886.hp2 others(10): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(6): Show | a0001c0001t0002g0056a0001c0001t0014g0176a0001c0001t0015g0079others(9): Show | 13 | 350 | 0.0371 | -2 | c.641 others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99199640 | CTG | C | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(16): Show | a0001c0001t0001g0173a0001c0001t0001g0184a0001c0001t0001g0208others(24): Show | 27 | 350 | 0.0771 | -2 | c.641 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99217301 | CAT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | 350 | 0.1400 | -2 | c.640 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99222897 | CTT | C | intron_variant | MODIFIER | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0002t0003a0001c0002t0019 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | 350 | 0.0086 | -2 | c.640 others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99234855 | CAA | C | intron_variant | MODIFIER | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(16): Show | a0001c0001t0002g0061a0001c0001t0002g0067a0001c0001t0002g0068others(31): Show | 35 | 350 | 0.1000 | -2 | c.428 others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99267544 | ACC | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(265): Show | 269 | 350 | 0.7686 | -2 | c.58+ others(17): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99269875 | TAA | T | intron_variant | MODIFIER | HG02293.hp1 HG02293.hp2 HG02683.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(6): Show | a0001c0001t0001g0193a0001c0001t0002g0115a0001c0001t0002g0118others(8): Show | 11 | 350 | 0.0314 | -2 | c.58+ others(17): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99275474 | TAC | T | upstream_gene_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(139): Show | 142 | 350 | 0.4057 | -2 | c.-42 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3278 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99276142 | CAA | C | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(124): Show | 127 | 350 | 0.3629 | -2 | c.-49 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3946 | chr14 | TogoVar | ||||||
BCL11B_chr14_99164287_99277197 | 99276486 | TTA | T | upstream_gene_variant | MODIFIER | NA18968.hp1 NA18995.hp1 NA19012.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012a0001c0001t0022others(1): Show | a0001c0001t0001g0232a0001c0001t0012g0147a0001c0001t0012g0148others(3): Show | 6 | 350 | 0.0171 | -2 | c.-52 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4290 | chr14 | TogoVar | ||||||
BCL2L10_chr15_52104263_52117775 | 52104996 | CTT | C | downstream_gene_variant | MODIFIER | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0002c0002t0001g0024others(20): Show | 25 | 458 | 0.0546 | -2 | c.*48 others(13): Show |
BCL2L10 | ENSG00000137875.4 | transcript | ENST00000260442.3 | protein_coding | 4266 | chr15 | TogoVar | ||||||
BCL2L10_chr15_52104263_52117775 | 52105401 | CAG | C | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(33): Show | 112 | 458 | 0.2445 | -2 | c.*44 others(13): Show |
BCL2L10 | ENSG00000137875.4 | transcript | ENST00000260442.3 | protein_coding | 3861 | chr15 | TogoVar | ||||||
BCL2L10_chr15_52104263_52117775 | 52111173 | AAC | A | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp2 HG00738.hp1 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0004g0149others(4): Show | 32 | 458 | 0.0699 | -2 | c.489 others(19): Show |
BCL2L10 | ENSG00000137875.4 | transcript | ENST00000260442.3 | protein_coding | 1/1 | chr15 | TogoVar | ||||||
BCL2L10_chr15_52104263_52117775 | 52115153 | TAC | T | upstream_gene_variant | MODIFIER | HG01934.hp2 HG01952.hp2 HG02004.hp1 others(10): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0004 | a0002c0002t0001g0024a0002c0002t0001g0032a0002c0002t0001g0100others(4): Show | 13 | 458 | 0.0284 | -2 | c.-24 others(13): Show |
BCL2L10 | ENSG00000137875.4 | transcript | ENST00000260442.3 | protein_coding | 2379 | chr15 | TogoVar | ||||||
BCL2L10_chr15_52104263_52117775 | 52116918 | CTT | C | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(23): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0005a0002c0002t0009others(1): Show | a0002c0002t0001g0033a0002c0002t0001g0051a0002c0002t0001g0109others(15): Show | 26 | 458 | 0.0568 | -2 | c.-41 others(13): Show |
BCL2L10 | ENSG00000137875.4 | transcript | ENST00000260442.3 | protein_coding | 4144 | chr15 | TogoVar | ||||||
BCL2L11_chr2_111115914_111173444 | 111118751 | CAG | C | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 69 | 398 | 0.1734 | -2 | c.-24 others(13): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 2162 | chr2 | TogoVar | ||||||
BCL2L11_chr2_111115914_111173444 | 111135100 | CCT | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(50): Show | 69 | 398 | 0.1734 | -2 | c.394 others(21): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BCL2L11_chr2_111115914_111173444 | 111137673 | CAT | C | intron_variant | MODIFIER | HG02055.hp2 HG02559.hp1 HG03209.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | 398 | 0.0101 | -2 | c.395 others(21): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BCL2L11_chr2_111115914_111173444 | 111147346 | TCA | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG01069.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(9): Show | a0001c0001t0002g0280a0001c0001t0002g0292a0001c0001t0004g0024others(23): Show | 29 | 398 | 0.0729 | -2 | c.395 others(19): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BCL2L11_chr2_111115914_111173444 | 111158296 | CAG | C | intron_variant | MODIFIER | HG02055.hp2 HG02559.hp1 HG03209.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | 398 | 0.0101 | -2 | c.499 others(19): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 3/3 | chr2 | TogoVar | ||||||
BCL2L11_chr2_111115914_111173444 | 111163861 | CTT | C | intron_variant | MODIFIER | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0002g0279a0001c0001t0002g0281a0001c0001t0003g0157others(34): Show | 38 | 398 | 0.0955 | -2 | c.499 others(17): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BCL2L11_chr2_111115914_111173444 | 111169212 | AGT | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(226): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(192): Show | 229 | 398 | 0.5754 | -2 | c.*49 others(13): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 769 | chr2 | TogoVar | ||||||
BCL2L11_chr2_111115914_111173444 | 111169437 | ACT | A | downstream_gene_variant | MODIFIER | NA18969.hp1 NA18981.hp1 NA18998.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0114a0001c0001t0004g0122a0001c0001t0004g0126 | 3 | 398 | 0.0075 | -2 | c.*52 others(13): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 994 | chr2 | TogoVar | ||||||
BCL2L11_chr2_111115914_111173444 | 111170699 | CAA | C | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(55): Show | 72 | 398 | 0.1809 | -2 | c.*64 others(13): Show |
BCL2L11 | ENSG00000153094.25 | transcript | ENST00000393256.8 | protein_coding | 2256 | chr2 | TogoVar | ||||||
BCL2L13_chr22_17633757_17735855 | 17645225 | ATT | A | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(58): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0007a0003c0004others(4): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(15): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0003g0002others(58): Show | 61 | 306 | 0.1994 | -2 | c.-51 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17646888 | TTG | T | intron_variant | MODIFIER | HG01256.hp2 HG02280.hp2 HG02698.hp1 others(8): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0003a0001c0002t0001a0001c0002t0006others(2): Show | a0001c0001t0003g0021a0001c0001t0003g0048a0001c0001t0003g0049others(8): Show | 11 | 306 | 0.0360 | -2 | c.-51 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17649871 | CTT | C | intron_variant | MODIFIER | HG01069.hp1 HG01109.hp1 HG02280.hp2 others(9): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0003g0048others(9): Show | 12 | 306 | 0.0392 | -2 | c.-50 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17653495 | ATT | A | intron_variant | MODIFIER | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004others(1): Show | a0001c0001t0024a0001c0002t0014a0003c0004t0015others(4): Show | a0001c0001t0024g0243a0001c0001t0024g0244a0001c0002t0014g0063others(13): Show | 16 | 306 | 0.0523 | -2 | c.-50 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17656335 | CTT | C | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0003a0001c0001t0008a0001c0001t0024others(4): Show | a0001c0001t0003g0251a0001c0001t0008g0223a0001c0001t0008g0227others(6): Show | 9 | 306 | 0.0294 | -2 | c.121 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17659056 | TAA | T | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(42): Show |
a0001a0004a0007others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0003a0001c0001t0009a0001c0001t0023others(11): Show | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(42): Show | 45 | 306 | 0.1471 | -2 | c.121 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17664415 | ACC | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
a0001 | a0001c0001a0001c0009a0001c0012others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | 306 | 0.5261 | -2 | c.121 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17667963 | CTT | C | intron_variant | MODIFIER | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(24): Show |
a0001a0003a0004 | a0001c0001a0003c0004a0003c0005others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0002g0099a0001c0001t0003g0054a0001c0001t0004g0191others(24): Show | 27 | 306 | 0.0882 | -2 | c.121 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17669030 | CTT | C | intron_variant | MODIFIER | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0014a0001c0002t0027a0001c0002t0037 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(3): Show | 6 | 306 | 0.0196 | -2 | c.121 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17671393 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
a0001a0004a0005others(2): Show | a0001c0001a0001c0002a0001c0007others(7): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(54): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(206): Show | 209 | 306 | 0.6830 | -2 | c.122 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17673361 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
a0001 | a0001c0001a0001c0009a0001c0012 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(25): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(106): Show | 109 | 306 | 0.3562 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17673533 | ATT | A | intron_variant | MODIFIER | HG01070.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
a0001a0007 | a0001c0001a0007c0013 | a0001c0001t0002a0001c0001t0003a0007c0013t0003 | a0001c0001t0002g0128a0001c0001t0003g0024a0001c0001t0003g0025others(9): Show | 12 | 306 | 0.0392 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17674605 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
a0001a0003a0005others(2): Show | a0001c0001a0001c0002a0001c0007others(8): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(61): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(234): Show | 237 | 306 | 0.7745 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17675075 | TAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0009a0001c0012others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(49): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(178): Show | 181 | 306 | 0.5915 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17679264 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
a0001a0003 | a0001c0001a0001c0009a0001c0012others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(43): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | 306 | 0.5261 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17680540 | AAG | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG01069.hp1 others(28): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(11): Show | a0001c0001t0002g0141a0001c0001t0002g0144a0001c0001t0002g0150others(28): Show | 31 | 306 | 0.1013 | -2 | c.122 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17685760 | CTT | C | intron_variant | MODIFIER | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
a0003 | a0003c0004a0003c0005 | a0003c0004t0015a0003c0004t0016a0003c0005t0006 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0016g0087others(6): Show | 9 | 306 | 0.0294 | -2 | c.229 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17691358 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0009a0001c0012others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(50): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(179): Show | 182 | 306 | 0.5948 | -2 | c.386 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17693372 | GTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
a0001 | a0001c0001a0001c0009a0001c0012others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(29): Show | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0002g0138others(94): Show | 97 | 306 | 0.3170 | -2 | c.387 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17699445 | CAA | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(5): Show | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | 306 | 0.0719 | -2 | c.457 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
BCL2L13_chr22_17633757_17735855 | 17701915 | CAA | C | intron_variant | MODIFIER | HG00408.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0005a0001c0001t0028a0005c0008t0019 | a0001c0001t0005g0161a0001c0001t0005g0241a0001c0001t0028g0302others(3): Show | 6 | 306 | 0.0196 | -2 | c.457 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | TogoVar |