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 | 50685420 | TC | T | intron_variant | MODIFIER | HG02895.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0024a0001c0001t0042 | a0001c0001t0024g0058a0001c0001t0042g0048 | 2 | 106 | 0.0189 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50687153 | AT | A | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(45): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(21): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(45): Show | 48 | 106 | 0.4528 | -1 | c.103 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50691528 | GA | G | intron_variant | MODIFIER | NA18944.hp2 NA19068.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | 106 | 0.0189 | -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 | 50699224 | AG | A | intron_variant | MODIFIER | HG00621.hp1 HG00741.hp1 HG01071.hp1 others(36): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(15): Show | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0019others(36): Show | 39 | 106 | 0.3679 | -1 | c.103 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50700685 | CT | C | intron_variant | MODIFIER | HG00621.hp2 HG01192.hp1 HG01243.hp2 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(9): Show | a0001c0001t0004g0072a0001c0001t0004g0102a0001c0001t0005g0018others(17): Show | 20 | 106 | 0.1887 | -1 | c.103 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50701112 | TA | T | intron_variant | MODIFIER | HG01071.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0030a0001c0001t0035others(1): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0030g0053others(2): Show | 5 | 106 | 0.0472 | -1 | c.103 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50702075 | TC | T | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(103): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | a0001c0001t0001g0086a0001c0001t0002g0010a0001c0001t0002g0013others(103): Show | 106 | 106 | 1.0000 | -1 | c.103 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50702156 | 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(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50704113 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(27): Show | 30 | 106 | 0.2830 | -1 | c.103 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50705299 | TG | T | intron_variant | MODIFIER | HG01071.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0030a0001c0001t0035others(1): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0030g0053others(2): Show | 5 | 106 | 0.0472 | -1 | c.119 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 16/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50709377 | TG | T | intron_variant | MODIFIER | HG00621.hp2 HG01192.hp1 HG01243.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(7): Show | a0001c0001t0004g0072a0001c0001t0004g0102a0001c0001t0005g0018others(15): Show | 18 | 106 | 0.1698 | -1 | c.128 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50709469 | TA | T | intron_variant | MODIFIER | HG02055.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0010a0001c0001t0032others(1): Show | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0010g0030others(2): Show | 5 | 106 | 0.0472 | -1 | c.128 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50714058 | CA | C | intron_variant | MODIFIER | HG00621.hp1 HG00741.hp1 HG01071.hp1 others(44): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(23): Show | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0019others(44): Show | 47 | 106 | 0.4434 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50714407 | GA | G | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(14): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(29): Show | 32 | 106 | 0.3019 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50716899 | AT | A | intron_variant | MODIFIER | HG01071.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0030a0001c0001t0035others(1): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0030g0053others(2): Show | 5 | 106 | 0.0472 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50723788 | GA | G | intron_variant | MODIFIER | HG00621.hp2 HG01192.hp1 HG01243.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(13): Show | a0001c0001t0004g0072a0001c0001t0004g0102a0001c0001t0005g0018others(25): Show | 28 | 106 | 0.2642 | -1 | c.128 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50729543 | TG | T | intron_variant | MODIFIER | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0037a0001c0001t0046 | a0001c0001t0017g0057a0001c0001t0037g0034a0001c0001t0046g0104 | 3 | 106 | 0.0283 | -1 | c.128 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50738790 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(60): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(32): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(60): Show | 63 | 106 | 0.5943 | -1 | c.128 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50740275 | GA | G | intron_variant | MODIFIER | HG00621.hp2 HG01192.hp1 HG01243.hp2 others(19): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(10): Show | a0001c0001t0004g0072a0001c0001t0004g0102a0001c0001t0005g0018others(19): Show | 22 | 106 | 0.2076 | -1 | c.128 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50740661 | AT | A | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp2 HG02698.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0012a0001c0001t0040 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0067others(3): Show | 6 | 106 | 0.0566 | -1 | c.128 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50742698 | AT | A | intron_variant | MODIFIER | HG02647.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0097a0001c0001t0011g0099 | 2 | 106 | 0.0189 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50743103 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(27): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(13): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(27): Show | 30 | 106 | 0.2830 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50747881 | CA | C | intron_variant | MODIFIER | HG01071.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0030a0001c0001t0035others(1): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0030g0053others(2): Show | 5 | 106 | 0.0472 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50748710 | TA | T | intron_variant | MODIFIER | HG01071.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0030a0001c0001t0048 | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0030g0053others(1): Show | 4 | 106 | 0.0377 | -1 | c.128 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50753792 | GA | G | intron_variant | MODIFIER | HG01071.hp2 HG01243.hp2 HG02055.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0013a0001c0001t0016a0001c0001t0030others(2): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0016g0003others(3): Show | 6 | 106 | 0.0566 | -1 | c.139 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50757684 | TG | T | intron_variant | MODIFIER | NA18906.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0037 | a0001c0001t0017g0057a0001c0001t0037g0034 | 2 | 106 | 0.0189 | -1 | c.139 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50762120 | TC | T | intron_variant | MODIFIER | HG00280.hp2 HG04115.hp1 NA18944.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0026 | a0001c0001t0002g0042a0001c0001t0004g0078a0001c0001t0004g0079others(4): Show | 7 | 106 | 0.0660 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50772769 | GA | G | intron_variant | MODIFIER | HG02647.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0097a0001c0001t0011g0099 | 2 | 106 | 0.0189 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50775949 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(66): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(36): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(66): Show | 69 | 106 | 0.6509 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50777640 | AT | A | intron_variant | MODIFIER | HG00621.hp2 HG01071.hp2 HG01192.hp1 others(28): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(17): Show | a0001c0001t0005g0018a0001c0001t0005g0021a0001c0001t0005g0022others(28): Show | 31 | 106 | 0.2925 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50779670 | CT | C | intron_variant | MODIFIER | HG00621.hp2 HG01192.hp1 HG01884.hp1 others(22): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(12): Show | a0001c0001t0005g0018a0001c0001t0005g0021a0001c0001t0005g0022others(22): Show | 25 | 106 | 0.2359 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50779912 | AG | A | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(41): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(21): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(41): Show | 44 | 106 | 0.4151 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50781187 | TG | T | intron_variant | MODIFIER | HG02109.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0007a0001c0001t0015a0002c0003t0018 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0039others(2): Show | 5 | 106 | 0.0472 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50781486 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(16): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(35): Show | 38 | 106 | 0.3585 | -1 | c.139 others(11): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50785741 | TG | T | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0010a0001c0001t0027others(5): Show | a0001c0001t0009g0085a0001c0001t0009g0100a0001c0001t0009g0101others(8): Show | 11 | 106 | 0.1038 | -1 | c.139 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50786912 | TA | T | intron_variant | MODIFIER | HG01071.hp2 HG01243.hp2 HG02055.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0013a0001c0001t0016a0001c0001t0030others(2): Show | a0001c0001t0013g0009a0001c0001t0013g0068a0001c0001t0016g0003others(3): Show | 6 | 106 | 0.0566 | -1 | c.139 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50790750 | AG | A | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0010a0001c0001t0027others(5): Show | a0001c0001t0009g0085a0001c0001t0009g0100a0001c0001t0009g0101others(8): Show | 11 | 106 | 0.1038 | -1 | c.139 others(10): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | chr8 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 50792080 | AT | A | intron_variant | MODIFIER | HG01071.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(13): Show | a0001c0001t0004g0090a0001c0001t0007g0036a0001c0001t0007g0037others(17): Show | 20 | 106 | 0.1887 | -1 | c.139 others(9): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50799728 | AT | A | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(5): Show | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0015others(20): Show | 23 | 106 | 0.2170 | -1 | c.*69 others(6): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 3037 | chr8 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 950680 | TC | T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00673.hp2 HG01074.hp1 others(24): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(7): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0004others(12): Show | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0057others(24): Show | 27 | 190 | 0.1421 | -1 | c.-31 others(5): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 168 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 952662 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(61): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0002c0003others(17): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(18): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(61): Show | 64 | 190 | 0.3368 | -1 | c.72+ others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 956043 | GC | G | intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG02895.hp1 others(10): Show |
a0001a0003a0004others(4): Show | a0001c0002a0003c0007a0003c0008others(6): Show | a0001c0002t0001a0001c0002t0002a0003c0007t0001others(8): Show | a0001c0002t0001g0069a0001c0002t0002g0002a0001c0002t0002g0076others(10): Show | 13 | 190 | 0.0684 | -1 | c.72+ others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 956249 | GC | G | intron_variant | MODIFIER | HG03225.hp1 HG03471.hp1 NA20129.hp1 |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0006 | a0001c0002t0002a0004c0014t0002a0005c0006t0002 | a0001c0002t0002g0002a0004c0014t0002g0001a0005c0006t0002g0003 | 3 | 190 | 0.0158 | -1 | c.72+ others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 956256 | CG | C | intron_variant | MODIFIER | HG03225.hp1 HG03471.hp1 NA20129.hp1 |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0006 | a0001c0002t0002a0004c0014t0002a0005c0006t0002 | a0001c0002t0002g0002a0004c0014t0002g0001a0005c0006t0002g0003 | 3 | 190 | 0.0158 | -1 | c.72+ others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 959107 | TA | T | intron_variant | MODIFIER | HG02109.hp2 HG02895.hp1 HG02970.hp1 others(6): Show |
a0001a0003a0004others(4): Show | a0001c0002a0003c0007a0003c0008others(5): Show | a0001c0002t0001a0001c0002t0002a0003c0007t0001others(6): Show | a0001c0002t0001g0069a0001c0002t0002g0002a0003c0007t0001g0068others(6): Show | 9 | 190 | 0.0474 | -1 | c.72+ others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 965105 | CT | C | intron_variant | MODIFIER | HG00673.hp1 HG02015.hp2 NA18942.hp1 others(2): Show |
a0001a0002a0006 | a0001c0002a0002c0003a0002c0005others(1): Show | a0001c0002t0001a0002c0003t0001a0002c0005t0001others(1): Show | a0001c0002t0001g0115a0002c0003t0001g0113a0002c0005t0001g0114others(2): Show | 5 | 190 | 0.0263 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 965164 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(19): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0002c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(8): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | 190 | 0.1158 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 965280 | CT | C | intron_variant | MODIFIER | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
a0001a0003a0004others(4): Show | a0001c0002a0003c0008a0004c0004others(5): Show | a0001c0002t0001a0003c0008t0001a0004c0004t0001others(5): Show | a0001c0002t0001g0041a0003c0008t0001g0044a0004c0004t0001g0047others(6): Show | 9 | 190 | 0.0474 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 966303 | AT | A | intron_variant | MODIFIER | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
a0001a0003a0004others(1): Show | a0001c0002a0003c0007a0004c0004others(1): Show | a0001c0002t0001a0003c0007t0001a0004c0004t0001others(1): Show | a0001c0002t0001g0133a0003c0007t0001g0080a0003c0007t0001g0108others(3): Show | 6 | 190 | 0.0316 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 966455 | AT | A | intron_variant | MODIFIER | HG00140.hp2 HG00673.hp2 HG01074.hp1 others(31): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(12): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(16): Show | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0058others(31): Show | 34 | 190 | 0.1790 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |