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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARL8B_chr3_5117292_5185911 | 5162987 | C | CTTTT | intron_variant | MODIFIER | HG02257.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011a0001c0001t0012 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0096others(3): Show | 6 | 304 | 0.0197 | 4 | c.124 others(21): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARL8B_chr3_5117292_5185911 | 5169305 | T | TTGTG | intron_variant | MODIFIER | HG02280.hp2 NA18941.hp1 NA18984.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0022 | a0001c0001t0001g0083a0001c0001t0001g0106a0001c0001t0002g0295others(1): Show | 4 | 304 | 0.0132 | 4 | c.124 others(21): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARL8B_chr3_5117292_5185911 | 5173713 | T | TCAAA | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0118a0001c0001t0001g0154a0001c0001t0001g0177others(23): Show | 26 | 304 | 0.0855 | 4 | c.373 others(19): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARL9_chr4_56500791_56529453 | 56502496 | C | CATAT | upstream_gene_variant | MODIFIER | HG01361.hp1 HG01993.hp1 HG02040.hp1 others(34): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0035others(19): Show | 37 | 416 | 0.0889 | 4 | c.-33 others(15): Show |
ARL9 | ENSG00000196503.5 | transcript | ENST00000640821.3 | protein_coding | 3294 | chr4 | TogoVar | ||||||
ARL9_chr4_56500791_56529453 | 56506786 | T | TTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00738.hp1 others(22): Show |
a0001a0003 | a0001c0001a0001c0014a0003c0007 | a0001c0001t0001a0001c0001t0008a0001c0014t0001others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0042others(15): Show | 25 | 416 | 0.0601 | 4 | c.279 others(19): Show |
ARL9 | ENSG00000196503.5 | transcript | ENST00000640821.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARL9_chr4_56500791_56529453 | 56506786 | T | TTTTG | intron_variant | MODIFIER | HG00438.hp2 HG01256.hp2 HG01361.hp1 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0001others(2): Show | a0001c0001t0001g0238a0002c0002t0001g0098a0002c0002t0001g0099others(8): Show | 13 | 416 | 0.0313 | 4 | c.279 others(19): Show |
ARL9 | ENSG00000196503.5 | transcript | ENST00000640821.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARMC10_chr7_103070140_103104759 | 103103946 | G | GGTGT | downstream_gene_variant | MODIFIER | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0019 | 4 | 390 | 0.0103 | 4 | c.*53 others(15): Show |
ARMC10 | ENSG00000170632.14 | transcript | ENST00000323716.8 | protein_coding | 4188 | chr7 | TogoVar | ||||||
ARMC12_chr6_35732032_35754079 | 35742496 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0040others(25): Show | 36 | 438 | 0.0822 | 4 | c.444 others(21): Show |
ARMC12 | ENSG00000157343.9 | transcript | ENST00000373866.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC1_chr8_65597458_65639177 | 65601030 | G | GAAAA | downstream_gene_variant | MODIFIER | HG00408.hp1 HG01109.hp2 HG01346.hp1 others(24): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0002t0002others(5): Show | a0001c0001t0005g0300a0001c0001t0005g0308a0001c0001t0006g0035others(23): Show | 27 | 390 | 0.0692 | 4 | c.*33 others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1427 | chr8 | TogoVar | ||||||
ARMC1_chr8_65597458_65639177 | 65609872 | A | AAAAG | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(88): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0022a0001c0001t0023others(2): Show | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(73): Show | 91 | 390 | 0.2333 | 4 | c.465 others(21): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | TogoVar | ||||||
ARMC1_chr8_65597458_65639177 | 65609879 | A | AAAAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(19): Show | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(228): Show | 279 | 390 | 0.7154 | 4 | c.465 others(21): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | TogoVar | ||||||
ARMC1_chr8_65597458_65639177 | 65623786 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0022a0001c0002t0003 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0025others(31): Show | 44 | 390 | 0.1128 | 4 | c.184 others(21): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | TogoVar | ||||||
ARMC2_chr6_108843422_108979476 | 108857602 | C | CTCTT | intron_variant | MODIFIER | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0007 | a0001c0001t0005g0089a0001c0001t0005g0090a0001c0001t0007g0088 | 3 | 290 | 0.0103 | 4 | c.219 others(19): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108880777 | C | CTCCT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0001c0006others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 253 | 290 | 0.8724 | 4 | c.671 others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108885227 | G | GGTGT | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101others(20): Show | 23 | 290 | 0.0793 | 4 | c.671 others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108901098 | A | ATTTT | intron_variant | MODIFIER | HG01106.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0003a0004c0005t0001 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0072others(6): Show | 9 | 290 | 0.0310 | 4 | c.847 others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108910826 | A | ATGTT | intron_variant | MODIFIER | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0265a0002c0002t0001g0267a0002c0002t0001g0268others(21): Show | 24 | 290 | 0.0828 | 4 | c.102 others(19): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108923383 | A | AGTGG | intron_variant | MODIFIER | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0148a0001c0001t0001g0205a0001c0001t0001g0206others(24): Show | 27 | 290 | 0.0931 | 4 | c.135 others(23): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108923618 | C | CTTTT | intron_variant | MODIFIER | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0265a0002c0002t0001g0267a0002c0002t0001g0268others(21): Show | 24 | 290 | 0.0828 | 4 | c.135 others(23): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108932516 | C | CTTTT | intron_variant | MODIFIER | HG00597.hp1 HG01358.hp1 HG01952.hp1 others(27): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(2): Show | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0093others(27): Show | 30 | 290 | 0.1035 | 4 | c.149 others(23): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108936246 | T | TTTTG | intron_variant | MODIFIER | HG02572.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0069a0001c0001t0001g0202a0001c0001t0002g0068others(1): Show | 4 | 290 | 0.0138 | 4 | c.149 others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC2_chr6_108843422_108979476 | 108938599 | C | CTTTT | intron_variant | MODIFIER | HG01243.hp2 HG01358.hp2 HG01981.hp2 others(11): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0130others(11): Show | 14 | 290 | 0.0483 | 4 | c.159 others(23): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 22952717 | C | CAAGA | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(19): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0004t0001others(5): Show | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0002t0002g0285others(19): Show | 22 | 302 | 0.0729 | 4 | c.167 others(21): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 23018514 | A | ATTTT | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp1 HG01257.hp1 others(22): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0002a0002c0003t0001a0002c0003t0005 | a0001c0002t0002g0131a0001c0002t0002g0132a0001c0002t0002g0287others(22): Show | 25 | 302 | 0.0828 | 4 | c.204 others(23): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 23024391 | C | CAGAT | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0087a0001c0004t0003g0106a0001c0004t0003g0108others(1): Show | 4 | 302 | 0.0133 | 4 | c.204 others(23): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 23024391 | C | CATAT | intron_variant | MODIFIER | HG01884.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
a0001a0002 | a0001c0002a0001c0004a0002c0003 | a0001c0002t0002a0001c0004t0002a0002c0003t0005 | a0001c0002t0002g0009a0001c0002t0002g0079a0001c0002t0002g0131others(6): Show | 9 | 302 | 0.0298 | 4 | c.204 others(23): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 23024393 | C | CATAG | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(2): Show | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0001g0196others(19): Show | 22 | 302 | 0.0729 | 4 | c.204 others(23): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ARMC3_chr10_22923053_23043523 | 23042370 | C | CGTGT | downstream_gene_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(4): Show | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0048others(89): Show | 92 | 302 | 0.3046 | 4 | c.*48 others(15): Show |
ARMC3 | ENSG00000165309.14 | transcript | ENST00000298032.10 | protein_coding | 3848 | chr10 | TogoVar | ||||||
ARMC5_chr16_31454501_31472165 | 31454873 | A | AAAAT | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01256.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0018a0001c0025others(1): Show | a0001c0001t0001a0001c0018t0001a0001c0025t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(5): Show | 14 | 418 | 0.0335 | 4 | c.-46 others(15): Show |
ARMC5 | ENSG00000140691.18 | transcript | ENST00000268314.9 | protein_coding | 4627 | chr16 | TogoVar | ||||||
ARMC5_chr16_31454501_31472165 | 31455042 | A | AACAC | upstream_gene_variant | MODIFIER | HG01891.hp1 HG02080.hp1 HG02486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002a0001c0002t0001g0005 | 5 | 418 | 0.0120 | 4 | c.-44 others(15): Show |
ARMC5 | ENSG00000140691.18 | transcript | ENST00000268314.9 | protein_coding | 4458 | chr16 | TogoVar | ||||||
ARMC5_chr16_31454501_31472165 | 31460678 | C | CAATG | intron_variant | MODIFIER | HG02630.hp2 HG02723.hp2 NA19030.hp1 |
a0001 | a0001c0008 | a0001c0008t0003 | a0001c0008t0003g0018 | 3 | 418 | 0.0072 | 4 | c.475 others(19): Show |
ARMC5 | ENSG00000140691.18 | transcript | ENST00000268314.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ARMC6_chr19_19028603_19063176 | 19038898 | T | TACAC | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 199 | 322 | 0.6180 | 4 | c.30- others(19): Show |
ARMC6 | ENSG00000105676.14 | transcript | ENST00000535612.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARMC6_chr19_19028603_19063176 | 19045077 | C | CTCAG | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 HG01257.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002a0001c0001t0002g0046a0001c0001t0002g0110others(6): Show | 14 | 322 | 0.0435 | 4 | c.279 others(21): Show |
ARMC6 | ENSG00000105676.14 | transcript | ENST00000535612.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARMC6_chr19_19028603_19063176 | 19046927 | G | GTTTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0005a0004c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(146): Show | 185 | 322 | 0.5745 | 4 | c.279 others(21): Show |
ARMC6 | ENSG00000105676.14 | transcript | ENST00000535612.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARMC6_chr19_19028603_19063176 | 19051371 | C | CTGTG | intron_variant | MODIFIER | HG01109.hp1 HG02970.hp2 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026a0001c0001t0001g0159 | 3 | 322 | 0.0093 | 4 | c.280 others(19): Show |
ARMC6 | ENSG00000105676.14 | transcript | ENST00000535612.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARMC6_chr19_19028603_19063176 | 19051375 | C | CTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0016others(15): Show | 28 | 322 | 0.0870 | 4 | c.280 others(19): Show |
ARMC6 | ENSG00000105676.14 | transcript | ENST00000535612.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138186571 | G | GCACA | upstream_gene_variant | MODIFIER | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | 246 | 0.0285 | 4 | c.-98 others(13): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 729 | chr3 | TogoVar | ||||||
ARMC8_chr3_138182301_138303373 | 138201436 | C | CTTTT | intron_variant | MODIFIER | HG01074.hp1 HG01106.hp1 HG01516.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117a0001c0001t0001g0190a0001c0001t0001g0202others(4): Show | 7 | 246 | 0.0285 | 4 | c.46- others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138229134 | G | GTATA | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03688.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0206 | 3 | 246 | 0.0122 | 4 | c.528 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138252746 | G | GCCCC | intron_variant | MODIFIER | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0045others(45): Show | 48 | 246 | 0.1951 | 4 | c.113 others(23): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138256402 | C | CTTTT | intron_variant | MODIFIER | HG02723.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | 246 | 0.0203 | 4 | c.113 others(23): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138274233 | A | ATGTG | intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 HG02559.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0112 | 3 | 246 | 0.0122 | 4 | c.163 others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231221830 | C | CAAAA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(69): Show | 72 | 200 | 0.3600 | 4 | c.505 others(19): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231237175 | C | CGTGT | intron_variant | MODIFIER | HG01175.hp2 HG01978.hp1 HG02738.hp2 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0011a0001c0001t0029others(3): Show | a0001c0001t0001g0078a0001c0001t0001g0129a0001c0001t0011g0165others(4): Show | 7 | 200 | 0.0350 | 4 | c.780 others(21): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231237757 | A | ATATG | intron_variant | MODIFIER | HG03942.hp1 NA18951.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0002t0022 | a0001c0001t0008g0153a0001c0002t0022g0145 | 2 | 200 | 0.0100 | 4 | c.781 others(21): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231255180 | A | AACAC | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp1 HG01978.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0034a0001c0002t0002others(1): Show | a0001c0001t0001g0113a0001c0001t0034g0061a0001c0002t0002g0043others(1): Show | 4 | 200 | 0.0200 | 4 | c.880 others(21): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231272500 | G | GTGTT | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(26): Show | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0087others(38): Show | 41 | 200 | 0.2050 | 4 | c.121 others(21): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231328814 | C | CTTTT | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp2 HG01943.hp1 others(8): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0002a0001c0002t0003a0001c0002t0006others(2): Show | a0001c0002t0002g0133a0001c0002t0002g0161a0001c0002t0002g0174others(8): Show | 11 | 200 | 0.0550 | 4 | c.177 others(23): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231341640 | T | TGATA | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(43): Show | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0001g0179others(68): Show | 71 | 200 | 0.3550 | 4 | c.187 others(23): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARMC9_chr2_231193631_231381848 | 231352661 | G | GGATA | intron_variant | MODIFIER | HG00544.hp1 HG02602.hp1 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009a0001c0001t0019 | a0001c0001t0001g0099a0001c0001t0009g0176a0001c0001t0019g0067 | 3 | 200 | 0.0150 | 4 | c.199 others(23): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |