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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CPNE8_chr12_38647203_38910591 | 38808756 | TAATAA | T | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp2 HG01071.hp1 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105others(28): Show | 31 | 342 | 0.0906 | -5 | c.407 others(24): Show |
CPNE8 | ENSG00000139117.14 | transcript | ENST00000331366.10 | protein_coding | 6/19 | chr12 | TogoVar | ||||||
CPNE8_chr12_38647203_38910591 | 38897664 | ATATAT | A | intron_variant | MODIFIER | HG01884.hp1 HG03453.hp1 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | 342 | 0.0088 | -5 | c.98+ others(20): Show |
CPNE8 | ENSG00000139117.14 | transcript | ENST00000331366.10 | protein_coding | 1/19 | chr12 | TogoVar | ||||||
CPNE8_chr12_38647203_38910591 | 38898587 | CTTAAT | C | intron_variant | MODIFIER | HG02698.hp2 HG03017.hp2 HG03239.hp1 |
a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0001a0001c0003t0011g0002a0001c0003t0011g0003 | 3 | 342 | 0.0088 | -5 | c.98+ others(20): Show |
CPNE8 | ENSG00000139117.14 | transcript | ENST00000331366.10 | protein_coding | 1/19 | chr12 | TogoVar | ||||||
CPO_chr2_206934518_206974474 | 206941142 | ATAAAC | A | intron_variant | MODIFIER | HG00323.hp2 HG01243.hp1 HG01496.hp1 |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0039a0002c0003t0001g0362 | 3 | 422 | 0.0071 | -5 | c.68+ others(20): Show |
CPO | ENSG00000144410.5 | transcript | ENST00000272852.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CPO_chr2_206934518_206974474 | 206943702 | AGATAG | A | intron_variant | MODIFIER | HG01070.hp1 NA18945.hp2 NA20129.hp2 |
a0001a0002 | a0001c0001a0001c0004a0002c0003 | a0001c0001t0001a0001c0004t0001a0002c0003t0001 | a0001c0001t0001g0278a0001c0004t0001g0130a0002c0003t0001g0334 | 3 | 422 | 0.0071 | -5 | c.68+ others(20): Show |
CPO | ENSG00000144410.5 | transcript | ENST00000272852.4 | protein_coding | 1/8 | chr2 | TogoVar | ||||||
CPPED1_chr16_12654799_12808887 | 12703733 | AAAGAG | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0006others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(52): Show | a0001c0001t0001g0138a0001c0001t0001g0168a0001c0001t0001g0188others(121): Show | 124 | 290 | 0.4276 | -5 | c.715 others(20): Show |
CPPED1 | ENSG00000103381.12 | transcript | ENST00000381774.9 | protein_coding | 3/3 | chr16 | TogoVar | ||||||
CPPED1_chr16_12654799_12808887 | 12740025 | GAAAGA | G | intron_variant | MODIFIER | HG01358.hp1 HG01975.hp2 HG02129.hp1 others(15): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0004others(3): Show | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(13): Show | a0001c0001t0001g0138a0001c0001t0004g0288a0002c0002t0001g0009others(15): Show | 18 | 290 | 0.0621 | -5 | c.290 others(24): Show |
CPPED1 | ENSG00000103381.12 | transcript | ENST00000381774.9 | protein_coding | 2/3 | chr16 | TogoVar | ||||||
CPQ_chr8_96640242_97148501 | 96651700 | ATATTT | A | intron_variant | MODIFIER | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(43): Show | 46 | 126 | 0.3651 | -5 | c.-35 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96687149 | TTTTTC | T | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
a0001a0003a0009 | a0001c0001a0001c0002a0003c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | 126 | 0.0476 | -5 | c.-35 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96687175 | TTTCTC | T | intron_variant | MODIFIER | HG01255.hp2 NA18990.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104a0001c0001t0001g0117 | 2 | 126 | 0.0159 | -5 | c.-35 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96707688 | AATGAT | A | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
a0001a0003a0009 | a0001c0001a0001c0002a0003c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | 126 | 0.0476 | -5 | c.-35 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | TogoVar | ||||||
CPQ_chr8_96640242_97148501 | 96734711 | AAAAAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
a0001a0003a0006others(2): Show | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | 126 | 0.5556 | -5 | c.-34 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96765545 | ATTTAT | A | intron_variant | MODIFIER | NA18989.hp2 NA19060.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | 126 | 0.0159 | -5 | c.-34 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96777753 | TATATA | T | intron_variant | MODIFIER | HG02257.hp1 HG03579.hp1 NA18949.hp2 others(2): Show |
a0001a0004 | a0001c0002a0004c0006 | a0001c0002t0001a0004c0006t0001 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0119others(2): Show | 5 | 126 | 0.0397 | -5 | c.-34 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | TogoVar | ||||||
CPQ_chr8_96640242_97148501 | 96779256 | GATGTT | G | intron_variant | MODIFIER | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | 126 | 0.0318 | -5 | c.-34 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96806265 | AAAATT | A | intron_variant | MODIFIER | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | 126 | 0.0318 | -5 | c.433 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | TogoVar | ||||||
CPQ_chr8_96640242_97148501 | 96945683 | TATAAA | T | intron_variant | MODIFIER | NA18522.hp2 NA19030.hp1 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | 126 | 0.0159 | -5 | c.850 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96964088 | CTTTCT | C | intron_variant | MODIFIER | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0002t0001a0001c0008t0001 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | 126 | 0.0556 | -5 | c.850 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 96976247 | CAAAAA | C | intron_variant | MODIFIER | HG00733.hp2 HG01261.hp2 HG02109.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | 126 | 0.0476 | -5 | c.961 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 97035697 | TTTGTA | T | intron_variant | MODIFIER | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(11): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | 126 | 0.7222 | -5 | c.105 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 97119328 | CAAAAA | C | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0021a0001c0002t0001g0005a0001c0002t0001g0006others(6): Show | 9 | 126 | 0.0714 | -5 | c.125 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 97123100 | TAAATA | T | intron_variant | MODIFIER | HG01081.hp2 HG02615.hp1 HG02809.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0031a0001c0001t0001g0080a0001c0002t0001g0049others(7): Show | 10 | 126 | 0.0794 | -5 | c.125 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 97123148 | TAAATA | T | intron_variant | MODIFIER | HG01081.hp2 HG01261.hp1 HG01517.hp2 others(58): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 61 | 126 | 0.4841 | -5 | c.125 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPQ_chr8_96640242_97148501 | 97123206 | AAAAAT | A | intron_variant | MODIFIER | HG02040.hp1 HG02109.hp2 HG03579.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004a0001c0007 | a0001c0002t0001a0001c0002t0002a0001c0004t0001others(1): Show | a0001c0002t0001g0060a0001c0002t0002g0039a0001c0004t0001g0107others(1): Show | 4 | 126 | 0.0318 | -5 | c.125 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CPS1_chr2_210551599_210684107 | 210674479 | AAAACC | A | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0029a0002c0002others(12): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(19): Show | a0001c0001t0003g0081a0001c0001t0003g0091a0001c0001t0003g0092others(53): Show | 56 | 340 | 0.1647 | -5 | c.410 others(22): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CPSF2_chr14_92116969_92177145 | 92157521 | AAAAAT | A | intron_variant | MODIFIER | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0094 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | 388 | 0.0129 | -5 | c.159 others(22): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
CPSF2_chr14_92116969_92177145 | 92157946 | GATAAC | G | intron_variant | MODIFIER | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0094 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | 388 | 0.0129 | -5 | c.182 others(20): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
CPSF2_chr14_92116969_92177145 | 92167770 | TTAATG | T | 3_prime_UTR_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | 388 | 0.2345 | -5 | c.*60 others(16): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6030 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||
CPSF2_chr14_92116969_92177145 | 92173438 | TATATA | T | downstream_gene_variant | MODIFIER | HG03041.hp1 HG03486.hp2 HG06807.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0042 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | 388 | 0.0103 | -5 | c.*11 others(18): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1294 | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92173440 | TATATA | T | downstream_gene_variant | MODIFIER | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0022a0001c0001t0042a0001c0001t0114others(3): Show | a0001c0001t0022g0038a0001c0001t0042g0257a0001c0001t0114g0254others(3): Show | 6 | 388 | 0.0155 | -5 | c.*11 others(18): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1296 | chr14 | TogoVar | ||||||
CPSF3_chr2_9418654_9478101 | 9459638 | CTTTTT | C | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 12 | 230 | 0.0522 | -5 | c.178 others(20): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CPSF3_chr2_9418654_9478101 | 9468619 | CTTTTT | C | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(38): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0001 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(37): Show | 41 | 230 | 0.1783 | -5 | c.185 others(22): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CPSF4L_chr17_73243449_73266880 | 73262938 | CAGAAA | C | upstream_gene_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(15): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0002 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0056others(8): Show | 18 | 398 | 0.0452 | -5 | c.-11 others(16): Show |
CPSF4L | ENSG00000187959.9 | transcript | ENST00000344935.8 | protein_coding | 1059 | chr17 | TogoVar | ||||||
CPSF4_chr7_99433943_99462373 | 99437310 | ATTTCT | A | upstream_gene_variant | MODIFIER | HG02895.hp1 HG02897.hp1 NA18963.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0002t0001g0262 | 3 | 364 | 0.0082 | -5 | c.-17 others(16): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1632 | chr7 | TogoVar | ||||||
CPSF6_chr12_69234569_69279358 | 69236391 | ATATAT | A | upstream_gene_variant | MODIFIER | HG00558.hp1 HG01069.hp1 HG01071.hp2 others(43): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0073a0001c0001t0074a0001c0002t0001others(10): Show | a0001c0001t0073g0180a0001c0001t0074g0001a0001c0002t0001g0014others(41): Show | 46 | 392 | 0.1174 | -5 | c.-32 others(16): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3177 | chr12 | TogoVar | ||||||
CPSF6_chr12_69234569_69279358 | 69275710 | TAAAAG | T | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
a0001 | a0001c0002a0001c0005 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(19): Show | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(101): Show | 123 | 392 | 0.3138 | -5 | c.*62 others(16): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1353 | chr12 | TogoVar | ||||||
CPSF7_chr11_61397729_61434975 | 61427026 | CAAAAA | C | intron_variant | MODIFIER | HG02630.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0117a0001c0001t0003g0006a0001c0001t0003g0114others(3): Show | 8 | 190 | 0.0421 | -5 | c.54+ others(20): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | TogoVar | ||||||
CPT1A_chr11_68749883_68846916 | 68803712 | AAAAAT | A | intron_variant | MODIFIER | HG00438.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(6): Show | a0001c0001t0001g0020a0001c0001t0001g0089a0001c0001t0001g0109others(18): Show | 21 | 236 | 0.0890 | -5 | c.555 others(20): Show |
CPT1A | ENSG00000110090.13 | transcript | ENST00000265641.10 | protein_coding | 5/18 | chr11 | TogoVar | ||||||
CPT1C_chr19_49686116_49718731 | 49691376 | GGGCCT | G | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | 350 | 0.0486 | -5 | c.-84 others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CPT1C_chr19_49686116_49718731 | 49708002 | CAAAAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(26): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(24): Show | 29 | 350 | 0.0829 | -5 | c.144 others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CPXCR1_chrX_88742225_88759781 | 88748322 | TTAATG | T | intron_variant | MODIFIER | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0012a0001c0001t0002g0028a0001c0001t0002g0048others(3): Show | 9 | 308 | 0.0292 | -5 | c.-11 others(22): Show |
CPXCR1 | ENSG00000147183.10 | transcript | ENST00000276127.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
CPXM2_chr10_123740639_123896807 | 123744955 | ATTTCT | A | downstream_gene_variant | MODIFIER | HG01192.hp1 HG01255.hp1 HG01346.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0003a0001c0002t0003a0001c0002t0008others(1): Show | a0001c0001t0003g0241a0001c0002t0003g0090a0001c0002t0003g0097others(10): Show | 13 | 288 | 0.0451 | -5 | c.*18 others(16): Show |
CPXM2 | ENSG00000121898.13 | transcript | ENST00000241305.4 | protein_coding | 683 | chr10 | TogoVar | ||||||
CPZ_chr4_8587765_8624752 | 8624584 | GAAAAA | G | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(41): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0006a0001c0010others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(15): Show | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0305others(29): Show | 44 | 442 | 0.0996 | -5 | c.*49 others(16): Show |
CPZ | ENSG00000109625.19 | transcript | ENST00000360986.9 | protein_coding | 4833 | chr4 | TogoVar | ||||||
CP_chr3_149167497_149226829 | 149213630 | GGGTGT | G | intron_variant | MODIFIER | HG01243.hp2 NA18990.hp1 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0108a0001c0001t0001g0347a0002c0002t0002g0276 | 3 | 376 | 0.0080 | -5 | c.147 others(20): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | TogoVar | ||||||
CR1L_chr1_207640133_207728703 | 207650538 | GAAATA | G | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
a0001a0007a0008 | a0001c0001a0001c0017a0007c0007others(1): Show | a0001c0001t0001a0001c0017t0001a0007c0007t0001others(1): Show | a0001c0001t0001g0171a0001c0017t0001g0125a0001c0017t0001g0170others(3): Show | 6 | 346 | 0.0173 | -5 | c.97+ others(20): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CR1L_chr1_207640133_207728703 | 207677307 | CAAAAA | C | intron_variant | MODIFIER | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(16): Show |
a0002a0005a0006others(2): Show | a0002c0002a0005c0005a0006c0006others(2): Show | a0002c0002t0001a0005c0005t0001a0006c0006t0001others(2): Show | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0045others(16): Show | 19 | 346 | 0.0549 | -5 | c.98- others(16): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CR1L_chr1_207640133_207728703 | 207692730 | CTACGT | C | intron_variant | MODIFIER | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
a0002a0006a0014others(2): Show | a0002c0002a0006c0006a0014c0023others(2): Show | a0002c0002t0001a0006c0006t0001a0014c0023t0001others(2): Show | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | 346 | 0.0260 | -5 | c.464 others(22): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CR1L_chr1_207640133_207728703 | 207698664 | CTTCTT | C | intron_variant | MODIFIER | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
a0014a0015 | a0014c0023a0015c0024 | a0014c0023t0001a0015c0024t0001 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | 346 | 0.0116 | -5 | c.114 others(22): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CR1_chr1_207491157_207646765 | 207623911 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
a0001a0002a0004others(13): Show | a0001c0001a0001c0021a0001c0051others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0146others(83): Show | 86 | 360 | 0.2389 | -5 | c.735 others(22): Show |
CR1 | ENSG00000203710.12 | transcript | ENST00000367049.9 | protein_coding | 45/46 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CR2_chr1_207449328_207494892 | 207486230 | CAAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0001c0031others(9): Show | a0001c0001t0001a0001c0007t0001a0001c0031t0001others(9): Show | a0001c0001t0001g0086a0001c0001t0001g0103a0001c0001t0001g0110others(19): Show | 29 | 378 | 0.0767 | -5 | c.*18 others(20): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |