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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
THSD7B_chr2_136760545_137682718 | 136948477 | CAT | C | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01358.hp2 others(17): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0012others(15): Show | a0001c0001t0002a0001c0004t0003a0001c0012t0011others(16): Show | a0001c0001t0002g0034a0001c0004t0003g0091a0001c0012t0011g0096others(17): Show | 20 | 98 | 0.2041 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136957435 | ACG | A | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01358.hp2 others(18): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0012others(15): Show | a0001c0001t0002a0001c0004t0003a0001c0012t0011others(17): Show | a0001c0001t0002g0034a0001c0004t0003g0091a0001c0012t0011g0096others(18): Show | 21 | 98 | 0.2143 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136957608 | ATG | A | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01358.hp2 others(17): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0012others(15): Show | a0001c0001t0002a0001c0004t0003a0001c0012t0011others(16): Show | a0001c0001t0002g0034a0001c0004t0003g0091a0001c0012t0011g0096others(17): Show | 20 | 98 | 0.2041 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136962403 | CTT | C | intron_variant | MODIFIER | HG00609.hp1 HG01167.hp1 HG02976.hp2 others(1): Show |
a0001a0004a0019 | a0001c0017a0004c0007a0004c0008others(1): Show | a0001c0017t0001a0004c0007t0001a0004c0008t0010others(1): Show | a0001c0017t0001g0045a0004c0007t0001g0044a0004c0008t0010g0079others(1): Show | 4 | 98 | 0.0408 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136965010 | CAA | C | intron_variant | MODIFIER | HG00735.hp2 HG01255.hp2 HG01358.hp2 others(16): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0005a0001c0021others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(14): Show | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0002g0034others(16): Show | 19 | 98 | 0.1939 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136966223 | ATT | A | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(32): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0005others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(28): Show | a0001c0001t0001g0027a0001c0001t0002g0025a0001c0001t0002g0034others(32): Show | 35 | 98 | 0.3571 | -2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136971639 | TAC | T | intron_variant | MODIFIER | HG02257.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
a0001a0003a0005 | a0001c0036a0003c0002a0003c0025others(1): Show | a0001c0036t0002a0003c0002t0001a0003c0025t0001others(1): Show | a0001c0036t0002g0051a0003c0002t0001g0047a0003c0025t0001g0006others(1): Show | 4 | 98 | 0.0408 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136983502 | GTT | G | intron_variant | MODIFIER | HG00735.hp2 HG01358.hp2 HG02257.hp2 others(15): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0012others(13): Show | a0001c0001t0002a0001c0004t0003a0001c0012t0011others(14): Show | a0001c0001t0002g0034a0001c0004t0003g0091a0001c0012t0011g0096others(15): Show | 18 | 98 | 0.1837 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136989995 | CTT | C | intron_variant | MODIFIER | NA18993.hp2 NA19084.hp2 |
a0001a0004 | a0001c0056a0004c0055 | a0001c0056t0003a0004c0055t0003 | a0001c0056t0003g0086a0004c0055t0003g0076 | 2 | 98 | 0.0204 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136993821 | CAT | C | intron_variant | MODIFIER | HG00438.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
a0001a0002a0004others(4): Show | a0001c0004a0001c0012a0001c0019others(8): Show | a0001c0004t0003a0001c0012t0011a0001c0019t0016others(10): Show | a0001c0004t0003g0091a0001c0012t0011g0096a0001c0019t0016g0090others(10): Show | 13 | 98 | 0.1327 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136995339 | CAG | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0010others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(21): Show | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0002g0025others(27): Show | 30 | 98 | 0.3061 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136998261 | CAA | C | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0005others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(22): Show | a0001c0001t0001g0052a0001c0001t0002g0025a0001c0001t0002g0034others(25): Show | 28 | 98 | 0.2857 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136998909 | GAC | G | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01169.hp1 others(8): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0004a0001c0005others(7): Show | a0001c0001t0001a0001c0004t0006a0001c0005t0010others(8): Show | a0001c0001t0001g0027a0001c0004t0006g0023a0001c0005t0010g0078others(8): Show | 11 | 98 | 0.1122 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137004296 | TAC | T | intron_variant | MODIFIER | HG02056.hp2 HG02809.hp1 HG02976.hp2 others(4): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0006others(3): Show | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0002g0034others(4): Show | 7 | 98 | 0.0714 | -2 | c.140 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137057456 | TTA | T | intron_variant | MODIFIER | HG02647.hp1 HG03540.hp1 NA20300.hp1 |
a0003a0005 | a0003c0014a0003c0040a0005c0057 | a0003c0014t0002a0003c0040t0011a0005c0057t0013 | a0003c0014t0002g0001a0003c0040t0011g0080a0005c0057t0013g0013 | 3 | 98 | 0.0306 | -2 | c.950 others(17): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137063203 | CAT | C | intron_variant | MODIFIER | HG00438.hp1 HG01255.hp1 HG01358.hp2 others(18): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0005a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0027a0001c0001t0002g0034a0001c0001t0003g0081others(18): Show | 21 | 98 | 0.2143 | -2 | c.950 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137067565 | AAG | A | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01358.hp1 others(17): Show |
a0001a0002a0003others(7): Show | a0001c0010a0001c0031a0001c0053others(16): Show | a0001c0010t0002a0001c0031t0004a0001c0053t0005others(17): Show | a0001c0010t0002g0020a0001c0031t0004g0060a0001c0053t0005g0084others(17): Show | 20 | 98 | 0.2041 | -2 | c.950 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137080367 | GTT | G | intron_variant | MODIFIER | HG01167.hp1 HG02056.hp2 HG03041.hp1 others(4): Show |
a0001a0002a0004 | a0001c0004a0001c0021a0002c0006others(2): Show | a0001c0004t0002a0001c0004t0006a0001c0021t0004others(4): Show | a0001c0004t0002g0039a0001c0004t0006g0023a0001c0021t0004g0071others(4): Show | 7 | 98 | 0.0714 | -2 | c.951 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137089245 | GGT | G | intron_variant | MODIFIER | HG02056.hp2 HG03041.hp1 HG03139.hp2 others(4): Show |
a0001a0002a0004others(1): Show | a0001c0004a0002c0006a0002c0020others(3): Show | a0001c0004t0002a0001c0004t0006a0002c0006t0001others(4): Show | a0001c0004t0002g0039a0001c0004t0006g0023a0002c0006t0001g0067others(4): Show | 7 | 98 | 0.0714 | -2 | c.951 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137089289 | CAT | C | intron_variant | MODIFIER | HG00438.hp1 HG01255.hp1 HG01358.hp2 others(24): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0005others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0027a0001c0001t0002g0034a0001c0001t0003g0081others(24): Show | 27 | 98 | 0.2755 | -2 | c.951 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137114821 | CCT | C | intron_variant | MODIFIER | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
a0001a0002a0016others(1): Show | a0001c0004a0001c0053a0002c0029others(2): Show | a0001c0004t0001a0001c0053t0005a0002c0029t0001others(2): Show | a0001c0004t0001g0058a0001c0053t0005g0084a0002c0029t0001g0024others(2): Show | 5 | 98 | 0.0510 | -2 | c.120 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137127056 | AAT | A | intron_variant | MODIFIER | HG02109.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
a0001a0003a0005others(2): Show | a0001c0036a0003c0002a0005c0045others(2): Show | a0001c0036t0002a0003c0002t0001a0005c0045t0012others(2): Show | a0001c0036t0002g0051a0003c0002t0001g0005a0005c0045t0012g0057others(2): Show | 5 | 98 | 0.0510 | -2 | c.136 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137141494 | TCA | T | intron_variant | MODIFIER | HG00738.hp1 HG01358.hp1 HG02258.hp2 others(13): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0001c0013others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(11): Show | a0001c0001t0001g0052a0001c0001t0002g0034a0001c0001t0008g0012others(13): Show | 16 | 98 | 0.1633 | -2 | c.137 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137141684 | CGT | C | intron_variant | MODIFIER | HG00735.hp2 HG02280.hp1 HG03540.hp2 others(4): Show |
a0001a0002a0005others(1): Show | a0001c0004a0001c0019a0002c0006others(3): Show | a0001c0004t0003a0001c0019t0016a0002c0006t0002others(4): Show | a0001c0004t0003g0091a0001c0019t0016g0090a0002c0006t0002g0035others(4): Show | 7 | 98 | 0.0714 | -2 | c.137 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137152006 | ATT | A | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(6): Show |
a0001a0002a0010others(1): Show | a0001c0001a0001c0005a0001c0012others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0005t0010others(6): Show | a0001c0001t0001g0026a0001c0001t0003g0081a0001c0005t0010g0078others(6): Show | 9 | 98 | 0.0918 | -2 | c.137 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137158642 | CAT | C | intron_variant | MODIFIER | HG01358.hp2 HG02257.hp2 HG02280.hp2 others(17): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0010a0001c0031others(14): Show | a0001c0001t0001a0001c0001t0008a0001c0010t0002others(15): Show | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0008g0012others(17): Show | 20 | 98 | 0.2041 | -2 | c.137 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 5/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137165762 | TAC | T | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(77): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0005others(42): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(66): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(77): Show | 80 | 98 | 0.8163 | -2 | c.152 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137176939 | CAG | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01169.hp1 others(12): Show |
a0001a0002a0010 | a0001c0001a0001c0004a0001c0005others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(12): Show | a0001c0001t0001g0026a0001c0001t0003g0081a0001c0004t0001g0058others(12): Show | 15 | 98 | 0.1531 | -2 | c.172 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137196376 | GTT | G | intron_variant | MODIFIER | HG00738.hp1 HG01358.hp1 HG02056.hp1 others(7): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0053a0002c0044others(6): Show | a0001c0001t0001a0001c0053t0005a0002c0044t0007others(6): Show | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0053t0005g0084others(7): Show | 10 | 98 | 0.1020 | -2 | c.172 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137205906 | CAG | C | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(55): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0005a0001c0012others(36): Show | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(48): Show | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0062others(55): Show | 58 | 98 | 0.5918 | -2 | c.172 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 7/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137220243 | GAA | G | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(55): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0005a0001c0012others(36): Show | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(48): Show | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0062others(55): Show | 58 | 98 | 0.5918 | -2 | c.172 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137221423 | CTG | C | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(50): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0005a0001c0017others(32): Show | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(44): Show | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0008g0012others(50): Show | 53 | 98 | 0.5408 | -2 | c.172 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137231587 | CTA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0005others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(31): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0003g0081others(37): Show | 40 | 98 | 0.4082 | -2 | c.191 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137237113 | CAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(44): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0004a0001c0005others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(41): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0052others(44): Show | 47 | 98 | 0.4796 | -2 | c.215 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137241396 | CAA | C | intron_variant | MODIFIER | HG02280.hp2 HG02717.hp1 HG02809.hp1 |
a0001a0002 | a0001c0001a0001c0053a0002c0044 | a0001c0001t0001a0001c0053t0005a0002c0044t0007 | a0001c0001t0001g0052a0001c0053t0005g0084a0002c0044t0007g0059 | 3 | 98 | 0.0306 | -2 | c.215 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137264247 | CTT | C | intron_variant | MODIFIER | HG02109.hp2 HG03225.hp2 NA18993.hp2 others(1): Show |
a0001a0004a0022 | a0001c0021a0004c0008a0004c0055others(1): Show | a0001c0021t0004a0004c0008t0001a0004c0055t0003others(1): Show | a0001c0021t0004g0071a0004c0008t0001g0040a0004c0055t0003g0076others(1): Show | 4 | 98 | 0.0408 | -2 | c.226 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137273025 | TAC | T | intron_variant | MODIFIER | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0005a0001c0012others(7): Show | a0001c0001t0002a0001c0005t0001a0001c0012t0004others(8): Show | a0001c0001t0002g0034a0001c0005t0001g0022a0001c0012t0004g0011others(9): Show | 12 | 98 | 0.1225 | -2 | c.239 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137288792 | AAT | A | intron_variant | MODIFIER | HG02717.hp1 NA19240.hp2 |
a0001a0002 | a0001c0053a0002c0003 | a0001c0053t0005a0002c0003t0001 | a0001c0053t0005g0084a0002c0003t0001g0056 | 2 | 98 | 0.0204 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137289056 | CTT | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(33): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0005others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(30): Show | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0029others(33): Show | 36 | 98 | 0.3674 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137299687 | CTG | C | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0010a0001c0013others(5): Show | a0001c0001t0001a0001c0010t0002a0001c0013t0002others(6): Show | a0001c0001t0001g0062a0001c0010t0002g0020a0001c0010t0002g0053others(7): Show | 10 | 98 | 0.1020 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137316768 | AAG | A | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01255.hp1 others(18): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0019others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(16): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0003g0081others(18): Show | 21 | 98 | 0.2143 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137323280 | CAG | C | intron_variant | MODIFIER | HG02622.hp2 HG03195.hp2 HG03225.hp2 |
a0001 | a0001c0012a0001c0013a0001c0021 | a0001c0012t0004a0001c0013t0002a0001c0021t0004 | a0001c0012t0004g0011a0001c0013t0002g0030a0001c0021t0004g0071 | 3 | 98 | 0.0306 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137324457 | CTG | C | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0002others(14): Show | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0002g0025others(17): Show | 20 | 98 | 0.2041 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137339134 | CAA | C | intron_variant | MODIFIER | HG00735.hp2 HG02258.hp1 HG02630.hp2 others(9): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0010a0002c0006others(7): Show | a0001c0001t0001a0001c0010t0002a0002c0006t0002others(8): Show | a0001c0001t0001g0062a0001c0010t0002g0020a0001c0010t0002g0053others(9): Show | 12 | 98 | 0.1225 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137346478 | TTC | T | intron_variant | MODIFIER | NA19030.hp2 NA19043.hp1 |
a0005 | a0005c0009 | a0005c0009t0001a0005c0009t0007 | a0005c0009t0001g0009a0005c0009t0007g0008 | 2 | 98 | 0.0204 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137347555 | ATT | A | intron_variant | MODIFIER | HG01169.hp2 HG01255.hp1 HG02280.hp2 others(12): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0003a0002c0029others(8): Show | a0001c0001t0001a0002c0003t0009a0002c0029t0001others(9): Show | a0001c0001t0001g0018a0001c0001t0001g0027a0002c0003t0009g0073others(12): Show | 15 | 98 | 0.1531 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137356967 | GAC | G | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(33): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0005others(21): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(31): Show | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0003g0081others(33): Show | 36 | 98 | 0.3674 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137372323 | CTT | C | intron_variant | MODIFIER | HG01169.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
a0001a0004 | a0001c0004a0001c0005a0004c0055 | a0001c0004t0001a0001c0005t0002a0001c0005t0010others(1): Show | a0001c0004t0001g0058a0001c0005t0002g0021a0001c0005t0010g0078others(1): Show | 4 | 98 | 0.0408 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137385647 | CTT | C | intron_variant | MODIFIER | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
a0001a0002a0003others(2): Show | a0001c0012a0001c0013a0001c0021others(6): Show | a0001c0012t0004a0001c0013t0002a0001c0021t0004others(6): Show | a0001c0012t0004g0011a0001c0013t0002g0030a0001c0021t0004g0071others(6): Show | 9 | 98 | 0.0918 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137389402 | ATT | A | intron_variant | MODIFIER | HG00438.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0005others(19): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(26): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(29): Show | 32 | 98 | 0.3265 | -2 | c.250 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |