view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TSPAN15_chr10_69446465_69512666 | 69508440 | CAA | C | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(52): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(48): Show |
55 | 340 | 0.1618 | -2 | c.*14 others(13): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 775 | chr10 | TogoVar | |||||||
TSPAN15_chr10_69446465_69512666 | 69509082 | GGA | G | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
a0001a0003 | a0001c0001a0003c0003a0003c0004 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(5): Show | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(24): Show |
33 | 340 | 0.0971 | -2 | c.*21 others(13): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1417 | chr10 | TogoVar | |||||||
TSPAN16_chr19_11291160_11320967 | 11293071 | TTG | T | upstream_gene_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0002g0041 a0001c0001t0004g0005 a0001c0001t0004g0056 others(14): Show |
24 | 382 | 0.0628 | -2 | c.-32 others(13): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3088 | chr19 | TogoVar | |||||||
TSPAN16_chr19_11291160_11320967 | 11293076 | ATT | A | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
105 | 382 | 0.2749 | -2 | c.-32 others(13): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3083 | chr19 | TogoVar | |||||||
TSPAN16_chr19_11291160_11320967 | 11298435 | ATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
a0001a0002a0004 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
171 | 382 | 0.4476 | -2 | c.267 others(17): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TSPAN16_chr19_11291160_11320967 | 11299985 | GAA | G | intron_variant | MODIFIER | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0005 | a0001c0001t0001g0265 a0001c0001t0001g0268 a0001c0001t0004g0186 others(7): Show |
12 | 382 | 0.0314 | -2 | c.342 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TSPAN16_chr19_11291160_11320967 | 11302528 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(112): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
115 | 382 | 0.3011 | -2 | c.450 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TSPAN16_chr19_11291160_11320967 | 11302660 | CAT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004 | a0001c0001t0002g0034 a0001c0001t0002g0099 a0001c0001t0002g0105 others(10): Show |
15 | 382 | 0.0393 | -2 | c.450 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TSPAN16_chr19_11291160_11320967 | 11303575 | ATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(96): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0007t0001 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
99 | 382 | 0.2592 | -2 | c.450 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | TogoVar | |||||||
TSPAN16_chr19_11291160_11320967 | 11303576 | TTA | T | intron_variant | MODIFIER | HG00621.hp2 HG01106.hp1 HG01261.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0048 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
12 | 382 | 0.0314 | -2 | c.450 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | TogoVar | |||||||
TSPAN16_chr19_11291160_11320967 | 11310515 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
138 | 382 | 0.3613 | -2 | c.604 others(19): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
TSPAN16_chr19_11291160_11320967 | 11316117 | GGT | G | downstream_gene_variant | MODIFIER | HG00735.hp2 HG02145.hp1 NA18967.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0035 a0001c0001t0002g0099 a0001c0001t0002g0124 |
3 | 382 | 0.0079 | -2 | c.*28 others(11): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 151 | chr19 | TogoVar | |||||||
TSPAN17_chr5_176642484_176664051 | 176659325 | CAG | C | downstream_gene_variant | MODIFIER | HG02559.hp2 HG02809.hp2 HG02896.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
10 | 410 | 0.0244 | -2 | c.*16 others(13): Show |
TSPAN17 | ENSG00000048140.18 | transcript | ENST00000508164.6 | protein_coding | 275 | chr5 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44725663 | GCA | G | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0009others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0262 a0001c0001t0002g0004 a0001c0001t0002g0005 others(118): Show |
122 | 290 | 0.4207 | -2 | c.-18 others(13): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1298 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44731596 | TTG | T | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(13): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0014a0001c0001t0028a0001c0001t0055others(7): Show | a0001c0001t0014g0087 a0001c0001t0014g0089 a0001c0001t0014g0096 others(13): Show |
16 | 290 | 0.0552 | -2 | c.-24 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44739797 | GTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(100): Show | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0020 others(159): Show |
163 | 290 | 0.5621 | -2 | c.-24 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44741447 | ATG | A | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(64): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0014a0001c0001t0016a0001c0001t0017others(54): Show | a0001c0001t0014g0087 a0001c0001t0014g0089 a0001c0001t0014g0096 others(64): Show |
67 | 290 | 0.2310 | -2 | c.-24 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44742677 | CAG | C | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0014a0001c0001t0017a0001c0001t0024others(14): Show | a0001c0001t0014g0087 a0001c0001t0014g0089 a0001c0001t0014g0096 others(24): Show |
27 | 290 | 0.0931 | -2 | c.-24 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44752566 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(125): Show | a0001c0001t0001g0196 a0001c0001t0001g0262 a0001c0001t0002g0004 others(263): Show |
267 | 290 | 0.9207 | -2 | c.-23 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44768892 | ATT | A | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(104): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | a0001c0001t0002g0033 a0001c0001t0003g0013 a0001c0001t0003g0183 others(104): Show |
107 | 290 | 0.3690 | -2 | c.-15 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44786623 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | a0001c0001t0001g0196 a0001c0001t0001g0262 a0001c0001t0002g0020 others(130): Show |
133 | 290 | 0.4586 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44790544 | GTT | G | intron_variant | MODIFIER | HG02486.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0024a0001c0001t0119a0001c0003t0102 | a0001c0001t0024g0007 a0001c0001t0024g0117 a0001c0001t0024g0121 others(2): Show |
5 | 290 | 0.0172 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44790563 | CGT | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(2): Show | a0001c0001t0004g0240 a0001c0001t0004g0266 a0001c0001t0008g0241 others(4): Show |
7 | 290 | 0.0241 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44790611 | CGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(18): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(10): Show | a0001c0001t0003g0199 a0001c0001t0006g0201 a0001c0001t0012g0252 others(18): Show |
21 | 290 | 0.0724 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44807527 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | a0001c0001t0001g0262 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
141 | 290 | 0.4862 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44811125 | AAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(14): Show | a0001c0001t0004g0179 a0001c0001t0004g0203 a0001c0001t0008g0215 others(18): Show |
21 | 290 | 0.0724 | -2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44857893 | CAT | C | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(28): Show | a0001c0001t0003g0013 a0001c0001t0003g0183 a0001c0001t0003g0197 others(40): Show |
43 | 290 | 0.1483 | -2 | c.-15 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44861793 | TCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0196 a0001c0001t0001g0262 a0001c0001t0002g0004 others(89): Show |
93 | 290 | 0.3207 | -2 | c.-11 others(19): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44878895 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(90): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0007others(4): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(45): Show | a0001c0001t0002g0020 a0001c0001t0003g0013 a0001c0001t0003g0155 others(90): Show |
93 | 290 | 0.3207 | -2 | c.-11 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44879424 | AAG | A | intron_variant | MODIFIER | HG01243.hp1 HG01517.hp1 HG02559.hp2 |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0012a0001c0001t0089 | a0001c0001t0009g0070 a0001c0001t0012g0252 a0001c0001t0089g0143 |
3 | 290 | 0.0103 | -2 | c.-11 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44880393 | AGG | A | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp2 HG01070.hp2 others(17): Show |
a0001a0002a0004 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(8): Show | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0183 others(17): Show |
20 | 290 | 0.0690 | -2 | c.-11 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44882577 | CAG | C | intron_variant | MODIFIER | HG02129.hp1 NA18959.hp1 NA18999.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0077a0002c0002t0007 | a0001c0001t0002g0033 a0001c0001t0077g0109 a0002c0002t0007g0031 |
3 | 290 | 0.0103 | -2 | c.-11 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44900680 | CTT | C | intron_variant | MODIFIER | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0017others(11): Show | a0001c0001t0003g0155 a0001c0001t0003g0197 a0001c0001t0006g0174 others(13): Show |
16 | 290 | 0.0552 | -2 | c.-10 others(19): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44924097 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(49): Show | a0001c0001t0001g0196 a0001c0001t0003g0013 a0001c0001t0003g0155 others(131): Show |
135 | 290 | 0.4655 | -2 | c.616 others(19): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN19_chr12_85009317_85041277 | 85015541 | TAC | T | intron_variant | MODIFIER | HG00639.hp2 HG01109.hp1 HG01261.hp1 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(1): Show | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
37 | 350 | 0.1057 | -2 | c.678 others(17): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 8/8 | chr12 | TogoVar | |||||||
TSPAN19_chr12_85009317_85041277 | 85028154 | TTC | T | intron_variant | MODIFIER | HG02615.hp1 HG02723.hp1 HG02976.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 3 | 350 | 0.0086 | -2 | c.140 others(17): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 3/8 | chr12 | TogoVar | |||||||
TSPAN19_chr12_85009317_85041277 | 85029682 | CTA | C | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp2 HG02630.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
14 | 350 | 0.0400 | -2 | c.139 others(15): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 3/8 | chr12 | TogoVar | |||||||
TSPAN1_chr1_46170087_46190962 | 46179964 | AGT | A | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp1 HG03654.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 a0001c0001t0001g0077 a0001c0001t0001g0125 others(1): Show |
5 | 436 | 0.0115 | -2 | c.-14 others(19): Show |
TSPAN1 | ENSG00000117472.10 | transcript | ENST00000372003.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TSPAN1_chr1_46170087_46190962 | 46186488 | CTT | C | downstream_gene_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(3): Show |
9 | 436 | 0.0206 | -2 | c.*95 others(11): Show |
TSPAN1 | ENSG00000117472.10 | transcript | ENST00000372003.6 | protein_coding | 527 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115049989 | GAC | G | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(40): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0003a0001c0001t0010a0001c0001t0012others(3): Show | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0041 others(24): Show |
43 | 362 | 0.1188 | -2 | c.*49 others(11): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 499 | chr1 | TogoVar | ||||||
TSPAN2_chr1_115043011_115094503 | 115077332 | TAA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0001g0229 a0001c0001t0003g0005 a0001c0001t0003g0006 others(31): Show |
52 | 362 | 0.1437 | -2 | c.70- others(17): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115079137 | CCA | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0001g0229 a0001c0001t0003g0005 a0001c0001t0003g0006 others(27): Show |
52 | 362 | 0.1437 | -2 | c.70- others(17): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115079167 | ACG | A | intron_variant | MODIFIER | HG03831.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | 362 | 0.0138 | -2 | c.70- others(17): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | TogoVar | |||||||
TSPAN31_chr12_57740039_57755219 | 57742964 | CAT | C | upstream_gene_variant | MODIFIER | HG00544.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0013a0001c0001t0017others(5): Show | a0001c0001t0005g0003 a0001c0001t0013g0003 a0001c0001t0017g0001 others(5): Show |
27 | 372 | 0.0726 | -2 | c.-21 others(13): Show |
TSPAN31 | ENSG00000135452.10 | transcript | ENST00000257910.8 | protein_coding | 2074 | chr12 | TogoVar | |||||||
TSPAN31_chr12_57740039_57755219 | 57745631 | TCA | T | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0013 | a0001c0001t0005g0003 a0001c0001t0013g0003 |
16 | 372 | 0.0430 | -2 | c.64- others(15): Show |
TSPAN31 | ENSG00000135452.10 | transcript | ENST00000257910.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TSPAN31_chr12_57740039_57755219 | 57749141 | GTC | G | 3_prime_UTR_variant | MODIFIER | HG00544.hp2 HG02572.hp1 HG02683.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0023a0001c0001t0046others(1): Show | a0001c0001t0017g0001 a0001c0001t0023g0001 a0001c0001t0046g0001 others(1): Show |
7 | 372 | 0.0188 | -2 | c.*18 others(13): Show |
TSPAN31 | ENSG00000135452.10 | transcript | ENST00000257910.8 | protein_coding | 6/6 | 1855 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TSPAN32_chr11_2297013_2323204 | 2304567 | CTA | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0008others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0021 others(210): Show |
257 | 412 | 0.6238 | -2 | c.279 others(17): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN32_chr11_2297013_2323204 | 2306007 | AGT | A | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(50): Show |
a0001 | a0001c0001a0001c0002a0001c0008others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0008t0001others(1): Show | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0150 others(40): Show |
53 | 412 | 0.1286 | -2 | c.279 others(19): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN32_chr11_2297013_2323204 | 2319532 | CAA | C | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0012others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0016 others(199): Show |
251 | 412 | 0.6092 | -2 | c.*16 others(13): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1329 | chr11 | TogoVar | |||||||
TSPAN32_chr11_2297013_2323204 | 2319551 | AAT | A | downstream_gene_variant | MODIFIER | HG01433.hp2 HG02723.hp1 HG03471.hp2 others(18): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0054 a0001c0001t0001g0310 a0001c0002t0001g0005 others(13): Show |
21 | 412 | 0.0510 | -2 | c.*16 others(13): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1348 | chr11 | TogoVar |