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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM120B_chr12_121707752_121787068 | 121747693 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0272 | 1 | 229 | 0.0044 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747713 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG01943.hp2 NA18940.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0022 a0001c0001t0004g0107 |
2 | 237 | 0.0084 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747713 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0119 | 1 | 236 | 0.0042 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747793 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00673.hp1 HG02165.hp2 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0003a0002c0002t0010 | a0002c0002t0001g0245 a0002c0002t0003g0244 a0002c0002t0010g0161 |
3 | 250 | 0.0120 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747813 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0003 | a0003c0006 | a0003c0006t0047 | a0003c0006t0047g0144 | 1 | 236 | 0.0042 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747827 | C | CGGGAGGC others(15): Show |
intron_variant | MODIFIER | HG02451.hp2 HG03579.hp1 |
a0002 | a0002c0002 | a0002c0002t0016 | a0002c0002t0016g0009 a0002c0002t0016g0286 |
2 | 282 | 0.0071 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747833 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01346.hp2 |
a0002 | a0002c0002 | a0002c0002t0024 | a0002c0002t0024g0197 a0002c0002t0024g0205 |
2 | 263 | 0.0076 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747979 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0021 | 1 | 244 | 0.0041 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747984 | G | GGTAGAAG others(15): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020 | 1 | 309 | 0.0032 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121747993 | T | TGGGAGGC others(15): Show |
intron_variant | MODIFIER | NA19007.hp1 | a0002 | a0002c0002 | a0002c0002t0013 | a0002c0002t0013g0038 | 1 | 216 | 0.0046 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748021 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0056 | 1 | 270 | 0.0037 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748063 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(46): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0079 a0001c0001t0001g0092 a0001c0001t0001g0108 others(46): Show |
49 | 289 | 0.1696 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748085 | A | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG02155.hp2 | a0004 | a0004c0005 | a0004c0005t0003 | a0004c0005t0003g0130 | 1 | 297 | 0.0034 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | |||||||
TMEM120B_chr12_121707752_121787068 | 121748105 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG02071.hp1 HG02109.hp2 HG02572.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0016a0001c0001t0018others(2): Show | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0253 others(7): Show |
11 | 294 | 0.0374 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748125 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01433.hp1 HG02056.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0104 a0001c0001t0003g0235 a0001c0001t0006g0052 others(6): Show |
9 | 81 | 0.1111 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748187 | G | GCTGGGGT others(15): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002a0002c0002t0003others(29): Show | a0002c0002t0001g0170 a0002c0002t0001g0177 a0002c0002t0001g0184 others(75): Show |
78 | 279 | 0.2796 | 22 | c.189 others(37): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105521599 | T | TTCTTTCT others(15): Show |
upstream_gene_variant | MODIFIER | HG00438.hp2 HG01167.hp1 HG02818.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0002 | a0001c0001t0001g0001 a0002c0002t0001g0001 a0002c0002t0002g0001 others(1): Show |
8 | 223 | 0.0359 | 22 | c.-51 others(33): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 4983 | chr14 | TogoVar | |||||||
TMEM121_chr14_105521583_105535198 | 105521599 | T | TTCTTTCT others(15): Show |
upstream_gene_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG02559.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0001 a0002c0002t0002g0001 |
3 | 218 | 0.0138 | 22 | c.-51 others(33): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 4983 | chr14 | TogoVar | |||||||
TMEM121_chr14_105521583_105535198 | 105521601 | C | CTTTCTTT others(15): Show |
upstream_gene_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 314 | 0.0032 | 22 | c.-51 others(33): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 4981 | chr14 | TogoVar | |||||||
TMEM123_chr11_102391332_102457765 | 102395301 | G | GTTTTTGT others(15): Show |
downstream_gene_variant | MODIFIER | HG02970.hp1 HG03471.hp1 |
a0001 | a0001c0004 | a0001c0004t0008a0001c0004t0024 | a0001c0004t0008g0002 a0001c0004t0024g0177 |
2 | 25 | 0.0800 | 22 | c.*35 others(33): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1030 | chr11 | TogoVar | |||||||
TMEM130_chr7_98841490_98875014 | 98842378 | A | AATATATA others(15): Show |
downstream_gene_variant | MODIFIER | HG02922.hp2 NA18522.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 a0001c0002t0001g0242 |
2 | 371 | 0.0054 | 22 | c.*56 others(33): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 4111 | chr7 | TogoVar | |||||||
TMEM130_chr7_98841490_98875014 | 98842382 | A | AATATATA others(15): Show |
downstream_gene_variant | MODIFIER | HG00140.hp1 HG01081.hp1 HG01167.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0004 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0002t0001g0045 others(3): Show |
8 | 155 | 0.0516 | 22 | c.*56 others(33): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 4107 | chr7 | TogoVar | |||||||
TMEM130_chr7_98841490_98875014 | 98850273 | A | ATATATAT others(15): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 | 1 | 23 | 0.0435 | 22 | c.100 others(41): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 6/7 | chr7 | TogoVar | |||||||
TMEM130_chr7_98841490_98875014 | 98850273 | A | ATATATTT others(15): Show |
intron_variant | MODIFIER | HG02922.hp2 NA18522.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 a0001c0002t0001g0242 |
2 | 24 | 0.0833 | 22 | c.100 others(41): Show |
TMEM130 | ENSG00000166448.15 | transcript | ENST00000339375.9 | protein_coding | 6/7 | chr7 | TogoVar | |||||||
TMEM131L_chr4_153461360_153641711 | 153493345 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG02970.hp1 NA19043.hp2 |
a0001a0004 | a0001c0005a0004c0027 | a0001c0005t0001a0004c0027t0001 | a0001c0005t0001g0247 a0004c0027t0001g0248 |
2 | 118 | 0.0169 | 22 | c.239 others(41): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
TMEM131_chr2_97751336_98000948 | 97943037 | A | AAAAGAAA others(15): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0262 | 1 | 210 | 0.0048 | 22 | c.188 others(41): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | TogoVar | |||||||
TMEM132B_chr12_125181386_125667369 | 125270112 | T | TTGTGTGT others(15): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0002 | a0002c0001 | a0002c0001t0030 | a0002c0001t0030g0093 | 1 | 25 | 0.0400 | 22 | c.68- others(39): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132B_chr12_125181386_125667369 | 125277502 | A | AACACACA others(15): Show |
intron_variant | MODIFIER | HG03139.hp1 HG03453.hp2 |
a0005 | a0005c0009 | a0005c0009t0007 | a0005c0009t0007g0025 a0005c0009t0007g0059 |
2 | 38 | 0.0526 | 22 | c.68- others(39): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132B_chr12_125181386_125667369 | 125432366 | A | AAAATATA others(15): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0004 | a0001c0004t0036 | a0001c0004t0036g0023 | 1 | 73 | 0.0137 | 22 | c.110 others(43): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132B_chr12_125181386_125667369 | 125575057 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG02015.hp2 NA18964.hp1 |
a0001a0002 | a0001c0004a0002c0006 | a0001c0004t0038a0002c0006t0033 | a0001c0004t0038g0036 a0002c0006t0033g0048 |
2 | 12 | 0.1667 | 22 | c.129 others(41): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128269347 | C | CGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG01081.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
a0003a0005a0006others(3): Show | a0003c0010a0003c0071a0005c0012others(4): Show | a0003c0010t0003a0003c0071t0002a0005c0012t0004others(4): Show | a0003c0010t0003g0164 a0003c0071t0002g0082 a0005c0012t0004g0035 others(4): Show |
7 | 69 | 0.1014 | 22 | c.85+ others(37): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128489562 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 76 | 0.0132 | 22 | c.975 others(41): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128622360 | A | AAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0006 | a0006c0017 | a0006c0017t0003 | a0006c0017t0003g0064 | 1 | 78 | 0.0128 | 22 | c.130 others(41): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM132C_chr12_128262170_128712911 | 128711534 | C | CAAAAAAA others(15): Show |
downstream_gene_variant | MODIFIER | HG01243.hp1 HG02735.hp2 HG02895.hp1 |
a0002a0003 | a0002c0004a0003c0009 | a0002c0004t0003a0003c0009t0001 | a0002c0004t0003g0039 a0003c0009t0001g0076 a0003c0009t0001g0153 |
3 | 7 | 0.4286 | 22 | c.*52 others(33): Show |
TMEM132C | ENSG00000181234.10 | transcript | ENST00000435159.3 | protein_coding | 3624 | chr12 | TogoVar | |||||||
TMEM132D_chr12_129066726_129909025 | 129147261 | T | TATGTGCA others(15): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0016 | 1 | 66 | 0.0152 | 22 | c.144 others(43): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | |||||||
TMEM132D_chr12_129066726_129909025 | 129147261 | T | TATGTGCA others(15): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG01884.hp2 others(23): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0014others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0002g0027 others(23): Show |
26 | 91 | 0.2857 | 22 | c.144 others(43): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 5/8 | chr12 | TogoVar | |||||||
TMEM132D_chr12_129066726_129909025 | 129374269 | C | CAGAGAGA others(15): Show |
intron_variant | MODIFIER | HG01192.hp2 HG02809.hp1 HG02965.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0001c0001t0006a0002c0003t0009 | a0001c0001t0003g0084 a0001c0001t0006g0068 a0002c0003t0009g0018 |
3 | 20 | 0.1500 | 22 | c.111 others(43): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 3/8 | chr12 | TogoVar | |||||||
TMEM132D_chr12_129066726_129909025 | 129636737 | T | TGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG01978.hp1 HG02040.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0005a0001c0006t0002 | a0001c0001t0005g0038 a0001c0006t0002g0076 |
2 | 20 | 0.1000 | 22 | c.968 others(41): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 2/8 | chr12 | TogoVar | |||||||
TMEM132E_chr17_34574582_34644318 | 34613211 | A | ACACACAC others(15): Show |
intron_variant | MODIFIER | HG01978.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0183 | 1 | 182 | 0.0055 | 22 | c.68- others(39): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TMEM132E_chr17_34574582_34644318 | 34613211 | A | ACACACAC others(15): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0184 | 1 | 182 | 0.0055 | 22 | c.68- others(39): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TMEM132E_chr17_34574582_34644318 | 34627467 | C | CGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG03486.hp1 HG03516.hp2 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0126 a0001c0001t0026g0198 a0001c0001t0026g0334 |
3 | 55 | 0.0545 | 22 | c.998 others(37): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TMEM132E_chr17_34574582_34644318 | 34627467 | C | CGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02735.hp1 HG02922.hp1 others(10): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(4): Show | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0003g0292 others(10): Show |
13 | 65 | 0.2000 | 22 | c.998 others(37): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TMEM132E_chr17_34574582_34644318 | 34627473 | T | TGCGTGCG others(15): Show |
intron_variant | MODIFIER | HG03225.hp1 HG03471.hp2 |
a0001 | a0001c0003 | a0001c0003t0063a0001c0003t0081 | a0001c0003t0063g0393 a0001c0003t0081g0014 |
2 | 400 | 0.0050 | 22 | c.998 others(37): Show |
TMEM132E | ENSG00000181291.8 | transcript | ENST00000631683.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87131341 | A | AATCCCCT others(15): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(147): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0044 others(147): Show |
150 | 272 | 0.5515 | 22 | c.397 others(41): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87159593 | G | GCGCACAC others(15): Show |
intron_variant | MODIFIER | HG02965.hp1 HG03195.hp2 NA21309.hp2 |
a0001a0003a0005 | a0001c0001a0003c0003a0005c0004 | a0001c0001t0003a0003c0003t0003a0005c0004t0043 | a0001c0001t0003g0267 a0003c0003t0003g0147 a0005c0004t0043g0260 |
3 | 192 | 0.0156 | 22 | c.462 others(39): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87159617 | A | ACACACAC others(15): Show |
intron_variant | MODIFIER | HG02602.hp2 HG02723.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0021a0002c0002t0001 | a0001c0001t0021g0060 a0002c0002t0001g0092 |
2 | 186 | 0.0108 | 22 | c.462 others(39): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87159617 | A | ACACACAC others(15): Show |
intron_variant | MODIFIER | NA18959.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0087 | 1 | 185 | 0.0054 | 22 | c.462 others(39): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM135_chr11_87032934_87333824 | 87159617 | A | ACACACAC others(15): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0015 | 1 | 185 | 0.0054 | 22 | c.462 others(39): Show |
TMEM135 | ENSG00000166575.17 | transcript | ENST00000305494.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TMEM144_chr4_158205486_158260416 | 158249887 | G | GGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0173 | 1 | 24 | 0.0417 | 22 | c.955 others(39): Show |
TMEM144 | ENSG00000164124.11 | transcript | ENST00000296529.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
TMEM144_chr4_158205486_158260416 | 158255590 | G | GTATATAT others(15): Show |
downstream_gene_variant | MODIFIER | HG02896.hp1 HG02897.hp2 |
a0002 | a0002c0004 | a0002c0004t0049a0002c0004t0050 | a0002c0004t0049g0019 a0002c0004t0050g0019 |
2 | 234 | 0.0085 | 22 | c.*20 others(33): Show |
TMEM144 | ENSG00000164124.11 | transcript | ENST00000296529.11 | protein_coding | 175 | chr4 | TogoVar |