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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MUC4_chr3_195741771_195816929 | 195786583 | GGAAGAGG others(41): Show |
G | disruptive_inframe_deletion | MODERATE | NA19070.hp1 | a0065 | a0065c0196 | a0065c0196t0003 | a0065c0196t0003g0208 | 1 | 249 | 0.0040 | -48 | c.494 others(57): Show |
p.His others(15): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 2/25 | 5108/16756 | 4949/16239 | 1650/5412 | chr3 | TogoVar | ||
MUC4_chr3_195741771_195816929 | 195786647 | GACCTGTG others(41): Show |
G | conservative_inframe_deletion | MODERATE | HG01361.hp2 | a0176 | a0176c0037 | a0176c0037t0002 | a0176c0037t0002g0197 | 1 | 249 | 0.0040 | -48 | c.488 others(57): Show |
p.Asp others(15): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 2/25 | 5044/16756 | 4885/16239 | 1629/5412 | chr3 | TogoVar | ||
MUC4_chr3_195741771_195816929 | 195788495 | CGGTGACA others(41): Show |
C | conservative_inframe_deletion | MODERATE | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(7): Show |
a0011a0034a0035others(5): Show | a0011c0008a0011c0028a0034c0152others(6): Show | a0011c0008t0001a0011c0028t0001a0034c0152t0014others(6): Show | a0011c0008t0001g0058a0011c0008t0001g0059a0011c0028t0001g0057others(7): Show | 10 | 249 | 0.0402 | -48 | c.303 others(57): Show |
p.Ser others(15): Show |
MUC4 | ENSG00000145113.22 | transcript | ENST00000463781.8 | protein_coding | 2/25 | 3196/16756 | 3037/16239 | 1013/5412 | chr3 | TogoVar | ||
MXRA8_chr1_1347691_1363555 | 1350955 | CTGGACGG others(41): Show |
C | downstream_gene_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0003 | 1 | 338 | 0.0030 | -48 | c.*26 others(59): Show |
MXRA8 | ENSG00000162576.17 | transcript | ENST00000309212.11 | protein_coding | 1735 | chr1 | TogoVar | ||||||
MYDGF_chr19_4652545_4675342 | 4672111 | TTATATAT others(41): Show |
T | upstream_gene_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 410 | 0.0024 | -48 | c.-18 others(59): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1770 | chr19 | TogoVar | ||||||
MYDGF_chr19_4652545_4675342 | 4672249 | ATATTCAT others(41): Show |
A | upstream_gene_variant | MODIFIER | HG01243.hp1 HG02015.hp2 HG02451.hp1 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0084a0002c0002t0002g0086a0002c0002t0002g0087others(4): Show | 7 | 410 | 0.0171 | -48 | c.-19 others(59): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1908 | chr19 | TogoVar | ||||||
MYDGF_chr19_4652545_4675342 | 4672301 | ATTCATAT others(41): Show |
A | upstream_gene_variant | MODIFIER | NA18964.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0120 | 1 | 410 | 0.0024 | -48 | c.-20 others(59): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1960 | chr19 | TogoVar | ||||||
MYL10_chr7_101608330_101634296 | 101609727 | CCCTTCCT others(41): Show |
C | downstream_gene_variant | MODIFIER | HG02818.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0034a0002c0003t0001g0062a0002c0003t0001g0063 | 4 | 398 | 0.0101 | -48 | c.*37 others(59): Show |
MYL10 | ENSG00000106436.8 | transcript | ENST00000223167.5 | protein_coding | 3602 | chr7 | TogoVar | ||||||
MYMK_chr9_133509586_133529959 | 133512124 | GTATATGT others(41): Show |
G | downstream_gene_variant | MODIFIER | HG02723.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0053a0001c0001t0002g0089a0001c0001t0002g0106others(2): Show | 5 | 456 | 0.0110 | -48 | c.*24 others(59): Show |
MYMK | ENSG00000187616.5 | transcript | ENST00000339996.4 | protein_coding | 2461 | chr9 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108997318 | AAGAAAGA others(41): Show |
A | intron_variant | MODIFIER | NA18964.hp1 NA18969.hp1 NA18989.hp1 others(4): Show |
a0001a0008a0014others(1): Show | a0001c0002a0008c0058a0014c0056others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0017others(3): Show | a0001c0002t0001g0142a0001c0002t0002g0027a0001c0002t0002g0101others(4): Show | 7 | 152 | 0.0461 | -48 | c.244 others(67): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
MYO18B_chr22_25737188_26036045 | 25999524 | CTCCCCCT others(41): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG02486.hp1 HG02622.hp2 others(7): Show |
a0004a0006a0029others(5): Show | a0004c0073a0006c0062a0006c0093others(7): Show | a0004c0073t0001a0006c0062t0001a0006c0093t0001others(7): Show | a0004c0073t0001g0226a0006c0062t0001g0228a0006c0093t0001g0098others(7): Show | 10 | 228 | 0.0439 | -48 | c.628 others(67): Show |
MYO18B | ENSG00000133454.16 | transcript | ENST00000335473.12 | protein_coding | 40/43 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
MYO3B_chr2_170173147_170660167 | 170649358 | TATATTAT others(41): Show |
T | intron_variant | MODIFIER | HG03490.hp2 HG03492.hp1 |
a0003a0005 | a0003c0003a0005c0012 | a0003c0003t0003a0005c0012t0003 | a0003c0003t0003g0048a0005c0012t0003g0158 | 2 | 174 | 0.0115 | -48 | c.373 others(67): Show |
MYO3B | ENSG00000071909.19 | transcript | ENST00000408978.9 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MYO5C_chr15_52187322_52300804 | 52294413 | TGGAGATG others(41): Show |
T | intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0002 | a0002c0002t0035 | a0002c0002t0035g0105 | 1 | 360 | 0.0028 | -48 | c.27+ others(63): Show |
MYO5C | ENSG00000128833.13 | transcript | ENST00000261839.12 | protein_coding | 1/40 | chr15 | TogoVar | ||||||
MYO7B_chr2_127530683_127642726 | 127632734 | AGTCCATG others(41): Show |
A | intron_variant | MODIFIER | HG03209.hp1 | a0022 | a0022c0064 | a0022c0064t0002 | a0022c0064t0002g0140 | 1 | 282 | 0.0036 | -48 | c.540 others(65): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MYO9A_chr15_71817291_72123150 | 71925149 | TCACATAT others(41): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(247): Show |
a0001a0002a0004others(19): Show | a0001c0001a0001c0002a0001c0011others(26): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(66): Show | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0114others(247): Show | 250 | 308 | 0.8117 | -48 | c.256 others(67): Show |
MYO9A | ENSG00000066933.17 | transcript | ENST00000356056.10 | protein_coding | 18/41 | chr15 | TogoVar | ||||||
MYO9A_chr15_71817291_72123150 | 72101465 | GGCGGGGT others(41): Show |
G | intron_variant | MODIFIER | HG00597.hp1 NA18989.hp1 |
a0002 | a0002c0003 | a0002c0003t0003a0002c0003t0009 | a0002c0003t0003g0252a0002c0003t0009g0240 | 2 | 308 | 0.0065 | -48 | c.-72 others(67): Show |
MYO9A | ENSG00000066933.17 | transcript | ENST00000356056.10 | protein_coding | 1/41 | chr15 | TogoVar | ||||||
MYOF_chr10_93301429_93487334 | 93334348 | GCTGAAAG others(41): Show |
G | intron_variant | MODIFIER | HG01081.hp1 HG01109.hp2 HG01891.hp1 others(3): Show |
a0001 | a0001c0002a0001c0004a0001c0005others(1): Show | a0001c0002t0001a0001c0004t0003a0001c0005t0001others(1): Show | a0001c0002t0001g0007a0001c0002t0001g0037a0001c0004t0003g0233others(3): Show | 6 | 240 | 0.0250 | -48 | c.456 others(65): Show |
MYOF | ENSG00000138119.17 | transcript | ENST00000359263.9 | protein_coding | 41/53 | chr10 | TogoVar | ||||||
MYOM2_chr8_2040046_2150456 | 2055087 | GAAGTACC others(41): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
a0001a0002a0003others(49): Show | a0001c0002a0001c0003a0001c0009others(100): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(115): Show | a0001c0002t0001g0216a0001c0002t0001g0220a0001c0002t0001g0282others(192): Show | 196 | 403 | 0.4864 | -48 | c.264 others(65): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 3/36 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
MYOM2_chr8_2040046_2150456 | 2085544 | CCCACTGT others(41): Show |
C | intron_variant | MODIFIER | HG01261.hp2 HG01516.hp2 HG02523.hp1 others(7): Show |
a0001a0002a0005others(4): Show | a0001c0003a0002c0006a0002c0048others(6): Show | a0001c0003t0001a0001c0003t0004a0002c0006t0001others(7): Show | a0001c0003t0001g0251a0001c0003t0004g0252a0002c0006t0001g0006others(7): Show | 10 | 403 | 0.0248 | -48 | c.164 others(65): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 14/36 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
MYOM2_chr8_2040046_2150456 | 2086230 | CCCCCACT others(41): Show |
C | intron_variant | MODIFIER | HG01123.hp2 HG04228.hp2 NA18983.hp1 |
a0001a0013 | a0001c0003a0013c0074 | a0001c0003t0001a0013c0074t0001 | a0001c0003t0001g0032a0001c0003t0001g0188a0013c0074t0001g0335 | 3 | 403 | 0.0074 | -48 | c.164 others(65): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 14/36 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
MYOM2_chr8_2040046_2150456 | 2100109 | TTTCTTTC others(41): Show |
T | intron_variant | MODIFIER | HG03130.hp2 | a0038 | a0038c0131 | a0038c0131t0001 | a0038c0131t0001g0045 | 1 | 403 | 0.0025 | -48 | c.244 others(65): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 19/36 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
MYRFL_chr12_69820227_69964097 | 69891589 | CTTTCTTT others(41): Show |
C | intron_variant | MODIFIER | HG00741.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0005 | a0001c0001t0003a0001c0003t0001a0002c0005t0002 | a0001c0001t0003g0248a0001c0003t0001g0152a0001c0003t0001g0153others(2): Show | 5 | 322 | 0.0155 | -48 | c.903 others(63): Show |
MYRFL | ENSG00000166268.11 | transcript | ENST00000552032.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
MYT1L_chr2_1784113_2336275 | 1829254 | TTCCCATA others(41): Show |
T | intron_variant | MODIFIER | HG02257.hp2 HG02717.hp2 |
a0001 | a0001c0013a0001c0025 | a0001c0013t0019a0001c0025t0005 | a0001c0013t0019g0065a0001c0025t0005g0019 | 2 | 104 | 0.0192 | -48 | c.308 others(67): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 21/24 | chr2 | TogoVar | ||||||
MYT1L_chr2_1784113_2336275 | 1842866 | AGCTTCCG others(41): Show |
A | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0073 | 1 | 104 | 0.0096 | -48 | c.277 others(67): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 19/24 | chr2 | TogoVar | ||||||
MYT1L_chr2_1784113_2336275 | 2004972 | ATGCCTTC others(41): Show |
A | intron_variant | MODIFIER | HG02559.hp2 HG03225.hp2 |
a0001 | a0001c0005a0001c0012 | a0001c0005t0002a0001c0012t0004 | a0001c0005t0002g0076a0001c0012t0004g0005 | 2 | 104 | 0.0192 | -48 | c.-15 others(67): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 4/24 | chr2 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64212162 | AGTGGGGG others(41): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0071a0001c0001t0001g0175a0001c0001t0002g0155others(35): Show | 39 | 223 | 0.1749 | -48 | c.151 others(64): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
MYT1_chr20_64159452_64247253 | 64235172 | ATGTGACC others(41): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(29): Show | a0001c0001t0002g0142a0001c0001t0002g0214a0001c0001t0003g0008others(118): Show | 122 | 223 | 0.5471 | -48 | c.289 others(67): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
MYT1_chr20_64159452_64247253 | 64235729 | TGGCTGGC others(41): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp2 HG01175.hp2 others(20): Show |
a0001 | a0001c0002a0001c0017 | a0001c0002t0002a0001c0002t0005a0001c0002t0018others(1): Show | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0032others(19): Show | 23 | 223 | 0.1031 | -48 | c.289 others(65): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
MYT1_chr20_64159452_64247253 | 64236027 | CGGTGGGT others(41): Show |
C | intron_variant | MODIFIER | HG01346.hp2 HG03540.hp2 HG04199.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0146a0001c0002t0002g0178a0001c0002t0002g0184 | 3 | 223 | 0.0135 | -48 | c.289 others(65): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
MYT1_chr20_64159452_64247253 | 64236267 | TGGTGGGT others(41): Show |
T | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0155 | 1 | 223 | 0.0045 | -48 | c.289 others(65): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
MYZAP_chr15_57586904_57690364 | 57624391 | CCCCATTT others(41): Show |
C | intron_variant | MODIFIER | NA18975.hp1 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0070 | 1 | 352 | 0.0028 | -48 | c.412 others(65): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
NAALADL2_chr3_174854334_175815548 | 175131844 | GGACGGGG others(41): Show |
G | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01074.hp2 others(42): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0013a0002c0005others(17): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0030others(42): Show | a0001c0001t0002g0012a0001c0001t0012g0031a0001c0001t0030g0030others(42): Show | 45 | 64 | 0.7031 | -48 | c.545 others(67): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NAP1L5_chr4_88690913_88702829 | 88698076 | GTAGCTGC others(41): Show |
G | upstream_gene_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 414 | 0.0024 | -48 | c.-37 others(57): Show |
NAP1L5 | ENSG00000177432.8 | transcript | ENST00000323061.7 | protein_coding | 248 | chr4 | TogoVar | ||||||
NAP1L5_chr4_88690913_88702829 | 88698989 | TTTCCTCA others(41): Show |
T | upstream_gene_variant | MODIFIER | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(31): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0000a0001c0001t0003g0000a0001c0002t0001g0000 | 34 | 414 | 0.0821 | -48 | c.-12 others(59): Show |
NAP1L5 | ENSG00000177432.8 | transcript | ENST00000323061.7 | protein_coding | 1161 | chr4 | TogoVar | ||||||
NARF_chr17_82453741_82495537 | 82468274 | GTACTGTA others(41): Show |
G | intron_variant | MODIFIER | NA18961.hp2 NA19060.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0043 | 2 | 356 | 0.0056 | -48 | c.253 others(63): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NAV1_chr1_201534127_201831969 | 201756794 | CTCTTTCT others(41): Show |
C | intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0026 | a0001c0026t0069 | a0001c0026t0069g0169 | 1 | 210 | 0.0048 | -48 | c.208 others(69): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NAV3_chr12_77825894_78218010 | 78142689 | ATATACAT others(41): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG01192.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(11): Show | a0001c0001t0002g0139a0001c0001t0005g0040a0001c0001t0005g0072others(16): Show | 19 | 186 | 0.1022 | -48 | c.468 others(67): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 20/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NBEA_chr13_34937270_35677736 | 35355173 | CTCACTTG others(41): Show |
C | intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031 | 1 | 122 | 0.0082 | -48 | c.617 others(67): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 38/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
NBPF8_chr1_120410035_120474676 | 120431321 | AATATATA others(41): Show |
A | intron_variant | MODIFIER | HG01099.hp2 HG01106.hp2 HG01169.hp2 others(13): Show |
a0001a0012 | a0001c0002a0001c0010a0001c0011others(2): Show | a0001c0002t0002a0001c0002t0008a0001c0010t0032others(5): Show | a0001c0002t0002g0001a0001c0002t0002g0014a0001c0002t0002g0020others(12): Show | 16 | 292 | 0.0548 | -48 | c.-29 others(67): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6504176 | TATATACA others(41): Show |
T | intron_variant | MODIFIER | HG01243.hp1 HG02886.hp1 HG03195.hp2 others(3): Show |
a0001 | a0001c0004a0001c0031a0001c0033 | a0001c0004t0001a0001c0004t0004a0001c0004t0011others(2): Show | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0004g0194others(3): Show | 6 | 432 | 0.0139 | -48 | c.128 others(65): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD3_chr11_134145113_134228967 | 134154531 | CGGGTGGT others(41): Show |
C | intron_variant | MODIFIER | HG01081.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0035 | 1 | 370 | 0.0027 | -48 | c.425 others(67): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 32/34 | chr11 | TogoVar | ||||||
NCBP2L_chrX_107772733_107800829 | 107782214 | TATATATA others(41): Show |
T | intron_variant | MODIFIER | HG02486.hp1 HG06807.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0033a0001c0002t0002g0035 | 2 | 303 | 0.0066 | -48 | c.-73 others(65): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107782252 | TATATATA others(41): Show |
T | intron_variant | MODIFIER | HG02622.hp1 HG03486.hp2 HG03540.hp1 |
a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0226a0001c0002t0005g0227a0001c0002t0005g0228 | 3 | 303 | 0.0099 | -48 | c.-73 others(65): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107782278 | TATATATA others(41): Show |
T | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0098 | 1 | 303 | 0.0033 | -48 | c.-73 others(65): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36872623 | TTGGAGGT others(41): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
a0001a0003a0004 | a0001c0001a0001c0004a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(171): Show | 235 | 434 | 0.5415 | -48 | c.627 others(63): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867085 | TTTCTTTC others(41): Show |
T | intron_variant | MODIFIER | NA21309.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0180 | 1 | 232 | 0.0043 | -48 | c.-19 others(65): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867089 | TTTCTTTC others(41): Show |
T | intron_variant | MODIFIER | HG00544.hp2 HG02135.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | 232 | 0.0086 | -48 | c.-19 others(65): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCOA6_chr20_34709774_34830651 | 34817161 | ATGTATAT others(41): Show |
A | intron_variant | MODIFIER | HG01070.hp1 NA19068.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103a0001c0001t0001g0153 | 2 | 290 | 0.0069 | -48 | c.-16 others(67): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 1/14 | chr20 | TogoVar | ||||||
NCOR2_chr12_124319415_124572612 | 124333808 | GTGCCTGT others(41): Show |
G | intron_variant | MODIFIER | HG03209.hp1 | a0003 | a0003c0072 | a0003c0072t0062 | a0003c0072t0062g0136 | 1 | 234 | 0.0043 | -48 | c.660 others(65): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 43/48 | chr12 | TogoVar | ||||||
NCOR2_chr12_124319415_124572612 | 124373796 | AATCATGA others(41): Show |
A | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(67): Show |
a0001a0002a0003others(15): Show | a0001c0005a0001c0009a0001c0022others(46): Show | a0001c0005t0002a0001c0005t0003a0001c0005t0008others(64): Show | a0001c0005t0002g0099a0001c0005t0002g0100a0001c0005t0003g0186others(67): Show | 70 | 234 | 0.2992 | -48 | c.221 others(65): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar |