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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CUX1_chr7_101812626_102263233 | 101831734 | TTTA | T | intron_variant | MODIFIER | HG02615.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0005 | a0001c0001t0011a0001c0001t0019a0001c0003t0005others(1): Show | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0019g0001others(2): Show | 5 | 136 | 0.0368 | -3 | c.30+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101837828 | CAAA | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG01099.hp1 others(13): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0017others(10): Show | a0001c0001t0003g0036a0001c0001t0006g0009a0001c0001t0017g0037others(13): Show | 16 | 136 | 0.1177 | -3 | c.30+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101848051 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01123.hp2 HG01255.hp1 others(21): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0020others(10): Show | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0047others(21): Show | 24 | 136 | 0.1765 | -3 | c.30+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101870150 | TTTG | T | intron_variant | MODIFIER | HG01515.hp2 HG02055.hp2 HG02976.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0017a0001c0001t0060a0001c0002t0001others(2): Show | a0001c0001t0017g0037a0001c0001t0060g0064a0001c0002t0001g0035others(4): Show | 7 | 136 | 0.0515 | -3 | c.31- others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101958370 | TGCA | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(70): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0024others(111): Show | 114 | 136 | 0.8382 | -3 | c.141 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101984090 | ATAT | A | intron_variant | MODIFIER | HG01192.hp1 HG01496.hp1 HG01515.hp1 others(6): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0001a0001c0002t0012a0001c0002t0024others(4): Show | a0001c0002t0001g0093a0001c0002t0001g0098a0001c0002t0012g0032others(6): Show | 9 | 136 | 0.0662 | -3 | c.142 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 101993167 | TAAA | T | intron_variant | MODIFIER | HG02559.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0019a0001c0003t0005 | a0001c0001t0003g0036a0001c0001t0019g0001a0001c0001t0019g0006others(1): Show | 4 | 136 | 0.0294 | -3 | c.142 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102014858 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01123.hp2 HG01258.hp1 others(40): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0020others(27): Show | a0001c0001t0003g0024a0001c0001t0003g0040a0001c0001t0006g0043others(40): Show | 43 | 136 | 0.3162 | -3 | c.142 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102017429 | TCTC | T | intron_variant | MODIFIER | HG01884.hp1 HG02897.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0047a0002c0005t0013 | a0001c0001t0047g0084a0002c0005t0013g0078 | 2 | 136 | 0.0147 | -3 | c.142 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102021923 | CCTT | C | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(1): Show | a0001c0001t0003g0036a0001c0001t0017g0007a0001c0001t0019g0001others(2): Show | 5 | 136 | 0.0368 | -3 | c.142 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102065897 | TCTC | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(71): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0024others(117): Show | 120 | 136 | 0.8824 | -3 | c.190 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102076059 | ATCT | A | intron_variant | MODIFIER | HG02970.hp2 HG03041.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0002t0001 | a0001c0001t0020g0022a0001c0001t0020g0044a0001c0002t0001g0035 | 3 | 136 | 0.0221 | -3 | c.268 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102077059 | AAAG | A | intron_variant | MODIFIER | HG01123.hp2 HG01258.hp1 HG01496.hp2 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0004t0002a0001c0004t0016others(2): Show | a0001c0001t0006g0043a0001c0001t0006g0082a0001c0004t0002g0052others(4): Show | 7 | 136 | 0.0515 | -3 | c.268 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102083687 | AGAT | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0022a0001c0001t0056a0001c0002t0001others(3): Show | a0001c0001t0022g0099a0001c0001t0056g0113a0001c0002t0001g0100others(3): Show | 6 | 136 | 0.0441 | -3 | c.268 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102084266 | TTTA | T | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0022a0001c0001t0056a0001c0002t0001others(3): Show | a0001c0001t0022g0099a0001c0001t0056g0113a0001c0002t0001g0100others(3): Show | 6 | 136 | 0.0441 | -3 | c.269 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102084307 | TGTA | T | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0022a0001c0001t0056a0001c0002t0001others(3): Show | a0001c0001t0022g0099a0001c0001t0056g0113a0001c0002t0001g0100others(3): Show | 6 | 136 | 0.0441 | -3 | c.269 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102084858 | CTTT | C | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(13): Show | a0001c0001t0003g0040a0001c0001t0003g0047a0001c0001t0010g0085others(18): Show | 21 | 136 | 0.1544 | -3 | c.269 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102092934 | AAAG | A | intron_variant | MODIFIER | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(22): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0003a0001c0001t0011a0001c0001t0022others(15): Show | a0001c0001t0003g0047a0001c0001t0011g0003a0001c0001t0011g0004others(22): Show | 25 | 136 | 0.1838 | -3 | c.269 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102101914 | TAAA | T | intron_variant | MODIFIER | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0010a0001c0001t0011a0001c0001t0020others(8): Show | a0001c0001t0010g0045a0001c0001t0010g0111a0001c0001t0011g0048others(11): Show | 14 | 136 | 0.1029 | -3 | c.407 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102106079 | CTTT | C | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(27): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0020others(21): Show | a0001c0001t0003g0024a0001c0001t0003g0040a0001c0001t0010g0045others(27): Show | 30 | 136 | 0.2206 | -3 | c.530 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102151727 | CAAA | C | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(19): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0003a0003c0015others(2): Show | a0001c0001t0003a0001c0001t0047a0001c0001t0049others(12): Show | a0001c0001t0003g0008a0001c0001t0003g0024a0001c0001t0003g0040others(19): Show | 22 | 136 | 0.1618 | -3 | c.675 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102168925 | TTTC | T | intron_variant | MODIFIER | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0020others(7): Show | a0001c0001t0006g0009a0001c0001t0006g0029a0001c0001t0010g0045others(9): Show | 12 | 136 | 0.0882 | -3 | c.724 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102168930 | TTTA | T | intron_variant | MODIFIER | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0022a0001c0001t0047others(3): Show | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0048others(5): Show | 8 | 136 | 0.0588 | -3 | c.724 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102176558 | CTTT | C | intron_variant | MODIFIER | HG00639.hp2 HG01123.hp2 HG01258.hp1 others(28): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0006a0001c0003t0001a0001c0003t0004others(18): Show | a0001c0001t0006g0043a0001c0001t0006g0082a0001c0003t0001g0023others(28): Show | 31 | 136 | 0.2279 | -3 | c.829 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102177432 | AAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(17): Show |
a0001a0005a0007 | a0001c0003a0005c0010a0007c0008 | a0001c0003t0005a0001c0003t0008a0001c0003t0009others(12): Show | a0001c0003t0005g0005a0001c0003t0005g0066a0001c0003t0005g0083others(17): Show | 20 | 136 | 0.1471 | -3 | c.829 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102180016 | CGTT | C | intron_variant | MODIFIER | HG02970.hp1 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0045 | a0001c0001t0003g0047a0001c0001t0045g0041 | 2 | 136 | 0.0147 | -3 | c.101 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102186590 | TATA | T | intron_variant | MODIFIER | HG00639.hp2 HG01258.hp1 HG01496.hp2 others(21): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0006a0001c0003t0001a0001c0003t0004others(14): Show | a0001c0001t0006g0043a0001c0001t0006g0082a0001c0003t0001g0101others(21): Show | 24 | 136 | 0.1765 | -3 | c.101 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 11/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102186592 | TATA | T | intron_variant | MODIFIER | HG01123.hp2 HG01515.hp1 HG01978.hp1 others(3): Show |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0002a0001c0004t0018others(1): Show | a0001c0003t0001g0023a0001c0004t0002g0049a0001c0004t0002g0052others(3): Show | 6 | 136 | 0.0441 | -3 | c.101 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 11/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102216533 | CCCA | C | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(24): Show |
a0001a0005a0007 | a0001c0002a0001c0003a0001c0006others(2): Show | a0001c0002t0001a0001c0003t0004a0001c0003t0005others(16): Show | a0001c0002t0001g0054a0001c0003t0004g0031a0001c0003t0004g0034others(24): Show | 27 | 136 | 0.1985 | -3 | c.313 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102226620 | AGTT | A | intron_variant | MODIFIER | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0010a0001c0001t0020a0001c0001t0022others(4): Show | a0001c0001t0010g0045a0001c0001t0010g0085a0001c0001t0010g0111others(7): Show | 10 | 136 | 0.0735 | -3 | c.313 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102231025 | ATTT | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0003a0001c0001t0045a0001c0001t0048others(30): Show | a0001c0001t0003g0024a0001c0001t0003g0047a0001c0001t0045g0041others(39): Show | 42 | 136 | 0.3088 | -3 | c.343 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102243632 | AAAT | A | intron_variant | MODIFIER | HG00639.hp2 HG02055.hp2 HG02109.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0003a0001c0001t0011a0001c0001t0017others(12): Show | a0001c0001t0003g0008a0001c0001t0003g0036a0001c0001t0011g0003others(22): Show | 25 | 136 | 0.1838 | -3 | c.388 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102259759 | AAAG | A | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(67): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(52): Show | a0001c0001t0002g0105a0001c0001t0003g0047a0001c0001t0006g0009others(67): Show | 70 | 136 | 0.5147 | -3 | c.*10 others(16): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1527 | chr7 | TogoVar | ||||||
CUX2_chr12_111029165_111355554 | 111033123 | TAAC | T | upstream_gene_variant | MODIFIER | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
a0001 | a0001c0004a0001c0008a0001c0011 | a0001c0004t0001a0001c0008t0001a0001c0011t0001 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | 100 | 0.0300 | -3 | c.-10 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1041 | chr12 | TogoVar | ||||||
CUX2_chr12_111029165_111355554 | 111087366 | CAAA | C | intron_variant | MODIFIER | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(21): Show |
a0001a0005a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(21): Show | 24 | 100 | 0.2400 | -3 | c.63+ others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111087418 | TGAA | T | intron_variant | MODIFIER | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
a0001 | a0001c0004a0001c0005a0001c0014 | a0001c0004t0004a0001c0005t0001a0001c0014t0001 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | 100 | 0.0300 | -3 | c.63+ others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111125180 | ATTT | A | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(23): Show | 26 | 100 | 0.2600 | -3 | c.64- others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111142529 | GAAA | G | intron_variant | MODIFIER | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0079others(18): Show | 21 | 100 | 0.2100 | -3 | c.64- others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111175341 | CTTT | C | intron_variant | MODIFIER | HG01081.hp1 HG01169.hp1 HG01884.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(21): Show | 24 | 100 | 0.2400 | -3 | c.64- others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111179593 | GGTT | G | intron_variant | MODIFIER | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(19): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(8): Show | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(19): Show | 22 | 100 | 0.2200 | -3 | c.64- others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111210811 | GACA | G | intron_variant | MODIFIER | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0005a0001c0002t0001others(6): Show | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | 100 | 0.1800 | -3 | c.64- others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111220743 | CAAA | C | intron_variant | MODIFIER | HG01099.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0001 | a0001c0001t0001g0091a0001c0001t0002g0056a0001c0003t0001g0033others(1): Show | 4 | 100 | 0.0400 | -3 | c.222 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111249400 | CTTT | C | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp1 HG02486.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0003a0001c0003t0001a0001c0004t0001others(4): Show | a0001c0001t0003g0045a0001c0003t0001g0011a0001c0003t0001g0017others(6): Show | 9 | 100 | 0.0900 | -3 | c.223 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111257278 | TTCC | T | intron_variant | MODIFIER | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
a0002 | a0002c0006 | a0002c0006t0001 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | 100 | 0.0300 | -3 | c.223 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111282625 | TAAA | T | intron_variant | MODIFIER | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(34): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0083others(34): Show | 37 | 100 | 0.3700 | -3 | c.302 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111294585 | CAAA | C | intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG01099.hp1 others(24): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0007others(6): Show | a0001c0001t0004a0001c0002t0001a0001c0007t0001others(6): Show | a0001c0001t0004g0054a0001c0002t0001g0004a0001c0002t0001g0023others(24): Show | 27 | 100 | 0.2700 | -3 | c.561 others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111301038 | CAAA | C | intron_variant | MODIFIER | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(10): Show | a0001c0001t0001g0091a0001c0003t0001g0017a0001c0004t0001g0002others(18): Show | 21 | 100 | 0.2100 | -3 | c.753 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111302899 | TAAA | T | intron_variant | MODIFIER | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(24): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(24): Show | 27 | 100 | 0.2700 | -3 | c.754 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111314639 | TAAA | T | intron_variant | MODIFIER | HG01884.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001 | a0001c0001t0002g0030a0001c0001t0002g0083a0001c0003t0001g0008others(6): Show | 9 | 100 | 0.0900 | -3 | c.200 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111318242 | TTTC | T | intron_variant | MODIFIER | HG01884.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0011others(1): Show | a0001c0001t0002a0001c0003t0001a0001c0011t0001others(1): Show | a0001c0001t0002g0030a0001c0001t0002g0083a0001c0003t0001g0008others(9): Show | 12 | 100 | 0.1200 | -3 | c.200 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |