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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CUL4B_chrX_120518858_120565962 | 120559495 | ACTT | A | intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 | 1 | 278 | 0.0036 | -3 | c.556 others(18): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | TogoVar | ||||||
CUL4B_chrX_120518858_120565962 | 120565670 | CAAA | C | upstream_gene_variant | MODIFIER | HG01884.hp1 HG02723.hp1 HG02922.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0003 | a0001c0001t0003g0035a0001c0001t0003g0148a0001c0005t0003g0156 | 3 | 278 | 0.0108 | -3 | c.-50 others(14): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 4709 | chrX | TogoVar | ||||||
CUL5_chr11_108003898_108112761 | 108006205 | AAAG | A | upstream_gene_variant | MODIFIER | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
a0001 | a0001c0002 | a0001c0002t0004a0001c0002t0011a0001c0002t0035 | a0001c0002t0004g0208a0001c0002t0004g0209a0001c0002t0004g0210others(8): Show | 11 | 312 | 0.0353 | -3 | c.-31 others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2692 | chr11 | TogoVar | ||||||
CUL5_chr11_108003898_108112761 | 108017389 | CAAA | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0001c0001t0012a0001c0001t0020others(4): Show | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0096others(60): Show | 64 | 312 | 0.2051 | -3 | c.24+ others(18): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108024426 | AAAT | A | intron_variant | MODIFIER | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
a0001 | a0001c0004 | a0001c0004t0014 | a0001c0004t0014g0005a0001c0004t0014g0082 | 3 | 312 | 0.0096 | -3 | c.25- others(18): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108038224 | ATGT | A | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
a0001 | a0001c0002a0001c0005 | a0001c0002t0003a0001c0002t0010a0001c0002t0033others(1): Show | a0001c0002t0003g0003a0001c0002t0003g0033a0001c0002t0003g0034others(20): Show | 25 | 312 | 0.0801 | -3 | c.134 others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108079057 | ATCT | A | intron_variant | MODIFIER | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0012a0001c0004t0014 | a0001c0002t0012g0162a0001c0004t0014g0005a0001c0004t0014g0082 | 4 | 312 | 0.0128 | -3 | c.117 others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108093275 | ATCT | A | intron_variant | MODIFIER | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0002t0005a0001c0002t0013others(2): Show | a0001c0002t0002g0080a0001c0002t0002g0087a0001c0002t0002g0088others(35): Show | 39 | 312 | 0.1250 | -3 | c.144 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108096564 | CTTT | C | intron_variant | MODIFIER | HG01123.hp1 HG02109.hp1 HG02572.hp2 others(12): Show |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0002a0001c0002t0013a0001c0003t0005others(1): Show | a0001c0002t0002g0080a0001c0002t0002g0166a0001c0002t0002g0167others(10): Show | 15 | 312 | 0.0481 | -3 | c.190 others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108111776 | GATT | G | downstream_gene_variant | MODIFIER | HG00741.hp2 HG01081.hp2 HG01261.hp1 others(27): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(3): Show | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0002g0087others(26): Show | 30 | 312 | 0.0962 | -3 | c.*73 others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4016 | chr11 | TogoVar | ||||||
CUL9_chr6_43177196_43229587 | 43191481 | ATTT | A | intron_variant | MODIFIER | HG02015.hp2 HG03017.hp1 NA18939.hp1 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0055others(3): Show | 6 | 276 | 0.0217 | -3 | c.218 others(22): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
CUL9_chr6_43177196_43229587 | 43198673 | TGGG | T | disruptive_inframe_deletion | MODERATE | HG00639.hp1 HG02486.hp1 HG02970.hp1 others(5): Show |
a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0012a0003c0005t0001g0123a0003c0005t0001g0124others(3): Show | 8 | 276 | 0.0290 | -3 | c.287 others(12): Show |
p.Gly others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 12/41 | 2934/7759 | 2871/7554 | 957/2517 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |
CUL9_chr6_43177196_43229587 | 43210427 | CCTT | C | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(68): Show |
a0001a0002a0003others(5): Show | a0001c0002a0001c0003a0001c0032others(8): Show | a0001c0002t0001a0001c0003t0002a0001c0032t0001others(8): Show | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(44): Show | 71 | 276 | 0.2573 | -3 | c.521 others(22): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
CUTC_chr10_99727234_99761134 | 99729459 | CAAA | C | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(192): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 195 | 410 | 0.4756 | -3 | c.-28 others(14): Show |
CUTC | ENSG00000119929.13 | transcript | ENST00000370476.10 | protein_coding | 2774 | chr10 | TogoVar | ||||||
CUTC_chr10_99727234_99761134 | 99734064 | ATTT | A | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(184): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 187 | 410 | 0.4561 | -3 | c.61+ others(18): Show |
CUTC | ENSG00000119929.13 | transcript | ENST00000370476.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101831734 | TTTA | T | intron_variant | MODIFIER | HG02615.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0002a0001c0002t0001g0001a0002c0003t0001g0003others(2): Show | 5 | 132 | 0.0379 | -3 | c.63+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101837828 | CAAA | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG01099.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0013others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(5): Show | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0002t0001g0050others(13): Show | 16 | 132 | 0.1212 | -3 | c.63+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101848051 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01255.hp1 HG01515.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(8): Show | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0124others(20): Show | 23 | 132 | 0.1742 | -3 | c.63+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101870150 | TTTG | T | intron_variant | MODIFIER | HG01515.hp2 HG02055.hp1 HG02976.hp1 others(4): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0005 | a0001c0002t0001a0002c0003t0001a0002c0005t0001 | a0001c0002t0001g0021a0001c0002t0001g0095a0001c0002t0001g0125others(4): Show | 7 | 132 | 0.0530 | -3 | c.64- others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101958370 | TGCA | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(108): Show | 111 | 132 | 0.8409 | -3 | c.174 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101984090 | ATAT | A | intron_variant | MODIFIER | HG01192.hp2 HG01496.hp1 HG01515.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(3): Show | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0008g0071others(7): Show | 10 | 132 | 0.0758 | -3 | c.175 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 101993167 | TAAA | T | intron_variant | MODIFIER | HG02559.hp2 HG02615.hp2 HG02976.hp1 |
a0001a0002 | a0001c0002a0002c0005 | a0001c0002t0001a0001c0002t0005a0002c0005t0001 | a0001c0002t0001g0001a0001c0002t0005g0129a0002c0005t0001g0017 | 3 | 132 | 0.0227 | -3 | c.175 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102014858 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01258.hp1 HG01258.hp2 others(36): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0025others(36): Show | 39 | 132 | 0.2955 | -3 | c.175 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102017429 | TCTC | T | intron_variant | MODIFIER | HG01884.hp2 HG02896.hp2 HG02897.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0014a0001c0001t0001g0015a0002c0004t0001g0018 | 3 | 132 | 0.0227 | -3 | c.175 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102021923 | CCTT | C | intron_variant | MODIFIER | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0005 | a0001c0002t0001a0001c0002t0005a0002c0003t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0005g0129a0002c0003t0001g0013others(2): Show | 5 | 132 | 0.0379 | -3 | c.175 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102065897 | TCTC | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(113): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(10): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(22): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(113): Show | 116 | 132 | 0.8788 | -3 | c.223 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102076059 | ATCT | A | intron_variant | MODIFIER | HG02970.hp2 HG03041.hp1 HG03486.hp1 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0067a0001c0002t0001g0077a0002c0003t0001g0128 | 3 | 132 | 0.0227 | -3 | c.301 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102077059 | AAAG | A | intron_variant | MODIFIER | HG01258.hp1 HG01496.hp2 HG02257.hp2 others(3): Show |
a0002a0003 | a0002c0003a0002c0005a0002c0007others(1): Show | a0002c0003t0002a0002c0005t0001a0002c0007t0001others(1): Show | a0002c0003t0002g0052a0002c0003t0002g0076a0002c0005t0001g0081others(3): Show | 6 | 132 | 0.0455 | -3 | c.301 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102083687 | AGAT | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(2): Show | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0002t0001g0034others(3): Show | 6 | 132 | 0.0455 | -3 | c.301 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102084266 | TTTA | T | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(2): Show | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0002t0001g0034others(3): Show | 6 | 132 | 0.0455 | -3 | c.302 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102084307 | TGTA | T | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(2): Show | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0002t0001g0034others(3): Show | 6 | 132 | 0.0455 | -3 | c.302 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102084858 | CTTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0013others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | 132 | 0.1591 | -3 | c.302 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102092934 | AAAG | A | intron_variant | MODIFIER | HG00639.hp2 HG01168.hp1 HG01255.hp1 others(21): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0013others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | a0001c0001t0001g0042a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 24 | 132 | 0.1818 | -3 | c.302 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102101914 | TAAA | T | intron_variant | MODIFIER | HG01192.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(3): Show | a0001c0001t0001g0029a0001c0002t0001g0008a0001c0002t0001g0032others(10): Show | 13 | 132 | 0.0985 | -3 | c.440 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102106079 | CTTT | C | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0007others(7): Show | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0049others(26): Show | 29 | 132 | 0.2197 | -3 | c.563 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102151727 | CAAA | C | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(18): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(7): Show | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0072others(18): Show | 21 | 132 | 0.1591 | -3 | c.708 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102165350 | CTTT | C | intron_variant | MODIFIER | HG02970.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0067a0001c0002t0001g0077a0001c0002t0001g0078others(1): Show | 4 | 132 | 0.0303 | -3 | c.757 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102168925 | TTTC | T | intron_variant | MODIFIER | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
a0001a0002a0004 | a0001c0002a0002c0003a0004c0010 | a0001c0002t0001a0002c0003t0001a0002c0003t0002others(1): Show | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0001g0050others(8): Show | 11 | 132 | 0.0833 | -3 | c.757 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102168930 | TTTA | T | intron_variant | MODIFIER | HG01192.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0003t0002others(2): Show | a0001c0002t0001g0034a0001c0002t0001g0095a0002c0003t0001g0003others(5): Show | 8 | 132 | 0.0606 | -3 | c.757 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102176558 | CTTT | C | intron_variant | MODIFIER | HG00639.hp2 HG01258.hp1 HG01496.hp2 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0013a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(27): Show | 30 | 132 | 0.2273 | -3 | c.862 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102177432 | AAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(18): Show |
a0001a0002a0006 | a0001c0001a0002c0005a0006c0008 | a0001c0001t0001a0001c0001t0008a0002c0005t0001others(3): Show | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0049others(18): Show | 21 | 132 | 0.1591 | -3 | c.862 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102180016 | CGTT | C | intron_variant | MODIFIER | HG02970.hp1 HG03195.hp2 |
a0002a0003 | a0002c0003a0003c0012 | a0002c0003t0001a0003c0012t0005 | a0002c0003t0001g0122a0003c0012t0005g0079 | 2 | 132 | 0.0152 | -3 | c.105 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102186590 | TATA | T | intron_variant | MODIFIER | HG00639.hp2 HG01258.hp1 HG01496.hp2 others(21): Show |
a0001a0002a0003 | a0001c0001a0001c0013a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(21): Show | 24 | 132 | 0.1818 | -3 | c.105 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 11/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102186592 | TATA | T | intron_variant | MODIFIER | HG01515.hp1 HG01978.hp1 HG03195.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0007a0003c0006 | a0001c0001t0001a0002c0007t0001a0003c0006t0001 | a0001c0001t0001g0009a0001c0001t0001g0025a0002c0007t0001g0083others(2): Show | 5 | 132 | 0.0379 | -3 | c.105 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 11/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102216533 | CCCA | C | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(24): Show |
a0001a0002a0006 | a0001c0001a0002c0003a0002c0004others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(6): Show | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0042others(24): Show | 27 | 132 | 0.2046 | -3 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102226620 | AGTT | A | intron_variant | MODIFIER | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(1): Show | a0001c0001t0001g0029a0001c0002t0001g0019a0001c0002t0001g0032others(7): Show | 10 | 132 | 0.0758 | -3 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102231025 | ATTT | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(11): Show | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0025others(39): Show | 42 | 132 | 0.3182 | -3 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102243632 | AAAT | A | intron_variant | MODIFIER | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(3): Show | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0048others(23): Show | 26 | 132 | 0.1970 | -3 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102259759 | AAAG | A | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(66): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(14): Show | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(66): Show | 69 | 132 | 0.5227 | -3 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102269572 | ATTT | A | intron_variant | MODIFIER | HG00423.hp2 HG00735.hp1 HG01192.hp2 others(11): Show |
a0002 | a0002c0004a0002c0007 | a0002c0004t0001a0002c0004t0009a0002c0007t0001 | a0002c0004t0001g0012a0002c0004t0001g0026a0002c0004t0001g0027others(11): Show | 14 | 132 | 0.1061 | -3 | c.125 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |