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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TCERG1L_chr10_131087391_131316721 | 131289342 | A | AGT | intron_variant | MODIFIER | HG00733.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0008 | a0001c0001t0002g0223a0001c0001t0002g0225a0001c0001t0002g0227others(4): Show | 7 | 324 | 0.0216 | 2 | c.670 others(21): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3/11 | chr10 | TogoVar | ||||||
TCERG1L_chr10_131087391_131316721 | 131289965 | G | GGT | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp2 HG00738.hp2 others(15): Show |
a0001a0010 | a0001c0001a0001c0003a0001c0008others(1): Show | a0001c0001t0011a0001c0001t0020a0001c0003t0001others(4): Show | a0001c0001t0011g0186a0001c0001t0011g0188a0001c0001t0011g0189others(15): Show | 18 | 324 | 0.0556 | 2 | c.670 others(21): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3/11 | chr10 | TogoVar | ||||||
TCERG1L_chr10_131087391_131316721 | 131290101 | T | TGA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
a0001a0004a0006others(1): Show | a0001c0001a0001c0002a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(164): Show | 167 | 324 | 0.5154 | 2 | c.670 others(21): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3/11 | chr10 | TogoVar | ||||||
TCERG1L_chr10_131087391_131316721 | 131291401 | C | CTT | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(6): Show | a0001c0001t0001g0020a0001c0001t0003g0017a0001c0001t0003g0053others(23): Show | 26 | 324 | 0.0803 | 2 | c.670 others(21): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3/11 | chr10 | TogoVar | ||||||
TCERG1L_chr10_131087391_131316721 | 131292856 | A | ATT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG01496.hp1 others(5): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(2): Show | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0003g0070others(5): Show | 8 | 324 | 0.0247 | 2 | c.670 others(21): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3/11 | chr10 | TogoVar | ||||||
TCERG1L_chr10_131087391_131316721 | 131315668 | C | CGT | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0058others(79): Show | 82 | 324 | 0.2531 | 2 | c.-40 others(13): Show |
TCERG1L | ENSG00000176769.9 | transcript | ENST00000368642.4 | protein_coding | 3948 | chr10 | TogoVar | ||||||
TCERG1_chr5_146442333_146516961 | 146451319 | C | CTT | intron_variant | MODIFIER | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0259a0001c0001t0001g0260others(19): Show | 24 | 320 | 0.0750 | 2 | c.60- others(17): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146460426 | A | ATT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 106 | 320 | 0.3313 | 2 | c.892 others(19): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146466020 | C | CAA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(115): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0015a0001c0018others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0015t0002others(4): Show | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(100): Show | 118 | 320 | 0.3688 | 2 | c.113 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146472701 | T | TTG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(101): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 104 | 320 | 0.3250 | 2 | c.160 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146477692 | C | CTT | intron_variant | MODIFIER | HG00738.hp2 HG01175.hp2 HG01257.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 32 | 320 | 0.1000 | 2 | c.160 others(19): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146484581 | G | GTA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
a0001a0003a0008 | a0001c0001a0001c0015a0001c0018others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0015t0002others(3): Show | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | 320 | 0.3094 | 2 | c.216 others(19): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146501346 | G | GAT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(160): Show | 185 | 320 | 0.5781 | 2 | c.243 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCERG1_chr5_146442333_146516961 | 146505717 | A | ACT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0008a0001c0015others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | 320 | 0.5344 | 2 | c.278 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56925240 | G | GCC | intron_variant | MODIFIER | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0204others(16): Show | 19 | 330 | 0.0576 | 2 | c.148 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56926312 | C | CAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(4): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(29): Show | 32 | 330 | 0.0970 | 2 | c.148 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56941104 | C | CAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(326): Show | 329 | 330 | 0.9970 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56942651 | C | CAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(326): Show | 329 | 330 | 0.9970 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56950745 | G | GCT | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG00735.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0002g0240others(10): Show | 13 | 330 | 0.0394 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 56952184 | G | GTA | intron_variant | MODIFIER | HG00735.hp1 HG01074.hp1 HG01109.hp2 others(32): Show |
a0001a0002 | a0001c0004a0002c0003a0002c0006 | a0001c0004t0005a0002c0003t0004a0002c0003t0010others(2): Show | a0001c0004t0005g0135a0001c0004t0005g0136a0001c0004t0005g0137others(32): Show | 35 | 330 | 0.1061 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56952189 | T | TAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
a0001a0004 | a0001c0001a0004c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0105a0001c0001t0001g0251a0001c0001t0002g0003others(143): Show | 146 | 330 | 0.4424 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56952193 | C | CAA | intron_variant | MODIFIER | HG01243.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0325a0001c0001t0011g0326a0001c0001t0011g0327others(1): Show | 4 | 330 | 0.0121 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56958676 | A | AGT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(7): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(27): Show | 30 | 330 | 0.0909 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56958678 | A | AGT | intron_variant | MODIFIER | HG01978.hp1 HG02071.hp2 HG02155.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0019a0001c0002t0001others(2): Show | a0001c0001t0001g0049a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | 330 | 0.0242 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56960430 | A | ATT | intron_variant | MODIFIER | HG00735.hp1 HG01074.hp1 HG01109.hp2 others(24): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0006 | a0001c0001t0008a0001c0001t0011a0002c0003t0004others(3): Show | a0001c0001t0008g0309a0001c0001t0008g0310a0001c0001t0008g0311others(24): Show | 27 | 330 | 0.0818 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56963027 | C | CTT | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp2 HG02074.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0018 | a0001c0001t0001g0251a0001c0001t0002g0265a0001c0001t0002g0286others(3): Show | 6 | 330 | 0.0182 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56969535 | A | ATT | intron_variant | MODIFIER | HG01168.hp2 HG01361.hp1 HG01975.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(2): Show | a0001c0001t0001g0039a0001c0001t0001g0076a0001c0001t0001g0077others(9): Show | 12 | 330 | 0.0364 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56984249 | G | GGT | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0070others(27): Show | 30 | 330 | 0.0909 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56990151 | C | CTT | intron_variant | MODIFIER | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0008a0001c0001t0009a0001c0002t0001others(1): Show | a0001c0001t0008g0310a0001c0001t0008g0311a0001c0001t0009g0225others(3): Show | 6 | 330 | 0.0182 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56990250 | C | CGT | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0008a0001c0001t0020others(1): Show | a0001c0001t0003g0217a0001c0001t0008g0310a0001c0001t0008g0311others(4): Show | 7 | 330 | 0.0212 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56990799 | C | CTT | intron_variant | MODIFIER | HG00597.hp2 HG02071.hp2 HG02083.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(1): Show | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0007g0200others(11): Show | 14 | 330 | 0.0424 | 2 | c.148 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56995231 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0053others(89): Show | 92 | 330 | 0.2788 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56996283 | A | ATG | intron_variant | MODIFIER | HG01255.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0009a0001c0005t0001 | a0001c0001t0009g0081a0001c0005t0001g0069a0001c0005t0001g0080others(4): Show | 7 | 330 | 0.0212 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56998457 | C | CAA | intron_variant | MODIFIER | HG01099.hp1 HG01167.hp1 HG02027.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(4): Show | a0001c0001t0002g0224a0001c0001t0002g0258a0001c0001t0003g0112others(16): Show | 19 | 330 | 0.0576 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 56999414 | C | CAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(326): Show | 329 | 330 | 0.9970 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57001004 | T | TAA | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0007a0001c0001t0008g0309a0001c0001t0008g0310others(3): Show | 6 | 330 | 0.0182 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57001012 | A | ATT | intron_variant | MODIFIER | HG00544.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(2): Show | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0170others(12): Show | 15 | 330 | 0.0455 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57017726 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0002c0003others(2): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(12): Show | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0009others(96): Show | 99 | 330 | 0.3000 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57024216 | C | CTT | intron_variant | MODIFIER | HG00423.hp2 HG02074.hp2 HG02809.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0035 | a0001c0001t0001g0076a0001c0001t0002g0241a0001c0001t0002g0242others(8): Show | 11 | 330 | 0.0333 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57030074 | C | CTA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(30): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(216): Show | 219 | 330 | 0.6636 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57052716 | A | ATG | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | 330 | 0.0152 | 2 | c.149 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57054773 | C | CTT | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0005a0004c0009 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(2): Show | a0001c0001t0001g0053a0001c0001t0008g0310a0001c0001t0011g0326others(4): Show | 7 | 330 | 0.0212 | 2 | c.149 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57056116 | G | GGT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(5): Show | a0001c0001t0001g0061a0001c0001t0001g0105a0001c0001t0001g0227others(36): Show | 39 | 330 | 0.1182 | 2 | c.149 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57064795 | C | CAA | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(4): Show | a0001c0001t0001g0079a0001c0001t0001g0095a0001c0001t0001g0118others(26): Show | 29 | 330 | 0.0879 | 2 | c.222 others(17): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57067538 | C | CAA | intron_variant | MODIFIER | HG02145.hp1 HG02630.hp2 HG02698.hp2 others(4): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(1): Show | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0002g0318others(4): Show | 7 | 330 | 0.0212 | 2 | c.222 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57073484 | C | CTT | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0007a0001c0001t0008g0309a0001c0001t0008g0310others(3): Show | 6 | 330 | 0.0182 | 2 | c.222 others(19): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57075806 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(2): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(8): Show | 11 | 330 | 0.0333 | 2 | c.222 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57075828 | C | CTT | intron_variant | MODIFIER | HG02074.hp2 HG02132.hp2 HG02735.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0001t0002g0249others(4): Show | 7 | 330 | 0.0212 | 2 | c.222 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57075835 | T | TTC | intron_variant | MODIFIER | HG01243.hp2 HG02559.hp1 NA19043.hp1 |
a0001a0004 | a0001c0001a0004c0009 | a0001c0001t0011a0004c0009t0036 | a0001c0001t0011g0327a0001c0001t0011g0328a0004c0009t0036g0155 | 3 | 330 | 0.0091 | 2 | c.222 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TCF12_chr15_56913644_57294853 | 57076638 | C | CAA | intron_variant | MODIFIER | HG00735.hp1 HG01074.hp1 HG01109.hp2 others(16): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0006 | a0001c0001t0001a0002c0003t0004a0002c0003t0010others(2): Show | a0001c0001t0001g0060a0002c0003t0004g0269a0002c0003t0004g0270others(16): Show | 19 | 330 | 0.0576 | 2 | c.222 others(21): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar |