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 | 136832175 | T | TTG | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(10): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0005a0001c0010others(9): Show | a0001c0001t0003a0001c0005t0002a0001c0005t0010others(10): Show | a0001c0001t0003g0081a0001c0005t0002g0021a0001c0005t0010g0078others(10): Show | 13 | 98 | 0.1327 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136832201 | G | GTA | intron_variant | MODIFIER | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0005a0002c0003others(3): Show | a0001c0001t0010a0001c0005t0003a0002c0003t0009others(4): Show | a0001c0001t0010g0087a0001c0005t0003g0077a0002c0003t0009g0073others(5): Show | 8 | 98 | 0.0816 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136841593 | C | CAA | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(21): Show |
a0001a0003a0004others(7): Show | a0001c0001a0001c0004a0001c0021others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(17): Show | a0001c0001t0001g0062a0001c0001t0002g0034a0001c0004t0001g0058others(21): Show | 24 | 98 | 0.2449 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136844462 | C | CAG | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp2 HG01167.hp1 others(26): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0005a0001c0010others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(26): Show | a0001c0001t0001g0052a0001c0001t0003g0081a0001c0001t0008g0012others(26): Show | 29 | 98 | 0.2959 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136851933 | C | CTA | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(68): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0004a0001c0005others(38): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(68): Show | 71 | 98 | 0.7245 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136860016 | A | ATT | intron_variant | MODIFIER | HG01167.hp2 HG01255.hp2 HG02257.hp1 others(2): Show |
a0003a0004a0007 | a0003c0002a0003c0025a0004c0007others(1): Show | a0003c0002t0001a0003c0002t0015a0003c0025t0001others(2): Show | a0003c0002t0001g0002a0003c0002t0015g0038a0003c0025t0001g0006others(2): Show | 5 | 98 | 0.0510 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136868120 | G | GCA | intron_variant | MODIFIER | HG01358.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
a0001a0003a0005others(6): Show | a0001c0001a0001c0004a0001c0005others(10): Show | a0001c0001t0002a0001c0004t0001a0001c0005t0003others(10): Show | a0001c0001t0002g0034a0001c0004t0001g0058a0001c0005t0003g0077others(12): Show | 15 | 98 | 0.1531 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136870071 | C | CAA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(19): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0005others(15): Show | a0001c0001t0002a0001c0004t0001a0001c0004t0002others(17): Show | a0001c0001t0002g0034a0001c0004t0001g0058a0001c0004t0002g0039others(19): Show | 22 | 98 | 0.2245 | 2 | c.-35 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136872814 | C | CAA | intron_variant | MODIFIER | HG01169.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0005others(11): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0010others(11): Show | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0004t0001g0058others(13): Show | 16 | 98 | 0.1633 | 2 | c.-35 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136873021 | T | TAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(30): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0005others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(30): Show | 33 | 98 | 0.3367 | 2 | c.-35 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136877922 | C | CTT | intron_variant | MODIFIER | HG02717.hp1 HG02886.hp1 NA20300.hp1 |
a0001a0005 | a0001c0053a0005c0054a0005c0057 | a0001c0053t0005a0005c0054t0002a0005c0057t0013 | a0001c0053t0005g0084a0005c0054t0002g0031a0005c0057t0013g0013 | 3 | 98 | 0.0306 | 2 | c.-35 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136883341 | T | TAA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(76): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0004a0001c0005others(42): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(76): Show | 79 | 98 | 0.8061 | 2 | c.139 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136887300 | T | TTG | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01255.hp1 others(10): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0004a0002c0003others(8): Show | a0001c0001t0001a0001c0004t0006a0002c0003t0009others(9): Show | a0001c0001t0001g0026a0001c0004t0006g0023a0002c0003t0009g0073others(10): Show | 13 | 98 | 0.1327 | 2 | c.139 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136888944 | G | GGT | intron_variant | MODIFIER | HG00735.hp2 HG01358.hp2 HG02109.hp2 others(7): Show |
a0001a0002a0003others(4): Show | a0001c0013a0001c0021a0001c0056others(6): Show | a0001c0013t0002a0001c0021t0004a0001c0056t0003others(6): Show | a0001c0013t0002g0072a0001c0021t0004g0071a0001c0056t0003g0086others(7): Show | 10 | 98 | 0.1020 | 2 | c.139 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 136890305 | T | TCC | intron_variant | MODIFIER | HG02630.hp2 HG03225.hp2 |
a0001 | a0001c0010a0001c0021 | a0001c0010t0002a0001c0021t0004 | a0001c0010t0002g0053a0001c0021t0004g0071 | 2 | 98 | 0.0204 | 2 | c.139 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136895514 | C | CTT | intron_variant | MODIFIER | HG01255.hp2 HG01358.hp2 HG02258.hp2 others(10): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0036a0002c0003others(5): Show | a0001c0001t0001a0001c0036t0002a0002c0003t0001others(8): Show | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0062others(10): Show | 13 | 98 | 0.1327 | 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 | 136895540 | T | TTA | intron_variant | MODIFIER | HG02886.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
a0001a0016a0018 | a0001c0001a0001c0013a0016c0026others(1): Show | a0001c0001t0003a0001c0013t0002a0016c0026t0005others(1): Show | a0001c0001t0003g0081a0001c0013t0002g0072a0016c0026t0005g0085others(1): Show | 4 | 98 | 0.0408 | 2 | c.139 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 2/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 136898646 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0005others(35): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(57): Show | 60 | 98 | 0.6122 | 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 | 136903925 | G | GGT | intron_variant | MODIFIER | HG01358.hp1 NA19084.hp1 |
a0004a0009 | a0004c0008a0009c0035 | a0004c0008t0001a0009c0035t0001 | a0004c0008t0001g0040a0009c0035t0001g0063 | 2 | 98 | 0.0204 | 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 | 136912321 | C | CAA | intron_variant | MODIFIER | HG00609.hp2 HG00735.hp2 HG01167.hp1 others(34): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0005others(25): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(29): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(34): Show | 37 | 98 | 0.3776 | 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 | 136926388 | T | TAA | intron_variant | MODIFIER | HG00609.hp1 HG01167.hp1 HG03041.hp1 others(4): Show |
a0001a0002a0003others(1): Show | a0001c0004a0001c0017a0002c0016others(3): Show | a0001c0004t0002a0001c0017t0001a0002c0016t0001others(4): Show | a0001c0004t0002g0039a0001c0017t0001g0045a0002c0016t0001g0028others(4): Show | 7 | 98 | 0.0714 | 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 | 136940727 | A | AAT | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp1 HG02886.hp2 others(11): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0012others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0005t0002others(11): Show | a0001c0001t0001g0062a0001c0001t0003g0081a0001c0005t0002g0021others(11): Show | 14 | 98 | 0.1429 | 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 | 136940740 | A | ATT | intron_variant | MODIFIER | HG01255.hp1 HG01358.hp1 HG02280.hp1 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0004a0001c0019a0002c0003others(3): Show | a0001c0004t0003a0001c0019t0016a0002c0003t0009others(4): Show | a0001c0004t0003g0091a0001c0019t0016g0090a0002c0003t0009g0073others(4): Show | 7 | 98 | 0.0714 | 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 | 136940742 | A | ATT | intron_variant | MODIFIER | HG00738.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
a0001a0005a0008others(2): Show | a0001c0001a0001c0004a0001c0010others(4): Show | a0001c0001t0001a0001c0001t0008a0001c0004t0001others(5): Show | a0001c0001t0001g0029a0001c0001t0008g0012a0001c0004t0001g0058others(5): Show | 8 | 98 | 0.0816 | 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 | 136940863 | G | GTT | intron_variant | MODIFIER | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
a0003a0005a0006 | a0003c0014a0005c0054a0005c0057others(1): Show | a0003c0014t0002a0005c0054t0002a0005c0057t0013others(1): Show | a0003c0014t0002g0001a0005c0054t0002g0031a0005c0057t0013g0013others(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 | 136948443 | T | TCA | intron_variant | MODIFIER | HG00438.hp1 NA18961.hp1 |
a0002a0012 | a0002c0003a0012c0050 | a0002c0003t0006a0012c0050t0001 | a0002c0003t0006g0041a0012c0050t0001g0019 | 2 | 98 | 0.0204 | 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 | 136961088 | C | CAA | intron_variant | MODIFIER | HG00609.hp1 HG01167.hp1 HG01255.hp2 others(31): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0002others(28): Show | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0052others(31): Show | 34 | 98 | 0.3469 | 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 | 136961224 | C | CTT | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01358.hp2 others(16): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0012others(14): Show | a0001c0001t0002a0001c0004t0003a0001c0012t0011others(15): Show | a0001c0001t0002g0034a0001c0004t0003g0091a0001c0012t0011g0096others(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 | 136962403 | C | CTT | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0021a0002c0030others(4): Show | a0001c0001t0002a0001c0001t0010a0001c0021t0004others(6): Show | a0001c0001t0002g0034a0001c0001t0010g0087a0001c0021t0004g0071others(7): Show | 10 | 98 | 0.1020 | 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 | T | TAC | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp2 HG01167.hp2 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0020a0003c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(7): Show | a0001c0001t0001g0027a0001c0001t0002g0025a0001c0001t0010g0087others(9): Show | 12 | 98 | 0.1225 | 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 | 136983377 | A | ACT | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
a0001a0002a0005others(1): Show | a0001c0004a0001c0012a0001c0019others(3): Show | a0001c0004t0003a0001c0012t0011a0001c0019t0016others(4): Show | a0001c0004t0003g0091a0001c0012t0011g0096a0001c0019t0016g0090others(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 | 136998909 | G | GAC | intron_variant | MODIFIER | HG00438.hp1 HG03225.hp1 HG04199.hp1 |
a0001a0012 | a0001c0001a0001c0005a0012c0050 | a0001c0001t0001a0001c0005t0001a0012c0050t0001 | a0001c0001t0001g0018a0001c0005t0001g0022a0012c0050t0001g0019 | 3 | 98 | 0.0306 | 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 | T | TAC | intron_variant | MODIFIER | HG00438.hp1 HG01358.hp1 HG02056.hp1 others(6): Show |
a0001a0002a0003others(5): Show | a0001c0005a0002c0044a0003c0002others(5): Show | a0001c0005t0001a0002c0044t0007a0003c0002t0001others(6): Show | a0001c0005t0001g0022a0002c0044t0007g0059a0003c0002t0001g0005others(6): Show | 9 | 98 | 0.0918 | 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 | 137024690 | T | TAC | intron_variant | MODIFIER | HG02622.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
a0002a0003a0006others(1): Show | a0002c0003a0003c0002a0006c0048others(1): Show | a0002c0003t0001a0003c0002t0001a0006c0048t0005others(1): Show | a0002c0003t0001g0056a0003c0002t0001g0047a0006c0048t0005g0093others(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 | 137029078 | C | CTT | intron_variant | MODIFIER | HG02965.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
a0001a0002a0005 | a0001c0005a0001c0012a0001c0013others(2): Show | a0001c0005t0002a0001c0012t0004a0001c0013t0002others(2): Show | a0001c0005t0002g0021a0001c0012t0004g0011a0001c0013t0002g0072others(2): Show | 5 | 98 | 0.0510 | 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 | 137037414 | G | GTA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(19): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0005a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(16): Show | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0062others(19): Show | 22 | 98 | 0.2245 | 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 | 137060399 | C | CTT | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01358.hp1 others(15): Show |
a0001a0002a0003others(6): Show | a0001c0010a0001c0031a0001c0053others(14): Show | a0001c0010t0002a0001c0031t0004a0001c0053t0005others(15): Show | a0001c0010t0002g0020a0001c0031t0004g0060a0001c0053t0005g0084others(15): Show | 18 | 98 | 0.1837 | 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 | 137061301 | C | CAA | intron_variant | MODIFIER | HG01167.hp1 HG02056.hp2 HG02622.hp1 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0004a0002c0006a0002c0020others(3): Show | a0001c0004t0002a0001c0004t0006a0002c0006t0001others(5): Show | a0001c0004t0002g0039a0001c0004t0006g0023a0002c0006t0001g0067others(5): Show | 8 | 98 | 0.0816 | 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 | 137080168 | A | ATG | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01358.hp1 others(23): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0005a0001c0010others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0002others(23): Show | a0001c0001t0001g0052a0001c0001t0002g0034a0001c0005t0002g0021others(23): Show | 26 | 98 | 0.2653 | 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 | G | GGT | intron_variant | MODIFIER | HG00609.hp1 HG02717.hp1 HG02809.hp2 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0017a0001c0036others(5): Show | a0001c0001t0001a0001c0017t0001a0001c0036t0002others(5): Show | a0001c0001t0001g0018a0001c0017t0001g0045a0001c0036t0002g0051others(5): Show | 8 | 98 | 0.0816 | 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 | 137097769 | G | GAC | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(22): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0012others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(21): Show | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0002g0025others(22): Show | 25 | 98 | 0.2551 | 2 | c.119 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137135849 | T | TAA | intron_variant | MODIFIER | HG02280.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0013a0002c0044others(4): Show | a0001c0001t0002a0001c0013t0002a0002c0044t0007others(5): Show | a0001c0001t0002g0025a0001c0013t0002g0030a0002c0044t0007g0059others(5): Show | 8 | 98 | 0.0816 | 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 | 137171970 | G | GCA | intron_variant | MODIFIER | HG00738.hp1 HG01358.hp1 HG02258.hp2 |
a0007a0008a0009 | a0007c0024a0008c0034a0009c0035 | a0007c0024t0014a0008c0034t0001a0009c0035t0001 | a0007c0024t0014g0037a0008c0034t0001g0064a0009c0035t0001g0063 | 3 | 98 | 0.0306 | 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 | 137195234 | G | GTA | intron_variant | MODIFIER | HG01358.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
a0003a0005a0006others(2): Show | a0003c0002a0005c0045a0006c0011others(3): Show | a0003c0002t0001a0005c0045t0012a0006c0011t0003others(3): Show | a0003c0002t0001g0002a0003c0002t0001g0003a0005c0045t0012g0057others(4): Show | 7 | 98 | 0.0714 | 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 | 137195251 | T | TAC | intron_variant | MODIFIER | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0019a0002c0006others(5): Show | a0001c0001t0001a0001c0019t0016a0002c0006t0002others(6): Show | a0001c0001t0001g0062a0001c0019t0016g0090a0002c0006t0002g0035others(6): Show | 9 | 98 | 0.0918 | 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 | 137213030 | T | TAA | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp2 HG01255.hp1 others(18): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0001c0017others(12): Show | a0001c0001t0001a0001c0005t0001a0001c0005t0003others(15): Show | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0062others(18): Show | 21 | 98 | 0.2143 | 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 | 137213373 | G | GTA | 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 | 137220211 | C | CTT | 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 | 137229350 | G | GGT | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
a0001a0003a0004 | a0001c0001a0001c0019a0001c0031others(8): Show | a0001c0001t0008a0001c0019t0016a0001c0031t0004others(14): Show | a0001c0001t0008g0012a0001c0019t0016g0090a0001c0031t0004g0060others(18): Show | 21 | 98 | 0.2143 | 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 | 137238534 | C | CTT | intron_variant | MODIFIER | HG00738.hp1 HG01169.hp1 HG01358.hp1 others(7): Show |
a0001a0002a0004others(3): Show | a0001c0004a0001c0005a0001c0012others(7): Show | a0001c0004t0002a0001c0005t0010a0001c0012t0011others(7): Show | a0001c0004t0002g0039a0001c0005t0010g0078a0001c0012t0011g0096others(7): Show | 10 | 98 | 0.1020 | 2 | c.215 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |