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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM120B_chr12_121707752_121787068 | 121747613 | G | GCA | intron_variant | MODIFIER | HG00280.hp1 HG00544.hp2 HG01169.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(11): Show | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0003g0254others(12): Show | 15 | 314 | 0.0478 | 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 | 121747633 | G | GCA | intron_variant | MODIFIER | HG01106.hp1 HG01169.hp2 HG01258.hp1 others(27): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0313a0001c0001t0002g0020a0001c0001t0002g0023others(27): Show | 30 | 314 | 0.0955 | 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 | 121747653 | G | GCA | intron_variant | MODIFIER | HG01099.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0008 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(13): Show | a0001c0001t0002g0020a0001c0001t0010g0032a0001c0001t0011g0206others(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 | 121747673 | G | GCA | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(28): Show | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0001g0313others(40): Show | 43 | 314 | 0.1369 | 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 | 121747693 | G | GCA | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(32): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | a0001c0001t0001g0313a0001c0001t0002g0023a0001c0001t0002g0028others(32): Show | 35 | 314 | 0.1115 | 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 | 121747713 | G | GCA | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(19): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0129others(19): Show | 22 | 314 | 0.0701 | 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 | 121747733 | G | GCA | intron_variant | MODIFIER | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(12): Show | a0001c0001t0001g0268a0001c0001t0002g0026a0001c0001t0006g0033others(17): Show | 20 | 314 | 0.0637 | 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 | 121747753 | G | GCA | intron_variant | MODIFIER | HG00280.hp2 HG01258.hp1 HG01891.hp1 others(22): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0007a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(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 | 121747773 | G | GCA | intron_variant | MODIFIER | HG00544.hp1 HG00558.hp1 HG01943.hp2 others(16): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0045a0001c0001t0002g0020a0001c0001t0002g0023others(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 | 121747793 | G | GCA | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp2 HG01257.hp2 others(22): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(13): Show | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0001g0129others(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 | 121747813 | G | GCA | intron_variant | MODIFIER | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(14): Show | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 23 | 314 | 0.0733 | 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 | 121747833 | G | GCA | intron_variant | MODIFIER | HG01257.hp1 HG01346.hp1 HG01884.hp1 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0002g0028others(15): Show | 18 | 314 | 0.0573 | 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 | 121747853 | G | GCA | intron_variant | MODIFIER | HG00423.hp2 HG01099.hp1 HG01109.hp2 others(27): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0099a0001c0001t0001g0313a0001c0001t0002g0022others(27): Show | 30 | 314 | 0.0955 | 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 | 121747895 | G | GCA | intron_variant | MODIFIER | HG00621.hp1 HG01099.hp1 HG01109.hp2 others(40): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0079a0001c0001t0001g0109a0001c0001t0001g0118others(40): Show | 43 | 314 | 0.1369 | 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 | 121747937 | G | GCA | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(25): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0092a0001c0001t0001g0272a0001c0001t0002g0026others(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 | 121747979 | G | GCA | intron_variant | MODIFIER | HG02074.hp1 NA18942.hp2 NA18956.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010a0001c0001t0062others(1): Show | a0001c0001t0002g0028a0001c0001t0002g0030a0001c0001t0002g0112others(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 | 121748020 | G | GAC | intron_variant | MODIFIER | HG02129.hp1 HG02698.hp2 HG02723.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(4): Show | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0059others(9): Show | 12 | 314 | 0.0382 | 2 | c.189 others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748021 | G | GCA | intron_variant | MODIFIER | HG01099.hp1 HG01891.hp1 HG02559.hp2 others(12): Show |
a0001a0006 | a0001c0001a0001c0004a0006c0008 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(8): Show | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0028others(12): Show | 15 | 314 | 0.0478 | 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 | 121748063 | G | GCA | intron_variant | MODIFIER | HG00423.hp1 HG01517.hp2 HG01934.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0268a0001c0001t0002g0022a0001c0001t0002g0028others(15): Show | 18 | 314 | 0.0573 | 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 | 121748105 | G | GCA | intron_variant | MODIFIER | HG00738.hp1 HG01123.hp2 HG01433.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(8): Show | a0001c0001t0001g0104a0001c0001t0004g0233a0001c0001t0006g0050others(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 | 121748125 | G | GCA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(93): Show | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(215): Show | 219 | 314 | 0.6975 | 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 | 121748145 | G | GCA | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0003a0001c0001t0016a0001c0001t0026others(4): Show | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(6): Show | 9 | 314 | 0.0287 | 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 | 121748186 | G | GAC | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0003a0001c0001t0016a0001c0001t0026others(2): Show | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(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 | 121748187 | G | GCA | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp1 HG00735.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0056others(15): Show | a0001c0001t0002g0112a0001c0001t0005g0042a0001c0001t0056g0047others(20): Show | 23 | 314 | 0.0733 | 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 | 121757520 | A | ATT | intron_variant | MODIFIER | HG02698.hp2 HG02738.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0015a0001c0001t0055 | a0001c0001t0005g0081a0001c0001t0015g0101a0001c0001t0055g0095 | 3 | 314 | 0.0096 | 2 | c.462 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121759122 | G | GTT | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
a0001a0002a0004 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(78): Show | 81 | 314 | 0.2580 | 2 | c.462 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM120B_chr12_121707752_121787068 | 121764159 | C | CAA | intron_variant | MODIFIER | HG02559.hp1 HG03516.hp1 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0035a0001c0001t0109others(1): Show | a0001c0001t0003g0148a0001c0001t0035g0133a0001c0001t0109g0182others(1): Show | 4 | 314 | 0.0127 | 2 | c.551 others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121769715 | C | CGT | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp1 HG02717.hp1 |
a0002a0005 | a0002c0002a0005c0006 | a0002c0002t0001a0005c0006t0047 | a0002c0002t0001g0236a0002c0002t0001g0237a0005c0006t0047g0144 | 3 | 314 | 0.0096 | 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 | 121778450 | C | CAA | 3_prime_UTR_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG01167.hp1 others(79): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(29): Show | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(79): Show | 82 | 314 | 0.2612 | 2 | c.*27 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2750 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
TMEM120B_chr12_121707752_121787068 | 121779950 | G | GGT | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0007others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(127): Show | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(301): Show | 305 | 314 | 0.9713 | 2 | c.*42 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4233 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
TMEM120B_chr12_121707752_121787068 | 121783316 | G | GCC | downstream_gene_variant | MODIFIER | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(15): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0001c0009others(3): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0015others(14): Show | a0001c0001t0003g0248a0001c0001t0010g0031a0001c0001t0015g0269others(15): Show | 18 | 314 | 0.0573 | 2 | c.*75 others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1249 | chr12 | TogoVar | ||||||
TMEM121B_chr22_17111297_17126360 | 17115587 | G | GAA | downstream_gene_variant | MODIFIER | HG01109.hp2 HG01257.hp1 HG02273.hp2 others(9): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0002t0045a0001c0003t0001others(4): Show | a0001c0001t0006g0000a0001c0002t0045g0000a0001c0003t0001g0000others(4): Show | 12 | 468 | 0.0256 | 2 | c.*38 others(13): Show |
TMEM121B | ENSG00000183307.4 | transcript | ENST00000331437.4 | protein_coding | 709 | chr22 | TogoVar | ||||||
TMEM121B_chr22_17111297_17126360 | 17125423 | C | CAA | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0004a0001c0001t0006a0001c0001t0015others(11): Show | a0001c0001t0004g0000a0001c0001t0006g0000a0001c0001t0015g0000others(11): Show | 32 | 468 | 0.0684 | 2 | c.-42 others(13): Show |
TMEM121B | ENSG00000183307.4 | transcript | ENST00000331437.4 | protein_coding | 4064 | chr22 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105522454 | T | TTG | upstream_gene_variant | MODIFIER | HG02895.hp1 HG03704.hp2 NA19002.hp2 others(1): Show |
a0002 | a0002c0002a0002c0003 | a0002c0002t0003a0002c0003t0001 | a0002c0002t0003g0002a0002c0003t0001g0003a0002c0003t0001g0007 | 4 | 352 | 0.0114 | 2 | c.-43 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 4128 | chr14 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105523064 | C | CAA | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0006 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(11): Show | 118 | 352 | 0.3352 | 2 | c.-37 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 3518 | chr14 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105523987 | A | ATG | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(45): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0002others(1): Show | a0001c0001t0001g0001a0001c0001t0005g0001a0002c0002t0002g0001others(3): Show | 48 | 352 | 0.1364 | 2 | c.-27 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 2595 | chr14 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105523997 | G | GTA | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0003t0001 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0003t0001g0003others(2): Show | 52 | 352 | 0.1477 | 2 | c.-27 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 2585 | chr14 | TogoVar | ||||||
TMEM121_chr14_105521583_105535198 | 105525112 | C | CTT | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0002t0002a0002c0002t0003others(1): Show | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0009others(6): Show | 41 | 352 | 0.1165 | 2 | c.-16 others(13): Show |
TMEM121 | ENSG00000184986.12 | transcript | ENST00000392519.7 | protein_coding | 1470 | chr14 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102395301 | G | GTT | downstream_gene_variant | MODIFIER | HG00621.hp2 HG01169.hp1 HG01169.hp2 others(18): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0061others(18): Show | 21 | 204 | 0.1029 | 2 | c.*35 others(13): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1030 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102406868 | C | CAA | intron_variant | MODIFIER | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(3): Show |
a0001a0004a0005 | a0001c0001a0004c0005a0005c0008 | a0001c0001t0001a0004c0005t0005a0005c0008t0005 | a0001c0001t0001g0121a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | 204 | 0.0294 | 2 | c.158 others(19): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102425583 | C | CTT | intron_variant | MODIFIER | HG01109.hp2 HG01261.hp1 HG01261.hp2 others(3): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0009a0004c0005t0005 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0102others(3): Show | 6 | 204 | 0.0294 | 2 | c.157 others(21): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102441733 | C | CAA | intron_variant | MODIFIER | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(1): Show | a0001c0001t0002g0040a0001c0001t0004g0020a0001c0001t0004g0021others(5): Show | 8 | 204 | 0.0392 | 2 | c.157 others(19): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102443104 | G | GAA | intron_variant | MODIFIER | HG00738.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0008a0001c0001t0003g0188a0001c0001t0003g0191others(2): Show | 6 | 204 | 0.0294 | 2 | c.157 others(19): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102443528 | A | ATT | intron_variant | MODIFIER | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
a0004a0005 | a0004c0005a0005c0008 | a0004c0005t0005a0005c0008t0005 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | 204 | 0.0245 | 2 | c.157 others(19): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | TogoVar | ||||||
TMEM123_chr11_102391332_102457765 | 102456064 | C | CTT | upstream_gene_variant | MODIFIER | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(3): Show |
a0001a0004a0005 | a0001c0001a0004c0005a0005c0008 | a0001c0001t0001a0004c0005t0005a0005c0008t0005 | a0001c0001t0001g0106a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | 204 | 0.0294 | 2 | c.-34 others(13): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3300 | chr11 | TogoVar | ||||||
TMEM125_chr1_43264983_43279002 | 43266572 | C | CTT | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(280): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(30): Show | 283 | 438 | 0.6461 | 2 | c.-39 others(13): Show |
TMEM125 | ENSG00000179178.11 | transcript | ENST00000439858.6 | protein_coding | 3410 | chr1 | TogoVar | ||||||
TMEM126A_chr11_85642967_85661542 | 85643204 | A | AGT | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(102): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0006 | a0001c0001t0002a0003c0003t0002a0004c0006t0002 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(15): Show | 105 | 398 | 0.2638 | 2 | c.-48 others(13): Show |
TMEM126A | ENSG00000171202.7 | transcript | ENST00000304511.7 | protein_coding | 4762 | chr11 | TogoVar | ||||||
TMEM126A_chr11_85642967_85661542 | 85648936 | G | GTT | intron_variant | MODIFIER | HG00741.hp2 HG01175.hp2 HG02970.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0011a0001c0001t0003g0034a0001c0001t0003g0085 | 9 | 398 | 0.0226 | 2 | c.-8+ others(15): Show |
TMEM126A | ENSG00000171202.7 | transcript | ENST00000304511.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM126A_chr11_85642967_85661542 | 85651069 | C | CAA | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp1 HG02155.hp1 others(7): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 10 | 398 | 0.0251 | 2 | c.86+ others(15): Show |
TMEM126A | ENSG00000171202.7 | transcript | ENST00000304511.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
TMEM126B_chr11_85623593_85641536 | 85625172 | G | GTC | upstream_gene_variant | MODIFIER | HG03654.hp1 NA18940.hp2 NA18965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025 | 5 | 414 | 0.0121 | 2 | c.-34 others(13): Show |
TMEM126B | ENSG00000171204.13 | transcript | ENST00000358867.11 | protein_coding | 3420 | chr11 | TogoVar |