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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MEI4_chr6_77648039_77932045 | 77680128 | A | AAAAAAAA others(30): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 328 | 0.0030 | 37 | c.-14 others(56): Show |
MEI4 | ENSG00000269964.4 | transcript | ENST00000684080.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MEI4_chr6_77648039_77932045 | 77834371 | C | CATATTAT others(30): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0179 | 1 | 358 | 0.0028 | 37 | c.900 others(54): Show |
MEI4 | ENSG00000269964.4 | transcript | ENST00000684080.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MEI4_chr6_77648039_77932045 | 77928850 | C | CTGGAAAC others(30): Show |
downstream_gene_variant | MODIFIER | NA19063.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0141 | 1 | 358 | 0.0028 | 37 | c.*55 others(48): Show |
MEI4 | ENSG00000269964.4 | transcript | ENST00000684080.1 | protein_coding | 1806 | chr6 | TogoVar | |||||||
MEMO1_chr2_31862823_32016008 | 31966732 | C | CAAAAAAA others(30): Show |
intron_variant | MODIFIER | HG01934.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136 | 1 | 187 | 0.0053 | 37 | c.62- others(54): Show |
MEMO1 | ENSG00000162959.14 | transcript | ENST00000404530.6 | protein_coding | 2/9 | chr2 | TogoVar | |||||||
MEP1A_chr6_46788389_46844778 | 46824894 | T | TATATATA others(30): Show |
intron_variant | MODIFIER | NA18968.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0290 | 1 | 295 | 0.0034 | 37 | c.557 others(52): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MEP1A_chr6_46788389_46844778 | 46825021 | A | ATATTTAA others(30): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | 350 | 0.0114 | 37 | c.557 others(52): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MERTK_chr2_111893607_112034561 | 111925292 | A | ATATATAT others(30): Show |
intron_variant | MODIFIER | HG00323.hp2 | a0005 | a0005c0005 | a0005c0005t0003 | a0005c0005t0003g0008 | 1 | 99 | 0.0101 | 37 | c.62- others(52): Show |
MERTK | ENSG00000153208.19 | transcript | ENST00000295408.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
METRNL_chr17_83074609_83100122 | 83090264 | A | ACACACAC others(30): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01258.hp2 HG03654.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0002 | a0001c0001t0002g0366 a0001c0003t0002g0008 |
3 | 378 | 0.0079 | 37 | c.557 others(54): Show |
METRNL | ENSG00000176845.13 | transcript | ENST00000320095.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
METRNL_chr17_83074609_83100122 | 83090298 | A | ACACACAC others(30): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0008a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
127 | 381 | 0.3333 | 37 | c.557 others(54): Show |
METRNL | ENSG00000176845.13 | transcript | ENST00000320095.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
METRNL_chr17_83074609_83100122 | 83090386 | C | CCCCCCAC others(30): Show |
intron_variant | MODIFIER | HG02074.hp2 NA18966.hp2 |
a0001 | a0001c0001a0001c0011 | a0001c0001t0002a0001c0011t0004 | a0001c0001t0002g0100 a0001c0011t0004g0106 |
2 | 295 | 0.0068 | 37 | c.557 others(54): Show |
METRNL | ENSG00000176845.13 | transcript | ENST00000320095.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
METTL27_chr7_73829590_73847516 | 73842642 | G | GCCCCCCC others(30): Show |
upstream_gene_variant | MODIFIER | HG01109.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0011 | 1 | 29 | 0.0345 | 37 | c.-15 others(46): Show |
METTL27 | ENSG00000165171.11 | transcript | ENST00000297873.9 | protein_coding | 127 | chr7 | TogoVar | |||||||
METTL8_chr2_171310746_171438990 | 171363792 | T | TATATATA others(30): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0307 | 1 | 133 | 0.0075 | 37 | c.144 others(54): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | TogoVar | |||||||
METTL9_chr16_21594577_21662471 | 21622141 | C | CTTTTTTT others(30): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0344 | 1 | 48 | 0.0208 | 37 | c.567 others(54): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
MEX3D_chr19_1549672_1573325 | 1550110 | A | ACCACACC others(30): Show |
downstream_gene_variant | MODIFIER | NA18959.hp2 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0206 | 1 | 370 | 0.0027 | 37 | c.*54 others(48): Show |
MEX3D | ENSG00000181588.17 | transcript | ENST00000402693.5 | protein_coding | 4561 | chr19 | TogoVar | |||||||
MFAP3L_chr4_169981602_170031395 | 170023173 | G | GGGTTCAT others(30): Show |
intron_variant | MODIFIER | NA19076.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0106 | 1 | 326 | 0.0031 | 37 | c.-13 others(56): Show |
MFAP3L | ENSG00000198948.12 | transcript | ENST00000361618.4 | protein_coding | 1/2 | chr4 | TogoVar | |||||||
MFGE8_chr15_88893683_88918379 | 88913993 | T | TAAAAAAA others(30): Show |
upstream_gene_variant | MODIFIER | HG02040.hp2 HG02135.hp2 NA18948.hp1 others(2): Show |
a0001a0002 | a0001c0002a0002c0001 | a0001c0002t0002a0002c0001t0002 | a0001c0002t0002g0007 a0001c0002t0002g0176 a0001c0002t0002g0227 others(1): Show |
5 | 162 | 0.0309 | 37 | c.-67 others(46): Show |
MFGE8 | ENSG00000140545.16 | transcript | ENST00000268150.13 | protein_coding | 615 | chr15 | TogoVar | |||||||
MFSD14B_chr9_94369569_94466042 | 94373681 | A | ATTTTTTT others(30): Show |
upstream_gene_variant | MODIFIER | HG00558.hp2 HG02071.hp1 HG02083.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0004 a0001c0001t0002g0161 a0001c0001t0002g0171 others(1): Show |
4 | 9 | 0.4444 | 37 | c.-11 others(48): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 887 | chr9 | TogoVar | |||||||
MFSD6_chr2_190403355_190507314 | 190414446 | T | TAAAAGAC others(30): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0243 | 1 | 342 | 0.0029 | 37 | c.-17 others(54): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142042834 | T | TATTATAT others(30): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 312 | 0.0032 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142043199 | A | ATATATTA others(30): Show |
intron_variant | MODIFIER | NA18978.hp1 NA19001.hp2 |
a0002a0008 | a0002c0008a0008c0019 | a0002c0008t0001a0008c0019t0001 | a0002c0008t0001g0079 a0008c0019t0001g0086 |
2 | 200 | 0.0100 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142043347 | C | CTATATTA others(30): Show |
intron_variant | MODIFIER | HG02155.hp2 NA18980.hp2 |
a0001a0003 | a0001c0003a0003c0005 | a0001c0003t0001a0003c0005t0001 | a0001c0003t0001g0210 a0003c0005t0001g0163 |
2 | 267 | 0.0075 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142043384 | C | CTATATTA others(30): Show |
intron_variant | MODIFIER | HG03490.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | 231 | 0.0087 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142043421 | C | CTATATTA others(30): Show |
intron_variant | MODIFIER | HG02074.hp1 HG03942.hp1 NA19088.hp2 |
a0002a0003 | a0002c0008a0003c0005 | a0002c0008t0001a0003c0005t0001 | a0002c0008t0001g0232 a0003c0005t0001g0003 a0003c0005t0001g0056 |
3 | 115 | 0.0261 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142045745 | A | AATATATA others(30): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(34): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0006others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(8): Show | a0001c0001t0001g0012 a0001c0001t0001g0240 a0001c0001t0001g0277 others(34): Show |
37 | 182 | 0.2033 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAM_chr7_141990879_142111747 | 142045755 | A | ATATACAT others(30): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0092 | 1 | 227 | 0.0044 | 37 | c.249 others(56): Show |
MGAM | ENSG00000257335.8 | transcript | ENST00000475668.6 | protein_coding | 21/70 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MGAT4A_chr2_98614106_98736132 | 98724722 | A | ATCGTTTG others(30): Show |
intron_variant | MODIFIER | HG03490.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0175 | 1 | 260 | 0.0038 | 37 | c.94+ others(52): Show |
MGAT4A | ENSG00000071073.13 | transcript | ENST00000393487.6 | protein_coding | 2/15 | chr2 | TogoVar | |||||||
MGAT5_chr2_134249072_134459621 | 134381364 | T | TAGATAGA others(30): Show |
intron_variant | MODIFIER | HG01255.hp2 NA18963.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0019a0001c0001t0033 | a0001c0001t0003g0154 a0001c0001t0019g0068 a0001c0001t0033g0172 |
3 | 263 | 0.0114 | 37 | c.138 others(58): Show |
MGAT5 | ENSG00000152127.9 | transcript | ENST00000281923.4 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MGA_chr15_41655405_41774940 | 41656344 | T | TCTCTCTC others(30): Show |
upstream_gene_variant | MODIFIER | NA18961.hp1 NA18984.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0113 a0001c0001t0002g0122 |
2 | 49 | 0.0408 | 37 | c.-42 others(48): Show |
MGA | ENSG00000174197.19 | transcript | ENST00000703841.1 | protein_coding | 4060 | chr15 | TogoVar | |||||||
MGRN1_chr16_4619826_4695972 | 4648524 | G | GGCTCTTC others(30): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0005 | 1 | 331 | 0.0030 | 37 | c.89- others(52): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | TogoVar | |||||||
MGRN1_chr16_4619826_4695972 | 4648623 | T | TCTCCGGG others(30): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0002 | 1 | 332 | 0.0030 | 37 | c.89- others(52): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
MIA_chr19_40770521_40782490 | 40777022 | T | TAGCATTG others(30): Show |
frameshift_variant | HIGH | NA19084.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0001 | 1 | 402 | 0.0025 | 37 | c.317 others(44): Show |
p.Val others(5): Show |
MIA | ENSG00000261857.7 | transcript | ENST00000263369.4 | protein_coding | 3/4 | 376/488 | 354/396 | 118/131 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||
MINAR1_chr15_79427336_79477304 | 79439295 | G | GGGTGGGT others(30): Show |
intron_variant | MODIFIER | NA18956.hp2 NA18957.hp1 NA18959.hp1 others(2): Show |
a0001 | a0001c0001a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0017t0001 | a0001c0001t0001g0033 a0001c0001t0001g0231 a0001c0001t0004g0032 others(1): Show |
5 | 387 | 0.0129 | 37 | c.-51 others(54): Show |
MINAR1 | ENSG00000169330.9 | transcript | ENST00000305428.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MINDY4_chr7_30766417_30897387 | 30843598 | A | ACCCCCAC others(30): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00609.hp2 HG01981.hp1 others(31): Show |
a0002a0003a0004others(4): Show | a0002c0022a0002c0029a0002c0034others(9): Show | a0002c0022t0002a0002c0029t0001a0002c0034t0001others(11): Show | a0002c0022t0002g0032 a0002c0022t0002g0290 a0002c0029t0001g0190 others(30): Show |
34 | 298 | 0.1141 | 37 | c.144 others(56): Show |
MINDY4 | ENSG00000106125.14 | transcript | ENST00000265299.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MLC1_chr22_50054391_50090426 | 50081009 | A | AAAAGAAA others(30): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0004 | a0004c0004 | a0004c0004t0021 | a0004c0004t0021g0163 | 1 | 65 | 0.0154 | 37 | c.268 others(52): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | TogoVar | |||||||
MLH3_chr14_75008775_75056467 | 75017201 | T | TCTATGGG others(30): Show |
splice_acceptor_variant others(1): Show |
HIGH | NA20300.hp1 | a0006 | a0006c0006 | a0006c0006t0001 | a0006c0006t0001g0047 | 1 | 260 | 0.0038 | 37 | c.424 others(51): Show |
MLH3 | ENSG00000119684.16 | transcript | ENST00000355774.7 | protein_coding | 12/12 | chr14 | TogoVar | |||||||
MLLT1_chr19_6205381_6284975 | 6238827 | C | CAAACGCC others(30): Show |
intron_variant | MODIFIER | HG02145.hp1 HG03579.hp1 NA19004.hp1 |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0012a0003c0008t0001 | a0001c0001t0012g0200 a0001c0001t0012g0201 a0003c0008t0001g0156 |
3 | 284 | 0.0106 | 37 | c.277 others(54): Show |
MLLT1 | ENSG00000130382.9 | transcript | ENST00000252674.9 | protein_coding | 3/11 | chr19 | TogoVar | |||||||
MLPH_chr2_237482251_237560322 | 237543405 | G | GGAGGGGA others(30): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0013 | a0013c0017 | a0013c0017t0010 | a0013c0017t0010g0250 | 1 | 251 | 0.0040 | 37 | c.153 others(54): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237543613 | G | GGGCACGG others(30): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0026 | a0026c0051 | a0026c0051t0001 | a0026c0051t0001g0074 | 1 | 263 | 0.0038 | 37 | c.153 others(54): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237543750 | T | TTGGGGGA others(30): Show |
intron_variant | MODIFIER | HG01358.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0135 | 1 | 248 | 0.0040 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | chr2 | TogoVar | |||||||
MLPH_chr2_237482251_237560322 | 237543806 | G | GGCACAGT others(30): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0140 | 1 | 255 | 0.0039 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | chr2 | TogoVar | |||||||
MLPH_chr2_237482251_237560322 | 237543922 | T | TGGGGGGA others(30): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0005 | a0005c0004 | a0005c0004t0001 | a0005c0004t0001g0022 | 1 | 228 | 0.0044 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237544076 | T | TGGGGGGA others(30): Show |
intron_variant | MODIFIER | HG02071.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0231 | 1 | 231 | 0.0043 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237544145 | T | TGGGGACA others(30): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02257.hp2 NA18906.hp1 others(1): Show |
a0002a0003a0028others(1): Show | a0002c0044a0003c0052a0028c0041others(1): Show | a0002c0044t0001a0003c0052t0003a0028c0041t0002others(1): Show | a0002c0044t0001g0080 a0003c0052t0003g0115 a0028c0041t0002g0265 others(1): Show |
4 | 192 | 0.0208 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237544315 | T | TGGGGGGA others(30): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0072 | 1 | 248 | 0.0040 | 37 | c.153 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MLPH_chr2_237482251_237560322 | 237544787 | T | TGGGGACA others(30): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01123.hp1 HG01167.hp2 others(37): Show |
a0001a0002a0004others(4): Show | a0001c0001a0002c0002a0002c0044others(6): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(13): Show | a0001c0001t0001g0204 a0001c0001t0002g0157 a0002c0002t0001g0044 others(37): Show |
40 | 211 | 0.1896 | 37 | c.154 others(56): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MMD2_chr7_4900998_4964187 | 4959883 | G | GGGGAGTG others(30): Show |
upstream_gene_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0044 | 1 | 273 | 0.0037 | 37 | c.-86 others(46): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 697 | chr7 | TogoVar | |||||||
MMP28_chr17_35760865_35800641 | 35786699 | C | CAAAAAAA others(30): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0217 | 1 | 163 | 0.0061 | 37 | c.112 others(54): Show |
MMP28 | ENSG00000271447.6 | transcript | ENST00000605424.6 | protein_coding | 1/7 | chr17 | TogoVar | |||||||
MND1_chr4_153339688_153420118 | 153415130 | C | CAAAAAAA others(30): Show |
downstream_gene_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0257 | 1 | 340 | 0.0029 | 37 | c.*27 others(46): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 13 | chr4 | TogoVar | |||||||
MNS1_chr15_56423724_56470137 | 56460009 | A | AAAAAAAA others(30): Show |
intron_variant | MODIFIER | HG02015.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 168 | 0.0060 | 37 | c.226 others(54): Show |
MNS1 | ENSG00000138587.6 | transcript | ENST00000260453.4 | protein_coding | 2/9 | chr15 | TogoVar | |||||||
MNS1_chr15_56423724_56470137 | 56460009 | A | AAAAAAAA others(30): Show |
intron_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0210 | 1 | 168 | 0.0060 | 37 | c.226 others(54): Show |
MNS1 | ENSG00000138587.6 | transcript | ENST00000260453.4 | protein_coding | 2/9 | chr15 | TogoVar |