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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM120A_chr7_75981831_75999595 | 75989053 | GCC | G | intron_variant | MODIFIER | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(42): Show |
a0001 | a0001c0001a0001c0010 | a0001c0001t0001a0001c0010t0001 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(31): Show | 45 | 368 | 0.1223 | -2 | c.377 others(17): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 4/11 | chr7 | TogoVar | ||||||
TMEM120A_chr7_75981831_75999595 | 75990897 | CAA | C | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 6 | 368 | 0.0163 | -2 | c.317 others(19): Show |
TMEM120A | ENSG00000189077.11 | transcript | ENST00000493111.7 | protein_coding | 3/11 | chr7 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121707799 | TAC | T | upstream_gene_variant | MODIFIER | HG01109.hp1 HG02083.hp2 NA20805.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0023a0002c0002t0001a0002c0002t0098 | a0001c0001t0023g0297a0002c0002t0001g0189a0002c0002t0098g0190 | 3 | 314 | 0.0096 | -2 | c.-50 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4952 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121718487 | CAG | C | intron_variant | MODIFIER | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0043a0001c0001t0044a0001c0001t0097others(1): Show | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | 314 | 0.0127 | -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 | 121734165 | CTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(163): Show | 166 | 314 | 0.5287 | -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 | 121734894 | CAA | C | intron_variant | MODIFIER | HG00140.hp1 HG01975.hp1 HG03654.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0092 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0092g0124 | 3 | 314 | 0.0096 | -2 | c.70- others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747308 | GGC | G | 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 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747309 | GCA | G | intron_variant | MODIFIER | HG01099.hp1 HG01257.hp1 HG01516.hp1 others(39): Show |
a0001a0002a0006 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0109a0001c0001t0002g0021a0001c0001t0002g0022others(39): Show | 42 | 314 | 0.1338 | -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 | 121747570 | GGC | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG01952.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0001c0001t0030a0002c0002t0001 | a0001c0001t0004g0217a0001c0001t0030g0162a0002c0002t0001g0209 | 3 | 314 | 0.0096 | -2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747571 | GCA | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(71): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0001g0313others(70): Show | 74 | 314 | 0.2357 | -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 | 121747872 | GGC | G | intron_variant | MODIFIER | HG02895.hp1 HG03516.hp2 NA18906.hp1 others(4): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0003a0001c0001t0042a0001c0001t0109others(4): Show | a0001c0001t0003g0254a0001c0001t0042g0252a0001c0001t0109g0182others(4): Show | 7 | 314 | 0.0223 | -2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747873 | GCA | G | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0006a0001c0001t0002g0057a0001c0001t0003g0003others(52): Show | 55 | 314 | 0.1752 | -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 | 121747915 | GCA | G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0026others(54): Show | 57 | 314 | 0.1815 | -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 | 121747957 | GCA | G | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(34): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0099a0001c0001t0001g0268a0001c0001t0002g0026others(34): Show | 37 | 314 | 0.1178 | -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 | 121747998 | GGC | G | intron_variant | MODIFIER | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0005a0001c0001t0079a0001c0004t0003others(2): Show | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | 314 | 0.0159 | -2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747999 | GCA | G | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(29): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(20): Show | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0129others(29): Show | 32 | 314 | 0.1019 | -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 | 121748041 | GCA | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(25): Show | 28 | 314 | 0.0892 | -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 | 121748083 | GCA | G | intron_variant | MODIFIER | HG00423.hp2 HG00738.hp1 HG01517.hp2 others(16): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(13): Show | a0001c0001t0001g0099a0001c0001t0001g0185a0001c0001t0005g0008others(16): Show | 19 | 314 | 0.0605 | -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 | 121748164 | GGC | G | intron_variant | MODIFIER | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0005a0001c0001t0079a0001c0004t0003others(2): Show | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | 314 | 0.0159 | -2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748165 | GCA | G | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG01261.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0001t0109others(5): Show | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182others(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 | 121753114 | AGG | A | intron_variant | MODIFIER | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(11): Show | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | 314 | 0.0796 | -2 | c.461 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121769162 | CAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(49): Show | a0001c0001t0001g0104a0001c0001t0004g0203a0001c0001t0005g0149others(120): Show | 124 | 314 | 0.3949 | -2 | c.552 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121769715 | CGT | C | intron_variant | MODIFIER | HG00423.hp2 HG02074.hp2 HG02165.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(5): Show | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0179others(9): Show | 12 | 314 | 0.0382 | -2 | c.552 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121773951 | CTT | C | intron_variant | MODIFIER | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
a0001a0003a0005 | a0001c0001a0001c0004a0003c0003others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0043others(7): Show | a0001c0001t0003g0255a0001c0001t0005g0025a0001c0001t0043g0310others(7): Show | 10 | 314 | 0.0319 | -2 | c.772 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121776954 | CTT | C | 3_prime_UTR_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0007a0002c0002others(4): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(45): Show | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(101): Show | 104 | 314 | 0.3312 | -2 | c.*12 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1249 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
TMEM121B_chr22_17111297_17126360 | 17112157 | CAT | C | downstream_gene_variant | MODIFIER | HG00639.hp1 HG01099.hp1 HG01167.hp1 others(33): Show |
a0001 | a0001c0001a0001c0010 | a0001c0001t0005a0001c0001t0006a0001c0001t0025others(1): Show | a0001c0001t0005g0000a0001c0001t0006g0000a0001c0001t0025g0000others(1): Show | 36 | 468 | 0.0769 | -2 | c.*72 others(13): Show |
TMEM121B | ENSG00000183307.4 | transcript | ENST00000331437.4 | protein_coding | 4139 | chr22 | TogoVar | ||||||
TMEM121B_chr22_17111297_17126360 | 17112998 | TTG | T | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(118): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0025others(19): Show | a0001c0001t0005g0000a0001c0001t0006g0000a0001c0001t0025g0000others(19): Show | 121 | 468 | 0.2586 | -2 | c.*63 others(13): Show |
TMEM121B | ENSG00000183307.4 | transcript | ENST00000331437.4 | protein_coding | 3298 | chr22 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105523812 | GTT | G | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(112): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(2): Show | a0001c0001t0001g0001a0002c0002t0001g0001a0002c0002t0001g0004others(10): Show | 115 | 352 | 0.3267 | -2 | c.-29 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 2770 | chr14 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105528414 | GGC | G | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(33): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0003a0002c0003t0001g0007a0002c0003t0001g0011 | 36 | 352 | 0.1023 | -2 | c.-11 others(19): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 1/1 | chr14 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102392548 | CTT | C | downstream_gene_variant | MODIFIER | HG02280.hp1 HG02622.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | 204 | 0.0098 | -2 | c.*63 others(13): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3783 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102393517 | AAC | A | downstream_gene_variant | MODIFIER | HG01346.hp2 HG02630.hp2 HG02895.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0018 | a0001c0001t0002g0024a0001c0001t0007g0016a0001c0001t0007g0017others(3): Show | 6 | 204 | 0.0294 | -2 | c.*53 others(13): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2814 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102401729 | ATT | A | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
a0001a0003 | a0001c0004a0001c0006a0003c0003 | a0001c0004t0008a0001c0004t0024a0001c0006t0012others(1): Show | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | 204 | 0.0588 | -2 | c.449 others(15): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102406868 | CAA | C | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
a0003 | a0003c0003 | a0003c0003t0006 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | 204 | 0.0245 | -2 | c.158 others(19): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102426858 | TTC | T | intron_variant | MODIFIER | HG02970.hp1 HG06807.hp1 |
a0001 | a0001c0004 | a0001c0004t0008a0001c0004t0024 | a0001c0004t0008g0012a0001c0004t0024g0177 | 2 | 204 | 0.0098 | -2 | c.157 others(21): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102432277 | TCC | T | intron_variant | MODIFIER | HG00323.hp2 HG02559.hp1 HG02735.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0160 | 3 | 204 | 0.0147 | -2 | c.157 others(21): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM125_chr1_43264983_43279002 | 43278763 | GTT | G | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(33): Show | 389 | 438 | 0.8881 | -2 | c.*53 others(13): Show |
TMEM125 | ENSG00000179178.11 | transcript | ENST00000439858.6 | protein_coding | 4762 | chr1 | TogoVar | ||||||
TMEM126A_chr11_85642967_85661542 | 85655883 | AAC | A | intron_variant | MODIFIER | HG00408.hp2 NA18984.hp1 NA18985.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014a0001c0001t0001g0059a0001c0001t0001g0061 | 7 | 398 | 0.0176 | -2 | c.395 others(17): Show |
TMEM126A | ENSG00000171202.7 | transcript | ENST00000304511.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM128_chr4_4230542_4253223 | 4236259 | TAA | T | splice_region_variant others(1): Show |
LOW | HG01943.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0002t0002a0001c0003t0002 | a0001c0001t0003g0019a0001c0001t0003g0123a0001c0002t0002g0054others(1): Show | 7 | 460 | 0.0152 | -2 | c.*10 others(13): Show |
TMEM128 | ENSG00000132406.12 | transcript | ENST00000382753.5 | protein_coding | 4/4 | chr4 | TogoVar | ||||||
TMEM128_chr4_4230542_4253223 | 4242523 | ATT | A | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(165): Show |
a0001a0002a0003 | a0001c0002a0001c0003a0001c0009others(2): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0005others(4): Show | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0014others(45): Show | 168 | 460 | 0.3652 | -2 | c.240 others(19): Show |
TMEM128 | ENSG00000132406.12 | transcript | ENST00000382753.5 | protein_coding | 2/4 | chr4 | TogoVar | ||||||
TMEM128_chr4_4230542_4253223 | 4252538 | TTG | T | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(83): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0003a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0003g0092a0001c0002t0001g0005a0001c0002t0001g0010others(23): Show | 86 | 460 | 0.1870 | -2 | c.-43 others(13): Show |
TMEM128 | ENSG00000132406.12 | transcript | ENST00000382753.5 | protein_coding | 4316 | chr4 | TogoVar | ||||||
TMEM129_chr4_1710952_1726323 | 1711051 | TAA | T | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0054others(22): Show | 167 | 388 | 0.4304 | -2 | c.*61 others(13): Show |
TMEM129 | ENSG00000168936.12 | transcript | ENST00000382936.8 | protein_coding | 4900 | chr4 | TogoVar | ||||||
TMEM129_chr4_1710952_1726323 | 1724379 | CTT | C | upstream_gene_variant | MODIFIER | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(12): Show |
a0002a0003 | a0002c0005a0003c0006 | a0002c0005t0007a0002c0005t0017a0003c0006t0004others(1): Show | a0002c0005t0007g0009a0002c0005t0017g0026a0003c0006t0004g0010others(1): Show | 15 | 388 | 0.0387 | -2 | c.-35 others(13): Show |
TMEM129 | ENSG00000168936.12 | transcript | ENST00000382936.8 | protein_coding | 3057 | chr4 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98842402 | TAC | T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(8): Show | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0022others(62): Show | 75 | 380 | 0.1974 | -2 | c.*56 others(13): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 4087 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98842426 | CAT | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 161 | 380 | 0.4237 | -2 | c.*56 others(13): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 4063 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98847504 | CTG | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0003a0001c0002t0003a0001c0004t0003 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0022others(41): Show | 54 | 380 | 0.1421 | -2 | c.*55 others(11): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 8/8 | 550 | chr7 | TogoVar | |||||
TMEM130_chr7_98841490_98875014 | 98850250 | CAT | C | intron_variant | MODIFIER | HG01070.hp1 HG01175.hp1 HG02257.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(4): Show | a0001c0001t0003g0040a0001c0001t0006g0239a0001c0001t0006g0273others(8): Show | 11 | 380 | 0.0290 | -2 | c.100 others(21): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 6/7 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98858632 | CTT | C | intron_variant | MODIFIER | HG02257.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0035a0001c0002t0001g0289a0001c0002t0001g0291others(2): Show | 6 | 380 | 0.0158 | -2 | c.551 others(19): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 3/7 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98860933 | ACT | A | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0005a0001c0002t0011others(2): Show | a0001c0002t0002g0312a0001c0002t0005g0298a0001c0002t0005g0304others(8): Show | 11 | 380 | 0.0290 | -2 | c.392 others(17): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 2/7 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98860942 | CAA | C | intron_variant | MODIFIER | HG00140.hp1 HG01243.hp2 HG01256.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0030a0001c0001t0001g0246a0001c0001t0001g0247others(14): Show | 18 | 380 | 0.0474 | -2 | c.392 others(17): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 2/7 | chr7 | TogoVar | ||||||
TMEM130_chr7_98841490_98875014 | 98862346 | CAG | C | intron_variant | MODIFIER | HG01123.hp1 HG01167.hp1 HG01257.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 11 | 380 | 0.0290 | -2 | c.391 others(17): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 2/7 | chr7 | TogoVar |