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 | 137252266 | C | CAA | intron_variant | MODIFIER | HG00609.hp2 HG02056.hp1 HG02056.hp2 others(13): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0004a0001c0010others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0006others(12): Show | a0001c0001t0001g0062a0001c0001t0003g0081a0001c0004t0006g0023others(13): Show | 16 | 98 | 0.1633 | 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 | 137252911 | C | CTT | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
a0001a0004a0020others(1): Show | a0001c0005a0001c0053a0004c0008others(3): Show | a0001c0005t0001a0001c0053t0005a0004c0008t0001others(3): Show | a0001c0005t0001g0022a0001c0053t0005g0084a0004c0008t0001g0040others(3): Show | 6 | 98 | 0.0612 | 2 | c.226 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137260921 | C | CTT | intron_variant | MODIFIER | HG02109.hp2 HG02280.hp2 HG03225.hp2 others(2): Show |
a0001a0002a0004others(1): Show | a0001c0021a0002c0044a0004c0008others(2): Show | a0001c0021t0004a0002c0044t0007a0004c0008t0001others(2): Show | a0001c0021t0004g0071a0002c0044t0007g0059a0004c0008t0001g0040others(2): Show | 5 | 98 | 0.0510 | 2 | c.226 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137263262 | A | AAT | intron_variant | MODIFIER | HG02258.hp1 HG03041.hp1 NA19030.hp2 others(1): Show |
a0001a0005a0020 | a0001c0004a0005c0009a0020c0038 | a0001c0004t0002a0005c0009t0001a0005c0009t0007others(1): Show | a0001c0004t0002g0039a0005c0009t0001g0009a0005c0009t0007g0008others(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 | 137271374 | C | CAT | intron_variant | MODIFIER | HG02717.hp1 NA19240.hp2 |
a0001a0002 | a0001c0053a0002c0003 | a0001c0053t0005a0002c0003t0001 | a0001c0053t0005g0084a0002c0003t0001g0056 | 2 | 98 | 0.0204 | 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 | 137271411 | T | TCA | intron_variant | MODIFIER | NA18993.hp2 NA19084.hp1 |
a0004 | a0004c0008a0004c0055 | a0004c0008t0001a0004c0055t0003 | a0004c0008t0001g0040a0004c0055t0003g0076 | 2 | 98 | 0.0204 | 2 | c.226 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 10/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137288792 | A | AAT | intron_variant | MODIFIER | HG02976.hp2 NA19043.hp2 |
a0001a0019 | a0001c0001a0019c0037 | a0001c0001t0008a0019c0037t0005 | a0001c0001t0008g0012a0019c0037t0005g0083 | 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 | 137290110 | C | CTT | intron_variant | MODIFIER | HG02647.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
a0001a0016a0017 | a0001c0001a0001c0005a0016c0026others(1): Show | a0001c0001t0008a0001c0005t0002a0016c0026t0005others(1): Show | a0001c0001t0008g0012a0001c0005t0002g0021a0016c0026t0005g0085others(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 | 137303694 | T | TTA | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
a0002a0003a0004others(1): Show | a0002c0003a0003c0002a0003c0014others(2): Show | a0002c0003t0006a0003c0002t0001a0003c0002t0002others(7): Show | a0002c0003t0006g0041a0003c0002t0001g0047a0003c0002t0002g0061others(8): Show | 11 | 98 | 0.1122 | 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 | 137303740 | T | TTA | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0001c0010a0001c0013others(4): Show | a0001c0001t0001a0001c0010t0002a0001c0013t0002others(5): Show | a0001c0001t0001g0062a0001c0010t0002g0020a0001c0010t0002g0053others(6): Show | 9 | 98 | 0.0918 | 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 | 137318786 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(4): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0013a0001c0021others(3): Show | a0001c0001t0003a0001c0013t0002a0001c0021t0004others(4): Show | a0001c0001t0003g0081a0001c0013t0002g0030a0001c0021t0004g0071others(4): Show | 7 | 98 | 0.0714 | 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 | 137334170 | T | TTC | intron_variant | MODIFIER | HG02109.hp2 HG02622.hp1 NA19030.hp2 others(1): Show |
a0002a0005a0006others(1): Show | a0002c0003a0005c0009a0006c0048others(1): Show | a0002c0003t0001a0005c0009t0001a0006c0048t0005others(1): Show | a0002c0003t0001g0056a0005c0009t0001g0009a0006c0048t0005g0093others(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 | 137346478 | T | TTC | intron_variant | MODIFIER | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0019a0001c0036others(4): Show | a0001c0001t0002a0001c0019t0016a0001c0036t0002others(4): Show | a0001c0001t0002g0034a0001c0019t0016g0090a0001c0036t0002g0051others(4): Show | 7 | 98 | 0.0714 | 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 | 137348703 | C | CTT | intron_variant | MODIFIER | HG00735.hp1 HG01515.hp2 HG03041.hp1 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0002c0052others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0002others(4): Show | a0001c0001t0001g0027a0001c0001t0002g0025a0001c0004t0002g0039others(4): Show | 7 | 98 | 0.0714 | 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 | 137356963 | C | CAG | intron_variant | MODIFIER | HG02257.hp1 HG02976.hp2 |
a0003a0019 | a0003c0025a0019c0037 | a0003c0025t0001a0019c0037t0005 | a0003c0025t0001g0006a0019c0037t0005g0083 | 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 | 137356967 | G | GAC | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 |
a0002a0006 | a0002c0030a0006c0023 | a0002c0030t0004a0006c0023t0002 | a0002c0030t0004g0050a0006c0023t0002g0014 | 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 | 137368050 | A | ACT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(72): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0005others(40): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | 98 | 0.7653 | 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 | 137369165 | A | ATT | intron_variant | MODIFIER | HG02257.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0012a0001c0013others(4): Show | a0001c0001t0002a0001c0012t0004a0001c0013t0002others(4): Show | a0001c0001t0002g0034a0001c0012t0004g0011a0001c0013t0002g0030others(4): Show | 7 | 98 | 0.0714 | 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 | 137369167 | A | ATT | intron_variant | MODIFIER | HG02280.hp2 HG02976.hp2 NA18906.hp1 |
a0002a0006a0019 | a0002c0044a0006c0011a0019c0037 | a0002c0044t0007a0006c0011t0005a0019c0037t0005 | a0002c0044t0007g0059a0006c0011t0005g0095a0019c0037t0005g0083 | 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 | 137372323 | C | CTT | intron_variant | MODIFIER | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0003a0002c0029others(6): Show | a0001c0001t0001a0001c0001t0010a0002c0003t0009others(7): Show | a0001c0001t0001g0027a0001c0001t0010g0087a0002c0003t0009g0073others(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 | 137380257 | G | GAA | intron_variant | MODIFIER | HG01169.hp2 HG01255.hp2 HG02109.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0029a0003c0002others(2): Show | a0001c0001t0003a0002c0029t0001a0003c0002t0001others(4): Show | a0001c0001t0003g0081a0002c0029t0001g0024a0003c0002t0001g0005others(4): Show | 7 | 98 | 0.0714 | 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 | 137389193 | C | CAT | intron_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
a0001a0002a0005others(1): Show | a0001c0004a0001c0005a0002c0006others(3): Show | a0001c0004t0001a0001c0005t0002a0002c0006t0001others(4): Show | a0001c0004t0001g0058a0001c0005t0002g0021a0002c0006t0001g0015others(4): Show | 7 | 98 | 0.0714 | 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 | 137389226 | A | AAT | intron_variant | MODIFIER | HG02280.hp1 HG03453.hp1 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0002a0001c0019t0016 | a0001c0001t0002g0034a0001c0019t0016g0090 | 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 | 137389402 | A | ATT | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp1 NA18747.hp1 others(3): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0019a0002c0003others(3): Show | a0001c0001t0008a0001c0019t0016a0002c0003t0006others(3): Show | a0001c0001t0008g0012a0001c0019t0016g0090a0002c0003t0006g0041others(3): Show | 6 | 98 | 0.0612 | 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 | 137404430 | G | GAT | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0004 | a0004c0007 | a0004c0007t0008 | a0004c0007t0008g0048a0004c0007t0008g0049 | 2 | 98 | 0.0204 | 2 | c.250 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137404470 | T | TAC | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 |
a0002 | a0002c0006a0002c0030 | a0002c0006t0001a0002c0030t0004 | a0002c0006t0001g0015a0002c0030t0004g0050 | 2 | 98 | 0.0204 | 2 | c.250 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137405198 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(27): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0003others(25): Show | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0010g0087others(27): Show | 30 | 98 | 0.3061 | 2 | c.250 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137415055 | C | CAA | intron_variant | MODIFIER | HG00735.hp2 HG01358.hp1 HG02056.hp1 others(28): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0005others(23): Show | a0001c0001t0001a0001c0001t0008a0001c0004t0003others(25): Show | a0001c0001t0001g0062a0001c0001t0008g0012a0001c0004t0003g0091others(28): Show | 31 | 98 | 0.3163 | 2 | c.295 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137415664 | G | GTT | intron_variant | MODIFIER | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0012a0001c0013others(4): Show | a0001c0001t0001a0001c0012t0004a0001c0013t0002others(4): Show | a0001c0001t0001g0027a0001c0012t0004g0011a0001c0013t0002g0030others(4): Show | 7 | 98 | 0.0714 | 2 | c.295 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137418913 | C | CTT | 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.295 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137419409 | G | GGC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0029others(34): Show | 37 | 98 | 0.3776 | 2 | c.295 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137439526 | T | TAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0004a0001c0005others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0029others(48): Show | 51 | 98 | 0.5204 | 2 | c.296 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137440462 | C | CTT | intron_variant | MODIFIER | HG00735.hp2 HG01358.hp1 HG01515.hp2 others(21): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0010a0002c0003others(18): Show | a0001c0001t0001a0001c0001t0008a0001c0010t0002others(20): Show | a0001c0001t0001g0062a0001c0001t0008g0012a0001c0010t0002g0020others(21): Show | 24 | 98 | 0.2449 | 2 | c.296 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137453326 | C | CTT | intron_variant | MODIFIER | HG00735.hp2 HG03225.hp1 NA18993.hp2 others(2): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0030a0004c0055others(1): Show | a0001c0001t0001a0001c0001t0003a0002c0030t0004others(2): Show | a0001c0001t0001g0018a0001c0001t0003g0081a0002c0030t0004g0050others(2): Show | 5 | 98 | 0.0510 | 2 | c.313 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137473093 | G | GTT | intron_variant | MODIFIER | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
a0003a0022 | a0003c0002a0022c0015 | a0003c0002t0001a0022c0015t0005 | a0003c0002t0001g0002a0003c0002t0001g0003a0003c0002t0001g0005others(1): Show | 4 | 98 | 0.0408 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137487374 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(34): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0010others(27): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0001others(32): Show | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0010g0087others(34): Show | 37 | 98 | 0.3776 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137493122 | C | CAA | intron_variant | MODIFIER | HG01515.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
a0002a0003a0004others(1): Show | a0002c0003a0002c0044a0002c0052others(3): Show | a0002c0003t0001a0002c0044t0007a0002c0052t0008others(3): Show | a0002c0003t0001g0056a0002c0044t0007g0059a0002c0052t0008g0042others(3): Show | 6 | 98 | 0.0612 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137497212 | G | GAC | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
a0001a0002a0005others(1): Show | a0001c0005a0001c0013a0001c0053others(5): Show | a0001c0005t0002a0001c0013t0002a0001c0053t0005others(5): Show | a0001c0005t0002g0021a0001c0013t0002g0072a0001c0053t0005g0084others(5): Show | 8 | 98 | 0.0816 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137508376 | A | ATT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(37): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0010others(26): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0001others(31): Show | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0029others(37): Show | 40 | 98 | 0.4082 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137510416 | T | TTA | intron_variant | MODIFIER | HG00609.hp1 HG01358.hp1 HG02056.hp1 others(7): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0012a0001c0017others(7): Show | a0001c0001t0001a0001c0012t0011a0001c0017t0001others(7): Show | a0001c0001t0001g0052a0001c0012t0011g0096a0001c0017t0001g0045others(7): Show | 10 | 98 | 0.1020 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137512382 | C | CTT | intron_variant | MODIFIER | HG00609.hp1 HG02056.hp1 HG02258.hp1 others(14): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0010a0001c0017others(13): Show | a0001c0001t0001a0001c0010t0002a0001c0017t0001others(13): Show | a0001c0001t0001g0062a0001c0010t0002g0020a0001c0010t0002g0053others(14): Show | 17 | 98 | 0.1735 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137516716 | C | CAT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(74): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0005others(44): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(63): Show | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0052others(74): Show | 77 | 98 | 0.7857 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137529596 | C | CTT | intron_variant | MODIFIER | HG02258.hp1 HG02280.hp1 HG02630.hp2 others(11): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0004a0001c0010others(9): Show | a0001c0001t0001a0001c0004t0003a0001c0010t0002others(10): Show | a0001c0001t0001g0062a0001c0004t0003g0091a0001c0010t0002g0020others(11): Show | 14 | 98 | 0.1429 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137534013 | T | TGC | intron_variant | MODIFIER | HG02109.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
a0001a0002a0005 | a0001c0004a0001c0005a0001c0013others(2): Show | a0001c0004t0002a0001c0005t0002a0001c0013t0002others(2): Show | a0001c0004t0002g0039a0001c0005t0002g0021a0001c0013t0002g0072others(2): Show | 5 | 98 | 0.0510 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137534018 | G | GCA | intron_variant | MODIFIER | HG02451.hp1 HG02451.hp2 HG03471.hp1 |
a0001a0002 | a0001c0012a0001c0031a0002c0006 | a0001c0012t0011a0001c0031t0004a0002c0006t0001 | a0001c0012t0011g0096a0001c0031t0004g0060a0002c0006t0001g0015 | 3 | 98 | 0.0306 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137534419 | A | AAT | intron_variant | MODIFIER | HG02258.hp2 HG03669.hp1 |
a0002a0007 | a0002c0003a0007c0024 | a0002c0003t0001a0007c0024t0014 | a0002c0003t0001g0070a0007c0024t0014g0037 | 2 | 98 | 0.0204 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137546395 | T | TAA | intron_variant | MODIFIER | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
a0002a0003a0022 | a0002c0052a0003c0002a0022c0015 | a0002c0052t0008a0003c0002t0001a0022c0015t0005 | a0002c0052t0008g0042a0003c0002t0001g0002a0003c0002t0001g0003others(1): Show | 4 | 98 | 0.0408 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137546448 | A | ATC | intron_variant | MODIFIER | HG02109.hp2 HG02895.hp1 HG02897.hp2 |
a0003a0022 | a0003c0002a0022c0015 | a0003c0002t0001a0022c0015t0005 | a0003c0002t0001g0002a0003c0002t0001g0003a0022c0015t0005g0098 | 3 | 98 | 0.0306 | 2 | c.313 others(23): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137562594 | T | TTG | intron_variant | MODIFIER | HG01358.hp2 HG01515.hp1 |
a0001a0021 | a0001c0001a0021c0039 | a0001c0001t0010a0021c0039t0002 | a0001c0001t0010g0087a0021c0039t0002g0004 | 2 | 98 | 0.0204 | 2 | c.313 others(19): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THSD7B_chr2_136760545_137682718 | 137579518 | G | GCA | intron_variant | MODIFIER | HG00609.hp1 HG01358.hp1 HG02056.hp1 others(7): Show |
a0001a0002a0003others(4): Show | a0001c0017a0001c0019a0002c0003others(7): Show | a0001c0017t0001a0001c0019t0016a0002c0003t0006others(7): Show | a0001c0017t0001g0045a0001c0019t0016g0090a0002c0003t0006g0041others(7): Show | 10 | 98 | 0.1020 | 2 | c.342 others(21): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |