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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TSPAN18_chr11_44721962_44937423 | 44762615 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG01168.hp2 others(4): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0010 | a0001c0001t0015a0001c0001t0018a0001c0001t0088others(2): Show | a0001c0001t0015g0122 a0001c0001t0018g0123 a0001c0001t0018g0125 others(4): Show |
7 | 290 | 0.0241 | 2 | c.-23 others(21): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44784736 | G | GGC | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0045 others(70): Show |
73 | 290 | 0.2517 | 2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44790415 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(16): Show | a0001c0001t0003g0199 a0001c0001t0006g0201 a0001c0001t0012g0252 others(24): Show |
27 | 290 | 0.0931 | 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 | 44800006 | G | GGT | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0009a0001c0001t0020a0001c0003t0015others(1): Show | a0001c0001t0009g0027 a0001c0001t0009g0028 a0001c0001t0020g0167 others(2): Show |
5 | 290 | 0.0172 | 2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44800006 | G | GTT | intron_variant | MODIFIER | HG01261.hp1 HG02055.hp1 HG03831.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0032a0001c0001t0041a0001c0001t0050others(2): Show | a0001c0001t0032g0202 a0001c0001t0041g0051 a0001c0001t0050g0084 others(5): Show |
8 | 290 | 0.0276 | 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 | 44802609 | G | GCA | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(63): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0262 a0001c0001t0002g0020 a0001c0001t0002g0033 others(62): Show |
66 | 290 | 0.2276 | 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 | 44810604 | C | CTT | intron_variant | MODIFIER | HG01106.hp1 HG01496.hp2 HG02886.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0043a0001c0001t0054others(8): Show | a0001c0001t0002g0026 a0001c0001t0002g0033 a0001c0001t0043g0081 others(9): Show |
12 | 290 | 0.0414 | 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 | A | AAC | intron_variant | MODIFIER | HG00323.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(16): Show | a0001c0001t0002g0033 a0001c0001t0003g0156 a0001c0001t0007g0042 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 | 44823475 | T | TTC | intron_variant | MODIFIER | HG01070.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(14): Show | a0001c0001t0003g0155 a0001c0001t0003g0199 a0001c0001t0003g0265 others(21): Show |
24 | 290 | 0.0828 | 2 | c.-15 others(23): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 2/9 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44851612 | A | ACC | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(25): Show | a0001c0001t0003g0218 a0001c0001t0004g0225 a0001c0001t0006g0206 others(26): Show |
29 | 290 | 0.1000 | 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 | 44854200 | T | TGG | intron_variant | MODIFIER | HG00544.hp1 HG01109.hp1 HG01168.hp1 others(25): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0002g0020 a0001c0001t0003g0183 a0001c0001t0004g0209 others(25): Show |
28 | 290 | 0.0966 | 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 | 44861792 | T | TTC | intron_variant | MODIFIER | HG00621.hp2 HG01069.hp1 HG04199.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0022a0002c0002t0002a0002c0002t0034 | a0001c0001t0022g0173 a0002c0002t0002g0002 a0002c0002t0034g0251 |
3 | 290 | 0.0103 | 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 | 44861793 | T | TCA | intron_variant | MODIFIER | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(27): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0002g0026 a0001c0001t0003g0250 a0001c0001t0004g0179 others(27): Show |
30 | 290 | 0.1035 | 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 | 44864286 | C | CAA | intron_variant | MODIFIER | HG00558.hp2 HG01175.hp2 HG01496.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0004a0001c0001t0013a0001c0001t0017others(11): Show | a0001c0001t0004g0214 a0001c0001t0013g0003 a0001c0001t0017g0168 others(13): Show |
16 | 290 | 0.0552 | 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 | 44867389 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(24): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0002g0005 a0001c0001t0003g0157 a0001c0001t0004g0214 others(24): Show |
27 | 290 | 0.0931 | 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 | 44882577 | C | CAG | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0024a0001c0001t0049 | a0001c0001t0006g0165 a0001c0001t0024g0007 a0001c0001t0049g0068 |
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 | 44882585 | G | GAC | intron_variant | MODIFIER | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(29): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0013others(17): Show | a0001c0001t0001g0262 a0001c0001t0010g0057 a0001c0001t0010g0058 others(29): Show |
32 | 290 | 0.1103 | 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 | 44882627 | C | CAG | intron_variant | MODIFIER | HG02602.hp2 NA18977.hp1 NA19000.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0007a0002c0002t0002others(1): Show | a0001c0001t0002g0020 a0001c0001t0007g0085 a0002c0002t0002g0041 others(1): Show |
4 | 290 | 0.0138 | 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 | 44907144 | C | CAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0005others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(132): Show | a0001c0001t0001g0196 a0001c0001t0001g0262 a0001c0001t0002g0005 others(271): Show |
275 | 290 | 0.9483 | 2 | c.63+ others(15): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44908769 | G | GAA | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG01069.hp1 others(37): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(34): Show | a0001c0001t0001g0262 a0001c0001t0002g0033 a0001c0001t0013g0003 others(37): Show |
40 | 290 | 0.1379 | 2 | c.64- others(15): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44908770 | A | AAG | intron_variant | MODIFIER | HG02559.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0033a0001c0001t0066a0001c0001t0084others(2): Show | a0001c0001t0033g0246 a0001c0001t0066g0016 a0001c0001t0084g0136 others(2): Show |
5 | 290 | 0.0172 | 2 | c.64- others(15): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 4/9 | chr11 | TogoVar | |||||||
TSPAN18_chr11_44721962_44937423 | 44908783 | G | GAA | intron_variant | MODIFIER | HG00280.hp2 HG01069.hp1 HG01106.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0013a0001c0001t0022a0001c0001t0025others(4): Show | a0001c0001t0013g0003 a0001c0001t0013g0062 a0001c0001t0022g0173 others(6): Show |
9 | 290 | 0.0310 | 2 | c.64- others(15): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44908787 | G | GAA | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0020others(12): Show | a0001c0001t0001g0262 a0001c0001t0002g0033 a0001c0001t0020g0167 others(12): Show |
15 | 290 | 0.0517 | 2 | c.64- others(15): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44920469 | C | CTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(97): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0011others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(74): Show | a0001c0001t0001g0262 a0001c0001t0002g0005 a0001c0001t0002g0033 others(97): Show |
100 | 290 | 0.3448 | 2 | c.615 others(17): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN18_chr11_44721962_44937423 | 44922117 | A | ATT | intron_variant | MODIFIER | HG01109.hp2 HG01175.hp2 HG01943.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0013a0001c0001t0030a0001c0001t0060others(7): Show | a0001c0001t0013g0003 a0001c0001t0013g0062 a0001c0001t0030g0142 others(8): Show |
11 | 290 | 0.0379 | 2 | c.615 others(19): Show |
TSPAN18 | ENSG00000157570.12 | transcript | ENST00000520358.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN19_chr12_85009317_85041277 | 85015537 | C | CAT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(52): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(23): Show |
55 | 350 | 0.1571 | 2 | c.678 others(17): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 8/8 | chr12 | TogoVar | |||||||
TSPAN19_chr12_85009317_85041277 | 85015541 | T | TAC | intron_variant | MODIFIER | HG02109.hp1 HG02602.hp2 HG02723.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0065 a0001c0001t0002g0003 a0001c0001t0002g0114 others(1): Show |
16 | 350 | 0.0457 | 2 | c.678 others(17): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 8/8 | chr12 | TogoVar | |||||||
TSPAN19_chr12_85009317_85041277 | 85035247 | G | GGT | intron_variant | MODIFIER | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 |
6 | 350 | 0.0171 | 2 | c.-28 others(17): Show |
TSPAN19 | ENSG00000231738.11 | transcript | ENST00000532498.7 | protein_coding | 1/8 | chr12 | TogoVar | |||||||
TSPAN1_chr1_46170087_46190962 | 46178354 | C | CAA | intron_variant | MODIFIER | HG00609.hp1 HG00673.hp1 HG02015.hp2 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
28 | 436 | 0.0642 | 2 | c.-14 others(21): Show |
TSPAN1 | ENSG00000117472.10 | transcript | ENST00000372003.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TSPAN1_chr1_46170087_46190962 | 46179964 | A | AGT | intron_variant | MODIFIER | HG01346.hp2 HG01934.hp2 HG02559.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0094 others(8): Show |
13 | 436 | 0.0298 | 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 | 46186664 | G | GTT | downstream_gene_variant | MODIFIER | HG00738.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0002 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(9): Show |
14 | 436 | 0.0321 | 2 | c.*11 others(13): Show |
TSPAN1 | ENSG00000117472.10 | transcript | ENST00000372003.6 | protein_coding | 703 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115048173 | G | GTA | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(11): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(107): Show |
153 | 362 | 0.4227 | 2 | c.*23 others(13): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2316 | chr1 | TogoVar | ||||||
TSPAN2_chr1_115043011_115094503 | 115048301 | A | ATT | 3_prime_UTR_variant | MODIFIER | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0032a0001c0002t0009 | a0001c0001t0009g0023 a0001c0001t0009g0062 a0001c0001t0009g0133 others(2): Show |
7 | 362 | 0.0193 | 2 | c.*21 others(13): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2188 | chr1 | TogoVar | ||||||
TSPAN2_chr1_115043011_115094503 | 115048306 | G | GAT | 3_prime_UTR_variant | MODIFIER | HG00621.hp1 HG00741.hp1 HG01167.hp1 others(48): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0004a0001c0001t0007a0001c0002t0004others(4): Show | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0046 others(30): Show |
51 | 362 | 0.1409 | 2 | c.*21 others(13): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2183 | chr1 | TogoVar | ||||||
TSPAN2_chr1_115043011_115094503 | 115055328 | A | ATT | intron_variant | MODIFIER | HG00544.hp1 HG01123.hp2 HG01952.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0032a0001c0003t0005 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0079 others(4): Show |
11 | 362 | 0.0304 | 2 | c.517 others(19): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115070374 | C | CTT | intron_variant | MODIFIER | HG00733.hp1 HG00741.hp2 HG01109.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(2): Show | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0214 others(8): Show |
18 | 362 | 0.0497 | 2 | c.172 others(19): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115071894 | G | GCT | intron_variant | MODIFIER | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0008a0001c0001t0025 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0059 others(5): Show |
14 | 362 | 0.0387 | 2 | c.172 others(19): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115079137 | C | CCA | intron_variant | MODIFIER | HG01175.hp1 HG01358.hp2 HG01884.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0010a0001c0003t0004 | a0001c0001t0001g0025 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
7 | 362 | 0.0193 | 2 | c.70- others(17): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | TogoVar | |||||||
TSPAN2_chr1_115043011_115094503 | 115087615 | C | CAA | intron_variant | MODIFIER | HG00544.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(3): Show | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0147 others(8): Show |
15 | 362 | 0.0414 | 2 | c.69+ others(17): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | TogoVar | |||||||
TSPAN32_chr11_2297013_2323204 | 2305370 | G | GCC | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(20): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0002t0001a0003c0004t0001 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0054 others(15): Show |
23 | 412 | 0.0558 | 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 | 2306046 | C | CTG | intron_variant | MODIFIER | HG02055.hp1 HG02738.hp2 HG03139.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0141 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | 412 | 0.0146 | 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 | 2314162 | T | TAA | intron_variant | MODIFIER | HG01255.hp1 HG02559.hp2 HG02698.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0168 others(6): Show |
9 | 412 | 0.0218 | 2 | c.457 others(17): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSPAN32_chr11_2297013_2323204 | 2319551 | A | AAT | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0039 others(10): Show |
21 | 412 | 0.0510 | 2 | c.*16 others(13): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1348 | chr11 | TogoVar | |||||||
TSPAN32_chr11_2297013_2323204 | 2319564 | A | ATG | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
a0001a0005a0010 | a0001c0001a0001c0002a0001c0013others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0232 a0001c0001t0001g0286 a0001c0002t0001g0005 others(40): Show |
48 | 412 | 0.1165 | 2 | c.*16 others(13): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1361 | chr11 | TogoVar | |||||||
TSPAN32_chr11_2297013_2323204 | 2319566 | A | ATG | downstream_gene_variant | MODIFIER | HG02083.hp2 HG02109.hp1 HG02809.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0027 a0001c0001t0001g0114 a0001c0001t0001g0152 others(5): Show |
8 | 412 | 0.0194 | 2 | c.*16 others(13): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1363 | chr11 | TogoVar | |||||||
TSPAN33_chr7_129139707_129174699 | 129139897 | C | CAA | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(105): Show |
160 | 432 | 0.3704 | 2 | c.-50 others(13): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4809 | chr7 | TogoVar | |||||||
TSPAN33_chr7_129139707_129174699 | 129139988 | C | CAA | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(128): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
131 | 432 | 0.3032 | 2 | c.-49 others(13): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4718 | chr7 | TogoVar | |||||||
TSPAN33_chr7_129139707_129174699 | 129141669 | A | AAC | upstream_gene_variant | MODIFIER | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0027 | a0001c0001t0001g0063 a0001c0001t0001g0072 a0001c0001t0001g0220 others(1): Show |
5 | 432 | 0.0116 | 2 | c.-33 others(13): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3037 | chr7 | TogoVar | |||||||
TSPAN33_chr7_129139707_129174699 | 129141897 | C | CTT | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02135.hp1 HG02486.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0044 others(4): Show |
8 | 432 | 0.0185 | 2 | c.-30 others(13): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 2809 | chr7 | TogoVar | |||||||
TSPAN33_chr7_129139707_129174699 | 129153657 | A | AAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
422 | 432 | 0.9769 | 2 | c.103 others(19): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |