view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TCF12_chr15_56913644_57294853 | 56963424 | C | CTTTAGCT others(7): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0173 | 1 | 330 | 0.0030 | 14 | c.148 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | chr15 | TogoVar | |||||||
TCF12_chr15_56913644_57294853 | 56984001 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01168.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0164 a0001c0001t0003g0169 |
2 | 330 | 0.0061 | 14 | c.148 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 56984249 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00639.hp1 HG01943.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0095 a0001c0001t0001g0119 a0001c0001t0003g0109 others(3): Show |
6 | 330 | 0.0182 | 14 | c.148 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57056116 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
a0001 | a0001c0004a0001c0005 | a0001c0004t0005a0001c0005t0001 | a0001c0004t0005g0145 a0001c0004t0005g0148 a0001c0005t0001g0085 others(1): Show |
4 | 330 | 0.0121 | 14 | c.149 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57064795 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG03041.hp2 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0060 a0001c0001t0008g0007 |
2 | 330 | 0.0061 | 14 | c.222 others(29): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57075800 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0172 | 1 | 330 | 0.0030 | 14 | c.222 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57075804 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | NA18978.hp2 NA19070.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0039 | a0001c0001t0003g0181 a0001c0001t0039g0150 |
2 | 330 | 0.0061 | 14 | c.222 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57075804 | T | TTCTTTCT others(7): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0175 | 1 | 330 | 0.0030 | 14 | c.222 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57075804 | T | TTCTTTCT others(7): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0210 | 1 | 330 | 0.0030 | 14 | c.222 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57075804 | T | TTCTTTCT others(7): Show |
intron_variant | MODIFIER | HG00621.hp1 HG02735.hp2 HG03831.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0038 | a0001c0001t0002g0220 a0001c0001t0002g0234 a0001c0001t0002g0258 others(4): Show |
7 | 330 | 0.0212 | 14 | c.222 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57123968 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(45): Show |
a0001a0005 | a0001c0001a0005c0009 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(3): Show | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0009 others(45): Show |
48 | 330 | 0.1455 | 14 | c.325 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57136958 | G | GTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02896.hp1 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0080 a0001c0005t0001g0083 |
2 | 330 | 0.0061 | 14 | c.326 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57177608 | C | CAGAGAGA others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG01071.hp1 others(26): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(26): Show |
29 | 330 | 0.0879 | 14 | c.390 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57197152 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01123.hp2 HG01255.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0025 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0252 others(5): Show |
8 | 330 | 0.0242 | 14 | c.527 others(29): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57208380 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 330 | 0.0030 | 14 | c.579 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57223643 | G | GTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00558.hp2 HG01081.hp2 HG01168.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0017a0001c0002t0003 | a0001c0001t0003g0112 a0001c0001t0003g0152 a0001c0001t0003g0160 others(8): Show |
11 | 330 | 0.0333 | 14 | c.580 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57223653 | T | TTTGTTTT others(7): Show |
intron_variant | MODIFIER | HG00597.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0221 a0001c0001t0002g0240 a0001c0001t0002g0252 others(2): Show |
5 | 330 | 0.0152 | 14 | c.580 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57223654 | T | TTGTTTTT others(7): Show |
intron_variant | MODIFIER | HG01168.hp1 NA19063.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0004 a0001c0001t0002g0289 |
2 | 330 | 0.0061 | 14 | c.580 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57223654 | T | TTTGTTTT others(7): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG02165.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0033 | a0001c0001t0002g0304 a0001c0001t0002g0319 a0001c0001t0002g0320 others(1): Show |
4 | 330 | 0.0121 | 14 | c.580 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57240879 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02615.hp2 |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0311 a0001c0001t0008g0312 |
2 | 330 | 0.0061 | 14 | c.103 others(33): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF12_chr15_56913644_57294853 | 57264195 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02622.hp1 NA19057.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0093 a0001c0001t0001g0228 a0001c0001t0011g0328 |
3 | 330 | 0.0091 | 14 | c.174 others(31): Show |
TCF12 | ENSG00000140262.18 | transcript | ENST00000333725.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TCF19_chr6_31153589_31169215 | 31155603 | C | CAAAAAAA others(7): Show |
upstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
a0001a0004a0006others(1): Show | a0001c0001a0004c0007a0006c0008others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(12): Show |
118 | 451 | 0.2616 | 14 | c.-36 others(25): Show |
TCF19 | ENSG00000137310.13 | transcript | ENST00000376257.8 | protein_coding | 2985 | chr6 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42161972 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0007 | a0007c0019 | a0007c0019t0002 | a0007c0019t0002g0243 | 1 | 355 | 0.0028 | 14 | c.*45 others(29): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42216079 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02630.hp1 NA18906.hp2 |
a0001a0005 | a0001c0002a0005c0009 | a0001c0002t0007a0005c0009t0001 | a0001c0002t0007g0102 a0005c0009t0001g0089 |
2 | 355 | 0.0056 | 14 | c.-36 others(29): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42219355 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(1): Show |
a0001a0003a0008 | a0001c0001a0001c0006a0003c0004others(1): Show | a0001c0001t0002a0001c0006t0002a0003c0004t0001others(1): Show | a0001c0001t0002g0248 a0001c0006t0002g0247 a0003c0004t0001g0108 others(1): Show |
4 | 355 | 0.0113 | 14 | c.-36 others(31): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42221739 | G | GTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0006a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0002others(4): Show | a0001c0001t0001g0245 a0001c0001t0001g0251 a0001c0001t0002g0091 others(9): Show |
12 | 355 | 0.0338 | 14 | c.-36 others(31): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42243292 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0074 | 1 | 355 | 0.0028 | 14 | c.-37 others(33): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | TogoVar | |||||||
TCF20_chr22_42155013_42275653 | 42254959 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02258.hp2 NA20300.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0002a0001c0006t0002 | a0001c0001t0002g0248 a0001c0006t0002g0246 a0001c0006t0002g0247 |
3 | 355 | 0.0085 | 14 | c.-37 others(33): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | TogoVar | |||||||
TCF25_chr16_89868592_89916379 | 89869053 | A | AAAAAACA others(7): Show |
upstream_gene_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 300 | 0.0033 | 14 | c.-46 others(25): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4538 | chr16 | TogoVar | |||||||
TCF25_chr16_89868592_89916379 | 89869053 | A | AAAATATA others(7): Show |
upstream_gene_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 300 | 0.0033 | 14 | c.-46 others(25): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4538 | chr16 | TogoVar | |||||||
TCF25_chr16_89868592_89916379 | 89907346 | A | ACCTCCCT others(7): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0267 | 1 | 300 | 0.0033 | 14 | c.179 others(29): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89907521 | T | TCCTCCCA others(7): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
a0001a0005a0010others(1): Show | a0001c0002a0005c0008a0010c0019others(1): Show | a0001c0002t0001a0001c0002t0005a0005c0008t0001others(2): Show | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0023 others(27): Show |
30 | 300 | 0.1000 | 14 | c.179 others(31): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89907550 | G | GCTCCTGG others(7): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0069 | 1 | 300 | 0.0033 | 14 | c.179 others(31): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89907563 | A | ACCTCCCT others(7): Show |
intron_variant | MODIFIER | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0272 others(13): Show |
16 | 300 | 0.0533 | 14 | c.179 others(31): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89907612 | A | ACCTCCCT others(7): Show |
intron_variant | MODIFIER | HG02040.hp2 HG02897.hp1 NA21309.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0003a0002c0003t0001 | a0001c0001t0001g0213 a0001c0001t0003g0292 a0002c0003t0001g0286 |
3 | 300 | 0.0100 | 14 | c.179 others(31): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89907617 | C | CCTCCTCC others(7): Show |
intron_variant | MODIFIER | HG00099.hp2 HG01167.hp1 HG02896.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0264 a0002c0003t0001g0005 a0002c0003t0001g0052 others(5): Show |
9 | 300 | 0.0300 | 14 | c.179 others(31): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89908731 | G | GCTCCCGC others(7): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(19): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0272 others(18): Show |
22 | 300 | 0.0733 | 14 | c.179 others(33): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89908812 | G | GCAGCTCC others(7): Show |
intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0045 | 1 | 300 | 0.0033 | 14 | c.179 others(33): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
TCF25_chr16_89868592_89916379 | 89914789 | T | TTGTGTGT others(7): Show |
downstream_gene_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG02040.hp1 others(8): Show |
a0001a0005 | a0001c0002a0005c0008 | a0001c0002t0001a0005c0008t0001 | a0001c0002t0001g0025 a0001c0002t0001g0028 a0001c0002t0001g0029 others(8): Show |
11 | 300 | 0.0367 | 14 | c.*35 others(25): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3411 | chr16 | TogoVar | |||||||
TCF3_chr19_1604292_1657615 | 1611178 | A | AATGTTTT others(7): Show |
3_prime_UTR_variant | MODIFIER | NA18969.hp1 | a0002 | a0002c0002 | a0002c0002t0054 | a0002c0002t0054g0157 | 1 | 352 | 0.0028 | 14 | c.*51 others(23): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 528 | chr19 | TogoVar | ||||||
TCF4_chr18_55217185_55593192 | 55246232 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0116 | 1 | 122 | 0.0082 | 14 | c.135 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 15/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55248960 | G | GCCTCGAA others(7): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 | 1 | 122 | 0.0082 | 14 | c.135 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 15/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55365156 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02615.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0025 | a0001c0001t0001g0113 a0001c0001t0025g0036 |
2 | 122 | 0.0164 | 14 | c.370 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 6/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55365191 | A | ATATATAT others(7): Show |
intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 122 | 0.0082 | 14 | c.370 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 6/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55399853 | A | ATCTCTCT others(7): Show |
intron_variant | MODIFIER | HG00323.hp2 | a0001 | a0001c0002 | a0001c0002t0036 | a0001c0002t0036g0003 | 1 | 122 | 0.0082 | 14 | c.369 others(31): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 6/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55434763 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01099.hp1 HG02280.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(4): Show | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | 122 | 0.0820 | 14 | c.304 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 5/19 | chr18 | TogoVar | |||||||
TCF4_chr18_55217185_55593192 | 55494157 | G | GACACACA others(7): Show |
intron_variant | MODIFIER | HG01109.hp1 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0029 | a0001c0001t0001g0086 a0001c0001t0029g0103 |
2 | 122 | 0.0164 | 14 | c.146 others(33): Show |
TCF4 | ENSG00000196628.20 | transcript | ENST00000354452.8 | protein_coding | 3/19 | chr18 | TogoVar | |||||||
TCF7L1_chr2_85128392_85315387 | 85153340 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG03041.hp1 HG03209.hp1 HG03669.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0092 a0001c0001t0001g0208 a0002c0002t0002g0039 |
3 | 236 | 0.0127 | 14 | c.441 others(33): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TCF7L1_chr2_85128392_85315387 | 85168192 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG01358.hp1 HG02572.hp1 HG03225.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(2): Show | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0196 others(7): Show |
10 | 236 | 0.0424 | 14 | c.441 others(33): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TCF7L1_chr2_85128392_85315387 | 85282794 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00597.hp1 HG02647.hp1 HG03130.hp2 |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0002 | a0001c0001t0001g0095 a0001c0001t0001g0163 a0005c0006t0002g0108 |
3 | 236 | 0.0127 | 14 | c.442 others(29): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |