view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM255B_chr13_113754226_113821995 | 113800082 | A | ATG | intron_variant | MODIFIER | HG04199.hp2 NA19030.hp2 NA19084.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0034 | a0001c0001t0001g0178a0001c0001t0003g0158a0001c0001t0034g0212 | 3 | 260 | 0.0115 | 2 | c.423 others(17): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
TMEM255B_chr13_113754226_113821995 | 113800301 | C | CTG | intron_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(40): Show |
a0001a0003a0007 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0194a0001c0001t0002g0122a0001c0001t0003g0145others(39): Show | 43 | 260 | 0.1654 | 2 | c.424 others(17): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
TMEM255B_chr13_113754226_113821995 | 113808792 | T | TGG | intron_variant | MODIFIER | HG00639.hp1 HG01081.hp1 HG02055.hp2 others(32): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | a0001c0001t0001g0182a0001c0001t0003g0158a0001c0001t0003g0208others(31): Show | 35 | 260 | 0.1346 | 2 | c.814 others(19): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
TMEM255B_chr13_113754226_113821995 | 113812873 | G | GCA | 3_prime_UTR_variant | MODIFIER | HG01496.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
a0001a0006 | a0001c0001a0001c0009a0006c0015others(1): Show | a0001c0001t0134a0001c0001t0137a0001c0001t0138others(5): Show | a0001c0001t0134g0030a0001c0001t0137g0031a0001c0001t0138g0217others(5): Show | 8 | 260 | 0.0308 | 2 | c.*97 others(11): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 9/9 | 971 | chr13 | TogoVar | ||||||
TMEM256_chr17_7397975_7409097 | 7399322 | C | CTT | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(3): Show | 17 | 398 | 0.0427 | 2 | c.*37 others(13): Show |
TMEM256 | ENSG00000205544.4 | transcript | ENST00000302422.4 | protein_coding | 3652 | chr17 | TogoVar | |||||||
TMEM256_chr17_7397975_7409097 | 7400314 | C | CAA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(1): Show | 56 | 398 | 0.1407 | 2 | c.*27 others(13): Show |
TMEM256 | ENSG00000205544.4 | transcript | ENST00000302422.4 | protein_coding | 2660 | chr17 | TogoVar | |||||||
TMEM256_chr17_7397975_7409097 | 7400431 | A | ATT | downstream_gene_variant | MODIFIER | HG01243.hp2 HG02602.hp1 HG02922.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 12 | 398 | 0.0302 | 2 | c.*26 others(13): Show |
TMEM256 | ENSG00000205544.4 | transcript | ENST00000302422.4 | protein_coding | 2543 | chr17 | TogoVar | |||||||
TMEM256_chr17_7397975_7409097 | 7403784 | A | ACC | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00733.hp2 others(44): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0023 | 47 | 398 | 0.1181 | 2 | c.86- others(13): Show |
TMEM256 | ENSG00000205544.4 | transcript | ENST00000302422.4 | protein_coding | 1/3 | chr17 | TogoVar | |||||||
TMEM256_chr17_7397975_7409097 | 7406653 | C | CGG | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(56): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 59 | 398 | 0.1482 | 2 | c.-25 others(13): Show |
TMEM256 | ENSG00000205544.4 | transcript | ENST00000302422.4 | protein_coding | 2557 | chr17 | TogoVar | |||||||
TMEM259_chr19_1004653_1026123 | 1022208 | G | GTT | upstream_gene_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
a0001 | a0001c0008a0001c0022 | a0001c0008t0002a0001c0022t0002 | a0001c0008t0002g0015a0001c0008t0002g0049a0001c0008t0002g0050others(2): Show | 10 | 430 | 0.0233 | 2 | c.-12 others(13): Show |
TMEM259 | ENSG00000182087.14 | transcript | ENST00000356663.8 | protein_coding | 1086 | chr19 | TogoVar | |||||||
TMEM259_chr19_1004653_1026123 | 1022211 | G | GTT | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(154): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(20): Show | a0001c0001t0001g0037a0001c0002t0001g0072a0001c0002t0001g0151others(65): Show | 157 | 430 | 0.3651 | 2 | c.-12 others(13): Show |
TMEM259 | ENSG00000182087.14 | transcript | ENST00000356663.8 | protein_coding | 1089 | chr19 | TogoVar | |||||||
TMEM259_chr19_1004653_1026123 | 1023704 | C | CAA | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(45): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0012others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0002t0002g0002others(24): Show | 48 | 430 | 0.1116 | 2 | c.-27 others(13): Show |
TMEM259 | ENSG00000182087.14 | transcript | ENST00000356663.8 | protein_coding | 2582 | chr19 | TogoVar | |||||||
TMEM259_chr19_1004653_1026123 | 1025585 | G | GTT | upstream_gene_variant | MODIFIER | HG03669.hp1 HG03831.hp1 HG04228.hp1 others(5): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0003t0001 | a0001c0002t0002g0003a0001c0002t0002g0017a0001c0003t0001g0004others(1): Show | 8 | 430 | 0.0186 | 2 | c.-45 others(13): Show |
TMEM259 | ENSG00000182087.14 | transcript | ENST00000356663.8 | protein_coding | 4463 | chr19 | TogoVar | |||||||
TMEM25_chr11_118526192_118540829 | 118539164 | A | ATT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(11): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0002t0001g0001others(12): Show | 91 | 398 | 0.2286 | 2 | c.*45 others(13): Show |
TMEM25 | ENSG00000149582.16 | transcript | ENST00000313236.10 | protein_coding | 3336 | chr11 | TogoVar | |||||||
TMEM260_chr14_56574798_56654515 | 56575553 | C | CTT | upstream_gene_variant | MODIFIER | HG00621.hp1 HG01243.hp1 HG01358.hp2 others(11): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0005others(2): Show | a0001c0001t0005a0001c0001t0008a0001c0004t0004others(3): Show | a0001c0001t0005g0325a0001c0001t0005g0329a0001c0001t0005g0330others(11): Show | 14 | 364 | 0.0385 | 2 | c.-43 others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4244 | chr14 | TogoVar | |||||||
TMEM260_chr14_56574798_56654515 | 56583990 | T | TTG | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG01433.hp1 others(16): Show |
a0001a0002a0003others(1): Show | a0001c0004a0001c0020a0002c0006others(2): Show | a0001c0004t0011a0001c0004t0015a0001c0020t0011others(5): Show | a0001c0004t0011g0310a0001c0004t0011g0311a0001c0004t0011g0312others(15): Show | 19 | 364 | 0.0522 | 2 | c.161 others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56593677 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0011a0002c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(6): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0130others(46): Show | 53 | 364 | 0.1456 | 2 | c.344 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56596381 | A | AGT | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
a0001a0002a0004others(4): Show | a0001c0002a0001c0004a0002c0003others(6): Show | a0001c0002t0001a0001c0002t0019a0001c0002t0023others(9): Show | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0022others(74): Show | 86 | 364 | 0.2363 | 2 | c.345 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56596423 | T | TAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(46): Show |
a0001a0002a0015 | a0001c0001a0002c0005a0015c0021 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(5): Show | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0201others(40): Show | 49 | 364 | 0.1346 | 2 | c.345 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56596782 | A | AAT | intron_variant | MODIFIER | HG00438.hp2 HG02258.hp2 HG03017.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0001c0001t0005a0002c0005t0012 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | 364 | 0.0275 | 2 | c.345 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | TogoVar | |||||||
TMEM260_chr14_56574798_56654515 | 56596784 | T | TAA | intron_variant | MODIFIER | HG01993.hp2 HG03017.hp2 HG03195.hp2 others(12): Show |
a0001a0002a0004 | a0001c0002a0002c0003a0004c0008 | a0001c0002t0001a0001c0002t0019a0002c0003t0001others(1): Show | a0001c0002t0001g0037a0001c0002t0001g0043a0001c0002t0001g0052others(12): Show | 15 | 364 | 0.0412 | 2 | c.345 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56602746 | C | CAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
a0001a0002a0004others(11): Show | a0001c0001a0001c0002a0001c0004others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(41): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 336 | 364 | 0.9231 | 2 | c.345 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56605467 | C | CTT | intron_variant | MODIFIER | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0008a0001c0001t0025 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | 364 | 0.0495 | 2 | c.523 others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | TogoVar | |||||||
TMEM260_chr14_56574798_56654515 | 56607712 | G | GTA | intron_variant | MODIFIER | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0008a0001c0001t0025 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(15): Show | 18 | 364 | 0.0495 | 2 | c.637 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56613895 | C | CAA | intron_variant | MODIFIER | HG00609.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0002c0006others(3): Show | a0001c0001t0002a0001c0001t0010a0001c0004t0004others(5): Show | a0001c0001t0002g0220a0001c0001t0010g0239a0001c0004t0004g0181others(7): Show | 10 | 364 | 0.0275 | 2 | c.857 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56622342 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(36): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0011others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0002g0207others(36): Show | 39 | 364 | 0.1071 | 2 | c.139 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56629271 | G | GTT | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
a0001 | a0001c0001a0001c0004a0001c0020 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(4): Show | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0216others(20): Show | 25 | 364 | 0.0687 | 2 | c.154 others(21): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56630042 | G | GAA | intron_variant | MODIFIER | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
a0001a0002 | a0001c0004a0001c0020a0002c0006 | a0001c0004t0003a0001c0004t0011a0001c0004t0014others(4): Show | a0001c0004t0003g0281a0001c0004t0003g0295a0001c0004t0003g0296others(37): Show | 41 | 364 | 0.1126 | 2 | c.154 others(21): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56631629 | A | AAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0011others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(8): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(107): Show | 119 | 364 | 0.3269 | 2 | c.154 others(21): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56633258 | A | ATT | intron_variant | MODIFIER | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(1): Show | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | 364 | 0.0550 | 2 | c.172 others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56633794 | T | TCA | intron_variant | MODIFIER | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(1): Show | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(17): Show | 20 | 364 | 0.0550 | 2 | c.172 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM260_chr14_56574798_56654515 | 56635844 | A | AAT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0005a0004c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(4): Show | a0001c0001t0001g0163a0001c0001t0002g0006a0001c0001t0002g0122others(60): Show | 69 | 364 | 0.1896 | 2 | c.177 others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
TMEM262_chr11_65083376_65094110 | 65091908 | A | AAT | upstream_gene_variant | MODIFIER | HG01106.hp2 HG02523.hp1 NA18941.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 8 | 382 | 0.0209 | 2 | c.-28 others(13): Show |
TMEM262 | ENSG00000187066.9 | transcript | ENST00000530719.6 | protein_coding | 2799 | chr11 | TogoVar | |||||||
TMEM262_chr11_65083376_65094110 | 65093247 | C | CTT | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0003g0005 | 9 | 382 | 0.0236 | 2 | c.-42 others(13): Show |
TMEM262 | ENSG00000187066.9 | transcript | ENST00000530719.6 | protein_coding | 4138 | chr11 | TogoVar | |||||||
TMEM263_chr12_106950907_106979035 | 106957165 | C | CGT | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0017 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(5): Show | 13 | 390 | 0.0333 | 2 | c.-7+ others(13): Show |
TMEM263 | ENSG00000151135.10 | transcript | ENST00000280756.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM263_chr12_106950907_106979035 | 106972860 | C | CTT | 3_prime_UTR_variant | MODIFIER | HG02257.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0011 | a0001c0001t0010g0030a0001c0001t0010g0050a0001c0001t0010g0161others(3): Show | 10 | 390 | 0.0256 | 2 | c.*14 others(13): Show |
TMEM263 | ENSG00000151135.10 | transcript | ENST00000280756.9 | protein_coding | 4/4 | 1489 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM265_chr16_30735642_30750196 | 30749204 | G | GGT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 232 | 284 | 0.8169 | 2 | c.*52 others(13): Show |
TMEM265 | ENSG00000281991.2 | transcript | ENST00000615541.3 | protein_coding | 4009 | chr16 | TogoVar | |||||||
TMEM266_chr15_76054985_76209963 | 76071908 | A | ATT | intron_variant | MODIFIER | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0008a0001c0001t0001g0144a0001c0001t0001g0270others(4): Show | 7 | 274 | 0.0256 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76075837 | C | CTT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0074others(62): Show | 65 | 274 | 0.2372 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76083233 | C | CTT | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(2): Show | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0111others(15): Show | 18 | 274 | 0.0657 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76084598 | G | GGT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(43): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0084others(43): Show | 46 | 274 | 0.1679 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | TogoVar | |||||||
TMEM266_chr15_76054985_76209963 | 76086928 | C | CGG | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp2 HG01169.hp2 others(19): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(4): Show | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0135others(19): Show | 22 | 274 | 0.0803 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76089093 | C | CAA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(68): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(68): Show | 71 | 274 | 0.2591 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76090491 | C | CAA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(35): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0074a0001c0001t0001g0084others(35): Show | 38 | 274 | 0.1387 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76096932 | A | ATT | intron_variant | MODIFIER | HG00597.hp2 HG00735.hp2 HG00741.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0190a0001c0001t0001g0272a0001c0001t0002g0038others(8): Show | 11 | 274 | 0.0402 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76103910 | C | CAA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0157others(29): Show | 32 | 274 | 0.1168 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76120758 | C | CAA | intron_variant | MODIFIER | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(1): Show | a0001c0001t0001g0102a0001c0001t0001g0135a0001c0001t0001g0143others(6): Show | 9 | 274 | 0.0329 | 2 | c.-12 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76126374 | C | CAT | intron_variant | MODIFIER | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0139a0001c0001t0001g0273a0001c0001t0002g0042others(12): Show | 15 | 274 | 0.0547 | 2 | c.-12 others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76127323 | C | CTT | intron_variant | MODIFIER | HG01243.hp1 HG01255.hp2 HG02257.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0025others(18): Show | 21 | 274 | 0.0766 | 2 | c.-12 others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
TMEM266_chr15_76054985_76209963 | 76132113 | A | ATT | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0024others(68): Show | 72 | 274 | 0.2628 | 2 | c.-12 others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar |