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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CUL1_chr7_148693903_148806110 | 148725219 | G | GCGCACAC others(7): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(5): Show | 8 | 338 | 0.0237 | 14 | c.-16 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL1_chr7_148693903_148806110 | 148725219 | G | GCGCGCAC others(7): Show |
intron_variant | MODIFIER | HG01516.hp2 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | 338 | 0.0059 | 14 | c.-16 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL1_chr7_148693903_148806110 | 148725219 | G | GCGCGCGC others(7): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 338 | 0.0030 | 14 | c.-16 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL1_chr7_148693903_148806110 | 148769397 | T | TCACACAC others(7): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02647.hp2 HG03579.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0047others(2): Show | 5 | 338 | 0.0148 | 14 | c.108 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL1_chr7_148693903_148806110 | 148776307 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02040.hp2 NA18979.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0273a0001c0001t0001g0312 | 2 | 338 | 0.0059 | 14 | c.108 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL1_chr7_148693903_148806110 | 148778070 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02559.hp1 HG03942.hp1 NA19009.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0163a0001c0001t0001g0230 | 3 | 338 | 0.0089 | 14 | c.108 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUL3_chr2_224465150_224590363 | 224528191 | C | CTAAAGCA others(7): Show |
intron_variant | MODIFIER | NA18965.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0085 | 1 | 382 | 0.0026 | 14 | c.378 others(31): Show |
CUL3 | ENSG00000036257.14 | transcript | ENST00000264414.9 | protein_coding | 3/15 | chr2 | TogoVar | ||||||
CUL4A_chr13_113204613_113272108 | 113260211 | A | AAAAAAAA others(7): Show |
intron_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0128 | 1 | 396 | 0.0025 | 14 | c.203 others(31): Show |
CUL4A | ENSG00000139842.15 | transcript | ENST00000375440.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108006590 | C | CATATATA others(7): Show |
upstream_gene_variant | MODIFIER | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0012a0001c0002t0006others(1): Show | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0107others(16): Show | 19 | 312 | 0.0609 | 14 | c.-27 others(25): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2307 | chr11 | TogoVar | ||||||
CUL5_chr11_108003898_108112761 | 108048648 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0164 | 1 | 312 | 0.0032 | 14 | c.235 others(31): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108091695 | T | TCACACAC others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01981.hp1 HG02486.hp1 others(6): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0005a0001c0002t0006others(2): Show | a0001c0002t0003g0047a0001c0002t0005g0014a0001c0002t0006g0071others(5): Show | 9 | 312 | 0.0289 | 14 | c.144 others(33): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108111782 | T | TAGGCATG others(7): Show |
downstream_gene_variant | MODIFIER | NA18985.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117 | 1 | 312 | 0.0032 | 14 | c.*73 others(25): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4022 | chr11 | TogoVar | ||||||
CUL9_chr6_43177196_43229587 | 43177228 | G | GTTTTTTT others(7): Show |
upstream_gene_variant | MODIFIER | HG02258.hp2 NA20752.hp1 |
a0001a0002 | a0001c0010a0002c0006 | a0001c0010t0002a0002c0006t0001 | a0001c0010t0002g0008a0002c0006t0001g0049 | 2 | 276 | 0.0073 | 14 | c.-50 others(25): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4967 | chr6 | TogoVar | ||||||
CUL9_chr6_43177196_43229587 | 43191252 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03098.hp2 HG03225.hp1 NA18522.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0076a0001c0003t0001g0119a0001c0003t0001g0120 | 3 | 276 | 0.0109 | 14 | c.218 others(33): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
CUL9_chr6_43177196_43229587 | 43191481 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0080 | 1 | 276 | 0.0036 | 14 | c.218 others(33): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101853584 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0071 | 1 | 132 | 0.0076 | 14 | c.63+ others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101984077 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03098.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0008a0001c0002t0001g0032 | 2 | 132 | 0.0152 | 14 | c.175 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102003295 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0028 | 1 | 132 | 0.0076 | 14 | c.175 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102043323 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042 | 1 | 132 | 0.0076 | 14 | c.222 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102073165 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02572.hp2 HG02717.hp2 |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0127a0001c0002t0001g0008a0002c0003t0001g0130 | 3 | 132 | 0.0227 | 14 | c.301 others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102108736 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01169.hp2 HG02257.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0074others(4): Show | 7 | 132 | 0.0530 | 14 | c.564 others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102126177 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01168.hp1 HG03041.hp1 HG03486.hp1 others(1): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0024a0001c0002t0001g0077a0001c0002t0001g0078others(1): Show | 4 | 132 | 0.0303 | 14 | c.707 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102219055 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00544.hp2 HG02897.hp2 others(3): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0006a0002c0003t0001others(2): Show | a0001c0002t0001g0065a0001c0002t0006g0046a0002c0003t0001g0068others(3): Show | 6 | 132 | 0.0455 | 14 | c.125 others(35): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102222811 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00621.hp1 HG01978.hp2 others(8): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0003t0012others(1): Show | a0001c0002t0001g0043a0001c0002t0001g0047a0001c0002t0001g0060others(8): Show | 11 | 132 | 0.0833 | 14 | c.125 others(35): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101853584 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0028 | 1 | 136 | 0.0074 | 14 | c.30+ others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101984077 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03098.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0002t0001 | a0001c0001t0010g0111a0001c0002t0001g0135 | 2 | 136 | 0.0147 | 14 | c.142 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102003295 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0059 | a0001c0001t0059g0107 | 1 | 136 | 0.0074 | 14 | c.142 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102003334 | A | ACACACAC others(7): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0040 | 1 | 136 | 0.0074 | 14 | c.142 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102043323 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0125 | 1 | 136 | 0.0074 | 14 | c.189 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102073165 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02572.hp1 HG02717.hp2 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0017a0001c0002t0001a0001c0003t0004 | a0001c0001t0017g0037a0001c0002t0001g0135a0001c0003t0004g0034 | 3 | 136 | 0.0221 | 14 | c.268 others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102108736 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01169.hp2 HG02257.hp1 others(5): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0003c0015others(2): Show | a0001c0001t0011a0001c0001t0056a0001c0003t0035others(5): Show | a0001c0001t0011g0048a0001c0001t0056g0113a0001c0003t0035g0123others(5): Show | 8 | 136 | 0.0588 | 14 | c.531 others(31): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102126177 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01168.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0012others(1): Show | a0001c0001t0010a0001c0001t0020a0001c0002t0001others(2): Show | a0001c0001t0010g0045a0001c0001t0020g0044a0001c0002t0001g0035others(2): Show | 5 | 136 | 0.0368 | 14 | c.674 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102219055 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00544.hp2 HG02897.hp2 others(4): Show |
a0001a0004 | a0001c0002a0001c0013a0004c0011 | a0001c0002t0001a0001c0002t0070a0001c0002t0072others(2): Show | a0001c0002t0001g0100a0001c0002t0001g0104a0001c0002t0001g0115others(4): Show | 7 | 136 | 0.0515 | 14 | c.313 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102222811 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00621.hp1 HG01123.hp1 others(9): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0026a0001c0002t0001a0001c0002t0024others(3): Show | a0001c0001t0026g0130a0001c0002t0001g0014a0001c0002t0001g0018others(9): Show | 12 | 136 | 0.0882 | 14 | c.313 others(33): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111134612 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0049 | 1 | 100 | 0.0100 | 14 | c.64- others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111134616 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0026 | 1 | 100 | 0.0100 | 14 | c.64- others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111134620 | C | CTCTGTGT others(7): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02486.hp2 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0038a0001c0005t0001g0039 | 2 | 100 | 0.0200 | 14 | c.64- others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111137364 | T | TTGTTGTT others(7): Show |
intron_variant | MODIFIER | HG02572.hp2 HG03471.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0001 | a0001c0001t0003g0045a0001c0004t0001g0005 | 2 | 100 | 0.0200 | 14 | c.64- others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111328972 | T | TCTCTCTC others(7): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0095 | 1 | 100 | 0.0100 | 14 | c.292 others(33): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111330716 | T | TATATACA others(7): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0006 | a0006c0020 | a0006c0020t0001 | a0006c0020t0001g0020 | 1 | 100 | 0.0100 | 14 | c.292 others(33): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUZD1_chr10_122827158_122850857 | 122843806 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | NA18948.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0051 | 1 | 422 | 0.0024 | 14 | c.82+ others(29): Show |
CUZD1 | ENSG00000138161.14 | transcript | ENST00000392790.6 | protein_coding | 1/8 | chr10 | TogoVar | ||||||
CWC27_chr5_64763930_65023750 | 64776068 | C | CGAGAGAG others(7): Show |
intron_variant | MODIFIER | HG01516.hp2 HG02055.hp1 HG02109.hp1 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0002 | a0001c0003t0001g0098a0001c0003t0002g0227a0001c0003t0002g0233 | 3 | 260 | 0.0115 | 14 | c.139 others(31): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64850225 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02559.hp1 HG02897.hp1 others(1): Show |
a0002a0003 | a0002c0002a0002c0006a0003c0008 | a0002c0002t0002a0002c0006t0002a0003c0008t0002 | a0002c0002t0002g0079a0002c0002t0002g0108a0002c0006t0002g0064others(1): Show | 4 | 260 | 0.0154 | 14 | c.939 others(33): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64878470 | T | TAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0050 | 1 | 260 | 0.0039 | 14 | c.939 others(31): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64885698 | G | GGGGTGTG others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01192.hp2 HG01515.hp2 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0001a0001c0005t0001 | a0001c0003t0001g0207a0001c0003t0001g0215a0001c0005t0001g0203 | 3 | 260 | 0.0115 | 14 | c.104 others(31): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64885698 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(36): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0133others(36): Show | 39 | 260 | 0.1500 | 14 | c.104 others(31): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64905200 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02257.hp2 HG02486.hp2 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0242a0002c0002t0002g0092a0002c0002t0002g0107 | 3 | 260 | 0.0115 | 14 | c.104 others(35): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64924956 | G | GACACACA others(7): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0011 | 1 | 260 | 0.0039 | 14 | c.104 others(35): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 65004891 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 260 | 0.0039 | 14 | c.125 others(35): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWF19L1_chr10_100227298_100272638 | 100228993 | G | GCACACAC others(7): Show |
downstream_gene_variant | MODIFIER | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(18): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0008 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0022others(16): Show | 21 | 364 | 0.0577 | 14 | c.*42 others(25): Show |
CWF19L1 | ENSG00000095485.18 | transcript | ENST00000354105.10 | protein_coding | 3304 | chr10 | TogoVar |