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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM117_chr12_43831081_44394758 | 44311823 | G | GTA | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02895.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0077others(1): Show | 4 | 110 | 0.0364 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311829 | A | ATG | intron_variant | MODIFIER | HG01981.hp1 HG02451.hp1 HG03098.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0064a0001c0001t0003g0016a0001c0001t0003g0036others(3): Show | 6 | 110 | 0.0546 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311831 | G | GTA | intron_variant | MODIFIER | HG01175.hp1 HG02258.hp2 HG02723.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0002g0057others(4): Show | 7 | 110 | 0.0636 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311847 | A | ATG | intron_variant | MODIFIER | HG02559.hp2 HG02809.hp2 HG02886.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0039a0001c0001t0002g0002a0001c0001t0002g0013others(7): Show | 10 | 110 | 0.0909 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44311873 | A | ATG | intron_variant | MODIFIER | HG01261.hp2 HG02055.hp1 HG02895.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0077others(1): Show | 4 | 110 | 0.0364 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44314567 | C | CTT | intron_variant | MODIFIER | HG02886.hp2 HG03209.hp1 HG03491.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0028a0001c0001t0002g0015a0001c0001t0002g0029others(2): Show | 5 | 110 | 0.0455 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44332712 | T | TAC | intron_variant | MODIFIER | HG00738.hp2 HG01192.hp1 HG01496.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0058others(7): Show | 10 | 110 | 0.0909 | 2 | c.768 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44345842 | A | ATT | intron_variant | MODIFIER | HG02486.hp2 HG02922.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0091a0001c0001t0002g0093 | 2 | 110 | 0.0182 | 2 | c.769 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44347074 | T | TAC | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(14): Show | 17 | 110 | 0.1546 | 2 | c.769 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44350279 | G | GTA | intron_variant | MODIFIER | HG02257.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0070a0001c0001t0004g0072a0001c0001t0004g0073others(2): Show | 5 | 110 | 0.0455 | 2 | c.769 others(21): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44373771 | C | CTT | intron_variant | MODIFIER | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0027others(11): Show | 14 | 110 | 0.1273 | 2 | c.769 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44374616 | T | TTG | intron_variant | MODIFIER | HG01168.hp1 HG01496.hp1 HG01496.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0030others(12): Show | 15 | 110 | 0.1364 | 2 | c.769 others(19): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM117_chr12_43831081_44394758 | 44390199 | G | GAC | downstream_gene_variant | MODIFIER | HG01169.hp1 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017a0001c0001t0001g0098 | 2 | 110 | 0.0182 | 2 | c.*15 others(13): Show |
TMEM117 | ENSG00000139173.10 | transcript | ENST00000266534.8 | protein_coding | 442 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108595360 | T | TAC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
a0001a0003a0004others(7): Show | a0001c0002a0001c0003a0001c0004others(13): Show | a0001c0002t0001a0001c0002t0005a0001c0002t0008others(31): Show | a0001c0002t0001g0002a0001c0002t0001g0013a0001c0002t0001g0022others(73): Show | 324 | 444 | 0.7297 | 2 | c.-15 others(19): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108596429 | A | AAC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
a0001a0002a0003others(4): Show | a0001c0002a0001c0004a0001c0006others(7): Show | a0001c0002t0001a0001c0002t0005a0001c0002t0008others(13): Show | a0001c0002t0001g0002a0001c0002t0001g0013a0001c0002t0001g0022others(24): Show | 105 | 444 | 0.2365 | 2 | c.-15 others(19): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108597457 | C | CCA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(158): Show |
a0001a0002a0007others(1): Show | a0001c0003a0001c0004a0001c0005others(4): Show | a0001c0003t0001a0001c0003t0009a0001c0003t0012others(10): Show | a0001c0003t0001g0003a0001c0003t0001g0008a0001c0003t0001g0009others(28): Show | 161 | 444 | 0.3626 | 2 | c.-15 others(17): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108601158 | T | TAA | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
a0001a0002a0007others(2): Show | a0001c0002a0001c0003a0001c0004others(5): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0009others(11): Show | a0001c0002t0001g0002a0001c0002t0001g0069a0001c0003t0001g0003others(26): Show | 159 | 444 | 0.3581 | 2 | c.-32 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3075 | chr12 | TogoVar | ||||||
TMEM119_chr12_108584851_108603084 | 108601621 | T | TAC | upstream_gene_variant | MODIFIER | HG02683.hp1 HG03490.hp2 HG03492.hp2 others(11): Show |
a0001a0002 | a0001c0006a0002c0001 | a0001c0006t0002a0002c0001t0001 | a0001c0006t0002g0006a0002c0001t0001g0001 | 14 | 444 | 0.0315 | 2 | c.-36 others(13): Show |
TMEM119 | ENSG00000183160.9 | transcript | ENST00000392806.4 | protein_coding | 3538 | chr12 | TogoVar | ||||||
TMEM11_chr17_21192954_21219161 | 21198865 | G | GGA | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01943.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013a0001c0001t0001g0041 | 7 | 422 | 0.0166 | 2 | c.63- others(13): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 1/1 | chr17 | TogoVar | ||||||
TMEM11_chr17_21192954_21219161 | 21203991 | C | CTT | intron_variant | MODIFIER | NA18950.hp2 NA18981.hp1 NA18983.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0083others(2): Show | 9 | 422 | 0.0213 | 2 | c.63- others(17): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 1/1 | chr17 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75989102 | A | AGG | intron_variant | MODIFIER | HG01175.hp1 HG01192.hp1 HG01346.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0004 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0139others(14): Show | 18 | 368 | 0.0489 | 2 | c.377 others(15): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 4/11 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75989109 | T | TGG | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(40): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0005 | a0001c0001t0001a0001c0004t0001a0003c0005t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(20): Show | 43 | 368 | 0.1169 | 2 | c.377 others(15): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 4/11 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75989109 | T | TTG | intron_variant | MODIFIER | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0198others(5): Show | 10 | 368 | 0.0272 | 2 | c.377 others(15): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 4/11 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75990897 | C | CAA | intron_variant | MODIFIER | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0052others(7): Show | 10 | 368 | 0.0272 | 2 | c.317 others(19): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 3/11 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75996617 | G | GAA | upstream_gene_variant | MODIFIER | NA18951.hp2 NA19068.hp2 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0192 | 3 | 368 | 0.0082 | 2 | c.-20 others(13): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 2023 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75998301 | A | ATT | upstream_gene_variant | MODIFIER | HG00642.hp2 HG00741.hp2 HG02027.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0050others(12): Show | 15 | 368 | 0.0408 | 2 | c.-37 others(13): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 3707 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75999495 | G | GTA | upstream_gene_variant | MODIFIER | HG00609.hp1 HG01081.hp2 HG01168.hp1 others(39): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(6): Show | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0039others(34): Show | 42 | 368 | 0.1141 | 2 | c.-49 others(13): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 4901 | chr7 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121707799 | T | TAC | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0185others(80): Show | 83 | 314 | 0.2643 | 2 | c.-50 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4952 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121716565 | C | CTT | intron_variant | MODIFIER | HG00621.hp1 HG01433.hp2 HG01884.hp1 others(32): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0002g0147others(32): Show | 35 | 314 | 0.1115 | 2 | c.69+ others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121724030 | C | CTT | intron_variant | MODIFIER | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0001t0012others(7): Show | a0001c0001t0005g0008a0001c0001t0009g0152a0001c0001t0012g0074others(9): Show | 12 | 314 | 0.0382 | 2 | c.69+ others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121726035 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(50): Show | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0099others(109): Show | 113 | 314 | 0.3599 | 2 | c.69+ others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121727873 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(71): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(27): Show | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(70): Show | 74 | 314 | 0.2357 | 2 | c.69+ others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121730647 | C | CAA | intron_variant | MODIFIER | HG00544.hp1 HG00621.hp1 HG01099.hp1 others(25): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0272a0001c0001t0002g0020a0001c0001t0002g0021others(25): Show | 28 | 314 | 0.0892 | 2 | c.70- others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121735185 | C | CAA | intron_variant | MODIFIER | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0033a0001c0001t0076others(3): Show | a0001c0001t0002g0147a0001c0001t0033g0145a0001c0001t0076g0287others(3): Show | 6 | 314 | 0.0191 | 2 | c.70- others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121736327 | G | GTT | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(6): Show | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(12): Show | 15 | 314 | 0.0478 | 2 | c.70- others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747269 | G | GCA | intron_variant | MODIFIER | HG01169.hp1 HG01255.hp2 HG01884.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0020a0001c0001t0109 | a0001c0001t0016g0308a0001c0001t0020g0122a0001c0001t0020g0126others(1): Show | 4 | 314 | 0.0127 | 2 | c.189 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747289 | G | GCA | intron_variant | MODIFIER | HG01884.hp1 HG02071.hp1 HG03540.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0046a0001c0001t0066others(1): Show | a0001c0001t0016g0308a0001c0001t0046g0067a0001c0001t0066g0138others(1): Show | 4 | 314 | 0.0127 | 2 | c.189 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747331 | G | GCA | intron_variant | MODIFIER | HG00423.hp2 HG01346.hp1 HG01433.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(3): Show | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0005g0059others(5): Show | 8 | 314 | 0.0255 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747351 | G | GCA | intron_variant | MODIFIER | HG00642.hp1 HG01167.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0012a0001c0001t0025a0001c0001t0082others(2): Show | a0001c0001t0012g0074a0001c0001t0025g0264a0001c0001t0082g0073others(2): Show | 5 | 314 | 0.0159 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747371 | G | GCA | intron_variant | MODIFIER | HG01884.hp1 HG03130.hp2 HG03540.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0016a0001c0001t0019a0002c0002t0012others(1): Show | a0001c0001t0016g0308a0001c0001t0019g0029a0002c0002t0012g0080others(1): Show | 4 | 314 | 0.0127 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747391 | G | GCA | intron_variant | MODIFIER | HG00423.hp2 HG01257.hp1 HG02027.hp1 others(10): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(9): Show | a0001c0001t0001g0099a0001c0001t0005g0025a0001c0001t0010g0031others(10): Show | 13 | 314 | 0.0414 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747411 | G | GCA | intron_variant | MODIFIER | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(13): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0105a0001c0001t0002g0021a0001c0001t0002g0035others(13): Show | 16 | 314 | 0.0510 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747431 | G | GCA | intron_variant | MODIFIER | HG01978.hp1 HG02004.hp2 HG02080.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(7): Show | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0005g0042others(11): Show | 14 | 314 | 0.0446 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747451 | G | GCA | intron_variant | MODIFIER | HG01358.hp1 HG02155.hp2 HG03491.hp1 others(3): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(2): Show | a0001c0001t0001g0006a0001c0001t0001g0105a0001c0001t0005g0025others(3): Show | 6 | 314 | 0.0191 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747471 | G | GCA | intron_variant | MODIFIER | HG01346.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(2): Show | a0001c0001t0001g0092a0001c0001t0005g0081a0001c0001t0007g0266others(2): Show | 5 | 314 | 0.0159 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747491 | G | GCA | intron_variant | MODIFIER | HG00621.hp1 HG01934.hp1 HG01943.hp2 others(18): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0003g0107others(18): Show | 21 | 314 | 0.0669 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747511 | G | GCA | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0272others(22): Show | 25 | 314 | 0.0796 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747531 | G | GCA | intron_variant | MODIFIER | HG01169.hp2 HG01891.hp1 HG01978.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(4): Show | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0025others(9): Show | 12 | 314 | 0.0382 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747551 | G | GCA | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(18): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(11): Show | a0001c0001t0002g0028a0001c0001t0002g0030a0001c0001t0005g0081others(18): Show | 21 | 314 | 0.0669 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121747593 | G | GCA | intron_variant | MODIFIER | HG00642.hp1 HG00735.hp1 HG02055.hp2 others(22): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0118a0001c0001t0002g0020a0001c0001t0002g0022others(22): Show | 25 | 314 | 0.0796 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |