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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
METRNL_chr17_83074609_83100122 | 83090397 | A | ACACCCCC | intron_variant | MODIFIER | NA18955.hp2 NA18969.hp1 NA19067.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0248a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | 399 | 0.0075 | 7 | c.557 others(24): Show |
METRNL | ENSG00000176845.13 | transcript | ENST00000320095.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
METRNL_chr17_83074609_83100122 | 83090403 | C | CAGGGTGG | intron_variant | MODIFIER | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 30 | 399 | 0.0752 | 7 | c.557 others(24): Show |
METRNL | ENSG00000176845.13 | transcript | ENST00000320095.12 | protein_coding | 2/3 | chr17 | TogoVar | ||||||
METRN_chr16_710118_724655 | 719796 | C | CAAAAAAA | downstream_gene_variant | MODIFIER | HG00323.hp1 HG01169.hp1 HG01175.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0019a0001c0001t0028 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0019g0002others(1): Show | 15 | 402 | 0.0373 | 7 | c.*24 others(18): Show |
METRN | ENSG00000103260.9 | transcript | ENST00000568223.7 | protein_coding | 142 | chr16 | TogoVar | ||||||
METTL13_chr1_171776660_171802716 | 171780724 | C | CAAAAAAA | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
a0001a0002a0003others(1): Show | a0001c0004a0001c0009a0001c0013others(5): Show | a0001c0004t0005a0001c0004t0008a0001c0009t0007others(6): Show | a0001c0004t0005g0007a0001c0004t0005g0014a0001c0004t0005g0062others(18): Show | 56 | 378 | 0.1482 | 7 | c.-12 others(18): Show |
METTL13 | ENSG00000010165.20 | transcript | ENST00000361735.4 | protein_coding | 935 | chr1 | TogoVar | ||||||
METTL15_chr11_28103388_28338507 | 28123568 | A | ATATCATT | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
a0001a0005a0006others(4): Show | a0001c0001a0001c0007a0001c0008others(7): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0008others(156): Show | 160 | 332 | 0.4819 | 7 | c.270 others(24): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
METTL15_chr11_28103388_28338507 | 28181259 | A | ATTTTTTT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(90): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0002a0001c0001t0010a0002c0002t0001others(4): Show | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(89): Show | 93 | 332 | 0.2801 | 7 | c.271 others(26): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
METTL15_chr11_28103388_28338507 | 28310965 | G | GTGGGTGT | intron_variant | MODIFIER | HG02809.hp2 NA18964.hp2 NA18983.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0005a0001c0001t0012others(1): Show | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0024others(4): Show | 8 | 332 | 0.0241 | 7 | c.778 others(26): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 6/6 | chr11 | TogoVar | ||||||
METTL15_chr11_28103388_28338507 | 28332936 | C | CAAAAAAA | 3_prime_UTR_variant | MODIFIER | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0017 | a0001c0001t0006g0160a0001c0001t0006g0176a0001c0001t0006g0187others(10): Show | 13 | 332 | 0.0392 | 7 | c.*21 others(18): Show |
METTL15 | ENSG00000169519.21 | transcript | ENST00000407364.8 | protein_coding | 7/7 | 2113 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
METTL16_chr17_2411049_2516888 | 2449520 | G | GAAAACAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(71): Show |
a0001a0004 | a0001c0001a0001c0007a0004c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0001t0001g0256others(71): Show | 74 | 298 | 0.2483 | 7 | c.729 others(24): Show |
METTL16 | ENSG00000127804.13 | transcript | ENST00000263092.11 | protein_coding | 6/9 | chr17 | TogoVar | ||||||
METTL22_chr16_8616698_8654654 | 8618339 | A | ATTTTGTT | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0005a0001c0006others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(256): Show | 338 | 390 | 0.8667 | 7 | c.-36 others(18): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 3358 | chr16 | TogoVar | ||||||
METTL22_chr16_8616698_8654654 | 8651386 | C | CAAAAAAA | downstream_gene_variant | MODIFIER | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0011a0004c0004t0006a0004c0004t0020others(1): Show | a0001c0001t0011g0220a0001c0001t0011g0221a0001c0001t0011g0222others(9): Show | 15 | 390 | 0.0385 | 7 | c.*52 others(18): Show |
METTL22 | ENSG00000067365.15 | transcript | ENST00000381920.8 | protein_coding | 1733 | chr16 | TogoVar | ||||||
METTL25B_chr1_156723469_156741960 | 156735565 | A | ATATATAT | intron_variant | MODIFIER | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(31): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0037a0001c0001t0001g0077a0001c0001t0001g0082others(22): Show | 34 | 390 | 0.0872 | 7 | c.112 others(24): Show |
METTL25B | ENSG00000143303.12 | transcript | ENST00000368216.9 | protein_coding | 6/7 | chr1 | TogoVar | ||||||
METTL26_chr16_629430_641305 | 637295 | C | CGGCAGGG | upstream_gene_variant | MODIFIER | NA18940.hp2 NA18956.hp1 NA18973.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0022 | 7 | 404 | 0.0173 | 7 | c.-10 others(18): Show |
METTL26 | ENSG00000130731.16 | transcript | ENST00000301686.13 | protein_coding | 991 | chr16 | TogoVar | ||||||
METTL2A_chr17_62418897_62458385 | 62425389 | C | CTTTTTTT | intron_variant | MODIFIER | HG01099.hp2 HG01168.hp1 HG02055.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0021a0001c0001t0028others(2): Show | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0013g0089others(10): Show | 14 | 363 | 0.0386 | 7 | c.203 others(22): Show |
METTL2A | ENSG00000087995.16 | transcript | ENST00000311506.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
METTL4_chr18_2532530_2576505 | 2536139 | T | TAAAAAAA | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
a0002a0003a0007 | a0002c0002a0002c0006a0002c0011others(2): Show | a0002c0002t0001a0002c0002t0011a0002c0002t0015others(4): Show | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(58): Show | 79 | 404 | 0.1955 | 7 | c.*28 others(18): Show |
METTL4 | ENSG00000101574.15 | transcript | ENST00000574538.2 | protein_coding | 1390 | chr18 | TogoVar | ||||||
METTL4_chr18_2532530_2576505 | 2566046 | C | CAAAAAAT | intron_variant | MODIFIER | HG00423.hp2 HG00642.hp2 HG01928.hp2 others(16): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0006 | a0001c0001t0005a0002c0002t0001a0002c0002t0015others(1): Show | a0001c0001t0005g0081a0002c0002t0001g0011a0002c0002t0001g0026others(12): Show | 19 | 404 | 0.0470 | 7 | c.396 others(22): Show |
METTL4 | ENSG00000101574.15 | transcript | ENST00000574538.2 | protein_coding | 2/8 | chr18 | TogoVar | ||||||
METTL9_chr16_21594577_21662471 | 21622141 | C | CTTTTTTT | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG01261.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143a0001c0001t0001g0180a0001c0001t0001g0183others(9): Show | 12 | 364 | 0.0330 | 7 | c.567 others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
MFAP5_chr12_8640943_8667826 | 8641508 | C | CTTTCTTT | downstream_gene_variant | MODIFIER | HG01169.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0057a0001c0001t0003g0210a0001c0001t0003g0212others(3): Show | 7 | 372 | 0.0188 | 7 | c.*65 others(18): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4434 | chr12 | TogoVar | ||||||
MFAP5_chr12_8640943_8667826 | 8666889 | C | CTTTTTTT | upstream_gene_variant | MODIFIER | HG01168.hp2 HG01169.hp1 HG02055.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0057a0001c0001t0003g0210a0001c0001t0003g0212others(3): Show | 6 | 372 | 0.0161 | 7 | c.-42 others(18): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4064 | chr12 | TogoVar | ||||||
MFHAS1_chr8_8778354_8898630 | 8877301 | C | CAAAAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(166): Show | 169 | 324 | 0.5216 | 7 | c.299 others(28): Show |
MFHAS1 | ENSG00000147324.11 | transcript | ENST00000276282.7 | protein_coding | 1/2 | chr8 | TogoVar | ||||||
MFN1_chr3_179342709_179399936 | 179372053 | T | TTATTATA | intron_variant | MODIFIER | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0045 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(7): Show | 11 | 402 | 0.0274 | 7 | c.976 others(24): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MFN1_chr3_179342709_179399936 | 179391111 | A | ACACATTT | intron_variant | MODIFIER | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0045 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | 402 | 0.0299 | 7 | c.214 others(24): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MFN2_chr1_11975444_12018508 | 11981920 | G | GTTTTTTT | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 116 | 394 | 0.2944 | 7 | c.-14 others(22): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MFN2_chr1_11975444_12018508 | 11991923 | C | CAAAAAAA | intron_variant | MODIFIER | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(17): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0130others(14): Show | 20 | 394 | 0.0508 | 7 | c.176 others(22): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MFSD11_chr17_76733119_76784341 | 76755813 | T | TATATATA | intron_variant | MODIFIER | HG00733.hp2 NA18993.hp2 NA19001.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149a0001c0001t0001g0263a0001c0001t0001g0268 | 3 | 348 | 0.0086 | 7 | c.682 others(24): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | TogoVar | ||||||
MFSD11_chr17_76733119_76784341 | 76781988 | A | ATTTTTTT | downstream_gene_variant | MODIFIER | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0006 | a0001c0001t0005g0004a0001c0001t0005g0022a0001c0001t0005g0023others(8): Show | 11 | 348 | 0.0316 | 7 | c.*36 others(18): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2648 | chr17 | TogoVar | ||||||
MFSD14A_chr1_100033095_100088377 | 100045710 | A | ATTTTATT | intron_variant | MODIFIER | HG00733.hp1 HG01069.hp1 HG01109.hp2 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(2): Show | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(30): Show | 38 | 242 | 0.1570 | 7 | c.85- others(22): Show |
MFSD14A | ENSG00000156875.14 | transcript | ENST00000370152.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MFSD14B_chr9_94369569_94466042 | 94409129 | C | CTTTTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0090others(6): Show | 9 | 350 | 0.0257 | 7 | c.109 others(24): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
MFSD14B_chr9_94369569_94466042 | 94439022 | G | GTTTTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0092others(49): Show | 53 | 350 | 0.1514 | 7 | c.395 others(22): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
MFSD14B_chr9_94369569_94466042 | 94455378 | A | ATTTTTTT | intron_variant | MODIFIER | HG00621.hp1 HG02148.hp1 HG02258.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0001g0262others(8): Show | 11 | 350 | 0.0314 | 7 | c.102 others(24): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
MFSD1_chr3_158797054_158834716 | 158827915 | G | GAGAGAGA | intron_variant | MODIFIER | HG01109.hp1 NA18948.hp1 NA18957.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0165others(1): Show | 4 | 402 | 0.0100 | 7 | c.139 others(24): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | TogoVar | ||||||
MFSD2A_chr1_39950145_39974956 | 39965169 | G | GCTCCAGC | intron_variant | MODIFIER | HG00642.hp1 HG02300.hp2 HG02717.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | 392 | 0.0204 | 7 | c.354 others(20): Show |
MFSD2A | ENSG00000168389.18 | transcript | ENST00000372811.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MFSD3_chr8_144504070_144516213 | 144513791 | C | CGTGGGCG | downstream_gene_variant | MODIFIER | HG00423.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0001a0002c0003t0001g0002 | 7 | 400 | 0.0175 | 7 | c.*26 others(18): Show |
MFSD3 | ENSG00000167700.9 | transcript | ENST00000301327.5 | protein_coding | 2579 | chr8 | TogoVar | ||||||
MFSD4A_chr1_205564014_205607918 | 205604005 | C | CAAAAAAA | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG01123.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0003a0002c0002t0002a0002c0002t0003others(1): Show | a0001c0001t0003g0024a0001c0001t0003g0243a0001c0001t0003g0250others(5): Show | 8 | 378 | 0.0212 | 7 | c.*35 others(18): Show |
MFSD4A | ENSG00000174514.13 | transcript | ENST00000367147.9 | protein_coding | 1088 | chr1 | TogoVar | ||||||
MFSD4B_chr6_111254339_111285005 | 111271775 | T | TAAAAAAA | 3_prime_UTR_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(43): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0015others(1): Show | a0001c0001t0146a0001c0002t0001a0001c0002t0012others(14): Show | a0001c0001t0146g0020a0001c0002t0001g0001a0001c0002t0001g0010others(23): Show | 46 | 364 | 0.1264 | 7 | c.*46 others(18): Show |
MFSD4B | ENSG00000173214.7 | transcript | ENST00000671876.2 | protein_coding | 4/4 | 4688 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||
MFSD6_chr2_190403355_190507314 | 190469733 | A | ATTTTTAT | splice_region_variant others(1): Show |
LOW | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0001c0010others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | 344 | 0.9041 | 7 | c.153 others(21): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MFSD6_chr2_190403355_190507314 | 190482903 | T | TTTTTTTG | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp1 HG01081.hp2 others(27): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0023others(4): Show | a0001c0001t0002g0081a0001c0001t0002g0327a0001c0001t0003g0017others(27): Show | 30 | 344 | 0.0872 | 7 | c.163 others(26): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | TogoVar | ||||||
MFSD8_chr4_127912805_127970173 | 127923552 | T | TTTATTTA | intron_variant | MODIFIER | HG02280.hp2 HG02572.hp2 HG02970.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0022a0002c0002t0005 | a0001c0001t0001g0101a0001c0001t0001g0127a0001c0001t0001g0282others(3): Show | 6 | 354 | 0.0170 | 7 | c.999 others(24): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | TogoVar | ||||||
MGAM2_chr7_142106718_142227324 | 142142524 | G | GTTTTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG01099.hp1 others(40): Show |
a0001a0002a0004others(12): Show | a0001c0001a0001c0004a0002c0002others(15): Show | a0001c0001t0001a0001c0004t0001a0002c0002t0001others(15): Show | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0160others(40): Show | 43 | 329 | 0.1307 | 7 | c.131 others(26): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM2_chr7_142106718_142227324 | 142174715 | C | CTTTTTTT | intron_variant | MODIFIER | HG02145.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
a0001a0006a0016others(3): Show | a0001c0001a0006c0033a0016c0020others(3): Show | a0001c0001t0001a0006c0033t0001a0016c0020t0001others(3): Show | a0001c0001t0001g0177a0006c0033t0001g0155a0016c0020t0001g0001others(3): Show | 7 | 329 | 0.0213 | 7 | c.368 others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042150 | A | ACATATAT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
a0007a0014a0015others(7): Show | a0007c0020a0014c0038a0015c0121others(8): Show | a0007c0020t0002a0014c0038t0002a0015c0121t0001others(8): Show | a0007c0020t0002g0062a0007c0020t0002g0231a0014c0038t0002g0029others(10): Show | 13 | 316 | 0.0411 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142042220 | C | CATATTAT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
a0007a0014a0015others(7): Show | a0007c0020a0014c0038a0015c0121others(8): Show | a0007c0020t0002a0014c0038t0002a0015c0121t0001others(8): Show | a0007c0020t0002g0062a0007c0020t0002g0231a0014c0038t0002g0029others(10): Show | 13 | 316 | 0.0411 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042278 | C | CATATAAT | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp1 HG02717.hp2 others(5): Show |
a0010a0061a0062others(2): Show | a0010c0017a0061c0115a0062c0113others(2): Show | a0010c0017t0001a0061c0115t0001a0062c0113t0001others(2): Show | a0010c0017t0001g0058a0010c0017t0001g0098a0010c0017t0001g0099others(5): Show | 8 | 316 | 0.0253 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042278 | C | CATATTAT | intron_variant | MODIFIER | HG02257.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
a0007a0016a0017others(2): Show | a0007c0020a0007c0037a0016c0128others(3): Show | a0007c0020t0002a0007c0037t0002a0016c0128t0003others(3): Show | a0007c0020t0002g0060a0007c0037t0002g0002a0007c0037t0002g0003others(4): Show | 7 | 316 | 0.0222 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042307 | C | CATATAAT | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
a0010a0061a0062others(2): Show | a0010c0017a0061c0115a0062c0113others(2): Show | a0010c0017t0001a0061c0115t0001a0062c0113t0001others(2): Show | a0010c0017t0001g0058a0010c0017t0001g0098a0010c0017t0001g0099others(4): Show | 7 | 316 | 0.0222 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042307 | C | CATATTAT | intron_variant | MODIFIER | HG02622.hp1 NA18947.hp1 NA19043.hp1 |
a0016a0028a0033 | a0016c0127a0028c0146a0033c0122 | a0016c0127t0001a0028c0146t0001a0033c0122t0001 | a0016c0127t0001g0119a0028c0146t0001g0044a0033c0122t0001g0100 | 3 | 316 | 0.0095 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042336 | C | CATATTAT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
a0007a0014a0015others(7): Show | a0007c0020a0014c0038a0015c0121others(8): Show | a0007c0020t0002a0014c0038t0002a0015c0121t0001others(8): Show | a0007c0020t0002g0062a0007c0020t0002g0231a0014c0038t0002g0029others(10): Show | 13 | 316 | 0.0411 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042365 | C | CATATTAT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
a0007a0014a0015others(7): Show | a0007c0020a0014c0038a0015c0121others(8): Show | a0007c0020t0002a0014c0038t0002a0015c0121t0001others(8): Show | a0007c0020t0002g0062a0007c0020t0002g0231a0014c0038t0002g0029others(10): Show | 13 | 316 | 0.0411 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042394 | C | CATATTAT | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
a0007a0014a0015others(7): Show | a0007c0020a0014c0038a0015c0121others(9): Show | a0007c0020t0002a0014c0038t0002a0015c0121t0001others(9): Show | a0007c0020t0002g0060a0007c0020t0002g0062a0007c0020t0002g0231others(12): Show | 15 | 316 | 0.0475 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MGAM_chr7_141990879_142111747 | 142042653 | T | TAATGTAA | intron_variant | MODIFIER | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
a0007a0015a0017others(3): Show | a0007c0020a0015c0121a0015c0125others(4): Show | a0007c0020t0002a0015c0121t0001a0015c0125t0001others(4): Show | a0007c0020t0002g0060a0007c0020t0002g0062a0015c0121t0001g0064others(5): Show | 8 | 316 | 0.0253 | 7 | c.249 others(26): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | chr7 | TogoVar |