view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNTG1_chr8_49906407_50801692 | 50488221 | GT | G | intron_variant | MODIFIER | HG00280.hp2 HG01884.hp2 HG02145.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0002g0033others(13): Show | 16 | 106 | 0.1509 | -1 | c.364 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50495463 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG01192.hp2 HG02109.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(14): Show | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0002g0033others(18): Show | 21 | 106 | 0.1981 | -1 | c.364 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50501425 | GT | G | intron_variant | MODIFIER | HG00621.hp2 HG01071.hp1 HG02300.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0002g0042a0001c0001t0003g0019a0001c0001t0003g0020others(8): Show | 11 | 106 | 0.1038 | -1 | c.364 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50501611 | AT | A | intron_variant | MODIFIER | HG00280.hp2 HG01167.hp2 HG01192.hp1 others(36): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0026others(36): Show | 39 | 106 | 0.3679 | -1 | c.364 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50503093 | AC | A | intron_variant | MODIFIER | HG00280.hp2 HG01192.hp2 HG01884.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0032others(23): Show | 26 | 106 | 0.2453 | -1 | c.466 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50507686 | CT | C | intron_variant | MODIFIER | HG00621.hp2 HG01071.hp1 HG01167.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0002g0017a0001c0001t0002g0042a0001c0001t0003g0019others(26): Show | 29 | 106 | 0.2736 | -1 | c.466 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50515387 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00741.hp1 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(13): Show | a0001c0001t0001g0086a0001c0001t0002g0013a0001c0001t0002g0026others(23): Show | 26 | 106 | 0.2453 | -1 | c.466 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50515416 | GT | G | intron_variant | MODIFIER | HG01192.hp1 HG01243.hp2 HG03209.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0001t0016a0001c0002t0014 | a0001c0001t0008g0061a0001c0001t0016g0003a0001c0002t0014g0014 | 3 | 106 | 0.0283 | -1 | c.466 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50522577 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG02698.hp2 HG02886.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0004g0079others(10): Show | 13 | 106 | 0.1226 | -1 | c.467 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50527183 | GT | G | intron_variant | MODIFIER | HG01167.hp2 HG01192.hp2 HG02886.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(6): Show | a0001c0001t0004g0072a0001c0001t0005g0035a0001c0001t0008g0071others(8): Show | 11 | 106 | 0.1038 | -1 | c.467 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50527973 | CA | C | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0020others(2): Show | a0001c0001t0002g0015a0001c0001t0003g0007a0001c0001t0003g0027others(3): Show | 6 | 106 | 0.0566 | -1 | c.467 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 9/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50530428 | AT | A | intron_variant | MODIFIER | HG00621.hp2 HG01071.hp1 HG01167.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0002g0017a0001c0001t0002g0042a0001c0001t0003g0019others(26): Show | 29 | 106 | 0.2736 | -1 | c.549 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50531328 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG02109.hp2 HG02622.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(7): Show | a0001c0001t0004g0074a0001c0001t0004g0094a0001c0001t0006g0051others(12): Show | 15 | 106 | 0.1415 | -1 | c.549 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50533576 | CA | C | intron_variant | MODIFIER | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0008a0001c0001t0016others(5): Show | a0001c0001t0002g0026a0001c0001t0008g0061a0001c0001t0016g0003others(5): Show | 8 | 106 | 0.0755 | -1 | c.550 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50534497 | TA | T | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0049 | a0001c0001t0006g0051a0001c0001t0006g0066a0001c0001t0049g0106 | 3 | 106 | 0.0283 | -1 | c.550 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50536335 | TA | T | intron_variant | MODIFIER | HG01167.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(4): Show | a0001c0001t0004g0072a0001c0001t0005g0035a0001c0001t0008g0071others(6): Show | 9 | 106 | 0.0849 | -1 | c.550 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50544527 | TA | T | intron_variant | MODIFIER | HG02886.hp1 HG03453.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0008 | a0001c0001t0004g0072a0001c0001t0005g0035a0001c0001t0008g0071 | 3 | 106 | 0.0283 | -1 | c.680 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50548629 | TA | T | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp2 HG01071.hp1 others(65): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(36): Show | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0017others(65): Show | 68 | 106 | 0.6415 | -1 | c.681 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50549257 | AG | A | intron_variant | MODIFIER | HG01167.hp2 HG01192.hp2 HG02698.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | a0001c0001t0004g0079a0001c0001t0004g0090a0001c0001t0007g0006others(11): Show | 14 | 106 | 0.1321 | -1 | c.681 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50554917 | GT | G | intron_variant | MODIFIER | HG02109.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0007a0001c0001t0015a0003c0004t0005 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0039others(2): Show | 5 | 106 | 0.0472 | -1 | c.810 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50554960 | TC | T | intron_variant | MODIFIER | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0002t0044 | a0001c0001t0002g0026a0001c0001t0006g0051a0001c0001t0006g0066others(1): Show | 4 | 106 | 0.0377 | -1 | c.810 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50557221 | CA | C | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02698.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(5): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0066others(6): Show | 9 | 106 | 0.0849 | -1 | c.810 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50564130 | TA | T | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(5): Show | 8 | 106 | 0.0755 | -1 | c.810 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50569399 | GA | G | intron_variant | MODIFIER | HG01192.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0007a0001c0001t0027a0001c0001t0033others(3): Show | a0001c0001t0007g0006a0001c0001t0027g0070a0001c0001t0033g0056others(3): Show | 6 | 106 | 0.0566 | -1 | c.810 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50569548 | CA | C | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0020others(7): Show | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0003g0007others(9): Show | 12 | 106 | 0.1132 | -1 | c.810 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50574789 | AT | A | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02698.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(5): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(7): Show | 10 | 106 | 0.0943 | -1 | c.811 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50577448 | GT | G | intron_variant | MODIFIER | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0002t0044 | a0001c0001t0002g0026a0001c0001t0006g0051a0001c0001t0006g0066others(1): Show | 4 | 106 | 0.0377 | -1 | c.811 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50583394 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0086a0001c0001t0002g0013a0001c0001t0002g0026others(23): Show | 26 | 106 | 0.2453 | -1 | c.811 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50589590 | TA | T | intron_variant | MODIFIER | HG01167.hp2 HG02698.hp2 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0010a0001c0002t0014others(3): Show | a0001c0001t0004g0072a0001c0002t0010g0012a0001c0002t0014g0014others(4): Show | 7 | 106 | 0.0660 | -1 | c.811 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50590634 | TA | T | intron_variant | MODIFIER | HG02109.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0007a0001c0001t0015a0003c0004t0005 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0039others(2): Show | 5 | 106 | 0.0472 | -1 | c.811 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50591332 | AT | A | intron_variant | MODIFIER | HG01192.hp2 HG02976.hp2 HG06807.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0033a0001c0001t0035a0001c0005t0019 | a0001c0001t0033g0056a0001c0001t0035g0031a0001c0005t0019g0044 | 3 | 106 | 0.0283 | -1 | c.849 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50594941 | CA | C | intron_variant | MODIFIER | HG02622.hp2 HG03041.hp2 NA21309.hp2 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0021a0002c0003t0018a0002c0003t0043 | a0001c0002t0021g0073a0002c0003t0018g0045a0002c0003t0043g0050 | 3 | 106 | 0.0283 | -1 | c.849 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50601152 | CA | C | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG01243.hp1 others(17): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(11): Show | a0001c0001t0002g0015a0001c0001t0002g0033a0001c0001t0004g0078others(17): Show | 20 | 106 | 0.1887 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50602899 | AT | A | intron_variant | MODIFIER | HG02451.hp2 HG02647.hp1 HG03098.hp1 others(7): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(5): Show | a0001c0001t0005g0024a0001c0001t0005g0035a0001c0001t0008g0071others(7): Show | 10 | 106 | 0.0943 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50606841 | CT | C | intron_variant | MODIFIER | HG00741.hp1 HG01167.hp2 HG02145.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(11): Show | 14 | 106 | 0.1321 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50612314 | TA | T | intron_variant | MODIFIER | HG02622.hp2 HG03041.hp2 |
a0002 | a0002c0003 | a0002c0003t0018a0002c0003t0043 | a0002c0003t0018g0045a0002c0003t0043g0050 | 2 | 106 | 0.0189 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50621063 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(30): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0086a0001c0001t0002g0010a0001c0001t0002g0013others(30): Show | 33 | 106 | 0.3113 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50623880 | CT | C | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(6): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(8): Show | 11 | 106 | 0.1038 | -1 | c.849 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50624320 | CA | C | intron_variant | MODIFIER | HG01167.hp2 HG02300.hp2 HG02451.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(5): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(7): Show | 10 | 106 | 0.0943 | -1 | c.850 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50630548 | AC | A | intron_variant | MODIFIER | HG01167.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(6): Show | a0001c0001t0002g0026a0001c0001t0004g0072a0001c0001t0006g0051others(8): Show | 11 | 106 | 0.1038 | -1 | c.850 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50643055 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp2 HG00741.hp2 others(37): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(37): Show | 40 | 106 | 0.3774 | -1 | c.850 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50645897 | GA | G | intron_variant | MODIFIER | HG02647.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0097a0001c0001t0011g0099 | 2 | 106 | 0.0189 | -1 | c.850 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50647890 | AC | A | intron_variant | MODIFIER | HG02647.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0097a0001c0001t0011g0099 | 2 | 106 | 0.0189 | -1 | c.850 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 13/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50658247 | AC | A | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(32): Show | 35 | 106 | 0.3302 | -1 | c.967 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 14/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50658260 | TA | T | intron_variant | MODIFIER | HG01192.hp2 HG02109.hp2 HG02647.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0007a0001c0001t0011a0001c0001t0015others(3): Show | a0001c0001t0007g0006a0001c0001t0007g0036a0001c0001t0007g0037others(7): Show | 10 | 106 | 0.0943 | -1 | c.967 others(8): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50660542 | AG | A | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(59): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0026others(59): Show | 62 | 106 | 0.5849 | -1 | c.103 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50669215 | TA | T | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(5): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(18): Show | 21 | 106 | 0.1981 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50672536 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(101): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0086a0001c0001t0002g0010a0001c0001t0002g0013others(101): Show | 104 | 106 | 0.9811 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50678165 | AT | A | intron_variant | MODIFIER | HG02109.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0007a0001c0001t0015a0002c0003t0018 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0039others(2): Show | 5 | 106 | 0.0472 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50681235 | GT | G | intron_variant | MODIFIER | HG01071.hp2 HG02109.hp1 HG02809.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0027a0001c0001t0030others(3): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0027g0070others(4): Show | 7 | 106 | 0.0660 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |