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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TPMT_chr6_18123311_18160077 | 18146166 | CAT | C | intron_variant | MODIFIER | HG02970.hp1 HG03130.hp2 NA19240.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0016a0001c0002t0002a0001c0002t0018 | a0001c0001t0016g0214a0001c0002t0002g0213a0001c0002t0018g0212 | 3 | 438 | 0.0069 | -2 | c.233 others(19): Show |
TPMT | ENSG00000137364.5 | transcript | ENST00000309983.5 | protein_coding | 3/8 | chr6 | TogoVar | ||||||
TPMT_chr6_18123311_18160077 | 18151184 | CTT | C | intron_variant | MODIFIER | HG00438.hp1 HG01109.hp2 HG01891.hp2 others(17): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0004 | a0001c0001t0001a0001c0001t0005a0002c0003t0001others(1): Show | a0001c0001t0001g0057a0001c0001t0005g0028a0001c0001t0005g0066others(8): Show | 20 | 438 | 0.0457 | -2 | c.-44 others(19): Show |
TPMT | ENSG00000137364.5 | transcript | ENST00000309983.5 | protein_coding | 1/8 | chr6 | TogoVar | ||||||
TPMT_chr6_18123311_18160077 | 18158323 | CAA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
a0001a0005 | a0001c0001a0001c0002a0005c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 149 | 438 | 0.3402 | -2 | c.-33 others(13): Show |
TPMT | ENSG00000137364.5 | transcript | ENST00000309983.5 | protein_coding | 3247 | chr6 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1459946 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
a0000a0001a0002others(5): Show | a0000c0019a0001c0001a0001c0004others(13): Show | a0000c0019t0004a0001c0001t0001a0001c0001t0002others(32): Show | a0000c0019t0004g0007a0001c0001t0001g0022a0001c0001t0001g0030others(87): Show | 91 | 130 | 0.7000 | -2 | c.819 others(19): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1470241 | TAA | T | intron_variant | MODIFIER | HG00741.hp1 HG02015.hp1 HG03239.hp2 others(3): Show |
a0003a0006a0013 | a0003c0003a0006c0009a0006c0013others(1): Show | a0003c0003t0005a0006c0009t0003a0006c0009t0006others(3): Show | a0003c0003t0005g0066a0006c0009t0003g0050a0006c0009t0006g0084others(3): Show | 6 | 130 | 0.0462 | -2 | c.820 others(19): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1480559 | TAC | T | intron_variant | MODIFIER | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0003others(4): Show | a0001c0001t0001g0079a0001c0001t0002g0033a0002c0002t0003g0053others(5): Show | 9 | 130 | 0.0692 | -2 | c.133 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1490429 | CAG | C | intron_variant | MODIFIER | HG00741.hp1 HG03239.hp2 |
a0006a0013 | a0006c0009a0013c0017 | a0006c0009t0006a0013c0017t0002 | a0006c0009t0006g0084a0013c0017t0002g0024 | 2 | 130 | 0.0154 | -2 | c.176 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 10/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1493462 | TCA | T | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
a0008 | a0008c0011a0008c0016a0008c0028 | a0008c0011t0006a0008c0011t0015a0008c0016t0003others(1): Show | a0008c0011t0006g0048a0008c0011t0006g0092a0008c0011t0015g0120others(2): Show | 5 | 130 | 0.0385 | -2 | c.176 others(19): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1510243 | CAG | C | intron_variant | MODIFIER | HG00423.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
a0003a0004a0007others(1): Show | a0003c0003a0003c0006a0004c0005others(2): Show | a0003c0003t0001a0003c0003t0004a0003c0003t0005others(5): Show | a0003c0003t0001g0010a0003c0003t0001g0046a0003c0003t0004g0016others(12): Show | 16 | 130 | 0.1231 | -2 | c.251 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1525303 | TCC | T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(14): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0002c0015others(4): Show | a0001c0001t0003a0002c0002t0003a0002c0002t0006others(5): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0002c0002t0003g0056others(14): Show | 17 | 130 | 0.1308 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1528124 | CCT | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 NA18612.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0003a0003c0006 | a0001c0001t0005a0003c0003t0005a0003c0006t0004 | a0001c0001t0005g0073a0003c0003t0005g0043a0003c0006t0004g0096others(1): Show | 4 | 130 | 0.0308 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1529505 | TTG | T | intron_variant | MODIFIER | HG00408.hp2 NA19011.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0005a0003c0003t0005 | a0001c0001t0005g0073a0003c0003t0005g0043 | 2 | 130 | 0.0154 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1529645 | CTG | C | intron_variant | MODIFIER | HG00423.hp1 NA18612.hp2 |
a0003 | a0003c0006 | a0003c0006t0004 | a0003c0006t0004g0096a0003c0006t0004g0097 | 2 | 130 | 0.0154 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1529786 | TGA | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
a0000a0001a0002others(16): Show | a0000c0019a0001c0001a0001c0004others(31): Show | a0000c0019t0004a0001c0001t0001a0001c0001t0002others(53): Show | a0000c0019t0004g0007a0001c0001t0001g0022a0001c0001t0001g0030others(106): Show | 111 | 130 | 0.8539 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1529971 | AAC | A | intron_variant | MODIFIER | HG00408.hp2 NA19011.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0005a0003c0003t0005 | a0001c0001t0005g0073a0003c0003t0005g0043 | 2 | 130 | 0.0154 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1530140 | ATC | A | intron_variant | MODIFIER | HG00423.hp1 NA18612.hp2 |
a0003 | a0003c0006 | a0003c0006t0004 | a0003c0006t0004g0096a0003c0006t0004g0097 | 2 | 130 | 0.0154 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1530282 | TCC | T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(30): Show |
a0000a0001a0002others(4): Show | a0000c0019a0001c0001a0001c0004others(10): Show | a0000c0019t0004a0001c0001t0002a0001c0001t0003others(16): Show | a0000c0019t0004g0007a0001c0001t0002g0065a0001c0001t0003g0077others(29): Show | 33 | 130 | 0.2539 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1530286 | CCG | C | intron_variant | MODIFIER | HG00423.hp1 HG03239.hp1 NA18612.hp2 others(1): Show |
a0003a0004 | a0003c0003a0003c0006a0004c0007 | a0003c0003t0005a0003c0006t0004a0004c0007t0004 | a0003c0003t0005g0066a0003c0006t0004g0096a0003c0006t0004g0097others(1): Show | 4 | 130 | 0.0308 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1530576 | CGA | C | intron_variant | MODIFIER | HG01928.hp2 HG03239.hp1 NA19058.hp1 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0007 | a0001c0001t0003a0003c0003t0005a0004c0007t0004 | a0001c0001t0003g0077a0003c0003t0005g0066a0004c0007t0004g0072 | 3 | 130 | 0.0231 | -2 | c.261 others(23): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1530828 | CTT | C | intron_variant | MODIFIER | HG00408.hp2 NA18998.hp1 NA19011.hp2 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0005 | a0001c0001t0005a0003c0003t0005a0004c0005t0005 | a0001c0001t0005g0073a0003c0003t0005g0043a0004c0005t0005g0071 | 3 | 130 | 0.0231 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1531040 | ACC | A | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(13): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0002c0015others(4): Show | a0001c0001t0003a0002c0002t0003a0002c0002t0006others(5): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0002c0002t0003g0056others(13): Show | 16 | 130 | 0.1231 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1531162 | ATC | A | intron_variant | MODIFIER | HG02040.hp1 NA18962.hp1 |
a0002a0006 | a0002c0002a0006c0013 | a0002c0002t0009a0006c0013t0012 | a0002c0002t0009g0062a0006c0013t0012g0067 | 2 | 130 | 0.0154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1531337 | CCT | C | intron_variant | MODIFIER | HG00423.hp1 HG00597.hp2 HG01192.hp2 others(4): Show |
a0003a0004a0007others(1): Show | a0003c0006a0004c0007a0004c0032others(2): Show | a0003c0006t0004a0004c0007t0004a0004c0007t0008others(3): Show | a0003c0006t0004g0096a0003c0006t0004g0097a0004c0007t0004g0116others(4): Show | 7 | 130 | 0.0539 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1531364 | TCC | T | intron_variant | MODIFIER | HG00408.hp2 NA18998.hp1 NA19011.hp2 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0005 | a0001c0001t0005a0003c0003t0005a0004c0005t0005 | a0001c0001t0005g0073a0003c0003t0005g0043a0004c0005t0005g0071 | 3 | 130 | 0.0231 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1531459 | ACT | A | intron_variant | MODIFIER | HG01081.hp1 NA19240.hp1 |
a0002a0004 | a0002c0002a0004c0007 | a0002c0002t0014a0004c0007t0008 | a0002c0002t0014g0008a0004c0007t0008g0049 | 2 | 130 | 0.0154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1531623 | AAC | A | intron_variant | MODIFIER | HG00423.hp1 NA18612.hp2 |
a0003 | a0003c0006 | a0003c0006t0004 | a0003c0006t0004g0096a0003c0006t0004g0097 | 2 | 130 | 0.0154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1531719 | ACT | A | intron_variant | MODIFIER | HG02040.hp1 NA18962.hp1 |
a0002a0006 | a0002c0002a0006c0013 | a0002c0002t0009a0006c0013t0012 | a0002c0002t0009g0062a0006c0013t0012g0067 | 2 | 130 | 0.0154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1531997 | ATC | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
a0000a0001a0002others(15): Show | a0000c0019a0001c0001a0001c0004others(24): Show | a0000c0019t0004a0001c0001t0001a0001c0001t0002others(45): Show | a0000c0019t0004g0007a0001c0001t0001g0022a0001c0001t0001g0030others(86): Show | 91 | 130 | 0.7000 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1532393 | CCA | C | intron_variant | MODIFIER | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(7): Show |
a0002a0003a0004others(2): Show | a0002c0002a0003c0006a0004c0007others(3): Show | a0002c0002t0014a0003c0006t0004a0004c0007t0004others(4): Show | a0002c0002t0014g0008a0003c0006t0004g0096a0003c0006t0004g0097others(7): Show | 10 | 130 | 0.0769 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1532508 | CCG | C | intron_variant | MODIFIER | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(8): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0005a0002c0002t0014a0003c0003t0005others(6): Show | a0001c0001t0005g0073a0002c0002t0014g0008a0003c0003t0005g0043others(8): Show | 11 | 130 | 0.0846 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1532566 | CCA | C | intron_variant | MODIFIER | HG00408.hp2 NA18998.hp1 NA19011.hp2 others(1): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0005 | a0001c0001t0005a0003c0003t0005a0004c0005t0005 | a0001c0001t0005g0073a0003c0003t0005g0043a0003c0003t0005g0066others(1): Show | 4 | 130 | 0.0308 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1532683 | CCA | C | intron_variant | MODIFIER | HG00597.hp2 HG01081.hp1 HG01192.hp2 others(5): Show |
a0002a0004a0007others(1): Show | a0002c0002a0004c0007a0004c0032others(2): Show | a0002c0002t0014a0004c0007t0004a0004c0007t0008others(3): Show | a0002c0002t0014g0008a0004c0007t0004g0109a0004c0007t0004g0116others(5): Show | 8 | 130 | 0.0615 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1532925 | ATC | A | intron_variant | MODIFIER | HG00597.hp2 HG01081.hp1 HG01192.hp2 others(5): Show |
a0002a0004a0007others(1): Show | a0002c0002a0004c0007a0004c0032others(2): Show | a0002c0002t0014a0004c0007t0004a0004c0007t0008others(3): Show | a0002c0002t0014g0008a0004c0007t0004g0109a0004c0007t0004g0116others(5): Show | 8 | 130 | 0.0615 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1533882 | CTG | C | intron_variant | MODIFIER | HG03239.hp1 NA19058.hp1 |
a0003a0004 | a0003c0003a0004c0007 | a0003c0003t0005a0004c0007t0004 | a0003c0003t0005g0066a0004c0007t0004g0072 | 2 | 130 | 0.0154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534046 | CCA | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG03654.hp2 others(11): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(10): Show | 14 | 130 | 0.1077 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534049 | CCA | C | intron_variant | MODIFIER | HG00597.hp2 HG01081.hp1 HG01192.hp2 others(6): Show |
a0002a0004a0006others(1): Show | a0002c0002a0004c0007a0004c0032others(2): Show | a0002c0002t0009a0002c0002t0014a0004c0007t0004others(4): Show | a0002c0002t0009g0062a0002c0002t0014g0008a0004c0007t0004g0109others(6): Show | 9 | 130 | 0.0692 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534242 | CAT | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1534360 | CTG | C | intron_variant | MODIFIER | HG00597.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0009others(7): Show | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0002g0039others(12): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534530 | CTG | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0002c0015others(4): Show | a0001c0001t0003a0002c0002t0003a0002c0002t0006others(5): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0002c0002t0003g0056others(15): Show | 18 | 130 | 0.1385 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534657 | CCA | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1534722 | TCC | T | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1534806 | ATC | A | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1535148 | TCC | T | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG00733.hp2 others(17): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0002c0015others(6): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(10): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0001c0001t0007g0013others(17): Show | 20 | 130 | 0.1539 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1535990 | TCC | T | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1536761 | CAT | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1536768 | CTG | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0015others(4): Show | a0001c0001t0003a0002c0002t0003a0002c0002t0006others(5): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0002c0002t0003g0056others(14): Show | 17 | 130 | 0.1308 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TPO_chr2_1408463_1548673 | 1537090 | CGT | C | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(12): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0015a0003c0003others(3): Show | a0001c0001t0005a0002c0015t0004a0003c0003t0004others(5): Show | a0001c0001t0005g0073a0002c0015t0004g0112a0003c0003t0004g0016others(11): Show | 15 | 130 | 0.1154 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1537767 | GTA | G | intron_variant | MODIFIER | HG02602.hp2 NA18962.hp2 NA19088.hp1 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0006 | a0002c0002t0003g0074a0002c0002t0003g0095a0002c0002t0006g0027 | 3 | 130 | 0.0231 | -2 | c.261 others(21): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1547860 | CCA | C | downstream_gene_variant | MODIFIER | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0004a0002c0002others(10): Show | a0001c0001t0003a0001c0004t0009a0002c0002t0003others(14): Show | a0001c0001t0003g0077a0001c0001t0003g0128a0001c0004t0009g0104others(27): Show | 30 | 130 | 0.2308 | -2 | c.*53 others(13): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 4188 | chr2 | TogoVar | ||||||
TPO_chr2_1408463_1548673 | 1547973 | CCA | C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
a0000a0001a0002others(16): Show | a0000c0019a0001c0001a0001c0004others(25): Show | a0000c0019t0004a0001c0001t0001a0001c0001t0002others(39): Show | a0000c0019t0004g0007a0001c0001t0001g0022a0001c0001t0001g0030others(82): Show | 86 | 130 | 0.6615 | -2 | c.*55 others(13): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 4301 | chr2 | TogoVar |