Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23316 |
|---|---|
| ensemblid | ENSG00000111249.14 |
| hgncid | 19347 |
| symbol | CUX2 |
| name | cut like homeobox 2 |
| refseq_nuc | NM_015267.4 |
| refseq_prot | NP_056082.2 |
| ensembl_nuc | ENST00000261726.11 |
| ensembl_prot | ENSP00000261726.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 111034165 |
| end | 111350554 |
| strand | + |
| ver | v1.2 |
| region | chr12:111034165-111350554 |
| region5000 | chr12:111029165-111355554 |
| regionname0 | CUX2_chr12_111034165_111350554 |
| regionname5000 | CUX2_chr12_111029165_111355554 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1486 | 92 | 75 | 9 | 2 | 0 | 6 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0002 | 0/0 | 1486 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0003 | 0/0 | 1486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0004 | 1/0 | 1486 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0005 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0006 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0007 | 0/1 | 1486 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4461 | 28 | 19 | 5 | 0 | 0 | 4 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0002 | 0/0 | 4461 | 23 | 19 | 2 | 1 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0003 | 0/0 | 4461 | 14 | 13 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0004 | 0/0 | 4461 | 8 | 7 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0005 | 0/0 | 4461 | 4 | 4 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0006 | 0/0 | 4461 | 3 | 1 | 0 | 0 | 0 | 2 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0007 | 0/0 | 4461 | 2 | 1 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0008 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0009 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0010 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0011 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0012 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0013 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0014 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0015 | 1/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0016 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0017 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0018 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0019 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0020 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0021 | 0/1 | 4461 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| c0022 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2243 | 65 | 54 | 5 | 2 | 0 | 4 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0002 | 1/1 | 2243 | 19 | 10 | 4 | 0 | 0 | 3 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0003 | 0/0 | 2243 | 5 | 4 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0004 | 0/0 | 2242 | 4 | 4 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0005 | 0/0 | 2243 | 3 | 2 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0006 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0007 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0008 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| t0009 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4461 | 28 | 19 | 5 | 0 | 0 | 4 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0002 | 0/0 | 4461 | 23 | 19 | 2 | 1 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0003 | 0/0 | 4461 | 14 | 13 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0004 | 0/0 | 4461 | 8 | 7 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0005 | 0/0 | 4461 | 4 | 4 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0007 | 0/0 | 4461 | 2 | 1 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0008 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0009 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0010 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0011 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0013 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0014 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0017 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0018 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0019 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0022 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0002c0006 | 0/0 | 4461 | 3 | 1 | 0 | 0 | 0 | 2 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0003c0016 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0004c0015 | 1/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0005c0012 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0006c0020 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0007c0021 | 0/1 | 4461 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6703 | 5 | 5 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0001t0002 | 0/0 | 6703 | 16 | 9 | 4 | 0 | 0 | 3 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0001t0003 | 0/0 | 6703 | 5 | 4 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0001t0004 | 0/0 | 6702 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0001t0005 | 0/0 | 6703 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0002t0001 | 0/0 | 6703 | 22 | 18 | 2 | 1 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0002t0007 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0003t0001 | 0/0 | 6703 | 13 | 12 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0003t0008 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0004t0001 | 0/0 | 6703 | 5 | 4 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0004t0004 | 0/0 | 6702 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0004t0005 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0004t0006 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0005t0001 | 0/0 | 6703 | 4 | 4 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0007t0001 | 0/0 | 6703 | 2 | 1 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0008t0001 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0008t0002 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0009t0001 | 0/0 | 6703 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0010t0001 | 0/0 | 6703 | 2 | 2 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0011t0001 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0013t0001 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0014t0001 | 0/0 | 6703 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0017t0001 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0018t0004 | 0/0 | 6702 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0019t0004 | 0/0 | 6702 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0001c0022t0005 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0002c0006t0001 | 0/0 | 6703 | 3 | 1 | 0 | 0 | 0 | 2 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0003c0016t0001 | 0/0 | 6703 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0004c0015t0002 | 1/0 | 6703 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0005c0012t0009 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0006c0020t0001 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| a0007c0021t0002 | 0/1 | 6703 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | copy fasta | chr12 | 111029165 | 111355554 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0002t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0003t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0004t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0008t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0008t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0009t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0010t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0010t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0013t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0014t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0017t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0018t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0019t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0001c0022t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0002c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0002c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0002c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0003c0016t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0004c0015t0002g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0005c0012t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0006c0020t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| a0007c0021t0002g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG00597 | hp2 | a0001 | c0007 | t0001 | g0098 | EAS | CHS | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01069 | hp2 | a0003 | c0016 | t0001 | g0068 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01081 | hp1 | a0001 | c0014 | t0001 | g0042 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0096 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0088 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01891 | hp1 | a0001 | c0008 | t0002 | g0022 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG01891 | hp2 | a0001 | c0019 | t0004 | g0077 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02280 | hp1 | a0001 | c0003 | t0008 | g0032 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02280 | hp2 | a0001 | c0004 | t0006 | g0075 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02615 | hp2 | a0001 | c0009 | t0001 | g0031 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02622 | hp2 | a0001 | c0004 | t0005 | g0007 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02698 | hp2 | a0002 | c0006 | t0001 | g0053 | SAS | PJL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02809 | hp2 | a0001 | c0018 | t0004 | g0029 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02896 | hp2 | a0005 | c0012 | t0009 | g0044 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02897 | hp2 | a0001 | c0022 | t0005 | g0034 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0002 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02922 | hp2 | a0001 | c0017 | t0001 | g0065 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02965 | hp1 | a0001 | c0010 | t0001 | g0050 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0027 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02976 | hp2 | a0006 | c0020 | t0001 | g0020 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03098 | hp1 | a0001 | c0010 | t0001 | g0049 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03209 | hp2 | a0001 | c0008 | t0001 | g0003 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | ESN | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03579 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | STU | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0055 | SAS | STU | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0097 | AFR | YRI | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | YRI | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA19030 | hp2 | a0001 | c0009 | t0001 | g0035 | AFR | LWK | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA19043 | hp1 | a0001 | c0011 | t0001 | g0001 | AFR | LWK | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | LWK | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20129 | hp2 | a0001 | c0013 | t0001 | g0063 | AFR | ASW | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0057 | SAS | GIH | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20905 | hp2 | a0002 | c0006 | t0001 | g0089 | SAS | GIH | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0041 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0028 | AFR | ACB | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | USA | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| HG06807 | hp2 | a0002 | c0006 | t0001 | g0084 | AFR | USA | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | USA | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0021 | t0002 | g0064 | REF | REF | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| homoSapiens_grch38 | hp1 | a0004 | c0015 | t0002 | g0036 | REF | REF | CUX2_chr12_111029165_111355554 | CUX2 | chr12 | 111029165 | 111355554 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111307201
|
G | T | 1 | a0007 | 1 | homoSapiens_chm13v2.hp1 | missense_variant&splice_region_variant | MODERATE | c.1053G>T | p.Lys351Asn | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 12/22 | 1066/6703 | 1053/4461 | 351/1486 | chr12 | 111307201 | ||
| chr12:111320279
|
C | T | 1 | a0006 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2270C>T | p.Ala757Val | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/22 | 2283/6703 | 2270/4461 | 757/1486 | chr12 | 111320279 | ||
| chr12:111320305
|
G | A | 1 | a0005 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.2296G>A | p.Ala766Thr | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/22 | 2309/6703 | 2296/4461 | 766/1486 | chr12 | 111320305 | ||
| chr12:111320395
|
C | T | 1 | a0003 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.2386C>T | p.Leu796Phe | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/22 | 2399/6703 | 2386/4461 | 796/1486 | chr12 | 111320395 | ||
| chr12:111347711
|
G | A | 1 | a0002 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.3847G>A | p.Glu1283Lys | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 3860/6703 | 3847/4461 | 1283/1486 | chr12 | 111347711 | ||
| chr12:111348278
|
G | C | 6 | a0001a0002a0003others(3): Show | 99 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(96): Show |
missense_variant | MODERATE | c.4414G>C | p.Val1472Leu | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 4427/6703 | 4414/4461 | 1472/1486 | chr12 | 111348278 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111293486
|
C | T | 1 | a0001c0022 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.477C>T | p.Thr159Thr | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/22 | 490/6703 | 477/4461 | 159/1486 | chr12 | 111293486 | ||
| chr12:111310159
|
C | T | 5 | a0001c0002a0001c0010a0001c0018others(2): Show | 28 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(25): Show |
synonymous_variant | LOW | c.1377C>T | p.Pro459Pro | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/22 | 1390/6703 | 1377/4461 | 459/1486 | chr12 | 111310159 | ||
| chr12:111310267
|
C | T | 6 | a0001c0004a0001c0005a0001c0008others(3): Show | 18 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.1485C>T | p.Ala495Ala | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/22 | 1498/6703 | 1485/4461 | 495/1486 | chr12 | 111310267 | ||
| chr12:111310411
|
G | A | 1 | a0001c0017 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1629G>A | p.Ala543Ala | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/22 | 1642/6703 | 1629/4461 | 543/1486 | chr12 | 111310411 | ||
| chr12:111312113
|
G | A | 1 | a0001c0018 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1914G>A | p.Pro638Pro | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/22 | 1927/6703 | 1914/4461 | 638/1486 | chr12 | 111312113 | ||
| chr12:111320286
|
C | A | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2277C>A | p.Leu759Leu | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/22 | 2290/6703 | 2277/4461 | 759/1486 | chr12 | 111320286 | ||
| chr12:111320388
|
C | T | 2 | a0001c0008a0001c0009 | 4 | HG01891.hp1 HG02615.hp2 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.2379C>T | p.Arg793Arg | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/22 | 2392/6703 | 2379/4461 | 793/1486 | chr12 | 111320388 | ||
| chr12:111322447
|
G | C | 8 | a0001c0002a0001c0010a0001c0013others(5): Show | 31 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(28): Show |
synonymous_variant | LOW | c.2793G>C | p.Val931Val | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/22 | 2806/6703 | 2793/4461 | 931/1486 | chr12 | 111322447 | ||
| chr12:111341988
|
C | T | 5 | a0001c0007a0001c0009a0001c0010others(2): Show | 10 | HG00597.hp2 HG01081.hp1 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.3594C>T | p.Ile1198Ile | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/22 | 3607/6703 | 3594/4461 | 1198/1486 | chr12 | 111341988 | ||
| chr12:111347782
|
T | C | 12 | a0001c0002a0001c0003a0001c0005others(9): Show | 55 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(52): Show |
synonymous_variant | LOW | c.3918T>C | p.Asp1306Asp | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 3931/6703 | 3918/4461 | 1306/1486 | chr12 | 111347782 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111348415
|
G | A | 1 | a0001c0004t0006 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 90 | chr12 | 111348415 | |||||
| chr12:111348730
|
C | G | 1 | a0001c0004t0006 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*405C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 405 | chr12 | 111348730 | |||||
| chr12:111348810
|
T | G | 1 | a0001c0001t0003 | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*485T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 485 | chr12 | 111348810 | |||||
| chr12:111348872
|
G | A | 4 | a0001c0001t0005a0001c0004t0005a0001c0004t0006others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 547 | chr12 | 111348872 | |||||
| chr12:111348973
|
C | T | 1 | a0005c0012t0009 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 648 | chr12 | 111348973 | |||||
| chr12:111349088
|
T | C | 27 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | 80 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*763T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 763 | chr12 | 111349088 | |||||
| chr12:111349275
|
G | A | 4 | a0001c0001t0004a0001c0004t0004a0001c0018t0004others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*950G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 950 | chr12 | 111349275 | |||||
| chr12:111349426
|
G | A | 1 | a0001c0002t0007 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 1101 | chr12 | 111349426 | |||||
| chr12:111349903
|
GC | G | 4 | a0001c0001t0004a0001c0004t0004a0001c0018t0004others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1579delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 1579 | chr12 | 111349903 | |||||
| chr12:111350365
|
G | A | 1 | a0001c0003t0008 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 22/22 | 2040 | chr12 | 111350365 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111034355
|
TGCCGGGG others(3): Show |
T | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.63+127_63+136delCC others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111034355 | |||||
| chr12:111034611
|
G | T | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+371G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111034611 | ||||||
| chr12:111035352
|
C | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+1112C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035352 | ||||||
| chr12:111035355
|
G | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+1115G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035355 | ||||||
| chr12:111035613
|
C | CT | 54 | a0001c0001t0001g0082a0001c0001t0002g0043a0001c0001t0002g0056others(51): Show | 54 | HG01069.hp1 HG01069.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.63+1389dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111035613 | |||||
| chr12:111035613
|
C | CTT | 11 | a0001c0001t0001g0091a0001c0001t0003g0099a0001c0002t0001g0090others(8): Show | 11 | HG00597.hp1 HG00597.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+1388_63+1389dup others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111035613 | |||||
| chr12:111035613
|
C | CTTTTT | 17 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+1385_63+1389dup others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111035613 | |||||
| chr12:111035613
|
C | CTTTTTT | 16 | a0001c0001t0001g0024a0001c0001t0002g0030a0001c0002t0001g0023others(13): Show | 16 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+1384_63+1389dup others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111035613 | |||||
| chr12:111035681
|
C | G | 7 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0085others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+1441C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035681 | ||||||
| chr12:111035763
|
C | T | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+1523C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035763 | ||||||
| chr12:111035833
|
G | T | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+1593G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035833 | ||||||
| chr12:111035876
|
A | T | 4 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(1): Show | 4 | HG01169.hp1 HG02055.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1636A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111035876 | ||||||
| chr12:111036516
|
A | G | 2 | a0001c0001t0002g0076a0001c0019t0004g0077 | 2 | HG01891.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.63+2276A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111036516 | ||||||
| chr12:111037048
|
A | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+2808A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111037048 | ||||||
| chr12:111037162
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+2922G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111037162 | ||||||
| chr12:111037263
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.63+3023C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111037263 | ||||||
| chr12:111037331
|
C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.63+3091C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111037331 | ||||||
| chr12:111037495
|
G | A | 3 | a0001c0001t0001g0006a0001c0003t0001g0008a0001c0004t0005g0007 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+3255G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111037495 | ||||||
| chr12:111038564
|
G | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+4324G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111038564 | ||||||
| chr12:111038690
|
T | C | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+4450T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111038690 | ||||||
| chr12:111038714
|
C | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(31): Show | 34 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+4474C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111038714 | ||||||
| chr12:111038835
|
C | G | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+4595C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111038835 | ||||||
| chr12:111039071
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+4831A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039071 | ||||||
| chr12:111039092
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+4852G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039092 | ||||||
| chr12:111039159
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+4919C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039159 | ||||||
| chr12:111039160
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+4920G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039160 | ||||||
| chr12:111039164
|
G | C | 2 | a0001c0001t0002g0076a0001c0019t0004g0077 | 2 | HG01891.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.63+4924G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039164 | ||||||
| chr12:111039228
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+4988G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039228 | ||||||
| chr12:111039265
|
G | C | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+5025G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039265 | ||||||
| chr12:111039575
|
C | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+5335C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039575 | ||||||
| chr12:111039854
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+5614G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039854 | ||||||
| chr12:111039973
|
T | C | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+5733T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111039973 | ||||||
| chr12:111040285
|
T | TA | 4 | a0001c0001t0001g0091a0001c0001t0003g0078a0001c0002t0001g0090others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6057dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111040285 | |||||
| chr12:111040703
|
C | G | 7 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0085others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6463C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111040703 | ||||||
| chr12:111040710
|
T | C | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+6470T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111040710 | ||||||
| chr12:111041361
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+7121G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111041361 | ||||||
| chr12:111041427
|
T | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+7187T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111041427 | ||||||
| chr12:111041849
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+7609G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111041849 | ||||||
| chr12:111041900
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+7660C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111041900 | ||||||
| chr12:111041992
|
C | T | 4 | a0001c0001t0002g0067a0001c0002t0001g0069a0001c0002t0001g0070others(1): Show | 4 | HG01069.hp2 HG01243.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+7752C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111041992 | ||||||
| chr12:111042096
|
A | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+7856A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042096 | ||||||
| chr12:111042125
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+7885C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042125 | ||||||
| chr12:111042154
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+7914C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042154 | ||||||
| chr12:111042246
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+8006G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042246 | ||||||
| chr12:111042249
|
G | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+8009G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042249 | ||||||
| chr12:111042291
|
C | G | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+8051C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042291 | ||||||
| chr12:111042300
|
C | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+8060C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042300 | ||||||
| chr12:111042555
|
T | C | 2 | a0001c0004t0001g0002a0001c0011t0001g0001 | 2 | HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.63+8315T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042555 | ||||||
| chr12:111042796
|
CT | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+8572delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111042796 | |||||
| chr12:111042828
|
G | T | 4 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0003t0001g0014others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8588G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042828 | ||||||
| chr12:111042996
|
G | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+8756G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111042996 | ||||||
| chr12:111043103
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+8863A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043103 | ||||||
| chr12:111043139
|
A | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+8899A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043139 | ||||||
| chr12:111043191
|
G | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+8951G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043191 | ||||||
| chr12:111043244
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+9004T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043244 | ||||||
| chr12:111043384
|
G | T | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+9144G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043384 | ||||||
| chr12:111043469
|
C | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(31): Show | 34 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+9229C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043469 | ||||||
| chr12:111043532
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+9292G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043532 | ||||||
| chr12:111043540
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+9300C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111043540 | ||||||
| chr12:111044059
|
G | A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+9819G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044059 | ||||||
| chr12:111044249
|
G | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+10009G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044249 | ||||||
| chr12:111044253
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+10013C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044253 | ||||||
| chr12:111044287
|
G | T | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+10047G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044287 | ||||||
| chr12:111044481
|
T | C | 3 | a0001c0001t0001g0006a0001c0003t0001g0008a0001c0004t0005g0007 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+10241T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044481 | ||||||
| chr12:111044520
|
GTTAGTTT others(5): Show |
G | 17 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+10283_63+10294d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111044520 | |||||
| chr12:111044527
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0002t0001g0004others(18): Show | 21 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+10287T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044527 | ||||||
| chr12:111044593
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+10353C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044593 | ||||||
| chr12:111044823
|
C | T | 1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.63+10583C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044823 | ||||||
| chr12:111044912
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+10672G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044912 | ||||||
| chr12:111044990
|
C | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+10750C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111044990 | ||||||
| chr12:111045087
|
C | G | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+10847C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111045087 | ||||||
| chr12:111045161
|
T | A | 8 | a0001c0001t0001g0024a0001c0002t0001g0018a0001c0002t0001g0023others(5): Show | 8 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+10921T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111045161 | ||||||
| chr12:111045169
|
C | T | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+10929C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111045169 | ||||||
| chr12:111045226
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(31): Show | 34 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+10986G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111045226 | ||||||
| chr12:111045936
|
C | T | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+11696C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111045936 | ||||||
| chr12:111046011
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63+11771C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046011 | ||||||
| chr12:111046168
|
C | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+11928C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046168 | ||||||
| chr12:111046276
|
G | T | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.63+12036G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046276 | ||||||
| chr12:111046666
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+12426T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046666 | ||||||
| chr12:111046669
|
T | A | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+12429T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046669 | ||||||
| chr12:111046741
|
C | T | 5 | a0001c0001t0001g0006a0001c0002t0001g0004a0001c0003t0001g0008others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+12501C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046741 | ||||||
| chr12:111046840
|
A | T | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+12600A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046840 | ||||||
| chr12:111046863
|
G | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12623G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046863 | ||||||
| chr12:111046880
|
T | C | 4 | a0001c0001t0003g0045a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+12640T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111046880 | ||||||
| chr12:111047188
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+12948G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047188 | ||||||
| chr12:111047202
|
G | C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12962G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047202 | ||||||
| chr12:111047368
|
C | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+13128C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047368 | ||||||
| chr12:111047413
|
G | A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+13173G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047413 | ||||||
| chr12:111047667
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+13427T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047667 | ||||||
| chr12:111047771
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+13531G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111047771 | ||||||
| chr12:111048178
|
G | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+13938G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048178 | ||||||
| chr12:111048567
|
A | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+14327A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048567 | ||||||
| chr12:111048640
|
G | A | 3 | a0001c0002t0001g0051a0001c0010t0001g0049a0001c0010t0001g0050 | 3 | HG02109.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63+14400G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048640 | ||||||
| chr12:111048747
|
A | G | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+14507A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048747 | ||||||
| chr12:111048877
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+14637C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048877 | ||||||
| chr12:111048902
|
G | C | 8 | a0001c0001t0001g0024a0001c0002t0001g0018a0001c0002t0001g0023others(5): Show | 8 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+14662G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111048902 | ||||||
| chr12:111049019
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.63+14779A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049019 | ||||||
| chr12:111049146
|
A | G | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.63+14906A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049146 | ||||||
| chr12:111049185
|
C | CCATCCAT others(9): Show |
1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.63+14955_63+14956i others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111049185 | |||||
| chr12:111049196
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.63+14956T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049196 | ||||||
| chr12:111049253
|
C | T | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+15013C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049253 | ||||||
| chr12:111049388
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+15148C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049388 | ||||||
| chr12:111049478
|
T | C | 2 | a0001c0001t0002g0100a0001c0003t0001g0052 | 2 | HG01069.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.63+15238T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049478 | ||||||
| chr12:111049601
|
T | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+15361T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049601 | ||||||
| chr12:111049605
|
A | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+15365A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049605 | ||||||
| chr12:111049616
|
G | A | 1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.63+15376G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049616 | ||||||
| chr12:111049691
|
A | G | 6 | a0001c0002t0001g0037a0001c0003t0001g0014a0001c0003t0001g0040others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+15451A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049691 | ||||||
| chr12:111049845
|
A | C | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+15605A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111049845 | ||||||
| chr12:111050179
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+15939C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111050179 | ||||||
| chr12:111050223
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+15983G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111050223 | ||||||
| chr12:111050398
|
C | G | 15 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(12): Show | 15 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+16158C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111050398 | ||||||
| chr12:111050936
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63+16696T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111050936 | ||||||
| chr12:111050955
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+16715T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111050955 | ||||||
| chr12:111051024
|
G | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+16784G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051024 | ||||||
| chr12:111051111
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+16871C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051111 | ||||||
| chr12:111051494
|
CT | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+17265delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111051494 | |||||
| chr12:111051501
|
T | G | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+17261T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051501 | ||||||
| chr12:111051511
|
G | C | 5 | a0001c0004t0001g0005a0001c0004t0004g0041a0001c0004t0006g0075others(2): Show | 5 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17271G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051511 | ||||||
| chr12:111051523
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+17283A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051523 | ||||||
| chr12:111051562
|
T | C | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+17322T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051562 | ||||||
| chr12:111051635
|
G | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(23): Show | 26 | HG01069.hp2 HG01099.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+17395G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051635 | ||||||
| chr12:111051784
|
A | G | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+17544A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051784 | ||||||
| chr12:111051812
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+17572T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051812 | ||||||
| chr12:111051869
|
GT | G | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+17639delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111051869 | |||||
| chr12:111051889
|
A | G | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17649A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051889 | ||||||
| chr12:111051938
|
T | A | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+17698T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111051938 | ||||||
| chr12:111052282
|
C | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+18042C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111052282 | ||||||
| chr12:111052320
|
T | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+18080T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111052320 | ||||||
| chr12:111052420
|
CA | C | 14 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0002t0001g0047others(11): Show | 14 | HG00597.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+18194delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111052420 | |||||
| chr12:111052420
|
CAA | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+18193_63+18194d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111052420 | |||||
| chr12:111052444
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+18204T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111052444 | ||||||
| chr12:111052689
|
C | CTG | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+18461_63+18462d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111052689 | |||||
| chr12:111052900
|
C | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+18660C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111052900 | ||||||
| chr12:111053019
|
G | A | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+18779G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053019 | ||||||
| chr12:111053038
|
A | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+18798A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053038 | ||||||
| chr12:111053080
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+18840C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053080 | ||||||
| chr12:111053176
|
C | T | 14 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(11): Show | 14 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+18936C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053176 | ||||||
| chr12:111053177
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.63+18937G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053177 | ||||||
| chr12:111053324
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+19084G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053324 | ||||||
| chr12:111053443
|
C | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+19203C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053443 | ||||||
| chr12:111053557
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19317C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053557 | ||||||
| chr12:111053661
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+19421C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053661 | ||||||
| chr12:111053662
|
G | A | 8 | a0001c0001t0002g0030a0001c0003t0008g0032a0001c0004t0001g0027others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+19422G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053662 | ||||||
| chr12:111053738
|
C | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19498C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053738 | ||||||
| chr12:111053855
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19615T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111053855 | ||||||
| chr12:111054091
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19851C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054091 | ||||||
| chr12:111054109
|
G | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19869G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054109 | ||||||
| chr12:111054139
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+19899A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054139 | ||||||
| chr12:111054423
|
C | G | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+20183C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054423 | ||||||
| chr12:111054553
|
A | AG | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20316dupG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111054553 | |||||
| chr12:111054560
|
CT | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20322delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111054560 | |||||
| chr12:111054627
|
C | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20387C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054627 | ||||||
| chr12:111054826
|
C | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20586C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054826 | ||||||
| chr12:111054848
|
A | T | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.63+20608A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054848 | ||||||
| chr12:111054914
|
A | C | 10 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+20674A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054914 | ||||||
| chr12:111054936
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20696C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054936 | ||||||
| chr12:111054987
|
T | G | 14 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(11): Show | 14 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+20747T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111054987 | ||||||
| chr12:111055044
|
G | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+20804G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055044 | ||||||
| chr12:111055207
|
T | C | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+20967T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055207 | ||||||
| chr12:111055234
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+20994C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055234 | ||||||
| chr12:111055281
|
T | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+21041T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055281 | ||||||
| chr12:111055415
|
C | T | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21175C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055415 | ||||||
| chr12:111055428
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+21188C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055428 | ||||||
| chr12:111055451
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+21211T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055451 | ||||||
| chr12:111055454
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+21214A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055454 | ||||||
| chr12:111055509
|
A | C | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+21269A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055509 | ||||||
| chr12:111055619
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.63+21379G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055619 | ||||||
| chr12:111055653
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+21413A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055653 | ||||||
| chr12:111055673
|
C | A | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.63+21433C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055673 | ||||||
| chr12:111055710
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+21470C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055710 | ||||||
| chr12:111055867
|
A | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+21627A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055867 | ||||||
| chr12:111055957
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+21717T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111055957 | ||||||
| chr12:111056079
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+21839G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056079 | ||||||
| chr12:111056088
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+21848T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056088 | ||||||
| chr12:111056331
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+22091C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056331 | ||||||
| chr12:111056509
|
G | A | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+22269G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056509 | ||||||
| chr12:111056553
|
C | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+22313C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056553 | ||||||
| chr12:111056589
|
C | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+22349C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056589 | ||||||
| chr12:111056665
|
G | T | 2 | a0001c0002t0001g0004a0001c0008t0002g0022 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.63+22425G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056665 | ||||||
| chr12:111056670
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(13): Show | 16 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+22430G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056670 | ||||||
| chr12:111056723
|
T | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+22483T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056723 | ||||||
| chr12:111056997
|
C | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+22757C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111056997 | ||||||
| chr12:111057015
|
G | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+22775G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111057015 | ||||||
| chr12:111057356
|
C | T | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+23116C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111057356 | ||||||
| chr12:111057714
|
A | G | 2 | a0001c0001t0002g0043a0007c0021t0002g0064 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.63+23474A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111057714 | ||||||
| chr12:111058491
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+24251T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058491 | ||||||
| chr12:111058561
|
G | GAGAC | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+24324_63+24325i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111058561 | |||||
| chr12:111058565
|
G | C | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+24325G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058565 | ||||||
| chr12:111058820
|
T | C | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+24580T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058820 | ||||||
| chr12:111058883
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+24643A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058883 | ||||||
| chr12:111058914
|
G | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+24674G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058914 | ||||||
| chr12:111058965
|
A | G | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+24725A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111058965 | ||||||
| chr12:111059080
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+24840C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059080 | ||||||
| chr12:111059251
|
C | T | 2 | a0001c0004t0006g0075a0001c0005t0001g0019 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.63+25011C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059251 | ||||||
| chr12:111059331
|
C | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+25091C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059331 | ||||||
| chr12:111059461
|
G | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.63+25221G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059461 | ||||||
| chr12:111059496
|
C | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+25256C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059496 | ||||||
| chr12:111059787
|
C | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+25547C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111059787 | ||||||
| chr12:111060191
|
G | A | 5 | a0001c0004t0001g0005a0001c0004t0004g0041a0001c0004t0006g0075others(2): Show | 5 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+25951G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111060191 | ||||||
| chr12:111060583
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+26343A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111060583 | ||||||
| chr12:111060829
|
G | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+26589G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111060829 | ||||||
| chr12:111061086
|
G | T | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+26846G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061086 | ||||||
| chr12:111061086
|
GC | G | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+26848delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061086 | |||||
| chr12:111061088
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0091others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.63+26848C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061088 | ||||||
| chr12:111061090
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+26850C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061090 | ||||||
| chr12:111061145
|
G | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+26905G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061145 | ||||||
| chr12:111061178
|
G | GCA | 28 | a0001c0001t0001g0091a0001c0001t0002g0058a0001c0001t0002g0059others(25): Show | 28 | HG01069.hp1 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+26975_63+26976d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
G | GCACA | 11 | a0001c0001t0001g0082a0001c0001t0002g0056a0001c0001t0002g0067others(8): Show | 11 | HG01099.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+26973_63+26976d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
G | GCACACA | 5 | a0001c0001t0003g0045a0001c0002t0001g0004a0001c0002t0001g0047others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+26971_63+26976d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0002g0076a0001c0019t0004g0077a0002c0006t0001g0053 | 3 | HG01891.hp2 HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.63+26967_63+26976d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
GCA | G | 3 | a0001c0001t0002g0043a0001c0005t0001g0019a0001c0007t0001g0021 | 3 | HG01169.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+26975_63+26976d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
GCACA | G | 12 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0079others(9): Show | 12 | HG01169.hp1 HG02055.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+26973_63+26976d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
GCACACAC others(1): Show |
G | 11 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(8): Show | 11 | HG01081.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+26969_63+26976d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061178
|
GCACACAC others(9): Show |
G | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+26961_63+26976d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111061178 | |||||
| chr12:111061420
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+27180C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061420 | ||||||
| chr12:111061484
|
A | G | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+27244A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061484 | ||||||
| chr12:111061526
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+27286G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061526 | ||||||
| chr12:111061568
|
C | T | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+27328C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061568 | ||||||
| chr12:111061889
|
AG | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.63+27650delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061889 | ||||||
| chr12:111061893
|
A | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+27653A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061893 | ||||||
| chr12:111061894
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(36): Show | 39 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+27654A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061894 | ||||||
| chr12:111061930
|
C | T | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.63+27690C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111061930 | ||||||
| chr12:111062062
|
G | A | 5 | a0001c0004t0001g0005a0001c0004t0004g0041a0001c0004t0006g0075others(2): Show | 5 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+27822G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062062 | ||||||
| chr12:111062186
|
G | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+27946G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062186 | ||||||
| chr12:111062256
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+28016T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062256 | ||||||
| chr12:111062273
|
T | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+28033T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062273 | ||||||
| chr12:111062379
|
CATTTTAT others(5): Show |
C | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+28142_63+28153d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111062379 | |||||
| chr12:111062401
|
T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+28161T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062401 | ||||||
| chr12:111062402
|
G | A | 7 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0004t0001g0002others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+28162G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062402 | ||||||
| chr12:111062532
|
C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(13): Show | 16 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+28292C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062532 | ||||||
| chr12:111062559
|
G | A | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+28319G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062559 | ||||||
| chr12:111062600
|
GCT | G | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+28364_63+28365d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111062600 | |||||
| chr12:111062605
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+28365C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062605 | ||||||
| chr12:111062738
|
A | G | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(23): Show | 26 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+28498A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062738 | ||||||
| chr12:111062877
|
C | G | 12 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(9): Show | 12 | HG00597.hp1 HG01243.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+28637C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062877 | ||||||
| chr12:111062998
|
G | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+28758G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111062998 | ||||||
| chr12:111063343
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+29103C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111063343 | ||||||
| chr12:111063345
|
C | G | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+29105C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111063345 | ||||||
| chr12:111063501
|
C | T | 4 | a0001c0004t0001g0002a0001c0005t0001g0019a0001c0008t0001g0003others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+29261C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111063501 | ||||||
| chr12:111063563
|
G | C | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.63+29323G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111063563 | ||||||
| chr12:111063716
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+29476C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111063716 | ||||||
| chr12:111064153
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+29913G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064153 | ||||||
| chr12:111064476
|
C | T | 33 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(30): Show | 33 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.63+30236C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064476 | ||||||
| chr12:111064524
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.63+30284T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064524 | ||||||
| chr12:111064732
|
C | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+30492C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064732 | ||||||
| chr12:111064754
|
G | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+30514G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064754 | ||||||
| chr12:111064761
|
CTCATATT others(17): Show |
C | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+30522_63+30545d others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064761 | ||||||
| chr12:111064995
|
T | C | 2 | a0001c0001t0002g0079a0001c0001t0003g0078 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.63+30755T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111064995 | ||||||
| chr12:111065259
|
A | T | 1 | a0001c0002t0001g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+31019A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065259 | ||||||
| chr12:111065293
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+31053G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065293 | ||||||
| chr12:111065294
|
A | G | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+31054A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065294 | ||||||
| chr12:111065396
|
C | T | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+31156C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065396 | ||||||
| chr12:111065518
|
T | G | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+31278T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065518 | ||||||
| chr12:111065524
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+31284C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065524 | ||||||
| chr12:111065813
|
C | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+31573C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065813 | ||||||
| chr12:111065873
|
T | G | 2 | a0001c0001t0004g0054a0005c0012t0009g0044 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+31633T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065873 | ||||||
| chr12:111065958
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+31718C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111065958 | ||||||
| chr12:111066229
|
T | C | 2 | a0001c0001t0002g0043a0007c0021t0002g0064 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.63+31989T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111066229 | ||||||
| chr12:111066259
|
C | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+32019C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111066259 | ||||||
| chr12:111066284
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+32044A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111066284 | ||||||
| chr12:111066860
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+32620C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111066860 | ||||||
| chr12:111066865
|
A | G | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+32625A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111066865 | ||||||
| chr12:111067007
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+32767T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067007 | ||||||
| chr12:111067462
|
T | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+33222T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067462 | ||||||
| chr12:111067493
|
C | T | 2 | a0001c0002t0001g0004a0001c0008t0002g0022 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.63+33253C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067493 | ||||||
| chr12:111067575
|
C | T | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+33335C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067575 | ||||||
| chr12:111067614
|
A | G | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.63+33374A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067614 | ||||||
| chr12:111067700
|
A | G | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+33460A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067700 | ||||||
| chr12:111067904
|
C | G | 4 | a0001c0004t0001g0002a0001c0005t0001g0019a0001c0008t0001g0003others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+33664C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067904 | ||||||
| chr12:111067963
|
T | C | 44 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(41): Show | 44 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.63+33723T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067963 | ||||||
| chr12:111067991
|
T | G | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+33751T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067991 | ||||||
| chr12:111067992
|
C | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(32): Show | 35 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+33752C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111067992 | ||||||
| chr12:111068374
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34134G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068374 | ||||||
| chr12:111068400
|
T | TCTTAAAA others(4): Show |
1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34160_63+34161i others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068400 | ||||||
| chr12:111068404
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34164T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068404 | ||||||
| chr12:111068406
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34166T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068406 | ||||||
| chr12:111068411
|
T | TCGAGGTG others(4): Show |
1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34171_63+34172i others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068411 | ||||||
| chr12:111068413
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34173A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068413 | ||||||
| chr12:111068414
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34174A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068414 | ||||||
| chr12:111068435
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34195G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068435 | ||||||
| chr12:111068451
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+34211C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068451 | ||||||
| chr12:111068460
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34220G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068460 | ||||||
| chr12:111068461
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34221G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068461 | ||||||
| chr12:111068480
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.63+34240G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068480 | ||||||
| chr12:111068497
|
T | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+34257T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068497 | ||||||
| chr12:111068572
|
G | A | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+34332G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068572 | ||||||
| chr12:111068819
|
C | A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+34579C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068819 | ||||||
| chr12:111068980
|
C | A | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+34740C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111068980 | ||||||
| chr12:111069037
|
G | C | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+34797G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069037 | ||||||
| chr12:111069053
|
C | T | 3 | a0001c0001t0001g0006a0001c0003t0001g0008a0001c0004t0005g0007 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+34813C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069053 | ||||||
| chr12:111069168
|
C | G | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+34928C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069168 | ||||||
| chr12:111069332
|
A | G | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+35092A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069332 | ||||||
| chr12:111069341
|
A | G | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+35101A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069341 | ||||||
| chr12:111069466
|
AC | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(35): Show | 38 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+35229delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069466 | |||||
| chr12:111069520
|
C | CTG | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0003t0001g0094 | 3 | HG02572.hp1 HG02717.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.63+35311_63+35312d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069520 | |||||
| chr12:111069533
|
T | TGTGTGTG others(19): Show |
4 | a0001c0001t0002g0056a0001c0001t0002g0076a0001c0002t0001g0061others(1): Show | 4 | HG01099.hp2 HG02698.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+35306_63+35331d others(28): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069533 | |||||
| chr12:111069533
|
T | TGTGTGTG others(21): Show |
1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.63+35312_63+35313i others(30): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069533 | |||||
| chr12:111069536
|
G | A | 7 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+35296G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069536 | ||||||
| chr12:111069536
|
G | GTGTA | 15 | a0001c0001t0002g0030a0001c0002t0001g0004a0001c0002t0001g0037others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+35299_63+35300i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069536 | |||||
| chr12:111069536
|
G | GTGTGTGT others(1): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(12): Show | 15 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+35303_63+35304i others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069536 | |||||
| chr12:111069537
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0002g0067a0001c0001t0005g0055 | 2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.63+35306_63+35307i others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069537 | |||||
| chr12:111069549
|
T | C | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+35309T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069549 | ||||||
| chr12:111069559
|
CGT | C | 3 | a0001c0004t0001g0002a0001c0005t0001g0019a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.63+35330_63+35331d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111069559 | |||||
| chr12:111069561
|
T | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+35321T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069561 | ||||||
| chr12:111069563
|
T | C | 4 | a0001c0004t0001g0002a0001c0005t0001g0019a0001c0007t0001g0021others(1): Show | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+35323T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069563 | ||||||
| chr12:111069600
|
G | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+35360G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069600 | ||||||
| chr12:111069732
|
A | G | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+35492A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069732 | ||||||
| chr12:111069801
|
T | C | 4 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+35561T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111069801 | ||||||
| chr12:111070047
|
C | T | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+35807C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070047 | ||||||
| chr12:111070095
|
C | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+35855C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070095 | ||||||
| chr12:111070152
|
A | G | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(29): Show | 32 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+35912A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070152 | ||||||
| chr12:111070376
|
TCTTCCTT others(25): Show |
T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+36153_63+36184d others(34): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070376 | |||||
| chr12:111070376
|
TCTTCCTT others(29): Show |
T | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+36153_63+36188d others(38): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070376 | |||||
| chr12:111070393
|
T | TTTCC | 3 | a0001c0002t0001g0095a0001c0003t0001g0094a0001c0004t0004g0041 | 3 | HG02486.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.63+36213_63+36216d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
T | TTTCCTTC others(5): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+36205_63+36216d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCC | T | 8 | a0001c0001t0002g0060a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+36213_63+36216d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCCTTC others(1): Show |
T | 10 | a0001c0001t0001g0006a0001c0001t0002g0059a0001c0001t0003g0080others(7): Show | 10 | HG01081.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+36209_63+36216d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCCTTC others(5): Show |
T | 16 | a0001c0001t0001g0082a0001c0001t0002g0043a0001c0001t0002g0079others(13): Show | 16 | HG01169.hp1 HG01169.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+36205_63+36216d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCCTTC others(9): Show |
T | 18 | a0001c0001t0001g0091a0001c0001t0002g0056a0001c0001t0002g0067others(15): Show | 18 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+36201_63+36216d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCCTTC others(13): Show |
T | 4 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0003t0001g0088others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+36197_63+36216d others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070393
|
TTTCCTTC others(17): Show |
T | 2 | a0001c0001t0002g0058a0001c0002t0001g0070 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.63+36193_63+36216d others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111070393 | |||||
| chr12:111070429
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+36189C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070429 | ||||||
| chr12:111070433
|
C | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+36193C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070433 | ||||||
| chr12:111070512
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+36272C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070512 | ||||||
| chr12:111070604
|
A | G | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+36364A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070604 | ||||||
| chr12:111070677
|
A | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(13): Show | 16 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+36437A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070677 | ||||||
| chr12:111070682
|
T | C | 2 | a0001c0001t0002g0083a0001c0004t0001g0005 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+36442T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070682 | ||||||
| chr12:111070717
|
C | A | 33 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(30): Show | 33 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.63+36477C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070717 | ||||||
| chr12:111070824
|
G | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+36584G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111070824 | ||||||
| chr12:111071083
|
G | GT | 20 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(17): Show | 20 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+36860dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111071083 | |||||
| chr12:111071083
|
GT | G | 8 | a0001c0001t0002g0058a0001c0002t0001g0051a0001c0002t0001g0070others(5): Show | 8 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+36860delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111071083 | |||||
| chr12:111071246
|
A | G | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+37006A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111071246 | ||||||
| chr12:111071287
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+37047G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111071287 | ||||||
| chr12:111071374
|
C | T | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+37134C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111071374 | ||||||
| chr12:111071693
|
G | GAT | 7 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+37454_63+37455d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111071693 | |||||
| chr12:111071873
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+37633T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111071873 | ||||||
| chr12:111071877
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+37637T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111071877 | ||||||
| chr12:111072001
|
T | C | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+37761T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072001 | ||||||
| chr12:111072037
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+37797G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072037 | ||||||
| chr12:111072355
|
T | C | 2 | a0001c0002t0001g0004a0001c0008t0002g0022 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.63+38115T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072355 | ||||||
| chr12:111072572
|
A | T | 7 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+38332A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072572 | ||||||
| chr12:111072734
|
A | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+38494A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072734 | ||||||
| chr12:111072788
|
C | A | 3 | a0001c0001t0001g0006a0001c0003t0001g0008a0001c0004t0005g0007 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+38548C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072788 | ||||||
| chr12:111072811
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+38571C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111072811 | ||||||
| chr12:111073116
|
C | T | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+38876C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073116 | ||||||
| chr12:111073150
|
T | A | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+38910T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073150 | ||||||
| chr12:111073156
|
A | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+38916A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073156 | ||||||
| chr12:111073158
|
G | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+38918G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073158 | ||||||
| chr12:111073160
|
TCCTTCGT others(686): Show |
T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+38922_63+39614d others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111073160 | |||||
| chr12:111073161
|
C | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+38921C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073161 | ||||||
| chr12:111073184
|
A | G | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+38944A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073184 | ||||||
| chr12:111073241
|
T | TCTTA | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+39004_63+39005i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111073241 | |||||
| chr12:111073251
|
A | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+39011A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073251 | ||||||
| chr12:111073546
|
T | C | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+39306T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073546 | ||||||
| chr12:111073674
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+39434C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073674 | ||||||
| chr12:111073727
|
A | T | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.63+39487A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073727 | ||||||
| chr12:111073854
|
C | G | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39614C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073854 | ||||||
| chr12:111073856
|
G | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39616G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073856 | ||||||
| chr12:111073860
|
C | G | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39620C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073860 | ||||||
| chr12:111073861
|
T | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39621T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073861 | ||||||
| chr12:111073862
|
G | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39622G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073862 | ||||||
| chr12:111073864
|
G | C | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39624G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073864 | ||||||
| chr12:111073866
|
C | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39626C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073866 | ||||||
| chr12:111073872
|
A | C | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39632A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073872 | ||||||
| chr12:111073873
|
A | C | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39633A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073873 | ||||||
| chr12:111073875
|
G | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39635G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073875 | ||||||
| chr12:111073877
|
C | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39637C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073877 | ||||||
| chr12:111073878
|
TTG | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39639_63+39640d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073878 | ||||||
| chr12:111073884
|
A | C | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39644A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073884 | ||||||
| chr12:111073885
|
G | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39645G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073885 | ||||||
| chr12:111073886
|
T | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39646T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073886 | ||||||
| chr12:111073888
|
C | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39648C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073888 | ||||||
| chr12:111073895
|
G | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39655G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073895 | ||||||
| chr12:111073896
|
C | T | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39656C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073896 | ||||||
| chr12:111073898
|
G | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39658G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073898 | ||||||
| chr12:111073899
|
T | A | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39659T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073899 | ||||||
| chr12:111073900
|
GAGCGATG others(1054): Show |
G | 2 | a0001c0009t0001g0035a0001c0022t0005g0034 | 2 | HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+39661_63+40721d others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073900 | ||||||
| chr12:111073956
|
A | G | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+39716A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111073956 | ||||||
| chr12:111074041
|
T | TAA | 5 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0008t0001g0003others(2): Show | 5 | HG01081.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+39811_63+39812d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111074041 | |||||
| chr12:111074057
|
ACATTGTT others(19): Show |
A | 7 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+39845_63+39870d others(28): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111074057 | |||||
| chr12:111074068
|
C | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+39828C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074068 | ||||||
| chr12:111074230
|
A | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+39990A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074230 | ||||||
| chr12:111074272
|
C | A | 3 | a0001c0002t0001g0051a0001c0010t0001g0049a0001c0010t0001g0050 | 3 | HG02109.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63+40032C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074272 | ||||||
| chr12:111074277
|
C | G | 7 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+40037C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074277 | ||||||
| chr12:111074408
|
G | A | 6 | a0001c0004t0001g0002a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+40168G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074408 | ||||||
| chr12:111074446
|
T | G | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+40206T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074446 | ||||||
| chr12:111074460
|
T | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+40220T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074460 | ||||||
| chr12:111074674
|
G | T | 1 | a0001c0001t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63+40434G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074674 | ||||||
| chr12:111074735
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+40495G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074735 | ||||||
| chr12:111074751
|
G | A | 3 | a0001c0002t0001g0051a0001c0010t0001g0049a0001c0010t0001g0050 | 3 | HG02109.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63+40511G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074751 | ||||||
| chr12:111074845
|
C | T | 7 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+40605C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111074845 | ||||||
| chr12:111075022
|
T | C | 12 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(9): Show | 12 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+40782T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075022 | ||||||
| chr12:111075195
|
A | G | 4 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0005t0001g0019others(1): Show | 4 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+40955A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075195 | ||||||
| chr12:111075260
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+41020C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075260 | ||||||
| chr12:111075300
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.63+41060G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075300 | ||||||
| chr12:111075425
|
T | C | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+41185T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075425 | ||||||
| chr12:111075595
|
T | A | 5 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0005t0001g0019others(2): Show | 5 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+41355T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075595 | ||||||
| chr12:111075757
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+41517G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075757 | ||||||
| chr12:111075855
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63+41615T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075855 | ||||||
| chr12:111075892
|
T | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+41652T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111075892 | ||||||
| chr12:111076021
|
A | G | 3 | a0001c0001t0001g0013a0001c0003t0001g0014a0001c0004t0001g0015 | 3 | HG01884.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.63+41781A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076021 | ||||||
| chr12:111076122
|
A | T | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+41882A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076122 | ||||||
| chr12:111076196
|
G | A | 2 | a0001c0001t0003g0099a0001c0008t0002g0022 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.63+41956G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076196 | ||||||
| chr12:111076205
|
G | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+41965G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076205 | ||||||
| chr12:111076225
|
A | G | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+41985A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076225 | ||||||
| chr12:111076653
|
G | A | 2 | a0001c0003t0001g0014a0001c0004t0001g0015 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.63+42413G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076653 | ||||||
| chr12:111076699
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.63+42459G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076699 | ||||||
| chr12:111076701
|
G | C | 4 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0005t0001g0019others(1): Show | 4 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+42461G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076701 | ||||||
| chr12:111076803
|
T | C | 4 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0005t0001g0019others(1): Show | 4 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+42563T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076803 | ||||||
| chr12:111076959
|
G | A | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+42719G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111076959 | ||||||
| chr12:111077216
|
G | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(63): Show | 66 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.63+42976G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111077216 | ||||||
| chr12:111077425
|
C | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+43185C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111077425 | ||||||
| chr12:111077465
|
G | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0076 | 2 | HG01099.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.63+43225G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111077465 | ||||||
| chr12:111077866
|
G | A | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+43626G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111077866 | ||||||
| chr12:111078182
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0003t0001g0014others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+43942C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078182 | ||||||
| chr12:111078283
|
A | C | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+44043A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078283 | ||||||
| chr12:111078394
|
C | T | 3 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.63+44154C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078394 | ||||||
| chr12:111078614
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+44374G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078614 | ||||||
| chr12:111078634
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+44394C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078634 | ||||||
| chr12:111078815
|
G | A | 14 | a0001c0001t0002g0030a0001c0002t0001g0004a0001c0002t0001g0037others(11): Show | 14 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+44575G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078815 | ||||||
| chr12:111078869
|
G | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+44629G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078869 | ||||||
| chr12:111078979
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+44739A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111078979 | ||||||
| chr12:111079141
|
G | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+44901G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111079141 | ||||||
| chr12:111079443
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+45203C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111079443 | ||||||
| chr12:111079748
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+45508C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111079748 | ||||||
| chr12:111079771
|
C | G | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+45531C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111079771 | ||||||
| chr12:111079866
|
C | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+45626C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111079866 | ||||||
| chr12:111080154
|
C | T | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+45914C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111080154 | ||||||
| chr12:111080284
|
C | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(37): Show | 40 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+46044C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111080284 | ||||||
| chr12:111080302
|
T | G | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+46062T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111080302 | ||||||
| chr12:111080516
|
T | TA | 5 | a0001c0001t0003g0045a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG01081.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+46290dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111080516 | |||||
| chr12:111080626
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+46386C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111080626 | ||||||
| chr12:111080675
|
A | AAAAAT | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+46441_63+46445d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111080675 | |||||
| chr12:111081130
|
G | A | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+46890G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081130 | ||||||
| chr12:111081135
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+46895C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081135 | ||||||
| chr12:111081151
|
T | C | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+46911T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081151 | ||||||
| chr12:111081312
|
T | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+47072T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081312 | ||||||
| chr12:111081418
|
A | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(40): Show | 43 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.63+47178A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081418 | ||||||
| chr12:111081840
|
T | C | 3 | a0001c0002t0001g0093a0001c0019t0004g0077a0002c0006t0001g0053 | 3 | HG01891.hp2 HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+47600T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111081840 | ||||||
| chr12:111082013
|
T | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+47773T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082013 | ||||||
| chr12:111082204
|
G | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+47964G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082204 | ||||||
| chr12:111082469
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+48229G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082469 | ||||||
| chr12:111082472
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+48232C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082472 | ||||||
| chr12:111082489
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+48249C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082489 | ||||||
| chr12:111082801
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+48561A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082801 | ||||||
| chr12:111082889
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+48649G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082889 | ||||||
| chr12:111082890
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+48650G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082890 | ||||||
| chr12:111082909
|
G | A | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+48669G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082909 | ||||||
| chr12:111082916
|
A | C | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+48676A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111082916 | ||||||
| chr12:111083069
|
C | T | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+48829C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083069 | ||||||
| chr12:111083257
|
A | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(40): Show | 43 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.63+49017A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083257 | ||||||
| chr12:111083385
|
C | T | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.63+49145C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083385 | ||||||
| chr12:111083410
|
G | T | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+49170G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083410 | ||||||
| chr12:111083440
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+49200G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083440 | ||||||
| chr12:111083930
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+49690C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111083930 | ||||||
| chr12:111084196
|
A | C | 6 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0002t0001g0095others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+49956A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111084196 | ||||||
| chr12:111084222
|
T | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(63): Show | 66 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.63+49982T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111084222 | ||||||
| chr12:111084480
|
A | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+50240A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111084480 | ||||||
| chr12:111084790
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+50550G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111084790 | ||||||
| chr12:111085518
|
T | C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+51278T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111085518 | ||||||
| chr12:111085578
|
G | C | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+51338G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111085578 | ||||||
| chr12:111085672
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+51432C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111085672 | ||||||
| chr12:111085852
|
C | A | 1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.63+51612C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111085852 | ||||||
| chr12:111086264
|
C | T | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+52024C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111086264 | ||||||
| chr12:111086579
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+52339G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111086579 | ||||||
| chr12:111086869
|
C | G | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+52629C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111086869 | ||||||
| chr12:111086935
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+52695A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111086935 | ||||||
| chr12:111087102
|
G | A | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+52862G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087102 | ||||||
| chr12:111087201
|
A | AAC | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+52973_63+52974d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087201 | |||||
| chr12:111087236
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+52996C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087236 | ||||||
| chr12:111087260
|
C | T | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+53020C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087260 | ||||||
| chr12:111087366
|
CA | C | 16 | a0001c0001t0002g0043a0001c0001t0002g0085a0001c0001t0002g0086others(13): Show | 16 | HG01069.hp1 HG01169.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+53154delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087366
|
CAA | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0002g0030others(44): Show | 47 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+53153_63+53154d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087366
|
CAAA | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(21): Show | 24 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.63+53152_63+53154d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087366
|
CAAAA | C | 4 | a0001c0001t0002g0056a0001c0004t0004g0041a0001c0005t0001g0019others(1): Show | 4 | HG01081.hp1 HG01099.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+53151_63+53154d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087366
|
CAAAAAAA others(2): Show |
C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+53146_63+53154d others(11): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087366
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+53138_63+53154d others(19): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087366 | |||||
| chr12:111087388
|
A | G | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+53148A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087388 | ||||||
| chr12:111087391
|
A | G | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+53151A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087391 | ||||||
| chr12:111087416
|
T | C | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+53176T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087416 | ||||||
| chr12:111087418
|
TGAA | T | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+53186_63+53188d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111087418 | |||||
| chr12:111087466
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+53226T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087466 | ||||||
| chr12:111087756
|
T | G | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+53516T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087756 | ||||||
| chr12:111087948
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+53708G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087948 | ||||||
| chr12:111087998
|
A | C | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.63+53758A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111087998 | ||||||
| chr12:111088007
|
C | G | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+53767C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088007 | ||||||
| chr12:111088111
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(10): Show | 13 | HG00597.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+53871C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088111 | ||||||
| chr12:111088352
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+54112G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088352 | ||||||
| chr12:111088421
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+54181A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088421 | ||||||
| chr12:111088575
|
G | A | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+54335G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088575 | ||||||
| chr12:111088691
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+54451G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088691 | ||||||
| chr12:111088834
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+54594T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088834 | ||||||
| chr12:111088995
|
G | C | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+54755G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111088995 | ||||||
| chr12:111089078
|
G | A | 1 | a0001c0004t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+54838G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089078 | ||||||
| chr12:111089529
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+55289A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089529 | ||||||
| chr12:111089571
|
T | C | 13 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(10): Show | 13 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+55331T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089571 | ||||||
| chr12:111089600
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+55360C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089600 | ||||||
| chr12:111089756
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+55516G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089756 | ||||||
| chr12:111089878
|
C | T | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+55638C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089878 | ||||||
| chr12:111089966
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+55726G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111089966 | ||||||
| chr12:111090127
|
G | A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+55887G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111090127 | ||||||
| chr12:111090167
|
G | T | 6 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+55927G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111090167 | ||||||
| chr12:111090350
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0056a0001c0001t0002g0076others(5): Show | 8 | HG01099.hp2 HG02698.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+56110G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111090350 | ||||||
| chr12:111090844
|
T | C | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+56604T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111090844 | ||||||
| chr12:111090971
|
C | G | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+56731C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111090971 | ||||||
| chr12:111091172
|
A | C | 1 | a0001c0002t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.63+56932A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091172 | ||||||
| chr12:111091185
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+56945C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091185 | ||||||
| chr12:111091330
|
C | T | 5 | a0001c0004t0004g0041a0001c0004t0006g0075a0001c0005t0001g0019others(2): Show | 5 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+57090C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091330 | ||||||
| chr12:111091370
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+57130A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091370 | ||||||
| chr12:111091391
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+57151G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091391 | ||||||
| chr12:111091399
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+57159A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091399 | ||||||
| chr12:111091405
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+57165A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091405 | ||||||
| chr12:111091450
|
G | C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+57210G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091450 | ||||||
| chr12:111091738
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+57498C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091738 | ||||||
| chr12:111091873
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+57633A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091873 | ||||||
| chr12:111091901
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+57661C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091901 | ||||||
| chr12:111091936
|
C | G | 1 | a0001c0004t0001g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+57696C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111091936 | ||||||
| chr12:111092508
|
A | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+58268A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092508 | ||||||
| chr12:111092527
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+58287G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092527 | ||||||
| chr12:111092566
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+58326C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092566 | ||||||
| chr12:111092642
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+58402G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092642 | ||||||
| chr12:111092659
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+58419G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092659 | ||||||
| chr12:111092706
|
G | A | 2 | a0001c0004t0006g0075a0001c0017t0001g0065 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.63+58466G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092706 | ||||||
| chr12:111092805
|
A | AT | 16 | a0001c0001t0002g0076a0001c0001t0002g0100a0001c0001t0005g0055others(13): Show | 16 | HG01069.hp1 HG01069.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+58592dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111092805 | |||||
| chr12:111092805
|
AT | A | 18 | a0001c0001t0002g0043a0001c0001t0002g0062a0001c0001t0002g0079others(15): Show | 18 | HG01169.hp1 HG01169.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+58592delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111092805 | |||||
| chr12:111092805
|
ATTTTTTT others(5): Show |
A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+58581_63+58592d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111092805 | |||||
| chr12:111092851
|
G | A | 3 | a0001c0004t0001g0002a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+58611G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111092851 | ||||||
| chr12:111093539
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+59299T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111093539 | ||||||
| chr12:111093882
|
G | A | 6 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+59642G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111093882 | ||||||
| chr12:111094185
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+59945G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111094185 | ||||||
| chr12:111094691
|
G | T | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+60451G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111094691 | ||||||
| chr12:111094761
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.63+60521C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111094761 | ||||||
| chr12:111094866
|
T | G | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+60626T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111094866 | ||||||
| chr12:111094963
|
C | T | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+60723C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111094963 | ||||||
| chr12:111095440
|
G | C | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+61200G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111095440 | ||||||
| chr12:111096656
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+62416G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111096656 | ||||||
| chr12:111096823
|
C | G | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+62583C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111096823 | ||||||
| chr12:111096900
|
C | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+62660C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111096900 | ||||||
| chr12:111096922
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+62682A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111096922 | ||||||
| chr12:111097653
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+63413C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111097653 | ||||||
| chr12:111097699
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+63459G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111097699 | ||||||
| chr12:111097706
|
G | A | 9 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+63466G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111097706 | ||||||
| chr12:111097765
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+63525G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111097765 | ||||||
| chr12:111098197
|
C | G | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+63957C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111098197 | ||||||
| chr12:111098399
|
C | CA | 8 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0003t0001g0014others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+64176dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111098399 | |||||
| chr12:111098463
|
T | C | 3 | a0001c0003t0001g0046a0001c0004t0006g0075a0001c0017t0001g0065 | 3 | HG02280.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+64223T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111098463 | ||||||
| chr12:111098470
|
G | A | 3 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+64230G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111098470 | ||||||
| chr12:111098784
|
G | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+64544G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111098784 | ||||||
| chr12:111098993
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+64753G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111098993 | ||||||
| chr12:111099018
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(91): Show | 94 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.63+64778A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099018 | ||||||
| chr12:111099053
|
G | A | 6 | a0001c0003t0001g0046a0001c0004t0004g0041a0001c0004t0006g0075others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+64813G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099053 | ||||||
| chr12:111099300
|
C | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+65060C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099300 | ||||||
| chr12:111099484
|
G | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+65244G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099484 | ||||||
| chr12:111099526
|
G | A | 2 | a0001c0001t0003g0099a0001c0008t0002g0022 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.63+65286G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099526 | ||||||
| chr12:111099643
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+65403T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099643 | ||||||
| chr12:111099766
|
C | T | 2 | a0001c0019t0004g0077a0002c0006t0001g0053 | 2 | HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.63+65526C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111099766 | ||||||
| chr12:111100181
|
C | CTG | 11 | a0001c0002t0001g0004a0001c0002t0001g0037a0001c0002t0001g0093others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+65961_63+65962d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111100181 | |||||
| chr12:111100181
|
CTG | C | 4 | a0001c0004t0001g0005a0001c0004t0004g0041a0001c0005t0001g0019others(1): Show | 4 | HG01081.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+65961_63+65962d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111100181 | |||||
| chr12:111100302
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0002g0012others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+66062C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100302 | ||||||
| chr12:111100321
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+66081C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100321 | ||||||
| chr12:111100852
|
CT | C | 2 | a0001c0004t0001g0027a0001c0005t0001g0028 | 2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.63+66614delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111100852 | |||||
| chr12:111100854
|
T | G | 1 | a0001c0001t0003g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+66614T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100854 | ||||||
| chr12:111100872
|
G | A | 2 | a0001c0003t0001g0046a0001c0004t0006g0075 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+66632G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100872 | ||||||
| chr12:111100917
|
T | C | 9 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+66677T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100917 | ||||||
| chr12:111100926
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.63+66686C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100926 | ||||||
| chr12:111100966
|
A | G | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+66726A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111100966 | ||||||
| chr12:111101093
|
A | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0002g0012others(30): Show | 33 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.63+66853A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111101093 | ||||||
| chr12:111101300
|
G | A | 9 | a0001c0001t0003g0045a0001c0003t0001g0033a0001c0003t0008g0032others(6): Show | 9 | HG01081.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+67060G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111101300 | ||||||
| chr12:111101564
|
G | C | 2 | a0001c0001t0003g0045a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.63+67324G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111101564 | ||||||
| chr12:111101652
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.63+67412C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111101652 | ||||||
| chr12:111101906
|
G | A | 13 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0002t0001g0037others(10): Show | 13 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+67666G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111101906 | ||||||
| chr12:111102087
|
T | C | 7 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(4): Show | 7 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+67847T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102087 | ||||||
| chr12:111102204
|
C | T | 2 | a0001c0002t0001g0004a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.63+67964C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102204 | ||||||
| chr12:111102227
|
C | T | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+67987C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102227 | ||||||
| chr12:111102234
|
C | T | 3 | a0001c0001t0001g0006a0001c0003t0001g0008a0001c0004t0005g0007 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+67994C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102234 | ||||||
| chr12:111102335
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+68095A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102335 | ||||||
| chr12:111102584
|
G | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+68344G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102584 | ||||||
| chr12:111102895
|
G | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+68655G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102895 | ||||||
| chr12:111102931
|
A | G | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+68691A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102931 | ||||||
| chr12:111102987
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+68747G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111102987 | ||||||
| chr12:111103041
|
A | G | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+68801A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111103041 | ||||||
| chr12:111103197
|
G | C | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+68957G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111103197 | ||||||
| chr12:111103434
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+69194G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111103434 | ||||||
| chr12:111103865
|
G | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.63+69625G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111103865 | ||||||
| chr12:111104010
|
G | A | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+69770G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104010 | ||||||
| chr12:111104014
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+69774C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104014 | ||||||
| chr12:111104067
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+69827G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104067 | ||||||
| chr12:111104097
|
A | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(31): Show | 34 | HG01081.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+69857A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104097 | ||||||
| chr12:111104161
|
T | C | 3 | a0001c0001t0003g0045a0001c0003t0001g0046a0001c0004t0001g0096 | 3 | HG01243.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+69921T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104161 | ||||||
| chr12:111104168
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+69928G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104168 | ||||||
| chr12:111104256
|
T | C | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+70016T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104256 | ||||||
| chr12:111104270
|
C | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+70030C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104270 | ||||||
| chr12:111104621
|
A | C | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+70381A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104621 | ||||||
| chr12:111104707
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+70467C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104707 | ||||||
| chr12:111104913
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+70673G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111104913 | ||||||
| chr12:111105009
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+70769C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111105009 | ||||||
| chr12:111105037
|
G | A | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+70797G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111105037 | ||||||
| chr12:111105083
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+70843G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111105083 | ||||||
| chr12:111105144
|
G | A | 7 | a0001c0001t0002g0076a0001c0001t0005g0055a0001c0002t0001g0061others(4): Show | 7 | HG02647.hp2 HG02698.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+70904G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111105144 | ||||||
| chr12:111105326
|
G | A | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+71086G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111105326 | ||||||
| chr12:111105485
|
C | CTG | 7 | a0001c0002t0001g0069a0001c0002t0001g0092a0001c0003t0001g0008others(4): Show | 7 | HG00597.hp1 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+71268_63+71269d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105485 | |||||
| chr12:111105485
|
C | CTGTG | 2 | a0001c0002t0001g0051a0001c0004t0001g0005 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.63+71266_63+71269d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105485 | |||||
| chr12:111105485
|
C | CTGTGTG | 5 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0019others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+71264_63+71269d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105485 | |||||
| chr12:111105485
|
C | CTGTGTGT others(1): Show |
6 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+71262_63+71269d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105485 | |||||
| chr12:111105508
|
T | TGTGC | 5 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+71269_63+71270i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105508 | |||||
| chr12:111105864
|
C | CT | 5 | a0001c0002t0001g0018a0001c0002t0001g0092a0001c0004t0001g0002others(2): Show | 5 | HG00597.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+71642dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105864 | |||||
| chr12:111105864
|
CT | C | 31 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(28): Show | 31 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+71642delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105864 | |||||
| chr12:111105864
|
CTT | C | 7 | a0001c0001t0001g0024a0001c0002t0001g0004a0001c0002t0001g0023others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+71641_63+71642d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111105864 | |||||
| chr12:111106021
|
C | T | 19 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(16): Show | 19 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+71781C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111106021 | ||||||
| chr12:111106141
|
A | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+71901A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111106141 | ||||||
| chr12:111106218
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+71978C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111106218 | ||||||
| chr12:111106464
|
A | T | 19 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(16): Show | 19 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+72224A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111106464 | ||||||
| chr12:111107401
|
C | A | 13 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+73161C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111107401 | ||||||
| chr12:111107429
|
A | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+73189A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111107429 | ||||||
| chr12:111107442
|
T | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(17): Show | 20 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+73202T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111107442 | ||||||
| chr12:111107453
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+73213A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111107453 | ||||||
| chr12:111107611
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.63+73371G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111107611 | ||||||
| chr12:111108045
|
C | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+73805C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108045 | ||||||
| chr12:111108340
|
A | C | 1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+74100A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108340 | ||||||
| chr12:111108342
|
G | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0008 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+74102G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108342 | ||||||
| chr12:111108361
|
T | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0056a0007c0021t0002g0064 | 3 | HG01099.hp2 HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.63+74121T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108361 | ||||||
| chr12:111108419
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0003t0001g0008others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+74179C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108419 | ||||||
| chr12:111108519
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+74279T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108519 | ||||||
| chr12:111108657
|
C | T | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.63+74417C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108657 | ||||||
| chr12:111108674
|
C | T | 11 | a0001c0001t0002g0030a0001c0002t0001g0037a0001c0003t0001g0033others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+74434C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108674 | ||||||
| chr12:111108707
|
TGCCCCAC others(7): Show |
T | 50 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(47): Show | 50 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.63+74482_63+74495d others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111108707 | |||||
| chr12:111108868
|
C | G | 4 | a0001c0002t0001g0018a0001c0004t0001g0002a0001c0008t0001g0003others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+74628C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111108868 | ||||||
| chr12:111109057
|
G | A | 7 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+74817G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111109057 | ||||||
| chr12:111109168
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+74928G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111109168 | ||||||
| chr12:111109224
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0007g0097 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+74984C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111109224 | ||||||
| chr12:111110042
|
AT | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(21): Show | 24 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.63+75821delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111110042 | |||||
| chr12:111110298
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+76058A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111110298 | ||||||
| chr12:111110440
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+76200G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111110440 | ||||||
| chr12:111110456
|
CA | C | 7 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+76217delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111110456 | ||||||
| chr12:111110521
|
G | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+76281G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111110521 | ||||||
| chr12:111110669
|
T | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+76429T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111110669 | ||||||
| chr12:111111024
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0002g0030others(15): Show | 18 | HG01081.hp1 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+76784A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111024 | ||||||
| chr12:111111108
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+76868C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111108 | ||||||
| chr12:111111234
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+76994G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111234 | ||||||
| chr12:111111251
|
G | T | 7 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+77011G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111251 | ||||||
| chr12:111111256
|
T | C | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+77016T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111256 | ||||||
| chr12:111111306
|
G | GA | 18 | a0001c0001t0001g0024a0001c0001t0002g0085a0001c0001t0002g0086others(15): Show | 18 | HG01099.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+77076dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111111306 | |||||
| chr12:111111487
|
T | C | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+77247T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111487 | ||||||
| chr12:111111549
|
C | T | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+77309C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111549 | ||||||
| chr12:111111644
|
T | G | 7 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+77404T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111644 | ||||||
| chr12:111111758
|
T | C | 2 | a0001c0019t0004g0077a0002c0006t0001g0053 | 2 | HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.63+77518T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111111758 | ||||||
| chr12:111111851
|
TAA | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+77620_63+77621d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111111851 | |||||
| chr12:111112256
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+78016T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111112256 | ||||||
| chr12:111112329
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+78089C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111112329 | ||||||
| chr12:111112384
|
G | A | 6 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+78144G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111112384 | ||||||
| chr12:111112809
|
C | G | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+78569C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111112809 | ||||||
| chr12:111113046
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+78806C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113046 | ||||||
| chr12:111113108
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+78868C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113108 | ||||||
| chr12:111113159
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+78919G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113159 | ||||||
| chr12:111113383
|
C | G | 10 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+79143C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113383 | ||||||
| chr12:111113390
|
C | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+79150C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113390 | ||||||
| chr12:111113577
|
CAG | C | 11 | a0001c0001t0002g0030a0001c0002t0001g0037a0001c0003t0001g0033others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+79340_63+79341d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111113577 | |||||
| chr12:111113685
|
G | C | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+79445G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113685 | ||||||
| chr12:111113880
|
A | G | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+79640A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111113880 | ||||||
| chr12:111114138
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+79898G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114138 | ||||||
| chr12:111114237
|
C | CTG | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+79997_63+79998i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114237 | ||||||
| chr12:111114239
|
C | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+79999C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114239 | ||||||
| chr12:111114240
|
C | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+80000C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114240 | ||||||
| chr12:111114242
|
G | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+80002G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114242 | ||||||
| chr12:111114243
|
C | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+80003C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114243 | ||||||
| chr12:111114259
|
T | C | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+80019T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114259 | ||||||
| chr12:111114346
|
T | A | 7 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+80106T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114346 | ||||||
| chr12:111114381
|
C | A | 2 | a0001c0002t0001g0004a0001c0002t0007g0097 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+80141C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114381 | ||||||
| chr12:111114398
|
T | C | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+80158T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111114398 | ||||||
| chr12:111115048
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+80808G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115048 | ||||||
| chr12:111115060
|
T | G | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+80820T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115060 | ||||||
| chr12:111115241
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0007g0097 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+81001C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115241 | ||||||
| chr12:111115279
|
C | CTT | 9 | a0001c0001t0002g0012a0001c0001t0002g0083a0001c0002t0001g0004others(6): Show | 9 | HG00597.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+81062_63+81063d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111115279 | |||||
| chr12:111115279
|
CT | C | 19 | a0001c0001t0002g0043a0001c0001t0002g0058a0001c0001t0002g0085others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+81063delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111115279 | |||||
| chr12:111115279
|
CTTTTTT | C | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+81058_63+81063d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111115279 | |||||
| chr12:111115279
|
CTTTTTTT | C | 4 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0073others(1): Show | 4 | HG02630.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+81057_63+81063d others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111115279 | |||||
| chr12:111115309
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(96): Show | 99 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.63+81069A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115309 | ||||||
| chr12:111115409
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+81169C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115409 | ||||||
| chr12:111115468
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+81228G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111115468 | ||||||
| chr12:111116193
|
A | T | 11 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+81953A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116193 | ||||||
| chr12:111116213
|
A | T | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+81973A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116213 | ||||||
| chr12:111116305
|
T | A | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.63+82065T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116305 | ||||||
| chr12:111116527
|
T | C | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+82287T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116527 | ||||||
| chr12:111116584
|
G | A | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+82344G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116584 | ||||||
| chr12:111116605
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+82365G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116605 | ||||||
| chr12:111116664
|
C | G | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+82424C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116664 | ||||||
| chr12:111116732
|
A | G | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.63+82492A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111116732 | ||||||
| chr12:111117279
|
T | A | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+83039T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111117279 | ||||||
| chr12:111117308
|
T | G | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+83068T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111117308 | ||||||
| chr12:111117667
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+83427A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111117667 | ||||||
| chr12:111117748
|
T | G | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+83508T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111117748 | ||||||
| chr12:111118164
|
G | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+83924G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111118164 | ||||||
| chr12:111118264
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+84024C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111118264 | ||||||
| chr12:111118401
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+84161C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111118401 | ||||||
| chr12:111118643
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+84403C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111118643 | ||||||
| chr12:111118698
|
C | T | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+84458C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111118698 | ||||||
| chr12:111119068
|
T | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(18): Show | 21 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+84828T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119068 | ||||||
| chr12:111119162
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+84922G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119162 | ||||||
| chr12:111119256
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63+85016C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119256 | ||||||
| chr12:111119351
|
C | G | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+85111C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119351 | ||||||
| chr12:111119384
|
G | A | 7 | a0001c0001t0002g0076a0001c0001t0005g0055a0001c0002t0001g0061others(4): Show | 7 | HG02647.hp2 HG02698.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+85144G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119384 | ||||||
| chr12:111119448
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+85208A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119448 | ||||||
| chr12:111119608
|
G | A | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+85368G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119608 | ||||||
| chr12:111119699
|
C | T | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+85459C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119699 | ||||||
| chr12:111119849
|
G | A | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+85609G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119849 | ||||||
| chr12:111119914
|
C | T | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+85674C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119914 | ||||||
| chr12:111119922
|
G | T | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+85682G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111119922 | ||||||
| chr12:111120399
|
C | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+86159C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111120399 | ||||||
| chr12:111120671
|
GA | G | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(23): Show | 26 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+86445delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111120671 | |||||
| chr12:111120750
|
A | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(19): Show | 22 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+86510A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111120750 | ||||||
| chr12:111120766
|
G | A | 3 | a0001c0004t0001g0027a0001c0005t0001g0028a0001c0013t0001g0063 | 3 | HG02559.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+86526G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111120766 | ||||||
| chr12:111121012
|
C | T | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+86772C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121012 | ||||||
| chr12:111121013
|
G | A | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+86773G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121013 | ||||||
| chr12:111121101
|
C | CA | 22 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0002g0030others(19): Show | 22 | HG01069.hp1 HG01069.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+86879dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121101 | |||||
| chr12:111121101
|
CA | C | 14 | a0001c0001t0002g0079a0001c0001t0002g0086a0001c0001t0003g0078others(11): Show | 14 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+86879delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121101 | |||||
| chr12:111121101
|
CAA | C | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(19): Show | 22 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+86878_63+86879d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121101 | |||||
| chr12:111121114
|
A | C | 5 | a0001c0001t0003g0045a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+86874A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121114 | ||||||
| chr12:111121173
|
T | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(49): Show | 52 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.63+86933T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121173 | ||||||
| chr12:111121369
|
CT | C | 55 | a0001c0001t0001g0091a0001c0001t0002g0043a0001c0001t0002g0056others(52): Show | 55 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.63+87154delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121369
|
CTT | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0073a0001c0002t0001g0074others(3): Show | 6 | HG02486.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+87153_63+87154d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121369
|
CTTTT | C | 6 | a0001c0001t0001g0024a0001c0002t0001g0004a0001c0002t0001g0023others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+87151_63+87154d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121369
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0002g0030a0001c0003t0001g0033a0001c0003t0008g0032others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+87146_63+87154d others(11): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121369
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+87145_63+87154d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121369
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+87143_63+87154d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121369 | |||||
| chr12:111121374
|
T | TTC | 6 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+87135_63+87136i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111121374 | |||||
| chr12:111121376
|
T | C | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+87136T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121376 | ||||||
| chr12:111121377
|
T | C | 9 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG00597.hp1 HG01081.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+87137T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121377 | ||||||
| chr12:111121379
|
T | C | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.63+87139T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121379 | ||||||
| chr12:111121380
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+87140T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121380 | ||||||
| chr12:111121381
|
T | C | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+87141T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121381 | ||||||
| chr12:111121386
|
T | C | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+87146T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121386 | ||||||
| chr12:111121388
|
T | C | 6 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0002g0085others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+87148T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121388 | ||||||
| chr12:111121400
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+87160G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121400 | ||||||
| chr12:111121652
|
A | G | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+87412A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111121652 | ||||||
| chr12:111122224
|
C | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+87984C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111122224 | ||||||
| chr12:111122797
|
G | A | 5 | a0001c0001t0003g0045a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+88557G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111122797 | ||||||
| chr12:111122854
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+88614G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111122854 | ||||||
| chr12:111123222
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.63+88982G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123222 | ||||||
| chr12:111123236
|
G | A | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+88996G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123236 | ||||||
| chr12:111123305
|
C | G | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+89065C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123305 | ||||||
| chr12:111123305
|
C | T | 2 | a0001c0004t0001g0005a0001c0007t0001g0021 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+89065C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123305 | ||||||
| chr12:111123353
|
T | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+89113T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123353 | ||||||
| chr12:111123498
|
T | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0008 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.63+89258T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123498 | ||||||
| chr12:111123517
|
G | T | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+89277G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123517 | ||||||
| chr12:111123543
|
A | AT | 4 | a0001c0002t0001g0004a0001c0002t0007g0097a0001c0004t0001g0005others(1): Show | 4 | HG02647.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+89313dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111123543 | |||||
| chr12:111123892
|
T | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(49): Show | 52 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.63+89652T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111123892 | ||||||
| chr12:111124193
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(20): Show | 23 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+89953A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124193 | ||||||
| chr12:111124495
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(44): Show | 47 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.64-89705C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124495 | ||||||
| chr12:111124689
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0002g0030others(20): Show | 23 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-89511T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124689 | ||||||
| chr12:111124732
|
C | T | 5 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-89468C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124732 | ||||||
| chr12:111124750
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-89450G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124750 | ||||||
| chr12:111124753
|
T | C | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-89447T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124753 | ||||||
| chr12:111124779
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(20): Show | 23 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-89421C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124779 | ||||||
| chr12:111124986
|
A | G | 6 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0002g0085others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-89214A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111124986 | ||||||
| chr12:111125019
|
G | T | 11 | a0001c0001t0002g0030a0001c0002t0001g0037a0001c0003t0001g0033others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-89181G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125019 | ||||||
| chr12:111125180
|
AT | A | 16 | a0001c0001t0001g0082a0001c0001t0003g0045a0001c0001t0004g0054others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-89003delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111125180 | |||||
| chr12:111125180
|
ATT | A | 11 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0083others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-89004_64-89003d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111125180 | |||||
| chr12:111125180
|
ATTT | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.64-89005_64-89003d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111125180 | |||||
| chr12:111125265
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(34): Show | 37 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.64-88935C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125265 | ||||||
| chr12:111125295
|
T | C | 2 | a0001c0001t0001g0006a0001c0003t0001g0008 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-88905T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125295 | ||||||
| chr12:111125431
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0002t0001g0037others(14): Show | 17 | HG01081.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-88769G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125431 | ||||||
| chr12:111125518
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-88682T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125518 | ||||||
| chr12:111125683
|
T | C | 44 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(41): Show | 44 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.64-88517T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125683 | ||||||
| chr12:111125863
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 38 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.64-88337T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111125863 | ||||||
| chr12:111126017
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(18): Show | 21 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-88183C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126017 | ||||||
| chr12:111126043
|
G | A | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64-88157G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126043 | ||||||
| chr12:111126045
|
G | A | 6 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0002g0085others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-88155G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126045 | ||||||
| chr12:111126050
|
G | C | 4 | a0001c0001t0003g0045a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-88150G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126050 | ||||||
| chr12:111126051
|
GGC | G | 11 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0083others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-88147_64-88146d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111126051 | |||||
| chr12:111126052
|
GC | G | 15 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(12): Show | 15 | HG01169.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-88147delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126052 | ||||||
| chr12:111126053
|
C | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0091others(44): Show | 47 | HG00597.hp1 HG01081.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.64-88147C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126053 | ||||||
| chr12:111126110
|
C | CT | 4 | a0001c0001t0001g0091a0001c0002t0001g0090a0001c0007t0001g0021others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-88074dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111126110 | |||||
| chr12:111126110
|
CT | C | 5 | a0001c0001t0003g0081a0001c0002t0001g0004a0001c0002t0007g0097others(2): Show | 5 | HG01081.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-88074delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111126110 | |||||
| chr12:111126140
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 38 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.64-88060A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126140 | ||||||
| chr12:111126164
|
G | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(31): Show | 34 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.64-88036G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126164 | ||||||
| chr12:111126202
|
A | G | 11 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0083others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-87998A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126202 | ||||||
| chr12:111126211
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-87989C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126211 | ||||||
| chr12:111126212
|
G | A | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-87988G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126212 | ||||||
| chr12:111126230
|
T | G | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64-87970T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126230 | ||||||
| chr12:111126258
|
G | A | 3 | a0001c0001t0001g0082a0001c0004t0001g0096a0001c0004t0006g0075 | 3 | HG01243.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-87942G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126258 | ||||||
| chr12:111126308
|
C | T | 11 | a0001c0001t0002g0030a0001c0002t0001g0037a0001c0002t0001g0093others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-87892C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126308 | ||||||
| chr12:111126811
|
C | T | 5 | a0001c0001t0001g0024a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-87389C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126811 | ||||||
| chr12:111126829
|
G | A | 18 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0067others(15): Show | 18 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-87371G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111126829 | ||||||
| chr12:111127026
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0002t0001g0037others(14): Show | 17 | HG01081.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-87174C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127026 | ||||||
| chr12:111127075
|
G | A | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-87125G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127075 | ||||||
| chr12:111127280
|
C | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-86920C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127280 | ||||||
| chr12:111127313
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0008 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-86887G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127313 | ||||||
| chr12:111127364
|
C | A | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-86836C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127364 | ||||||
| chr12:111127367
|
A | G | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-86833A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127367 | ||||||
| chr12:111127446
|
GT | G | 2 | a0001c0001t0001g0082a0001c0004t0006g0075 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-86753delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127446 | ||||||
| chr12:111127502
|
C | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0048a0001c0003t0001g0008 | 3 | HG02818.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.64-86698C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127502 | ||||||
| chr12:111127540
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64-86660A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127540 | ||||||
| chr12:111127575
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-86625G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127575 | ||||||
| chr12:111127703
|
C | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-86497C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127703 | ||||||
| chr12:111127792
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-86408C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127792 | ||||||
| chr12:111127863
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(44): Show | 47 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.64-86337C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127863 | ||||||
| chr12:111127917
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64-86283A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111127917 | ||||||
| chr12:111128165
|
G | A | 32 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(29): Show | 32 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.64-86035G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128165 | ||||||
| chr12:111128327
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-85873C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128327 | ||||||
| chr12:111128371
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-85829C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128371 | ||||||
| chr12:111128484
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-85716A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128484 | ||||||
| chr12:111128764
|
T | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-85436T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128764 | ||||||
| chr12:111128917
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-85283G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111128917 | ||||||
| chr12:111129407
|
TTCCA | T | 16 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0002t0001g0037others(13): Show | 16 | HG01081.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-84788_64-84785d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111129407 | |||||
| chr12:111129624
|
T | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64-84576T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111129624 | ||||||
| chr12:111129676
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-84524A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111129676 | ||||||
| chr12:111129681
|
C | T | 2 | a0001c0001t0002g0030a0001c0003t0001g0033 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-84519C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111129681 | ||||||
| chr12:111129692
|
G | A | 25 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(22): Show | 25 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-84508G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111129692 | ||||||
| chr12:111129837
|
G | A | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-84363G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111129837 | ||||||
| chr12:111130057
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0002g0030a0001c0001t0002g0062others(17): Show | 20 | HG01081.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-84143A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111130057 | ||||||
| chr12:111130205
|
G | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-83995G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111130205 | ||||||
| chr12:111130394
|
A | G | 3 | a0001c0001t0002g0086a0001c0002t0001g0087a0002c0006t0001g0084 | 3 | HG02109.hp1 HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-83806A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111130394 | ||||||
| chr12:111130640
|
C | CT | 44 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(41): Show | 44 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.64-83559dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111130640 | |||||
| chr12:111130743
|
T | C | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-83457T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111130743 | ||||||
| chr12:111130955
|
T | G | 9 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-83245T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111130955 | ||||||
| chr12:111131036
|
G | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-83164G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131036 | ||||||
| chr12:111131310
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(21): Show | 24 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-82890G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131310 | ||||||
| chr12:111131609
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-82591A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131609 | ||||||
| chr12:111131797
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-82403G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131797 | ||||||
| chr12:111131843
|
C | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-82357C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131843 | ||||||
| chr12:111131866
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-82334G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111131866 | ||||||
| chr12:111132011
|
G | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(43): Show | 46 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.64-82189G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111132011 | ||||||
| chr12:111132047
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-82153C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111132047 | ||||||
| chr12:111132310
|
C | A | 21 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0079others(18): Show | 21 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-81890C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111132310 | ||||||
| chr12:111132557
|
C | CT | 12 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0100others(9): Show | 12 | HG01069.hp1 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-81616dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111132557 | |||||
| chr12:111132557
|
C | CTTTTTTT others(33): Show |
1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-81616_64-81615i others(42): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111132557 | |||||
| chr12:111132557
|
CTT | C | 12 | a0001c0001t0002g0062a0001c0001t0002g0079a0001c0001t0003g0078others(9): Show | 12 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-81617_64-81616d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111132557 | |||||
| chr12:111132557
|
CTTTTTTT | C | 14 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(11): Show | 14 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-81622_64-81616d others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111132557 | |||||
| chr12:111132642
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-81558C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111132642 | ||||||
| chr12:111133381
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(36): Show | 39 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-80819T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111133381 | ||||||
| chr12:111133762
|
C | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(36): Show | 39 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-80438C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111133762 | ||||||
| chr12:111133821
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-80379G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111133821 | ||||||
| chr12:111134289
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(44): Show | 47 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.64-79911G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134289 | ||||||
| chr12:111134321
|
C | T | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-79879C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134321 | ||||||
| chr12:111134501
|
T | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(41): Show | 44 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.64-79699T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134501 | ||||||
| chr12:111134594
|
T | TTC | 5 | a0001c0001t0004g0054a0001c0001t0005g0055a0001c0002t0001g0071others(2): Show | 5 | HG02647.hp2 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-79580_64-79579d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134594 | |||||
| chr12:111134612
|
C | CTGTGTGT others(3): Show |
5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-79587_64-79586i others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134612 | |||||
| chr12:111134612
|
C | CTGTGTGT others(5): Show |
2 | a0001c0002t0001g0066a0001c0010t0001g0050 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.64-79587_64-79586i others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134612 | |||||
| chr12:111134612
|
C | CTGTGTGT others(7): Show |
1 | a0001c0010t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64-79587_64-79586i others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134612 | |||||
| chr12:111134612
|
C | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-79588C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134612 | ||||||
| chr12:111134614
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-79585_64-79584i others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134614 | |||||
| chr12:111134614
|
C | CTGTGTGT others(13): Show |
2 | a0001c0002t0001g0004a0001c0004t0001g0005 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64-79585_64-79584i others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134614 | |||||
| chr12:111134614
|
C | G | 9 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-79586C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134614 | ||||||
| chr12:111134616
|
C | CTGTGTGT others(1): Show |
2 | a0001c0004t0006g0075a0001c0017t0001g0065 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.64-79583_64-79582i others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134616 | |||||
| chr12:111134616
|
C | CTGTGTGT others(5): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0002t0001g0051others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-79583_64-79582i others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134616 | |||||
| chr12:111134616
|
C | CTGTGTGT others(7): Show |
1 | a0001c0002t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-79583_64-79582i others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134616 | |||||
| chr12:111134616
|
C | CTGTGTGT others(9): Show |
1 | a0001c0002t0001g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-79583_64-79582i others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134616 | |||||
| chr12:111134616
|
C | CTGTGTGT others(11): Show |
1 | a0001c0002t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64-79583_64-79582i others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134616 | |||||
| chr12:111134616
|
C | G | 13 | a0001c0001t0002g0079a0001c0001t0002g0085a0001c0001t0003g0045others(10): Show | 13 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-79584C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134616 | ||||||
| chr12:111134618
|
C | CTG | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-79581_64-79580i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134618 | |||||
| chr12:111134618
|
C | CTGTG | 2 | a0001c0001t0001g0082a0001c0001t0002g0060 | 2 | HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-79581_64-79580i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134618 | |||||
| chr12:111134618
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0002g0012a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.64-79581_64-79580i others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134618 | |||||
| chr12:111134618
|
C | CTGTGTGT others(9): Show |
1 | a0001c0003t0001g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-79581_64-79580i others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134618 | |||||
| chr12:111134618
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64-79581_64-79580i others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134618 | |||||
| chr12:111134618
|
C | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0079others(22): Show | 25 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-79582C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134618 | ||||||
| chr12:111134620
|
C | CTCTCTCT others(5): Show |
1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-79579_64-79578i others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTCTCTGT others(11): Show |
3 | a0001c0001t0002g0062a0001c0002t0001g0093a0001c0004t0001g0027 | 3 | HG02965.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.64-79579_64-79578i others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTCTCTGT others(13): Show |
2 | a0001c0003t0008g0032a0001c0013t0001g0063 | 2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-79579_64-79578i others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTCTGTGT others(7): Show |
2 | a0001c0005t0001g0038a0001c0005t0001g0039 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.64-79579_64-79578i others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTG | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0001c0008t0001g0003 | 3 | HG02559.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.64-79552_64-79551d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTGTGTGT others(9): Show |
2 | a0001c0002t0001g0037a0006c0020t0001g0020 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64-79566_64-79551d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | CTGTGTGT others(11): Show |
1 | a0001c0003t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.64-79568_64-79551d others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111134620 | |||||
| chr12:111134620
|
C | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(50): Show | 53 | HG01081.hp1 HG01081.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.64-79580C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134620 | ||||||
| chr12:111134649
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-79551_64-79550i others(25): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134649 | ||||||
| chr12:111134711
|
A | G | 42 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(39): Show | 42 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.64-79489A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134711 | ||||||
| chr12:111134849
|
C | G | 12 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-79351C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134849 | ||||||
| chr12:111134854
|
A | T | 12 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-79346A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111134854 | ||||||
| chr12:111135198
|
GA | G | 6 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-78992delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111135198 | |||||
| chr12:111135244
|
G | A | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-78956G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135244 | ||||||
| chr12:111135341
|
T | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-78859T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135341 | ||||||
| chr12:111135342
|
C | T | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-78858C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135342 | ||||||
| chr12:111135432
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-78768T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135432 | ||||||
| chr12:111135532
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-78668G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135532 | ||||||
| chr12:111135884
|
G | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(65): Show | 68 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(65): Show |
intron_variant | MODIFIER | c.64-78316G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135884 | ||||||
| chr12:111135940
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(4): Show | 7 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-78260C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135940 | ||||||
| chr12:111135947
|
C | T | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-78253C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111135947 | ||||||
| chr12:111136111
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-78089G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136111 | ||||||
| chr12:111136439
|
G | A | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-77761G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136439 | ||||||
| chr12:111136469
|
C | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(43): Show | 46 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.64-77731C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136469 | ||||||
| chr12:111136495
|
A | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-77705A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136495 | ||||||
| chr12:111136646
|
A | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(4): Show | 7 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-77554A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136646 | ||||||
| chr12:111136897
|
A | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(16): Show | 19 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-77303A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136897 | ||||||
| chr12:111136924
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(15): Show | 18 | HG01081.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-77276G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136924 | ||||||
| chr12:111136942
|
C | CT | 24 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0001g0091others(21): Show | 24 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-77245dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111136942 | |||||
| chr12:111136957
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-77243A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111136957 | ||||||
| chr12:111137104
|
AT | A | 29 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0085others(26): Show | 29 | HG01081.hp1 HG01099.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.64-77080delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137104 | |||||
| chr12:111137104
|
ATT | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-77081_64-77080d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137104 | |||||
| chr12:111137132
|
C | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-77068C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111137132 | ||||||
| chr12:111137357
|
GTTGTTGT | G | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(9): Show | 12 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-76836_64-76830d others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137357 | |||||
| chr12:111137364
|
T | TTG | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-76835_64-76834i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137364 | |||||
| chr12:111137364
|
T | TTGTTGTT others(4): Show |
1 | a0001c0010t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-76835_64-76834i others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137364 | |||||
| chr12:111137364
|
T | TTGTTGTT others(7): Show |
2 | a0001c0001t0003g0045a0001c0004t0001g0005 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64-76835_64-76834i others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137364 | |||||
| chr12:111137364
|
T | TTGTTGTT others(10): Show |
2 | a0001c0001t0002g0085a0001c0002t0001g0004 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.64-76835_64-76834i others(19): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111137364 | |||||
| chr12:111137371
|
A | T | 13 | a0001c0001t0002g0079a0001c0001t0002g0085a0001c0001t0003g0045others(10): Show | 13 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-76829A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111137371 | ||||||
| chr12:111137374
|
T | A | 6 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-76826T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111137374 | ||||||
| chr12:111137378
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(22): Show | 25 | HG01099.hp1 HG01169.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-76822C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111137378 | ||||||
| chr12:111137875
|
A | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(43): Show | 46 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.64-76325A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111137875 | ||||||
| chr12:111138060
|
T | G | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(23): Show | 26 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.64-76140T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138060 | ||||||
| chr12:111138123
|
C | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-76077C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138123 | ||||||
| chr12:111138144
|
G | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-76056G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138144 | ||||||
| chr12:111138325
|
G | A | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-75875G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138325 | ||||||
| chr12:111138658
|
G | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-75542G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138658 | ||||||
| chr12:111138987
|
G | A | 1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-75213G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111138987 | ||||||
| chr12:111139057
|
C | A | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-75143C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139057 | ||||||
| chr12:111139198
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-75002A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139198 | ||||||
| chr12:111139392
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-74808G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139392 | ||||||
| chr12:111139924
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-74276G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139924 | ||||||
| chr12:111139930
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(9): Show | 12 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-74270C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139930 | ||||||
| chr12:111139984
|
G | A | 2 | a0001c0007t0001g0021a0001c0017t0001g0065 | 2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64-74216G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111139984 | ||||||
| chr12:111140100
|
G | C | 12 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-74100G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140100 | ||||||
| chr12:111140300
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(44): Show | 47 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.64-73900T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140300 | ||||||
| chr12:111140404
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-73796T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140404 | ||||||
| chr12:111140547
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-73653C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140547 | ||||||
| chr12:111140688
|
TA | T | 2 | a0001c0004t0004g0041a0001c0014t0001g0042 | 2 | HG01081.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-73511delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140688 | ||||||
| chr12:111140730
|
G | A | 6 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-73470G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140730 | ||||||
| chr12:111140764
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(9): Show | 12 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-73436C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140764 | ||||||
| chr12:111140970
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0079others(18): Show | 21 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-73230G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111140970 | ||||||
| chr12:111141069
|
G | A | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(9): Show | 12 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-73131G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141069 | ||||||
| chr12:111141189
|
C | T | 21 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(18): Show | 21 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-73011C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141189 | ||||||
| chr12:111141227
|
A | AAC | 13 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(10): Show | 13 | HG00597.hp1 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-72945_64-72944d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACAC | 9 | a0001c0001t0002g0079a0001c0001t0002g0086a0001c0001t0003g0078others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-72947_64-72944d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACACAC | 11 | a0001c0001t0002g0062a0001c0001t0002g0085a0001c0001t0003g0045others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-72949_64-72944d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACACACA others(1): Show |
3 | a0001c0002t0001g0037a0001c0003t0008g0032a0001c0004t0001g0005 | 3 | HG02280.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64-72951_64-72944d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACACACA others(11): Show |
3 | a0001c0002t0001g0023a0001c0002t0001g0026a0006c0020t0001g0020 | 3 | HG01099.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64-72961_64-72944d others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACACACA others(13): Show |
8 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0002t0001g0025others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-72963_64-72944d others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141227
|
A | AACACACA others(17): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-72967_64-72944d others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111141227 | |||||
| chr12:111141390
|
T | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(40): Show | 43 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-72810T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141390 | ||||||
| chr12:111141422
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0085others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-72778G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141422 | ||||||
| chr12:111141621
|
A | G | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-72579A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141621 | ||||||
| chr12:111141716
|
G | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-72484G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141716 | ||||||
| chr12:111141847
|
G | A | 4 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-72353G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141847 | ||||||
| chr12:111141943
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-72257G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111141943 | ||||||
| chr12:111142075
|
C | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0002t0001g0037others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-72125C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142075 | ||||||
| chr12:111142226
|
T | G | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-71974T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142226 | ||||||
| chr12:111142272
|
C | T | 15 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0067others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-71928C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142272 | ||||||
| chr12:111142529
|
GA | G | 20 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(17): Show | 20 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-71653delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111142529 | |||||
| chr12:111142529
|
GAA | G | 4 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-71654_64-71653d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111142529 | |||||
| chr12:111142529
|
GAAA | G | 21 | a0001c0001t0001g0006a0001c0001t0002g0062a0001c0001t0002g0079others(18): Show | 21 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-71655_64-71653d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111142529 | |||||
| chr12:111142533
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-71667A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142533 | ||||||
| chr12:111142663
|
T | G | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-71537T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142663 | ||||||
| chr12:111142795
|
G | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(40): Show | 43 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-71405G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142795 | ||||||
| chr12:111142823
|
G | A | 9 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-71377G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142823 | ||||||
| chr12:111142835
|
C | T | 1 | a0001c0019t0004g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-71365C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142835 | ||||||
| chr12:111142870
|
C | G | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64-71330C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142870 | ||||||
| chr12:111142954
|
G | A | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-71246G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142954 | ||||||
| chr12:111142987
|
T | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64-71213T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111142987 | ||||||
| chr12:111143089
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-71111C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143089 | ||||||
| chr12:111143161
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-71039C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143161 | ||||||
| chr12:111143193
|
G | A | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-71007G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143193 | ||||||
| chr12:111143456
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-70744C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143456 | ||||||
| chr12:111143665
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-70535G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143665 | ||||||
| chr12:111143725
|
A | G | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-70475A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143725 | ||||||
| chr12:111143734
|
CG | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-70465delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143734 | ||||||
| chr12:111143810
|
G | T | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-70390G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143810 | ||||||
| chr12:111143974
|
C | G | 69 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(66): Show | 69 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-70226C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111143974 | ||||||
| chr12:111144052
|
C | A | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64-70148C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111144052 | ||||||
| chr12:111144338
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0002g0085others(18): Show | 21 | HG01081.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-69862C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111144338 | ||||||
| chr12:111144698
|
G | A | 5 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-69502G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111144698 | ||||||
| chr12:111144826
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(69): Show | 72 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(69): Show |
intron_variant | MODIFIER | c.64-69374T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111144826 | ||||||
| chr12:111145108
|
C | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-69092C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145108 | ||||||
| chr12:111145230
|
T | C | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-68970T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145230 | ||||||
| chr12:111145321
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0002g0079a0001c0001t0003g0078others(14): Show | 17 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-68879G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145321 | ||||||
| chr12:111145428
|
G | A | 4 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0002t0001g0004others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-68772G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145428 | ||||||
| chr12:111145578
|
G | C | 1 | a0001c0001t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-68622G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145578 | ||||||
| chr12:111145830
|
C | A | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-68370C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111145830 | ||||||
| chr12:111145833
|
T | TTTTG | 9 | a0001c0001t0002g0085a0001c0001t0003g0045a0001c0001t0004g0054others(6): Show | 9 | HG01081.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-68347_64-68344d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111145833 | |||||
| chr12:111145833
|
TTTTG | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-68347_64-68344d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111145833 | |||||
| chr12:111145854
|
TTTTTG | T | 10 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(7): Show | 10 | HG01099.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-68324_64-68320d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111145854 | |||||
| chr12:111146079
|
A | G | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-68121A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146079 | ||||||
| chr12:111146211
|
T | C | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-67989T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146211 | ||||||
| chr12:111146537
|
G | A | 2 | a0001c0019t0004g0077a0002c0006t0001g0053 | 2 | HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.64-67663G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146537 | ||||||
| chr12:111146537
|
G | C | 3 | a0001c0002t0001g0018a0001c0008t0001g0003a0001c0011t0001g0001 | 3 | HG02257.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-67663G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146537 | ||||||
| chr12:111146638
|
C | CAT | 98 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(95): Show | 98 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.64-67562_64-67561i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146638 | ||||||
| chr12:111146876
|
G | A | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-67324G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146876 | ||||||
| chr12:111146969
|
A | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-67231A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146969 | ||||||
| chr12:111146991
|
T | C | 3 | a0001c0001t0002g0086a0001c0002t0001g0087a0001c0003t0001g0088 | 3 | HG01884.hp2 HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-67209T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111146991 | ||||||
| chr12:111147060
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-67140G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147060 | ||||||
| chr12:111147220
|
T | C | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-66980T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147220 | ||||||
| chr12:111147285
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(96): Show | 99 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-66915T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147285 | ||||||
| chr12:111147455
|
C | A | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-66745C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147455 | ||||||
| chr12:111147622
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-66578G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147622 | ||||||
| chr12:111147828
|
G | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-66372G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147828 | ||||||
| chr12:111147876
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-66324A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111147876 | ||||||
| chr12:111148080
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-66120A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148080 | ||||||
| chr12:111148188
|
T | C | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-66012T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148188 | ||||||
| chr12:111148370
|
G | A | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-65830G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148370 | ||||||
| chr12:111148525
|
TTTATG | T | 4 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-65668_64-65664d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111148525 | |||||
| chr12:111148622
|
A | G | 22 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(19): Show | 22 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-65578A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148622 | ||||||
| chr12:111148827
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-65373T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148827 | ||||||
| chr12:111148871
|
C | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0079others(13): Show | 16 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-65329C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111148871 | ||||||
| chr12:111149028
|
A | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-65172A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149028 | ||||||
| chr12:111149061
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.64-65139C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149061 | ||||||
| chr12:111149227
|
A | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-64973A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149227 | ||||||
| chr12:111149286
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-64914G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149286 | ||||||
| chr12:111149314
|
G | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(65): Show | 68 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(65): Show |
intron_variant | MODIFIER | c.64-64886G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149314 | ||||||
| chr12:111149349
|
A | AC | 17 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-64847dupC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111149349 | |||||
| chr12:111149629
|
G | A | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-64571G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149629 | ||||||
| chr12:111149777
|
A | G | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-64423A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111149777 | ||||||
| chr12:111150126
|
A | G | 26 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(23): Show | 26 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.64-64074A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150126 | ||||||
| chr12:111150194
|
G | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-64006G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150194 | ||||||
| chr12:111150288
|
A | T | 1 | a0001c0001t0002g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-63912A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150288 | ||||||
| chr12:111150566
|
T | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64-63634T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150566 | ||||||
| chr12:111150600
|
G | C | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-63600G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150600 | ||||||
| chr12:111150886
|
T | C | 4 | a0001c0001t0003g0099a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-63314T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150886 | ||||||
| chr12:111150888
|
G | A | 1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-63312G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111150888 | ||||||
| chr12:111151166
|
C | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-63034C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151166 | ||||||
| chr12:111151272
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-62928C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151272 | ||||||
| chr12:111151584
|
G | A | 2 | a0001c0001t0002g0085a0001c0002t0001g0004 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.64-62616G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151584 | ||||||
| chr12:111151670
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-62530G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151670 | ||||||
| chr12:111151880
|
T | A | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-62320T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151880 | ||||||
| chr12:111151986
|
G | A | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-62214G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111151986 | ||||||
| chr12:111152130
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-62070A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111152130 | ||||||
| chr12:111152146
|
T | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-62054T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111152146 | ||||||
| chr12:111152284
|
CA | C | 11 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(8): Show | 11 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-61908delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111152284 | |||||
| chr12:111152688
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0091others(61): Show | 64 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(61): Show |
intron_variant | MODIFIER | c.64-61512T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111152688 | ||||||
| chr12:111153213
|
T | G | 12 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(9): Show | 12 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-60987T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153213 | ||||||
| chr12:111153256
|
A | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-60944A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153256 | ||||||
| chr12:111153261
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-60939C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153261 | ||||||
| chr12:111153423
|
C | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-60777C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153423 | ||||||
| chr12:111153491
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-60709T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153491 | ||||||
| chr12:111153625
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-60575A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153625 | ||||||
| chr12:111153640
|
G | A | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-60560G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153640 | ||||||
| chr12:111153648
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-60552G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153648 | ||||||
| chr12:111153786
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-60414G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153786 | ||||||
| chr12:111153993
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-60207T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111153993 | ||||||
| chr12:111154428
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-59772G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154428 | ||||||
| chr12:111154476
|
C | T | 3 | a0001c0002t0001g0093a0001c0019t0004g0077a0002c0006t0001g0053 | 3 | HG01891.hp2 HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-59724C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154476 | ||||||
| chr12:111154477
|
G | A | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-59723G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154477 | ||||||
| chr12:111154532
|
C | T | 4 | a0001c0001t0002g0012a0001c0003t0001g0009a0001c0003t0001g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-59668C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154532 | ||||||
| chr12:111154576
|
G | T | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0002c0006t0001g0089 | 3 | HG01243.hp2 HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.64-59624G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154576 | ||||||
| chr12:111154775
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-59425C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154775 | ||||||
| chr12:111154780
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-59420C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154780 | ||||||
| chr12:111154893
|
A | G | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-59307A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154893 | ||||||
| chr12:111154980
|
G | A | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0001c0004t0001g0096 | 3 | HG01243.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-59220G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111154980 | ||||||
| chr12:111155351
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-58849C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111155351 | ||||||
| chr12:111155923
|
TA | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(58): Show | 61 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-58265delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111155923 | |||||
| chr12:111155930
|
A | T | 23 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(20): Show | 23 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.64-58270A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111155930 | ||||||
| chr12:111155931
|
A | G | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-58269A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111155931 | ||||||
| chr12:111155932
|
A | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-58268A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111155932 | ||||||
| chr12:111155933
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-58267A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111155933 | ||||||
| chr12:111155934
|
AAT | A | 5 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-58264_64-58263d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111155934 | |||||
| chr12:111156258
|
G | T | 3 | a0001c0001t0002g0062a0001c0004t0001g0027a0001c0013t0001g0063 | 3 | HG02965.hp2 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-57942G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111156258 | ||||||
| chr12:111156791
|
A | G | 5 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-57409A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111156791 | ||||||
| chr12:111156851
|
C | T | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-57349C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111156851 | ||||||
| chr12:111156985
|
C | CA | 19 | a0001c0001t0002g0030a0001c0001t0002g0083a0001c0001t0002g0086others(16): Show | 19 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-57191dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111156985 | |||||
| chr12:111156985
|
C | CAA | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-57192_64-57191d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111156985 | |||||
| chr12:111156985
|
C | CAAAA | 7 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0003g0078others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-57194_64-57191d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111156985 | |||||
| chr12:111156985
|
C | CAAAAA | 17 | a0001c0001t0001g0091a0001c0001t0003g0081a0001c0002t0001g0048others(14): Show | 17 | HG01069.hp2 HG01169.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-57195_64-57191d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111156985 | |||||
| chr12:111156985
|
C | CAAAAAA | 8 | a0001c0001t0002g0059a0001c0001t0002g0067a0001c0001t0003g0099others(5): Show | 8 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-57196_64-57191d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111156985 | |||||
| chr12:111157008
|
AAC | A | 4 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(1): Show | 4 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-57190_64-57189d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111157008 | |||||
| chr12:111157012
|
G | A | 5 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(2): Show | 5 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-57188G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157012 | ||||||
| chr12:111157233
|
G | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-56967G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157233 | ||||||
| chr12:111157352
|
A | C | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-56848A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157352 | ||||||
| chr12:111157433
|
T | A | 23 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(20): Show | 23 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-56767T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157433 | ||||||
| chr12:111157521
|
A | C | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-56679A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157521 | ||||||
| chr12:111157533
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-56667A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157533 | ||||||
| chr12:111157619
|
A | G | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-56581A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157619 | ||||||
| chr12:111157632
|
C | G | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-56568C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157632 | ||||||
| chr12:111157732
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-56468A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157732 | ||||||
| chr12:111157836
|
A | G | 12 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(9): Show | 12 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-56364A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111157836 | ||||||
| chr12:111158035
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-56165T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158035 | ||||||
| chr12:111158166
|
C | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-56034C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158166 | ||||||
| chr12:111158315
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-55885A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158315 | ||||||
| chr12:111158487
|
A | AAAC | 11 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(8): Show | 11 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-55712_64-55711i others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111158487 | |||||
| chr12:111158487
|
A | AAC | 7 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0014others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-55712_64-55711i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111158487 | |||||
| chr12:111158608
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.64-55592G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158608 | ||||||
| chr12:111158801
|
C | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-55399C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158801 | ||||||
| chr12:111158832
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-55368G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111158832 | ||||||
| chr12:111159201
|
C | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-54999C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111159201 | ||||||
| chr12:111159279
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-54921G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111159279 | ||||||
| chr12:111159327
|
TTC | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(58): Show | 61 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-54872_64-54871d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111159327 | ||||||
| chr12:111159328
|
TC | T | 4 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-54870delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111159328 | |||||
| chr12:111159509
|
AT | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-54686delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111159509 | |||||
| chr12:111159552
|
C | A | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-54648C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111159552 | ||||||
| chr12:111159699
|
T | C | 20 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-54501T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111159699 | ||||||
| chr12:111160018
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-54182A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160018 | ||||||
| chr12:111160062
|
G | T | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-54138G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160062 | ||||||
| chr12:111160210
|
C | T | 11 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(8): Show | 11 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-53990C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160210 | ||||||
| chr12:111160398
|
C | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(47): Show | 50 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.64-53802C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160398 | ||||||
| chr12:111160645
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-53555A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160645 | ||||||
| chr12:111160697
|
C | T | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-53503C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160697 | ||||||
| chr12:111160848
|
G | A | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-53352G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160848 | ||||||
| chr12:111160885
|
G | A | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-53315G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111160885 | ||||||
| chr12:111161190
|
A | T | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-53010A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161190 | ||||||
| chr12:111161194
|
C | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-53006C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161194 | ||||||
| chr12:111161376
|
A | G | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-52824A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161376 | ||||||
| chr12:111161398
|
G | GTC | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(63): Show | 66 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(63): Show |
intron_variant | MODIFIER | c.64-52801_64-52800i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111161398 | |||||
| chr12:111161409
|
C | A | 1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-52791C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161409 | ||||||
| chr12:111161647
|
G | T | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-52553G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161647 | ||||||
| chr12:111161684
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-52516G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161684 | ||||||
| chr12:111161737
|
C | CT | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-52456dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111161737 | |||||
| chr12:111161751
|
T | G | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-52449T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161751 | ||||||
| chr12:111161812
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0003g0078 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64-52388G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161812 | ||||||
| chr12:111161813
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(25): Show | 28 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-52387T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161813 | ||||||
| chr12:111161829
|
G | A | 11 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(8): Show | 11 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-52371G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161829 | ||||||
| chr12:111161845
|
C | G | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-52355C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161845 | ||||||
| chr12:111161848
|
C | T | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-52352C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161848 | ||||||
| chr12:111161865
|
G | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0018others(1): Show | 4 | HG02257.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-52335G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111161865 | ||||||
| chr12:111162034
|
A | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(51): Show | 54 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.64-52166A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162034 | ||||||
| chr12:111162207
|
A | C | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-51993A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162207 | ||||||
| chr12:111162225
|
C | A | 11 | a0001c0001t0002g0062a0001c0001t0003g0045a0001c0002t0001g0037others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-51975C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162225 | ||||||
| chr12:111162330
|
G | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0056a0007c0021t0002g0064 | 3 | HG01099.hp2 HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.64-51870G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162330 | ||||||
| chr12:111162466
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087 | 3 | HG02109.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64-51734C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162466 | ||||||
| chr12:111162551
|
C | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-51649C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162551 | ||||||
| chr12:111162615
|
A | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(25): Show | 28 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-51585A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162615 | ||||||
| chr12:111162641
|
G | A | 5 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(2): Show | 5 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-51559G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162641 | ||||||
| chr12:111162657
|
C | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-51543C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162657 | ||||||
| chr12:111162739
|
C | T | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-51461C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162739 | ||||||
| chr12:111162985
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-51215G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111162985 | ||||||
| chr12:111163045
|
C | CA | 31 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0059others(28): Show | 31 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.64-51138dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111163045 | |||||
| chr12:111163232
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-50968C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163232 | ||||||
| chr12:111163427
|
G | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-50773G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163427 | ||||||
| chr12:111163473
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-50727C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163473 | ||||||
| chr12:111163653
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-50547C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163653 | ||||||
| chr12:111163671
|
G | A | 22 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(19): Show | 22 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-50529G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163671 | ||||||
| chr12:111163721
|
A | G | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-50479A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163721 | ||||||
| chr12:111163818
|
C | T | 1 | a0001c0004t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-50382C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111163818 | ||||||
| chr12:111164071
|
C | T | 4 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-50129C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164071 | ||||||
| chr12:111164075
|
G | C | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-50125G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164075 | ||||||
| chr12:111164083
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-50117C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164083 | ||||||
| chr12:111164302
|
A | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(63): Show | 66 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(63): Show |
intron_variant | MODIFIER | c.64-49898A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164302 | ||||||
| chr12:111164791
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-49409C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164791 | ||||||
| chr12:111164807
|
A | C | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-49393A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164807 | ||||||
| chr12:111164955
|
G | A | 13 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(10): Show | 13 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-49245G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164955 | ||||||
| chr12:111164955
|
G | C | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-49245G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111164955 | ||||||
| chr12:111165009
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.64-49191A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111165009 | ||||||
| chr12:111165049
|
C | T | 8 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-49151C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111165049 | ||||||
| chr12:111165459
|
C | A | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-48741C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111165459 | ||||||
| chr12:111165933
|
GATTAT | G | 3 | a0001c0004t0005g0007a0001c0009t0001g0035a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-48262_64-48258d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111165933 | |||||
| chr12:111166021
|
G | T | 25 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(22): Show | 25 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.64-48179G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166021 | ||||||
| chr12:111166626
|
AG | A | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-47570delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111166626 | |||||
| chr12:111166630
|
G | C | 4 | a0001c0002t0001g0093a0001c0011t0001g0001a0001c0019t0004g0077others(1): Show | 4 | HG01891.hp2 HG02698.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-47570G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166630 | ||||||
| chr12:111166632
|
C | A | 4 | a0001c0002t0001g0093a0001c0011t0001g0001a0001c0019t0004g0077others(1): Show | 4 | HG01891.hp2 HG02698.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-47568C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166632 | ||||||
| chr12:111166713
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64-47487C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166713 | ||||||
| chr12:111166787
|
G | A | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-47413G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166787 | ||||||
| chr12:111166846
|
C | T | 2 | a0001c0001t0003g0045a0001c0004t0006g0075 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.64-47354C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111166846 | ||||||
| chr12:111167357
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64-46843C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167357 | ||||||
| chr12:111167421
|
C | G | 1 | a0001c0004t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-46779C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167421 | ||||||
| chr12:111167669
|
GGTTT | G | 9 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-46498_64-46495d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111167669 | |||||
| chr12:111167674
|
G | T | 16 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0002g0086others(13): Show | 16 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-46526G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167674 | ||||||
| chr12:111167678
|
G | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-46522G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167678 | ||||||
| chr12:111167702
|
G | GTTTT | 17 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(14): Show | 17 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-46495_64-46494i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111167702 | |||||
| chr12:111167702
|
G | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(68): Show | 71 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-46498G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167702 | ||||||
| chr12:111167946
|
T | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-46254T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167946 | ||||||
| chr12:111167988
|
T | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0062others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-46212T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167988 | ||||||
| chr12:111167996
|
C | T | 6 | a0001c0001t0002g0062a0001c0002t0001g0095a0001c0003t0008g0032others(3): Show | 6 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-46204C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111167996 | ||||||
| chr12:111168097
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0062others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-46103A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168097 | ||||||
| chr12:111168228
|
A | G | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-45972A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168228 | ||||||
| chr12:111168232
|
T | G | 5 | a0001c0001t0002g0076a0001c0001t0004g0054a0001c0002t0001g0071others(2): Show | 5 | HG02647.hp2 HG02698.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-45968T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168232 | ||||||
| chr12:111168427
|
T | G | 12 | a0001c0001t0002g0062a0001c0001t0003g0045a0001c0002t0001g0037others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-45773T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168427 | ||||||
| chr12:111168840
|
G | A | 5 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(2): Show | 5 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-45360G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168840 | ||||||
| chr12:111168993
|
T | C | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-45207T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111168993 | ||||||
| chr12:111169015
|
G | A | 2 | a0001c0019t0004g0077a0002c0006t0001g0053 | 2 | HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.64-45185G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169015 | ||||||
| chr12:111169252
|
C | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0003t0001g0046 | 3 | HG02630.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.64-44948C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169252 | ||||||
| chr12:111169380
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-44820G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169380 | ||||||
| chr12:111169391
|
C | T | 4 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-44809C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169391 | ||||||
| chr12:111169424
|
C | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-44776C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169424 | ||||||
| chr12:111169489
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-44711G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169489 | ||||||
| chr12:111169834
|
A | G | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-44366A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169834 | ||||||
| chr12:111169844
|
G | A | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-44356G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111169844 | ||||||
| chr12:111170035
|
A | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-44165A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170035 | ||||||
| chr12:111170061
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-44139G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170061 | ||||||
| chr12:111170322
|
G | C | 22 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(19): Show | 22 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-43878G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170322 | ||||||
| chr12:111170441
|
G | GA | 32 | a0001c0001t0002g0030a0001c0001t0002g0043a0001c0001t0002g0056others(29): Show | 32 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.64-43746dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170441 | |||||
| chr12:111170441
|
G | GAA | 28 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0062others(25): Show | 28 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-43747_64-43746d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170441 | |||||
| chr12:111170441
|
G | GAAA | 34 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0002g0012others(31): Show | 34 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-43748_64-43746d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170441 | |||||
| chr12:111170545
|
C | CT | 8 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0001t0002g0100others(5): Show | 8 | HG01069.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-43629dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170545 | |||||
| chr12:111170545
|
C | CTTT | 5 | a0001c0001t0001g0024a0001c0001t0003g0045a0001c0002t0001g0037others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-43631_64-43629d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170545 | |||||
| chr12:111170545
|
CT | C | 31 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0067others(28): Show | 31 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.64-43629delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111170545 | |||||
| chr12:111170582
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-43618G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170582 | ||||||
| chr12:111170617
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-43583G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170617 | ||||||
| chr12:111170854
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-43346G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170854 | ||||||
| chr12:111170944
|
G | C | 12 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(9): Show | 12 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-43256G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170944 | ||||||
| chr12:111170961
|
C | T | 4 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-43239C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111170961 | ||||||
| chr12:111171332
|
T | C | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-42868T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171332 | ||||||
| chr12:111171416
|
C | T | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-42784C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171416 | ||||||
| chr12:111171417
|
G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | HG01099.hp1 HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.64-42783G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171417 | ||||||
| chr12:111171747
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-42453A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171747 | ||||||
| chr12:111171803
|
G | A | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-42397G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171803 | ||||||
| chr12:111171943
|
A | C | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64-42257A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171943 | ||||||
| chr12:111171959
|
G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(55): Show | 58 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-42241G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111171959 | ||||||
| chr12:111171975
|
C | CTG | 5 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-42214_64-42213d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111171975 | |||||
| chr12:111171979
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-42211_64-42196d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111171979 | |||||
| chr12:111172126
|
T | C | 3 | a0001c0004t0005g0007a0001c0009t0001g0035a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-42074T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172126 | ||||||
| chr12:111172166
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-42034T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172166 | ||||||
| chr12:111172315
|
T | A | 6 | a0001c0001t0002g0062a0001c0002t0001g0095a0001c0003t0008g0032others(3): Show | 6 | HG02280.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-41885T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172315 | ||||||
| chr12:111172370
|
G | A | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-41830G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172370 | ||||||
| chr12:111172501
|
T | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-41699T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172501 | ||||||
| chr12:111172509
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-41691A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172509 | ||||||
| chr12:111172521
|
C | A | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-41679C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172521 | ||||||
| chr12:111172594
|
C | G | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-41606C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172594 | ||||||
| chr12:111172616
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-41584C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172616 | ||||||
| chr12:111172919
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-41281T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111172919 | ||||||
| chr12:111173243
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-40957G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173243 | ||||||
| chr12:111173421
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-40779G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173421 | ||||||
| chr12:111173480
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-40720C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173480 | ||||||
| chr12:111173688
|
A | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-40512A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173688 | ||||||
| chr12:111173699
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-40501G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173699 | ||||||
| chr12:111173949
|
G | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-40251G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111173949 | ||||||
| chr12:111174137
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-40063G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111174137 | ||||||
| chr12:111174262
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-39938A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111174262 | ||||||
| chr12:111174487
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64-39713C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111174487 | ||||||
| chr12:111175026
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-39174C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111175026 | ||||||
| chr12:111175341
|
CT | C | 32 | a0001c0001t0002g0030a0001c0001t0002g0043a0001c0001t0002g0056others(29): Show | 32 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.64-38839delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111175341 | |||||
| chr12:111175341
|
CTT | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(37): Show | 40 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.64-38840_64-38839d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111175341 | |||||
| chr12:111175341
|
CTTT | C | 24 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(21): Show | 24 | HG01081.hp1 HG01169.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-38841_64-38839d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111175341 | |||||
| chr12:111175404
|
CA | C | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-38793delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111175404 | |||||
| chr12:111175589
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-38611A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111175589 | ||||||
| chr12:111175786
|
C | T | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-38414C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111175786 | ||||||
| chr12:111175842
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-38358T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111175842 | ||||||
| chr12:111176039
|
C | CT | 6 | a0001c0001t0002g0100a0001c0001t0005g0055a0001c0003t0001g0094others(3): Show | 6 | HG01069.hp1 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-38136dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111176039 | |||||
| chr12:111176039
|
CT | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(29): Show | 32 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.64-38136delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111176039 | |||||
| chr12:111176039
|
CTT | C | 13 | a0001c0001t0001g0082a0001c0001t0002g0062a0001c0001t0003g0045others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-38137_64-38136d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111176039 | |||||
| chr12:111176039
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-38146_64-38136d others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111176039 | |||||
| chr12:111176088
|
G | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-38112G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176088 | ||||||
| chr12:111176269
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-37931A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176269 | ||||||
| chr12:111176281
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-37919G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176281 | ||||||
| chr12:111176645
|
C | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-37555C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176645 | ||||||
| chr12:111176841
|
C | T | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-37359C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176841 | ||||||
| chr12:111176932
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(88): Show | 91 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.64-37268T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176932 | ||||||
| chr12:111176966
|
T | C | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-37234T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176966 | ||||||
| chr12:111176986
|
C | T | 4 | a0001c0001t0002g0062a0001c0003t0008g0032a0001c0004t0001g0027others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-37214C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111176986 | ||||||
| chr12:111177141
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-37059C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177141 | ||||||
| chr12:111177272
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-36928C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177272 | ||||||
| chr12:111177343
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-36857G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177343 | ||||||
| chr12:111177391
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-36809G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177391 | ||||||
| chr12:111177476
|
T | C | 1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-36724T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177476 | ||||||
| chr12:111177586
|
T | C | 13 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0003g0045others(10): Show | 13 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-36614T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177586 | ||||||
| chr12:111177634
|
G | A | 2 | a0001c0005t0001g0019a0001c0009t0001g0031 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-36566G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177634 | ||||||
| chr12:111177645
|
C | T | 2 | a0001c0004t0001g0027a0001c0013t0001g0063 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-36555C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111177645 | ||||||
| chr12:111178403
|
C | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(64): Show | 67 | HG01069.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.64-35797C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111178403 | ||||||
| chr12:111178502
|
C | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-35698C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111178502 | ||||||
| chr12:111179322
|
G | A | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-34878G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111179322 | ||||||
| chr12:111179406
|
C | G | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-34794C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111179406 | ||||||
| chr12:111179593
|
GGTT | G | 22 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(19): Show | 22 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-34582_64-34580d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111179593 | |||||
| chr12:111179682
|
G | GT | 13 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(10): Show | 13 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-34506dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111179682 | |||||
| chr12:111180011
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-34189C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180011 | ||||||
| chr12:111180058
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-34142C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180058 | ||||||
| chr12:111180206
|
C | A | 14 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(11): Show | 14 | HG01081.hp1 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-33994C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180206 | ||||||
| chr12:111180528
|
T | G | 22 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0060others(19): Show | 22 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-33672T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180528 | ||||||
| chr12:111180685
|
T | TGCAG | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-33515_64-33514i others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180685 | ||||||
| chr12:111180687
|
TC | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-33511delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111180687 | |||||
| chr12:111180689
|
C | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-33511C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180689 | ||||||
| chr12:111180857
|
C | G | 5 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-33343C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111180857 | ||||||
| chr12:111181005
|
A | G | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-33195A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181005 | ||||||
| chr12:111181474
|
G | A | 3 | a0001c0004t0005g0007a0001c0009t0001g0035a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-32726G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181474 | ||||||
| chr12:111181478
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-32722G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181478 | ||||||
| chr12:111181535
|
T | C | 46 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(43): Show | 46 | HG01069.hp2 HG01081.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.64-32665T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181535 | ||||||
| chr12:111181625
|
A | C | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-32575A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181625 | ||||||
| chr12:111181636
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(46): Show | 49 | HG01069.hp2 HG01081.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.64-32564T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181636 | ||||||
| chr12:111181896
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-32304A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181896 | ||||||
| chr12:111181921
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-32279A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111181921 | ||||||
| chr12:111182032
|
C | T | 5 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-32168C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182032 | ||||||
| chr12:111182094
|
T | C | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-32106T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182094 | ||||||
| chr12:111182231
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-31969G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182231 | ||||||
| chr12:111182396
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-31804G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182396 | ||||||
| chr12:111182920
|
A | T | 20 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(17): Show | 20 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-31280A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182920 | ||||||
| chr12:111182961
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-31239T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111182961 | ||||||
| chr12:111183122
|
A | C | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-31078A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183122 | ||||||
| chr12:111183167
|
A | C | 1 | a0001c0003t0001g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-31033A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183167 | ||||||
| chr12:111183312
|
T | C | 13 | a0001c0001t0002g0062a0001c0001t0002g0083a0001c0001t0003g0045others(10): Show | 13 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-30888T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183312 | ||||||
| chr12:111183441
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-30759C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183441 | ||||||
| chr12:111183654
|
C | T | 13 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(10): Show | 13 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-30546C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183654 | ||||||
| chr12:111183822
|
C | A | 4 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-30378C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111183822 | ||||||
| chr12:111183893
|
AC | A | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-30305delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111183893 | |||||
| chr12:111184106
|
T | C | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-30094T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111184106 | ||||||
| chr12:111184301
|
G | A | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-29899G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111184301 | ||||||
| chr12:111184573
|
C | CA | 23 | a0001c0001t0001g0091a0001c0001t0002g0062a0001c0001t0002g0100others(20): Show | 23 | HG00597.hp1 HG01069.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-29601dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111184573 | |||||
| chr12:111184573
|
CA | C | 4 | a0001c0001t0003g0081a0001c0005t0001g0038a0001c0008t0001g0003others(1): Show | 4 | HG01169.hp1 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-29601delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111184573 | |||||
| chr12:111184573
|
CAA | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0003g0045others(5): Show | 8 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-29602_64-29601d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111184573 | |||||
| chr12:111184573
|
CAAAA | C | 7 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-29604_64-29601d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111184573 | |||||
| chr12:111184573
|
CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0001g0006a0001c0001t0005g0055a0001c0002t0001g0018others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-29609_64-29601d others(11): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111184573 | |||||
| chr12:111184599
|
A | C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-29601A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111184599 | ||||||
| chr12:111184779
|
T | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-29421T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111184779 | ||||||
| chr12:111184871
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-29329G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111184871 | ||||||
| chr12:111185156
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-29044A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185156 | ||||||
| chr12:111185160
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64-29040A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185160 | ||||||
| chr12:111185165
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-29035A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185165 | ||||||
| chr12:111185176
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(74): Show | 77 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.64-29024A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185176 | ||||||
| chr12:111185289
|
A | T | 6 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-28911A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185289 | ||||||
| chr12:111185334
|
A | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(67): Show | 70 | HG01069.hp2 HG01081.hp1 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-28866A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185334 | ||||||
| chr12:111185817
|
G | C | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-28383G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185817 | ||||||
| chr12:111185839
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64-28361C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185839 | ||||||
| chr12:111185900
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-28300C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111185900 | ||||||
| chr12:111186141
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-28059G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186141 | ||||||
| chr12:111186218
|
A | C | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-27982A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186218 | ||||||
| chr12:111186451
|
C | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-27749C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186451 | ||||||
| chr12:111186664
|
A | G | 22 | a0001c0001t0002g0062a0001c0001t0002g0079a0001c0001t0002g0083others(19): Show | 22 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-27536A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186664 | ||||||
| chr12:111186776
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-27424G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186776 | ||||||
| chr12:111186782
|
G | GT | 30 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0062others(27): Show | 30 | HG01081.hp1 HG01169.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-27404dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111186782 | |||||
| chr12:111186782
|
G | GTT | 18 | a0001c0001t0002g0060a0001c0001t0002g0067a0001c0002t0001g0023others(15): Show | 18 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-27405_64-27404d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111186782 | |||||
| chr12:111186782
|
GTT | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-27405_64-27404d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111186782 | |||||
| chr12:111186940
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-27260G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111186940 | ||||||
| chr12:111187097
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-27103C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187097 | ||||||
| chr12:111187152
|
A | G | 17 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-27048A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187152 | ||||||
| chr12:111187254
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-26946G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187254 | ||||||
| chr12:111187584
|
C | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-26616C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187584 | ||||||
| chr12:111187600
|
G | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-26600G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187600 | ||||||
| chr12:111187663
|
G | A | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-26537G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187663 | ||||||
| chr12:111187737
|
G | C | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-26463G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187737 | ||||||
| chr12:111187810
|
G | A | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-26390G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187810 | ||||||
| chr12:111187914
|
C | T | 19 | a0001c0001t0002g0060a0001c0001t0002g0067a0001c0002t0001g0023others(16): Show | 19 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-26286C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111187914 | ||||||
| chr12:111188137
|
T | C | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-26063T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111188137 | ||||||
| chr12:111188602
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-25598T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111188602 | ||||||
| chr12:111188612
|
A | C | 1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-25588A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111188612 | ||||||
| chr12:111188650
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-25550G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111188650 | ||||||
| chr12:111188755
|
C | T | 9 | a0001c0001t0002g0083a0001c0001t0003g0045a0001c0002t0001g0037others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-25445C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111188755 | ||||||
| chr12:111189140
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-25060T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189140 | ||||||
| chr12:111189142
|
T | C | 2 | a0001c0002t0001g0092a0001c0007t0001g0098 | 2 | HG00597.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.64-25058T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189142 | ||||||
| chr12:111189244
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-24956C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189244 | ||||||
| chr12:111189287
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-24913A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189287 | ||||||
| chr12:111189298
|
C | T | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-24902C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189298 | ||||||
| chr12:111189347
|
C | T | 14 | a0001c0001t0002g0059a0001c0001t0002g0079a0001c0001t0003g0078others(11): Show | 14 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-24853C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189347 | ||||||
| chr12:111189523
|
G | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0012others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-24677G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189523 | ||||||
| chr12:111189564
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-24636G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189564 | ||||||
| chr12:111189585
|
C | T | 3 | a0001c0001t0002g0059a0001c0002t0001g0093a0002c0006t0001g0053 | 3 | HG02572.hp1 HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-24615C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111189585 | ||||||
| chr12:111190016
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-24184T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190016 | ||||||
| chr12:111190221
|
G | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-23979G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190221 | ||||||
| chr12:111190316
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-23884G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190316 | ||||||
| chr12:111190439
|
C | T | 4 | a0001c0001t0002g0059a0001c0002t0001g0093a0001c0011t0001g0001others(1): Show | 4 | HG02572.hp1 HG02698.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-23761C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190439 | ||||||
| chr12:111190457
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-23743A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190457 | ||||||
| chr12:111190500
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-23700G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190500 | ||||||
| chr12:111190611
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-23589C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190611 | ||||||
| chr12:111190790
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-23410G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190790 | ||||||
| chr12:111190899
|
G | A | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-23301G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111190899 | ||||||
| chr12:111191292
|
G | A | 3 | a0001c0001t0001g0013a0001c0003t0001g0014a0001c0004t0001g0015 | 3 | HG01884.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.64-22908G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111191292 | ||||||
| chr12:111191306
|
ATTAT | A | 19 | a0001c0001t0002g0016a0001c0001t0002g0060a0001c0001t0002g0067others(16): Show | 19 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-22855_64-22852d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111191306 | |||||
| chr12:111191306
|
ATTATTTA others(1): Show |
A | 29 | a0001c0001t0002g0030a0001c0001t0002g0062a0001c0001t0002g0076others(26): Show | 29 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.64-22859_64-22852d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111191306 | |||||
| chr12:111191306
|
ATTATTTA others(9): Show |
A | 2 | a0001c0002t0001g0004a0001c0003t0001g0094 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.64-22867_64-22852d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111191306 | |||||
| chr12:111191333
|
ATTTATTT others(9): Show |
A | 3 | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008 | 3 | HG02109.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64-22866_64-22851d others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111191333 | ||||||
| chr12:111191337
|
ATTTATTT others(5): Show |
A | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-22862_64-22851d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111191337 | ||||||
| chr12:111191481
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-22719G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111191481 | ||||||
| chr12:111191488
|
C | G | 16 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-22712C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111191488 | ||||||
| chr12:111192180
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-22020G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192180 | ||||||
| chr12:111192195
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0002g0085a0001c0003t0001g0009others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-22005C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192195 | ||||||
| chr12:111192236
|
T | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64-21964T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192236 | ||||||
| chr12:111192412
|
C | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-21788C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192412 | ||||||
| chr12:111192481
|
G | A | 3 | a0001c0004t0005g0007a0001c0009t0001g0035a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-21719G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192481 | ||||||
| chr12:111192501
|
T | A | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-21699T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192501 | ||||||
| chr12:111192715
|
C | T | 15 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0002t0001g0023others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-21485C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192715 | ||||||
| chr12:111192743
|
GT | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64-21454delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111192743 | |||||
| chr12:111192937
|
A | G | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-21263A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111192937 | ||||||
| chr12:111193904
|
G | T | 1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-20296G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193904 | ||||||
| chr12:111193929
|
C | T | 17 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0002t0001g0023others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-20271C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193929 | ||||||
| chr12:111193945
|
A | ACTCTC | 73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.64-20255_64-20254i others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193945 | ||||||
| chr12:111193947
|
G | GC | 73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.64-20253_64-20252i others(3): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193947 | ||||||
| chr12:111193948
|
G | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.64-20252G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193948 | ||||||
| chr12:111193961
|
G | A | 5 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0005t0001g0019others(2): Show | 5 | HG01243.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-20239G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111193961 | ||||||
| chr12:111194002
|
C | T | 2 | a0001c0001t0003g0045a0001c0004t0006g0075 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.64-20198C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194002 | ||||||
| chr12:111194031
|
A | G | 12 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(9): Show | 12 | HG00597.hp2 HG01069.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-20169A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194031 | ||||||
| chr12:111194098
|
A | G | 3 | a0001c0005t0001g0019a0001c0008t0002g0022a0001c0009t0001g0031 | 3 | HG01891.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-20102A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194098 | ||||||
| chr12:111194134
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-20066A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194134 | ||||||
| chr12:111194142
|
T | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(72): Show | 75 | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.64-20058T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194142 | ||||||
| chr12:111194146
|
G | T | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-20054G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194146 | ||||||
| chr12:111194200
|
C | G | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-20000C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194200 | ||||||
| chr12:111194284
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-19916G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194284 | ||||||
| chr12:111194315
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0085others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-19885C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194315 | ||||||
| chr12:111194379
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-19821C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194379 | ||||||
| chr12:111194582
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-19618C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194582 | ||||||
| chr12:111194601
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-19599C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194601 | ||||||
| chr12:111194739
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64-19461G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194739 | ||||||
| chr12:111194788
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-19412G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194788 | ||||||
| chr12:111194980
|
A | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(39): Show | 42 | HG01081.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.64-19220A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111194980 | ||||||
| chr12:111195030
|
A | G | 4 | a0001c0002t0001g0004a0001c0007t0001g0098a0002c0006t0001g0084others(1): Show | 4 | HG00597.hp2 HG01069.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-19170A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195030 | ||||||
| chr12:111195135
|
G | C | 3 | a0001c0002t0001g0004a0001c0007t0001g0098a0002c0006t0001g0084 | 3 | HG00597.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-19065G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195135 | ||||||
| chr12:111195248
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64-18952A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195248 | ||||||
| chr12:111195398
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-18802A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195398 | ||||||
| chr12:111195416
|
G | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-18784G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195416 | ||||||
| chr12:111195530
|
C | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-18670C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195530 | ||||||
| chr12:111195627
|
G | A | 2 | a0001c0002t0001g0093a0002c0006t0001g0053 | 2 | HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-18573G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195627 | ||||||
| chr12:111195693
|
A | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-18507A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195693 | ||||||
| chr12:111195914
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.64-18286C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195914 | ||||||
| chr12:111195919
|
T | A | 3 | a0001c0001t0001g0013a0001c0003t0001g0014a0001c0004t0001g0015 | 3 | HG01884.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.64-18281T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111195919 | ||||||
| chr12:111196091
|
C | G | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-18109C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196091 | ||||||
| chr12:111196168
|
A | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-18032A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196168 | ||||||
| chr12:111196260
|
T | C | 3 | a0001c0005t0001g0019a0001c0008t0002g0022a0001c0009t0001g0031 | 3 | HG01891.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-17940T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196260 | ||||||
| chr12:111196477
|
T | G | 22 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0062others(19): Show | 22 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-17723T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196477 | ||||||
| chr12:111196617
|
T | A | 2 | a0001c0001t0003g0045a0001c0004t0006g0075 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.64-17583T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196617 | ||||||
| chr12:111196658
|
T | C | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-17542T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196658 | ||||||
| chr12:111196940
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-17260G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196940 | ||||||
| chr12:111196953
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(38): Show | 41 | HG00597.hp2 HG01081.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-17247A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196953 | ||||||
| chr12:111196997
|
A | T | 5 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-17203A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111196997 | ||||||
| chr12:111197168
|
T | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-17032T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111197168 | ||||||
| chr12:111197301
|
T | C | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-16899T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111197301 | ||||||
| chr12:111197541
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-16659C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111197541 | ||||||
| chr12:111197636
|
G | A | 2 | a0001c0001t0002g0030a0001c0003t0001g0033 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-16564G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111197636 | ||||||
| chr12:111198440
|
A | C | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-15760A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111198440 | ||||||
| chr12:111198443
|
C | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-15757C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111198443 | ||||||
| chr12:111198474
|
C | CA | 58 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(55): Show | 58 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-15710dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111198474 | |||||
| chr12:111198474
|
C | CAA | 13 | a0001c0001t0001g0013a0001c0001t0002g0083a0001c0002t0001g0004others(10): Show | 13 | HG00597.hp2 HG01069.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-15711_64-15710d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111198474 | |||||
| chr12:111198776
|
T | G | 4 | a0001c0002t0001g0004a0001c0007t0001g0098a0002c0006t0001g0084others(1): Show | 4 | HG00597.hp2 HG01069.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-15424T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111198776 | ||||||
| chr12:111199520
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-14680G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111199520 | ||||||
| chr12:111199546
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-14654G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111199546 | ||||||
| chr12:111199620
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-14580C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111199620 | ||||||
| chr12:111199720
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-14480C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111199720 | ||||||
| chr12:111199882
|
G | T | 3 | a0001c0005t0001g0019a0001c0008t0002g0022a0001c0009t0001g0031 | 3 | HG01891.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-14318G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111199882 | ||||||
| chr12:111199909
|
CAG | C | 4 | a0001c0002t0001g0037a0001c0003t0001g0040a0001c0005t0001g0038others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-14288_64-14287d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111199909 | |||||
| chr12:111199950
|
CTGTT | C | 3 | a0001c0001t0003g0045a0001c0004t0001g0096a0001c0004t0006g0075 | 3 | HG01243.hp1 HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.64-14247_64-14244d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111199950 | |||||
| chr12:111200455
|
C | A | 2 | a0001c0001t0003g0045a0001c0004t0006g0075 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.64-13745C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200455 | ||||||
| chr12:111200588
|
G | A | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.64-13612G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200588 | ||||||
| chr12:111200613
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0004t0001g0005others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-13587A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200613 | ||||||
| chr12:111200641
|
G | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-13559G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200641 | ||||||
| chr12:111200644
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.64-13556G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200644 | ||||||
| chr12:111200693
|
G | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0007g0097 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-13507G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200693 | ||||||
| chr12:111200757
|
G | C | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-13443G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111200757 | ||||||
| chr12:111201030
|
G | A | 2 | a0001c0002t0001g0093a0002c0006t0001g0053 | 2 | HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-13170G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201030 | ||||||
| chr12:111201090
|
G | A | 2 | a0001c0002t0001g0093a0002c0006t0001g0053 | 2 | HG02698.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-13110G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201090 | ||||||
| chr12:111201294
|
G | C | 33 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0062others(30): Show | 33 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-12906G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201294 | ||||||
| chr12:111201451
|
G | A | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64-12749G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201451 | ||||||
| chr12:111201652
|
G | C | 71 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(68): Show | 71 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.64-12548G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201652 | ||||||
| chr12:111201744
|
C | T | 2 | a0001c0004t0001g0002a0002c0006t0001g0053 | 2 | HG02698.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-12456C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201744 | ||||||
| chr12:111201804
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0002t0001g0037others(4): Show | 7 | HG01243.hp1 HG02698.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-12396G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201804 | ||||||
| chr12:111201858
|
G | A | 1 | a0001c0004t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-12342G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201858 | ||||||
| chr12:111201867
|
T | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-12333T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111201867 | ||||||
| chr12:111202107
|
G | C | 2 | a0001c0002t0001g0037a0001c0003t0001g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-12093G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202107 | ||||||
| chr12:111202213
|
G | A | 17 | a0001c0001t0002g0079a0001c0001t0002g0083a0001c0001t0003g0078others(14): Show | 17 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-11987G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202213 | ||||||
| chr12:111202609
|
G | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64-11591G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202609 | ||||||
| chr12:111202644
|
C | T | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-11556C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202644 | ||||||
| chr12:111202693
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0082 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-11507C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202693 | ||||||
| chr12:111202870
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11330G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111202870 | ||||||
| chr12:111203105
|
G | A | 5 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0009t0001g0035others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11095G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111203105 | ||||||
| chr12:111203215
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-10985G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111203215 | ||||||
| chr12:111203231
|
C | CA | 8 | a0001c0001t0002g0067a0001c0003t0001g0011a0001c0003t0001g0046others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-10946dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203231 | |||||
| chr12:111203231
|
C | CAA | 5 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0002t0001g0004others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-10947_64-10946d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203231 | |||||
| chr12:111203231
|
CA | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0082others(26): Show | 29 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.64-10946delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203231 | |||||
| chr12:111203231
|
CAA | C | 38 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0079others(35): Show | 38 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.64-10947_64-10946d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203231 | |||||
| chr12:111203544
|
C | CA | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(3): Show | 6 | HG02615.hp1 HG02698.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10641dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203544 | |||||
| chr12:111203560
|
G | GA | 4 | a0001c0005t0001g0019a0001c0008t0002g0022a0001c0009t0001g0031others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-10632dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111203560 | |||||
| chr12:111203835
|
A | G | 3 | a0001c0001t0002g0058a0001c0002t0001g0004a0002c0006t0001g0084 | 3 | HG01081.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-10365A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111203835 | ||||||
| chr12:111204016
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64-10184G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204016 | ||||||
| chr12:111204026
|
C | A | 1 | a0001c0002t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64-10174C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204026 | ||||||
| chr12:111204065
|
C | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-10135C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204065 | ||||||
| chr12:111204088
|
C | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-10112C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204088 | ||||||
| chr12:111204332
|
C | T | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9868C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204332 | ||||||
| chr12:111204370
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9830G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204370 | ||||||
| chr12:111204480
|
A | C | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-9720A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204480 | ||||||
| chr12:111204533
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9667A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204533 | ||||||
| chr12:111204623
|
C | T | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.64-9577C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204623 | ||||||
| chr12:111204666
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-9534C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204666 | ||||||
| chr12:111204670
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-9530C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204670 | ||||||
| chr12:111204737
|
A | T | 1 | a0001c0001t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-9463A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204737 | ||||||
| chr12:111204810
|
A | G | 2 | a0001c0002t0001g0004a0002c0006t0001g0084 | 2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-9390A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204810 | ||||||
| chr12:111204818
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-9382T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204818 | ||||||
| chr12:111204892
|
G | T | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-9308G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111204892 | ||||||
| chr12:111205052
|
C | G | 5 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0009t0001g0035others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-9148C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205052 | ||||||
| chr12:111205124
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-9076C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205124 | ||||||
| chr12:111205141
|
CGTCTT | C | 18 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-9044_64-9040del others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111205141 | |||||
| chr12:111205320
|
C | T | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8880C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205320 | ||||||
| chr12:111205487
|
C | G | 1 | a0001c0002t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-8713C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205487 | ||||||
| chr12:111205948
|
T | C | 5 | a0001c0001t0002g0083a0001c0004t0001g0002a0001c0005t0001g0038others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-8252T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205948 | ||||||
| chr12:111205989
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-8211A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111205989 | ||||||
| chr12:111206044
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8156G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206044 | ||||||
| chr12:111206053
|
G | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64-8147G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206053 | ||||||
| chr12:111206430
|
G | A | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-7770G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206430 | ||||||
| chr12:111206526
|
G | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0004t0001g0096 | 3 | HG01243.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.64-7674G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206526 | ||||||
| chr12:111206727
|
T | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7473T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206727 | ||||||
| chr12:111206947
|
A | G | 18 | a0001c0001t0002g0079a0001c0001t0002g0083a0001c0001t0003g0078others(15): Show | 18 | HG01081.hp1 HG01169.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-7253A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206947 | ||||||
| chr12:111206996
|
G | A | 34 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(31): Show | 34 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.64-7204G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111206996 | ||||||
| chr12:111207239
|
A | G | 21 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(18): Show | 21 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-6961A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111207239 | ||||||
| chr12:111208110
|
G | C | 21 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(18): Show | 21 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-6090G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111208110 | ||||||
| chr12:111208682
|
C | T | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-5518C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111208682 | ||||||
| chr12:111208715
|
A | T | 46 | a0001c0001t0002g0012a0001c0001t0002g0059a0001c0001t0002g0062others(43): Show | 46 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.64-5485A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111208715 | ||||||
| chr12:111208725
|
G | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0004a0001c0002t0001g0051others(3): Show | 6 | HG02109.hp2 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-5475G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111208725 | ||||||
| chr12:111209049
|
C | G | 14 | a0001c0001t0002g0016a0001c0002t0001g0018a0001c0002t0001g0023others(11): Show | 14 | HG01099.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-5151C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209049 | ||||||
| chr12:111209061
|
G | C | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.64-5139G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209061 | ||||||
| chr12:111209222
|
A | AC | 4 | a0001c0001t0001g0013a0001c0003t0001g0014a0001c0004t0001g0015others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-4973dupC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111209222 | |||||
| chr12:111209243
|
A | T | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4957A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209243 | ||||||
| chr12:111209264
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-4936G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209264 | ||||||
| chr12:111209285
|
T | C | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-4915T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209285 | ||||||
| chr12:111209649
|
C | T | 31 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(28): Show | 31 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.64-4551C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209649 | ||||||
| chr12:111209861
|
C | T | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.64-4339C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111209861 | ||||||
| chr12:111210021
|
T | C | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-4179T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210021 | ||||||
| chr12:111210343
|
A | C | 9 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-3857A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210343 | ||||||
| chr12:111210368
|
T | G | 5 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(2): Show | 5 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3832T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210368 | ||||||
| chr12:111210449
|
T | C | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-3751T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210449 | ||||||
| chr12:111210613
|
T | C | 10 | a0001c0001t0002g0083a0001c0004t0001g0002a0001c0004t0004g0041others(7): Show | 10 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-3587T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210613 | ||||||
| chr12:111210811
|
GACA | G | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-3385_64-3383del others(3): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111210811 | |||||
| chr12:111210894
|
C | T | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-3306C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111210894 | ||||||
| chr12:111211167
|
G | A | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-3033G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211167 | ||||||
| chr12:111211375
|
G | A | 31 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(28): Show | 31 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.64-2825G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211375 | ||||||
| chr12:111211540
|
A | G | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-2660A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211540 | ||||||
| chr12:111211666
|
A | G | 6 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(3): Show | 6 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2534A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211666 | ||||||
| chr12:111211778
|
G | A | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2422G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211778 | ||||||
| chr12:111211788
|
G | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-2412G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211788 | ||||||
| chr12:111211822
|
G | C | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2378G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211822 | ||||||
| chr12:111211882
|
G | A | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-2318G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211882 | ||||||
| chr12:111211886
|
CA | C | 10 | a0001c0001t0002g0062a0001c0001t0002g0076a0001c0002t0001g0090others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-2298delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111211886 | |||||
| chr12:111211888
|
A | G | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-2312A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111211888 | ||||||
| chr12:111212014
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-2186A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111212014 | ||||||
| chr12:111212455
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-1745C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111212455 | ||||||
| chr12:111212535
|
A | G | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-1665A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111212535 | ||||||
| chr12:111212976
|
G | T | 55 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0012others(52): Show | 55 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.64-1224G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111212976 | ||||||
| chr12:111213076
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64-1124G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213076 | ||||||
| chr12:111213249
|
C | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-951C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213249 | ||||||
| chr12:111213302
|
T | C | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-898T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213302 | ||||||
| chr12:111213376
|
A | G | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-824A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213376 | ||||||
| chr12:111213476
|
A | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(15): Show | 18 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-724A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213476 | ||||||
| chr12:111213737
|
T | C | 1 | a0001c0005t0001g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64-463T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213737 | ||||||
| chr12:111213804
|
C | A | 4 | a0001c0001t0001g0013a0001c0003t0001g0014a0001c0004t0001g0015others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-396C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213804 | ||||||
| chr12:111213885
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.64-315T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213885 | ||||||
| chr12:111213905
|
G | C | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-295G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213905 | ||||||
| chr12:111213950
|
T | A | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-250T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111213950 | ||||||
| chr12:111214072
|
T | G | 5 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(2): Show | 5 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-128T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111214072 | ||||||
| chr12:111214144
|
AG | A | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-55delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111214144 | ||||||
| chr12:111214145
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(64): Show | 67 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.64-55G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | 111214145 | ||||||
| chr12:111214173
|
C | CT | 26 | a0001c0001t0002g0059a0001c0001t0002g0079a0001c0001t0003g0078others(23): Show | 26 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.64-11dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111214173 | |||||
| chr12:111214173
|
C | CTT | 14 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0083others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-12_64-11dupTT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111214173 | |||||
| chr12:111214173
|
CT | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0016others(14): Show | 17 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-11delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111214173 | |||||
| chr12:111214173
|
CTT | C | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-12_64-11delTT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 111214173 | |||||
| chr12:111214327
|
G | A | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.174+17G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111214327 | ||||||
| chr12:111214718
|
G | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(72): Show | 75 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.174+408G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111214718 | ||||||
| chr12:111214743
|
C | T | 1 | a0002c0006t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.174+433C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111214743 | ||||||
| chr12:111214750
|
G | T | 1 | a0001c0002t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.174+440G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111214750 | ||||||
| chr12:111215031
|
ACT | A | 55 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0012others(52): Show | 55 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.174+724_174+725del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 111215031 | |||||
| chr12:111215122
|
G | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+812G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111215122 | ||||||
| chr12:111215132
|
G | C | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+822G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111215132 | ||||||
| chr12:111215135
|
C | T | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+825C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111215135 | ||||||
| chr12:111215765
|
C | G | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.174+1455C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111215765 | ||||||
| chr12:111216199
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175-1691G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111216199 | ||||||
| chr12:111216417
|
T | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(11): Show | 14 | HG01099.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.175-1473T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111216417 | ||||||
| chr12:111216559
|
C | T | 55 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0002g0012others(52): Show | 55 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.175-1331C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111216559 | ||||||
| chr12:111216771
|
A | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.175-1119A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111216771 | ||||||
| chr12:111216785
|
TATCA | T | 18 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0005g0055others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.175-1100_175-1097d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 111216785 | |||||
| chr12:111217066
|
G | C | 11 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0002t0001g0004others(8): Show | 11 | HG02615.hp1 HG02647.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-824G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111217066 | ||||||
| chr12:111217657
|
GAA | G | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-231_175-230del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 111217657 | |||||
| chr12:111217709
|
C | T | 33 | a0001c0001t0001g0006a0001c0001t0002g0059a0001c0001t0002g0062others(30): Show | 33 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.175-181C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 2/21 | chr12 | 111217709 | ||||||
| chr12:111217948
|
G | C | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+11G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111217948 | ||||||
| chr12:111218044
|
G | A | 8 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(5): Show | 8 | HG01081.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+107G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218044 | ||||||
| chr12:111218157
|
C | A | 9 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+220C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218157 | ||||||
| chr12:111218192
|
C | G | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.222+255C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218192 | ||||||
| chr12:111218285
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+348G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218285 | ||||||
| chr12:111218326
|
C | T | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.222+389C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218326 | ||||||
| chr12:111218428
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(11): Show | 14 | HG01099.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.222+491G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218428 | ||||||
| chr12:111218559
|
G | C | 3 | a0001c0001t0002g0086a0001c0002t0001g0087a0001c0004t0001g0005 | 3 | HG02109.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.222+622G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218559 | ||||||
| chr12:111218683
|
T | G | 9 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+746T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218683 | ||||||
| chr12:111218765
|
C | A | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.222+828C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111218765 | ||||||
| chr12:111219095
|
T | C | 2 | a0001c0002t0001g0037a0001c0003t0001g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.222+1158T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111219095 | ||||||
| chr12:111219384
|
CA | C | 12 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+1462delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111219384 | |||||
| chr12:111219460
|
A | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0007g0097 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.222+1523A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111219460 | ||||||
| chr12:111219575
|
T | G | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222+1638T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111219575 | ||||||
| chr12:111219580
|
G | A | 5 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(2): Show | 5 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+1643G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111219580 | ||||||
| chr12:111219941
|
C | T | 33 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(30): Show | 33 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+2004C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111219941 | ||||||
| chr12:111220010
|
A | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+2073A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220010 | ||||||
| chr12:111220035
|
T | G | 1 | a0001c0018t0004g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222+2098T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220035 | ||||||
| chr12:111220036
|
C | G | 1 | a0001c0018t0004g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222+2099C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220036 | ||||||
| chr12:111220143
|
C | CA | 10 | a0001c0001t0002g0016a0001c0001t0002g0083a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+2221dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220143 | |||||
| chr12:111220143
|
C | CAA | 4 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+2220_222+2221d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220143 | |||||
| chr12:111220516
|
A | G | 5 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0009t0001g0035others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+2579A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220516 | ||||||
| chr12:111220526
|
T | C | 2 | a0001c0002t0001g0093a0001c0014t0001g0042 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222+2589T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220526 | ||||||
| chr12:111220530
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+2593C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220530 | ||||||
| chr12:111220743
|
C | CA | 7 | a0001c0002t0001g0023a0001c0002t0001g0026a0001c0002t0001g0047others(4): Show | 7 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+2843dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.222+2833_222+2843d others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CA | C | 17 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0002g0086others(14): Show | 17 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.222+2843delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAA | C | 12 | a0001c0001t0003g0081a0001c0001t0003g0099a0001c0001t0005g0055others(9): Show | 12 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+2842_222+2843d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAA | C | 4 | a0001c0001t0001g0091a0001c0001t0002g0056a0001c0003t0001g0033others(1): Show | 4 | HG01099.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+2841_222+2843d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAA | C | 11 | a0001c0001t0002g0030a0001c0001t0002g0067a0001c0001t0002g0076others(8): Show | 11 | HG00597.hp2 HG01081.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+2840_222+2843d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(3): Show | 6 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+2834_222+2843d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222+2833_222+2843d others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(6): Show |
C | 7 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(4): Show | 7 | HG02615.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+2831_222+2843d others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.222+2829_222+2843d others(17): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0002t0001g0037a0001c0003t0001g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.222+2827_222+2843d others(19): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220743
|
CAAAAAAA others(12): Show |
C | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+2825_222+2843d others(21): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220743 | |||||
| chr12:111220766
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222+2830_222+2844d others(17): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220766 | ||||||
| chr12:111220771
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0001g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.222+2835_222+2844d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220771 | ||||||
| chr12:111220781
|
T | A | 3 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051 | 3 | HG02109.hp2 HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.222+2844T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220781 | ||||||
| chr12:111220782
|
T | G | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.222+2845T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220782 | ||||||
| chr12:111220937
|
T | TA | 10 | a0001c0001t0001g0091a0001c0001t0002g0100a0001c0002t0001g0090others(7): Show | 10 | HG01069.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+3024dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220937 | |||||
| chr12:111220937
|
TA | T | 37 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0001t0002g0043others(34): Show | 37 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.222+3024delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111220937 | |||||
| chr12:111220955
|
A | T | 1 | a0001c0001t0003g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.222+3018A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220955 | ||||||
| chr12:111220980
|
C | T | 4 | a0001c0001t0001g0006a0001c0002t0001g0018a0001c0002t0001g0051others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+3043C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111220980 | ||||||
| chr12:111221107
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+3170A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221107 | ||||||
| chr12:111221110
|
T | C | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.222+3173T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221110 | ||||||
| chr12:111221128
|
A | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.222+3191A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221128 | ||||||
| chr12:111221231
|
G | A | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.222+3294G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221231 | ||||||
| chr12:111221261
|
C | G | 11 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0002t0001g0004others(8): Show | 11 | HG02615.hp1 HG02647.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+3324C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221261 | ||||||
| chr12:111221270
|
T | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.222+3333T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221270 | ||||||
| chr12:111221292
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(69): Show | 72 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.222+3355T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221292 | ||||||
| chr12:111221473
|
A | T | 5 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(2): Show | 5 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+3536A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221473 | ||||||
| chr12:111221562
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0002g0016a0001c0002t0001g0018others(6): Show | 9 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+3625C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221562 | ||||||
| chr12:111221819
|
G | A | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.222+3882G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111221819 | ||||||
| chr12:111222167
|
C | A | 1 | a0001c0001t0003g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.222+4230C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222167 | ||||||
| chr12:111222366
|
G | A | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.222+4429G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222366 | ||||||
| chr12:111222537
|
T | A | 5 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0009t0001g0035others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+4600T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222537 | ||||||
| chr12:111222601
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.222+4664G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222601 | ||||||
| chr12:111222768
|
C | T | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.222+4831C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222768 | ||||||
| chr12:111222795
|
G | T | 33 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(30): Show | 33 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+4858G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222795 | ||||||
| chr12:111222810
|
A | G | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+4873A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111222810 | ||||||
| chr12:111223316
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+5379G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223316 | ||||||
| chr12:111223352
|
G | A | 4 | a0001c0003t0001g0017a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+5415G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223352 | ||||||
| chr12:111223374
|
C | T | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.222+5437C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223374 | ||||||
| chr12:111223662
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+5725C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223662 | ||||||
| chr12:111223716
|
A | G | 9 | a0001c0001t0002g0083a0001c0004t0001g0002a0001c0004t0004g0041others(6): Show | 9 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+5779A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223716 | ||||||
| chr12:111223803
|
G | C | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.222+5866G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223803 | ||||||
| chr12:111223900
|
C | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.222+5963C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223900 | ||||||
| chr12:111223903
|
C | T | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.222+5966C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223903 | ||||||
| chr12:111223951
|
T | G | 3 | a0001c0001t0001g0013a0001c0002t0001g0037a0001c0003t0001g0040 | 3 | HG02257.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.222+6014T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111223951 | ||||||
| chr12:111224516
|
C | CT | 14 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0043others(11): Show | 14 | HG01169.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.222+6600dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111224516 | |||||
| chr12:111224516
|
CT | C | 28 | a0001c0001t0001g0013a0001c0001t0002g0059a0001c0001t0002g0062others(25): Show | 28 | HG01069.hp1 HG01069.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.222+6600delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111224516 | |||||
| chr12:111224516
|
CTT | C | 15 | a0001c0001t0002g0012a0001c0001t0002g0079a0001c0001t0002g0085others(12): Show | 15 | HG00597.hp2 HG01169.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.222+6599_222+6600d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111224516 | |||||
| chr12:111224774
|
G | A | 56 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(53): Show | 56 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.222+6837G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111224774 | ||||||
| chr12:111224940
|
C | G | 2 | a0001c0001t0001g0013a0001c0004t0001g0002 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.222+7003C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111224940 | ||||||
| chr12:111224992
|
G | A | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222+7055G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111224992 | ||||||
| chr12:111225081
|
G | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(79): Show | 82 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.222+7144G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225081 | ||||||
| chr12:111225180
|
A | G | 66 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(63): Show | 66 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.222+7243A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225180 | ||||||
| chr12:111225359
|
T | C | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+7422T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225359 | ||||||
| chr12:111225373
|
C | G | 43 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0059others(40): Show | 43 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.222+7436C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225373 | ||||||
| chr12:111225384
|
T | G | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+7447T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225384 | ||||||
| chr12:111225509
|
G | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+7572G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225509 | ||||||
| chr12:111225908
|
A | C | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+7971A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225908 | ||||||
| chr12:111225992
|
G | A | 2 | a0001c0002t0001g0093a0001c0014t0001g0042 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222+8055G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111225992 | ||||||
| chr12:111226036
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+8099C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226036 | ||||||
| chr12:111226163
|
C | T | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+8226C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226163 | ||||||
| chr12:111226223
|
C | T | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+8286C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226223 | ||||||
| chr12:111226224
|
G | A | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.222+8287G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226224 | ||||||
| chr12:111226240
|
G | C | 43 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0059others(40): Show | 43 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.222+8303G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226240 | ||||||
| chr12:111226257
|
T | G | 43 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0059others(40): Show | 43 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.222+8320T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226257 | ||||||
| chr12:111226305
|
C | G | 11 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(8): Show | 11 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8368C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226305 | ||||||
| chr12:111226334
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.222+8397C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226334 | ||||||
| chr12:111226600
|
C | T | 43 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0059others(40): Show | 43 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.222+8663C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226600 | ||||||
| chr12:111226613
|
T | A | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+8676T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226613 | ||||||
| chr12:111226923
|
C | T | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.222+8986C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111226923 | ||||||
| chr12:111227201
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.222+9264G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111227201 | ||||||
| chr12:111227396
|
C | G | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+9459C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111227396 | ||||||
| chr12:111227584
|
G | A | 40 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0062others(37): Show | 40 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.222+9647G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111227584 | ||||||
| chr12:111227630
|
C | G | 1 | a0001c0002t0001g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.222+9693C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111227630 | ||||||
| chr12:111227717
|
A | G | 30 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.222+9780A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111227717 | ||||||
| chr12:111228398
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+10461C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111228398 | ||||||
| chr12:111228415
|
G | GGT | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+10493_222+1049 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111228415 | |||||
| chr12:111228455
|
G | A | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222+10518G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111228455 | ||||||
| chr12:111228856
|
G | T | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+10919G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111228856 | ||||||
| chr12:111228921
|
T | C | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+10984T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111228921 | ||||||
| chr12:111229041
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222+11104C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229041 | ||||||
| chr12:111229171
|
G | A | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+11234G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229171 | ||||||
| chr12:111229180
|
C | T | 30 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.222+11243C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229180 | ||||||
| chr12:111229572
|
G | A | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+11635G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229572 | ||||||
| chr12:111229774
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+11837A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229774 | ||||||
| chr12:111229869
|
C | T | 5 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11932C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229869 | ||||||
| chr12:111229987
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+12050C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111229987 | ||||||
| chr12:111230013
|
C | CA | 6 | a0001c0001t0002g0030a0001c0001t0002g0086a0001c0005t0001g0019others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+12095dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111230013 | |||||
| chr12:111230013
|
CA | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+12095delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111230013 | |||||
| chr12:111230082
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.222+12145G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230082 | ||||||
| chr12:111230091
|
T | C | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+12154T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230091 | ||||||
| chr12:111230098
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.222+12161G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230098 | ||||||
| chr12:111230570
|
C | T | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.222+12633C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230570 | ||||||
| chr12:111230598
|
T | C | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+12661T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230598 | ||||||
| chr12:111230697
|
G | A | 2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.222+12760G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111230697 | ||||||
| chr12:111231100
|
G | C | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222+13163G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111231100 | ||||||
| chr12:111231231
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0009others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+13294C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111231231 | ||||||
| chr12:111231441
|
G | C | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.222+13504G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111231441 | ||||||
| chr12:111231546
|
A | G | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+13609A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111231546 | ||||||
| chr12:111231594
|
A | T | 3 | a0001c0001t0001g0091a0001c0002t0001g0090a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+13657A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111231594 | ||||||
| chr12:111232170
|
C | T | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+14233C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232170 | ||||||
| chr12:111232204
|
GAA | G | 8 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0002t0001g0090others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+14275_222+1427 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111232204 | |||||
| chr12:111232212
|
A | T | 2 | a0001c0011t0001g0001a0001c0017t0001g0065 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.222+14275A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232212 | ||||||
| chr12:111232212
|
AAT | A | 52 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(49): Show | 52 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.222+14289_222+1429 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111232212 | |||||
| chr12:111232295
|
T | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(24): Show | 27 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.222+14358T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232295 | ||||||
| chr12:111232565
|
A | G | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+14628A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232565 | ||||||
| chr12:111232569
|
A | G | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222+14632A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232569 | ||||||
| chr12:111232683
|
G | A | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+14746G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232683 | ||||||
| chr12:111232716
|
G | A | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+14779G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232716 | ||||||
| chr12:111232813
|
A | G | 1 | a0001c0004t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.222+14876A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232813 | ||||||
| chr12:111232876
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+14939G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232876 | ||||||
| chr12:111232878
|
G | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(79): Show | 82 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.222+14941G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232878 | ||||||
| chr12:111232970
|
C | G | 71 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(68): Show | 71 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.222+15033C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111232970 | ||||||
| chr12:111233033
|
T | C | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+15096T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111233033 | ||||||
| chr12:111233265
|
C | G | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.222+15328C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111233265 | ||||||
| chr12:111233272
|
G | A | 3 | a0001c0001t0005g0055a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG01243.hp2 HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.222+15335G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111233272 | ||||||
| chr12:111233283
|
T | C | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+15346T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111233283 | ||||||
| chr12:111233900
|
G | C | 11 | a0001c0001t0002g0083a0001c0003t0001g0017a0001c0004t0001g0002others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+15963G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111233900 | ||||||
| chr12:111234071
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.222+16134A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234071 | ||||||
| chr12:111234152
|
C | G | 7 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+16215C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234152 | ||||||
| chr12:111234225
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+16288G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234225 | ||||||
| chr12:111234274
|
A | G | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222+16337A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234274 | ||||||
| chr12:111234332
|
T | C | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+16395T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234332 | ||||||
| chr12:111234416
|
T | C | 3 | a0001c0003t0001g0014a0001c0004t0001g0015a0001c0004t0001g0027 | 3 | HG01884.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.222+16479T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234416 | ||||||
| chr12:111234553
|
T | C | 1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.222+16616T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234553 | ||||||
| chr12:111234716
|
C | CT | 12 | a0001c0001t0002g0083a0001c0003t0001g0017a0001c0004t0001g0002others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+16797dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111234716 | |||||
| chr12:111234716
|
CT | C | 10 | a0001c0001t0003g0045a0001c0002t0001g0023a0001c0002t0001g0025others(7): Show | 10 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+16797delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111234716 | |||||
| chr12:111234781
|
T | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.222+16844T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111234781 | ||||||
| chr12:111235169
|
G | A | 8 | a0001c0001t0002g0030a0001c0002t0001g0004a0001c0005t0001g0019others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+17232G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111235169 | ||||||
| chr12:111235372
|
G | A | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+17435G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111235372 | ||||||
| chr12:111235440
|
C | T | 32 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(29): Show | 32 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+17503C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111235440 | ||||||
| chr12:111235583
|
T | C | 30 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.222+17646T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111235583 | ||||||
| chr12:111235773
|
G | A | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+17836G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111235773 | ||||||
| chr12:111236085
|
A | G | 3 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | HG01099.hp1 HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.222+18148A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236085 | ||||||
| chr12:111236101
|
G | T | 2 | a0001c0002t0001g0037a0001c0003t0001g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.222+18164G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236101 | ||||||
| chr12:111236246
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222+18309A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236246 | ||||||
| chr12:111236317
|
T | C | 4 | a0001c0002t0001g0004a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+18380T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236317 | ||||||
| chr12:111236684
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.222+18747A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236684 | ||||||
| chr12:111236746
|
G | C | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+18809G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236746 | ||||||
| chr12:111236868
|
G | T | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.222+18931G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111236868 | ||||||
| chr12:111237062
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.222+19125T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237062 | ||||||
| chr12:111237063
|
C | T | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01169.hp1 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+19126C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237063 | ||||||
| chr12:111237132
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.222+19195G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237132 | ||||||
| chr12:111237253
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222+19316G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237253 | ||||||
| chr12:111237515
|
G | A | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+19578G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237515 | ||||||
| chr12:111237812
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222+19875C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237812 | ||||||
| chr12:111237837
|
C | G | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+19900C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111237837 | ||||||
| chr12:111238141
|
T | A | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.222+20204T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111238141 | ||||||
| chr12:111238214
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(5): Show | 8 | HG02257.hp1 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+20277T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111238214 | ||||||
| chr12:111238578
|
G | A | 4 | a0001c0001t0002g0083a0001c0005t0001g0038a0001c0005t0001g0039others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+20641G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111238578 | ||||||
| chr12:111238633
|
C | T | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.222+20696C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111238633 | ||||||
| chr12:111238717
|
T | TAC | 15 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+20792_222+2079 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111238717 | |||||
| chr12:111239148
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+21211G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111239148 | ||||||
| chr12:111239435
|
C | T | 1 | a0001c0004t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.222+21498C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111239435 | ||||||
| chr12:111239606
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.222+21669C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111239606 | ||||||
| chr12:111239758
|
G | GA | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+21821_222+2182 others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111239758 | ||||||
| chr12:111239790
|
C | G | 9 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(6): Show | 9 | HG01081.hp1 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+21853C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111239790 | ||||||
| chr12:111240047
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222+22110G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111240047 | ||||||
| chr12:111240654
|
A | T | 37 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0062others(34): Show | 37 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.222+22717A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111240654 | ||||||
| chr12:111240805
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.222+22868T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111240805 | ||||||
| chr12:111241410
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(58): Show | 61 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.223-22351C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241410 | ||||||
| chr12:111241591
|
C | T | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-22170C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241591 | ||||||
| chr12:111241605
|
A | G | 2 | a0001c0002t0001g0093a0001c0014t0001g0042 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223-22156A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241605 | ||||||
| chr12:111241808
|
C | A | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0030others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.223-21953C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241808 | ||||||
| chr12:111241943
|
C | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.223-21818C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241943 | ||||||
| chr12:111241952
|
T | G | 2 | a0001c0001t0002g0086a0001c0002t0001g0087 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.223-21809T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111241952 | ||||||
| chr12:111242022
|
T | G | 10 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-21739T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242022 | ||||||
| chr12:111242304
|
T | C | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223-21457T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242304 | ||||||
| chr12:111242347
|
A | G | 10 | a0001c0001t0002g0083a0001c0003t0001g0017a0001c0004t0001g0096others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-21414A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242347 | ||||||
| chr12:111242551
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(78): Show | 81 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.223-21210C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242551 | ||||||
| chr12:111242600
|
G | A | 4 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-21161G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242600 | ||||||
| chr12:111242769
|
C | T | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.223-20992C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242769 | ||||||
| chr12:111242935
|
C | T | 11 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0002t0001g0023others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.223-20826C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111242935 | ||||||
| chr12:111243081
|
A | G | 28 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0079others(25): Show | 28 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.223-20680A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243081 | ||||||
| chr12:111243496
|
C | CT | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(17): Show | 20 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.223-20240dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111243496 | |||||
| chr12:111243496
|
C | CTT | 10 | a0001c0001t0002g0016a0001c0003t0001g0014a0001c0003t0001g0088others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-20241_223-2024 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111243496 | |||||
| chr12:111243496
|
C | CTTT | 16 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0047others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.223-20242_223-2024 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111243496 | |||||
| chr12:111243496
|
C | CTTTT | 15 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(12): Show | 15 | HG00597.hp1 HG01069.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.223-20243_223-2024 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111243496 | |||||
| chr12:111243528
|
G | A | 3 | a0001c0002t0001g0037a0001c0003t0001g0017a0001c0003t0001g0040 | 3 | HG02886.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.223-20233G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243528 | ||||||
| chr12:111243528
|
G | C | 3 | a0001c0003t0001g0014a0001c0004t0001g0015a0001c0004t0001g0027 | 3 | HG01884.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.223-20233G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243528 | ||||||
| chr12:111243645
|
G | A | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.223-20116G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243645 | ||||||
| chr12:111243775
|
T | C | 14 | a0001c0001t0002g0030a0001c0001t0002g0086a0001c0003t0001g0014others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.223-19986T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243775 | ||||||
| chr12:111243817
|
C | T | 5 | a0001c0003t0001g0014a0001c0004t0001g0015a0001c0004t0001g0027others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-19944C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243817 | ||||||
| chr12:111243893
|
G | A | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.223-19868G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243893 | ||||||
| chr12:111243929
|
T | C | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-19832T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243929 | ||||||
| chr12:111243974
|
C | T | 4 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-19787C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111243974 | ||||||
| chr12:111244033
|
C | T | 9 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0017others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-19728C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244033 | ||||||
| chr12:111244075
|
G | A | 18 | a0001c0001t0002g0030a0001c0001t0002g0079a0001c0001t0003g0078others(15): Show | 18 | HG01169.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.223-19686G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244075 | ||||||
| chr12:111244092
|
GT | G | 10 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-19660delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111244092 | |||||
| chr12:111244093
|
T | G | 20 | a0001c0001t0002g0030a0001c0001t0002g0079a0001c0001t0002g0086others(17): Show | 20 | HG01169.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.223-19668T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244093 | ||||||
| chr12:111244117
|
A | G | 9 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0003t0001g0008others(6): Show | 9 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-19644A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244117 | ||||||
| chr12:111244277
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(1): Show | 4 | HG02559.hp2 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-19484C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244277 | ||||||
| chr12:111244427
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-19334G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244427 | ||||||
| chr12:111244801
|
G | A | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.223-18960G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111244801 | ||||||
| chr12:111245375
|
CA | C | 8 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0003t0001g0017others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-18375delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111245375 | |||||
| chr12:111245580
|
C | T | 15 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0083others(12): Show | 15 | HG02257.hp1 HG02280.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.223-18181C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111245580 | ||||||
| chr12:111245683
|
C | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.223-18078C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111245683 | ||||||
| chr12:111246345
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.223-17416C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111246345 | ||||||
| chr12:111246360
|
C | T | 2 | a0001c0003t0001g0014a0001c0004t0001g0015 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.223-17401C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111246360 | ||||||
| chr12:111246449
|
A | G | 33 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0004others(30): Show | 33 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-17312A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111246449 | ||||||
| chr12:111246657
|
A | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(79): Show | 82 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.223-17104A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111246657 | ||||||
| chr12:111246729
|
A | G | 14 | a0001c0001t0002g0012a0001c0001t0002g0083a0001c0001t0002g0085others(11): Show | 14 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.223-17032A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111246729 | ||||||
| chr12:111247964
|
T | C | 2 | a0001c0001t0002g0012a0001c0001t0002g0085 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.223-15797T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111247964 | ||||||
| chr12:111248052
|
C | G | 23 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0079others(20): Show | 23 | HG01169.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.223-15709C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111248052 | ||||||
| chr12:111248062
|
AT | A | 5 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-15691delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111248062 | |||||
| chr12:111248231
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-15530C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111248231 | ||||||
| chr12:111248285
|
CAG | C | 5 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(2): Show | 5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-15473_223-1547 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111248285 | |||||
| chr12:111248594
|
G | A | 1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-15167G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111248594 | ||||||
| chr12:111248617
|
G | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0085 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.223-15144G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111248617 | ||||||
| chr12:111249083
|
G | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-14678G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249083 | ||||||
| chr12:111249400
|
CT | C | 21 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0079others(18): Show | 21 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.223-14338delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111249400 | |||||
| chr12:111249400
|
CTT | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(4): Show | 7 | HG02615.hp1 HG02896.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-14339_223-1433 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111249400 | |||||
| chr12:111249400
|
CTTT | C | 9 | a0001c0001t0003g0045a0001c0003t0001g0011a0001c0003t0001g0017others(6): Show | 9 | HG01081.hp1 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-14340_223-1433 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111249400 | |||||
| chr12:111249423
|
T | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.223-14338T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249423 | ||||||
| chr12:111249436
|
CCTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0086others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.223-14324_223-1431 others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249436 | ||||||
| chr12:111249437
|
C | CT | 24 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(21): Show | 24 | HG01169.hp1 HG01243.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-14317dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111249437 | |||||
| chr12:111249444
|
TG | T | 8 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-14316delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249444 | ||||||
| chr12:111249445
|
G | GT | 5 | a0001c0002t0001g0018a0001c0003t0001g0033a0001c0003t0008g0032others(2): Show | 5 | HG00597.hp2 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-14297dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111249445 | |||||
| chr12:111249445
|
G | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 29 | HG00597.hp1 HG01169.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.223-14316G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249445 | ||||||
| chr12:111249471
|
G | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.223-14290G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249471 | ||||||
| chr12:111249548
|
C | G | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-14213C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249548 | ||||||
| chr12:111249592
|
G | C | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.223-14169G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249592 | ||||||
| chr12:111249953
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0085 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.223-13808G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111249953 | ||||||
| chr12:111250205
|
C | T | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.223-13556C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111250205 | ||||||
| chr12:111250335
|
C | T | 2 | a0001c0002t0001g0061a0001c0007t0001g0098 | 2 | HG00597.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223-13426C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111250335 | ||||||
| chr12:111250748
|
G | C | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.223-13013G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111250748 | ||||||
| chr12:111250906
|
G | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-12855G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111250906 | ||||||
| chr12:111251318
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0004g0054a0001c0005t0001g0019others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-12443A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111251318 | ||||||
| chr12:111251371
|
C | A | 23 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0083others(20): Show | 23 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.223-12390C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111251371 | ||||||
| chr12:111251391
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-12370G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111251391 | ||||||
| chr12:111251644
|
G | A | 2 | a0002c0006t0001g0053a0002c0006t0001g0089 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223-12117G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111251644 | ||||||
| chr12:111251900
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.223-11861C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111251900 | ||||||
| chr12:111252662
|
C | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(81): Show | 84 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.223-11099C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111252662 | ||||||
| chr12:111252775
|
T | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(81): Show | 84 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.223-10986T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111252775 | ||||||
| chr12:111252854
|
G | C | 8 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-10907G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111252854 | ||||||
| chr12:111252955
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(21): Show | 24 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-10806T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111252955 | ||||||
| chr12:111252975
|
T | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(29): Show | 32 | HG01169.hp1 HG01243.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.223-10786T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111252975 | ||||||
| chr12:111253161
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(24): Show | 27 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-10600C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111253161 | ||||||
| chr12:111253277
|
T | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(81): Show | 84 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.223-10484T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111253277 | ||||||
| chr12:111253604
|
C | T | 1 | a0001c0002t0001g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.223-10157C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111253604 | ||||||
| chr12:111253694
|
C | CTGAT | 8 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-10065_223-1006 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111253694 | |||||
| chr12:111253752
|
G | A | 24 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(21): Show | 24 | HG01169.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-10009G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111253752 | ||||||
| chr12:111253804
|
G | GT | 23 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(20): Show | 23 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.223-9950dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111253804 | |||||
| chr12:111253804
|
G | GTT | 7 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(4): Show | 7 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-9951_223-9950d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111253804 | |||||
| chr12:111253821
|
CTT | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(51): Show | 54 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.223-9927_223-9926d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111253821 | |||||
| chr12:111254004
|
G | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(24): Show | 27 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-9757G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254004 | ||||||
| chr12:111254099
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0083others(21): Show | 24 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.223-9662G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254099 | ||||||
| chr12:111254100
|
T | C | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-9661T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254100 | ||||||
| chr12:111254320
|
C | T | 27 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0076others(24): Show | 27 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.223-9441C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254320 | ||||||
| chr12:111254349
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(27): Show | 30 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.223-9412A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254349 | ||||||
| chr12:111254465
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.223-9296C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254465 | ||||||
| chr12:111254584
|
A | G | 9 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-9177A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254584 | ||||||
| chr12:111254695
|
G | T | 9 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-9066G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254695 | ||||||
| chr12:111254727
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(25): Show | 28 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-9034A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254727 | ||||||
| chr12:111254846
|
G | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(25): Show | 28 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-8915G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254846 | ||||||
| chr12:111254851
|
C | CT | 28 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(25): Show | 28 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-8901dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111254851 | |||||
| chr12:111254972
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.223-8789C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111254972 | ||||||
| chr12:111255127
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(25): Show | 28 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-8634G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255127 | ||||||
| chr12:111255191
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(16): Show | 19 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-8570G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255191 | ||||||
| chr12:111255242
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.223-8519A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255242 | ||||||
| chr12:111255284
|
C | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.223-8477C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255284 | ||||||
| chr12:111255367
|
G | C | 11 | a0001c0001t0002g0016a0001c0001t0003g0045a0001c0003t0001g0017others(8): Show | 11 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-8394G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255367 | ||||||
| chr12:111255394
|
G | A | 30 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0004others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.223-8367G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255394 | ||||||
| chr12:111255890
|
T | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.223-7871T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111255890 | ||||||
| chr12:111256144
|
G | A | 2 | a0001c0001t0002g0030a0001c0008t0002g0022 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.223-7617G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111256144 | ||||||
| chr12:111256590
|
G | C | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.223-7171G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111256590 | ||||||
| chr12:111256737
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-7024T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111256737 | ||||||
| chr12:111256861
|
T | C | 5 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-6900T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111256861 | ||||||
| chr12:111257065
|
G | A | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223-6696G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257065 | ||||||
| chr12:111257182
|
C | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.223-6579C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257182 | ||||||
| chr12:111257278
|
TTCC | T | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223-6470_223-6468d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257278 | |||||
| chr12:111257366
|
T | TCCTCCCA others(31): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-6293_223-6256d others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257366 | |||||
| chr12:111257403
|
C | A | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223-6358C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257403 | ||||||
| chr12:111257459
|
C | CCCCCTCC others(125): Show |
5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-6282_223-6281i others(134): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257459 | |||||
| chr12:111257461
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(5): Show | 8 | HG02559.hp2 HG02965.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-6300C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257461 | ||||||
| chr12:111257470
|
T | TTCTTCCT others(468): Show |
1 | a0007c0021t0002g0064 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.223-6256_223-6255i others(477): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257470 | |||||
| chr12:111257470
|
T | TTCTTCCT others(88): Show |
1 | a0001c0001t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.223-6256_223-6255i others(97): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257470 | |||||
| chr12:111257470
|
T | TTCTTCCT others(69): Show |
13 | a0001c0001t0002g0043a0001c0001t0002g0058a0001c0001t0002g0060others(10): Show | 13 | HG01069.hp1 HG01081.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.223-6263_223-6262i others(78): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257470 | |||||
| chr12:111257470
|
T | TTCTTCCT others(50): Show |
1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.223-6282_223-6281i others(59): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257470 | |||||
| chr12:111257477
|
TC | T | 18 | a0001c0001t0002g0062a0001c0002t0001g0018a0001c0002t0001g0047others(15): Show | 18 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-6279delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257477 | |||||
| chr12:111257478
|
C | CCCCCTCC others(11): Show |
6 | a0001c0001t0002g0059a0001c0002t0001g0004a0001c0002t0001g0023others(3): Show | 6 | HG01099.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-6278_223-6261d others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCCCCTCC others(30): Show |
4 | a0001c0002t0001g0025a0001c0013t0001g0063a0002c0006t0001g0053others(1): Show | 4 | HG02145.hp1 HG02698.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-6256_223-6255i others(39): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCCCCTCC others(49): Show |
7 | a0001c0001t0003g0045a0001c0003t0001g0033a0001c0004t0001g0002others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-6256_223-6255i others(58): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCCCCTCC others(68): Show |
8 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-6256_223-6255i others(77): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCCCCTCC others(125): Show |
2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-6263_223-6262i others(134): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCTCCTCC others(87): Show |
3 | a0001c0002t0001g0061a0001c0003t0001g0046a0001c0004t0006g0075 | 3 | HG02280.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.223-6282_223-6281i others(96): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCTCCTCC others(106): Show |
25 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(22): Show | 25 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-6282_223-6281i others(115): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257478
|
C | CCTCCTCC others(106): Show |
4 | a0001c0001t0002g0083a0001c0002t0001g0037a0001c0003t0001g0040others(1): Show | 4 | HG02970.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-6282_223-6281i others(115): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257478 | |||||
| chr12:111257487
|
A | T | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-6274A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257487 | ||||||
| chr12:111257557
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-6204C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257557 | ||||||
| chr12:111257641
|
TTCCTCCT others(6): Show |
T | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223-6110_223-6098d others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111257641 | |||||
| chr12:111257684
|
C | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.223-6077C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257684 | ||||||
| chr12:111257755
|
C | G | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223-6006C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111257755 | ||||||
| chr12:111258011
|
A | T | 4 | a0001c0002t0001g0061a0001c0007t0001g0098a0001c0010t0001g0049others(1): Show | 4 | HG00597.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-5750A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258011 | ||||||
| chr12:111258288
|
G | A | 8 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-5473G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258288 | ||||||
| chr12:111258315
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.223-5446C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258315 | ||||||
| chr12:111258319
|
A | C | 45 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(42): Show | 45 | HG01081.hp1 HG01169.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.223-5442A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258319 | ||||||
| chr12:111258442
|
G | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-5319G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258442 | ||||||
| chr12:111258512
|
C | CA | 12 | a0001c0001t0002g0067a0001c0001t0003g0078a0001c0002t0001g0023others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.223-5230dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111258512 | |||||
| chr12:111258571
|
A | T | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.223-5190A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258571 | ||||||
| chr12:111258608
|
A | G | 30 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(27): Show | 30 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.223-5153A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258608 | ||||||
| chr12:111258655
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.223-5106C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258655 | ||||||
| chr12:111258723
|
T | C | 21 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(18): Show | 21 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.223-5038T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258723 | ||||||
| chr12:111258724
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(82): Show | 85 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.223-5037T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258724 | ||||||
| chr12:111258766
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.223-4995G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258766 | ||||||
| chr12:111258788
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.223-4973C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111258788 | ||||||
| chr12:111259031
|
C | CTATGTGT others(3): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-4729_223-4728i others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTATGTGT others(5): Show |
2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-4729_223-4728i others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTG | 10 | a0001c0001t0002g0030a0001c0001t0002g0067a0001c0002t0001g0071others(7): Show | 10 | HG02615.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-4690_223-4689d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTGTG | 6 | a0001c0001t0002g0062a0001c0002t0001g0069a0001c0002t0001g0070others(3): Show | 6 | HG01069.hp2 HG01243.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-4692_223-4689d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTGTGTG | 8 | a0001c0001t0002g0059a0001c0002t0001g0047a0001c0002t0001g0048others(5): Show | 8 | HG00597.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-4694_223-4689d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTGTGTGT others(1): Show |
7 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0026others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-4696_223-4689d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
C | CTGTGTGT others(3): Show |
2 | a0001c0002t0001g0018a0001c0002t0001g0025 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.223-4698_223-4689d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTG | C | 2 | a0001c0002t0001g0090a0001c0003t0001g0033 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-4690_223-4689d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTGTG | C | 14 | a0001c0001t0002g0083a0001c0001t0003g0045a0001c0001t0004g0054others(11): Show | 14 | HG00597.hp2 HG02572.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.223-4692_223-4689d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTGTGTG | C | 4 | a0001c0003t0001g0017a0001c0004t0001g0002a0001c0004t0001g0096others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-4694_223-4689d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG01169.hp1 HG02055.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-4696_223-4689d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0002t0001g0037a0001c0003t0001g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.223-4698_223-4689d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259031
|
CTGTGTGT others(5): Show |
C | 12 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.223-4700_223-4689d others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259031 | |||||
| chr12:111259575
|
G | A | 21 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0083others(18): Show | 21 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.223-4186G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111259575 | ||||||
| chr12:111259612
|
C | T | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223-4149C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111259612 | ||||||
| chr12:111259793
|
C | CA | 11 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(8): Show | 11 | HG00597.hp1 HG01169.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-3950dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259793 | |||||
| chr12:111259793
|
CA | C | 34 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(31): Show | 34 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.223-3950delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111259793 | |||||
| chr12:111259849
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0004g0054a0001c0005t0001g0019others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-3912A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111259849 | ||||||
| chr12:111259971
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3790G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111259971 | ||||||
| chr12:111260023
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-3738C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260023 | ||||||
| chr12:111260122
|
C | CA | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3638dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111260122 | |||||
| chr12:111260168
|
T | A | 2 | a0001c0002t0001g0090a0001c0014t0001g0042 | 2 | HG01081.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.223-3593T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260168 | ||||||
| chr12:111260191
|
G | A | 5 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-3570G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260191 | ||||||
| chr12:111260333
|
G | A | 29 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(26): Show | 29 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.223-3428G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260333 | ||||||
| chr12:111260380
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3381C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260380 | ||||||
| chr12:111260428
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.223-3333C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260428 | ||||||
| chr12:111260431
|
T | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3330T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260431 | ||||||
| chr12:111260466
|
G | GA | 8 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(5): Show | 8 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-3283dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111260466 | |||||
| chr12:111260466
|
GA | G | 5 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021others(2): Show | 5 | HG01081.hp1 HG02109.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-3283delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111260466 | |||||
| chr12:111260512
|
T | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3249T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260512 | ||||||
| chr12:111260539
|
T | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-3222T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260539 | ||||||
| chr12:111260653
|
G | A | 65 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(62): Show | 65 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.223-3108G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260653 | ||||||
| chr12:111260812
|
C | G | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-2949C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260812 | ||||||
| chr12:111260850
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223-2911C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260850 | ||||||
| chr12:111260896
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-2865T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260896 | ||||||
| chr12:111260935
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-2826C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111260935 | ||||||
| chr12:111261213
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.223-2548G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111261213 | ||||||
| chr12:111261215
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-2546C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111261215 | ||||||
| chr12:111261342
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(83): Show | 86 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-2419A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111261342 | ||||||
| chr12:111261564
|
T | C | 5 | a0001c0001t0002g0030a0001c0005t0001g0019a0001c0008t0002g0022others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-2197T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111261564 | ||||||
| chr12:111261721
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-2040C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111261721 | ||||||
| chr12:111262379
|
C | CT | 63 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(60): Show | 63 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.223-1365dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111262379 | |||||
| chr12:111262454
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-1307T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111262454 | ||||||
| chr12:111262913
|
A | G | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.223-848A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111262913 | ||||||
| chr12:111262932
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223-829C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111262932 | ||||||
| chr12:111263260
|
G | A | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223-501G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111263260 | ||||||
| chr12:111263265
|
A | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-496A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111263265 | ||||||
| chr12:111263525
|
T | G | 30 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0004others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.223-236T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111263525 | ||||||
| chr12:111263625
|
A | AAAAAC | 2 | a0001c0001t0001g0013a0001c0003t0001g0017 | 2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.223-106_223-102dup others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111263625 | |||||
| chr12:111263625
|
AAAAAC | A | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-106_223-102del others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111263625 | |||||
| chr12:111263629
|
AC | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223-131delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111263629 | ||||||
| chr12:111263682
|
GA | G | 28 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0004others(25): Show | 28 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.223-69delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 111263682 | |||||
| chr12:111263733
|
G | A | 32 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(29): Show | 32 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.223-28G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | chr12 | 111263733 | ||||||
| chr12:111264378
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(9): Show | 12 | HG01169.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.301+539T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111264378 | ||||||
| chr12:111264501
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.301+662G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111264501 | ||||||
| chr12:111264637
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+798C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111264637 | ||||||
| chr12:111264841
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.301+1002C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111264841 | ||||||
| chr12:111264842
|
A | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(45): Show | 48 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.301+1003A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111264842 | ||||||
| chr12:111264893
|
TA | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(45): Show | 48 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.301+1056delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111264893 | |||||
| chr12:111265053
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.301+1214G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111265053 | ||||||
| chr12:111265309
|
T | TTTTTA | 16 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0001g0091others(13): Show | 16 | HG01069.hp1 HG01169.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.301+1515_301+1519d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111265309 | |||||
| chr12:111265309
|
T | TTTTTATT others(3): Show |
2 | a0001c0005t0001g0038a0001c0005t0001g0039 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.301+1510_301+1519d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111265309 | |||||
| chr12:111265309
|
TTTTTA | T | 13 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0003g0045others(10): Show | 13 | HG01081.hp1 HG01243.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+1515_301+1519d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111265309 | |||||
| chr12:111265309
|
TTTTTATT others(3): Show |
T | 23 | a0001c0001t0002g0016a0001c0001t0002g0059a0001c0001t0002g0062others(20): Show | 23 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.301+1510_301+1519d others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111265309 | |||||
| chr12:111265309
|
TTTTTATT others(8): Show |
T | 10 | a0001c0001t0002g0086a0001c0002t0001g0004a0001c0002t0001g0023others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+1505_301+1519d others(17): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111265309 | |||||
| chr12:111265427
|
C | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+1588C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111265427 | ||||||
| chr12:111265509
|
T | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(50): Show | 53 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.301+1670T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111265509 | ||||||
| chr12:111266187
|
A | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+2348A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266187 | ||||||
| chr12:111266272
|
T | C | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+2433T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266272 | ||||||
| chr12:111266338
|
G | T | 2 | a0001c0001t0001g0091a0006c0020t0001g0020 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.301+2499G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266338 | ||||||
| chr12:111266473
|
CA | C | 52 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(49): Show | 52 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.301+2650delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111266473 | |||||
| chr12:111266476
|
A | C | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+2637A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266476 | ||||||
| chr12:111266477
|
A | C | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.301+2638A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266477 | ||||||
| chr12:111266635
|
G | A | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+2796G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266635 | ||||||
| chr12:111266698
|
A | C | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301+2859A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266698 | ||||||
| chr12:111266735
|
G | A | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+2896G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266735 | ||||||
| chr12:111266909
|
G | C | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.301+3070G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111266909 | ||||||
| chr12:111267031
|
A | T | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301+3192A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267031 | ||||||
| chr12:111267033
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+3194A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267033 | ||||||
| chr12:111267195
|
CA | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0091others(63): Show | 66 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.301+3378delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111267195 | |||||
| chr12:111267195
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.301+3368_301+3378d others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111267195 | |||||
| chr12:111267214
|
A | G | 3 | a0001c0001t0002g0016a0001c0002t0001g0070a0001c0007t0001g0021 | 3 | HG01243.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+3375A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267214 | ||||||
| chr12:111267378
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+3539G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267378 | ||||||
| chr12:111267489
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+3650C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267489 | ||||||
| chr12:111267501
|
T | G | 1 | a0001c0001t0002g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301+3662T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267501 | ||||||
| chr12:111267531
|
G | C | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301+3692G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267531 | ||||||
| chr12:111267761
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+3922A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267761 | ||||||
| chr12:111267837
|
A | G | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+3998A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111267837 | ||||||
| chr12:111268085
|
C | T | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+4246C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268085 | ||||||
| chr12:111268089
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(73): Show | 76 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.301+4250A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268089 | ||||||
| chr12:111268201
|
G | T | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+4362G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268201 | ||||||
| chr12:111268207
|
GTTTGTTT | G | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+4393_301+4399d others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111268207 | |||||
| chr12:111268207
|
GTTTGTTT others(7): Show |
G | 3 | a0001c0001t0002g0016a0001c0001t0002g0086a0001c0007t0001g0021 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+4386_301+4399d others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111268207 | |||||
| chr12:111268211
|
G | GT | 21 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(18): Show | 21 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.301+4378dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111268211 | |||||
| chr12:111268350
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+4511G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268350 | ||||||
| chr12:111268411
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.301+4572A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268411 | ||||||
| chr12:111268532
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+4693T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268532 | ||||||
| chr12:111268863
|
C | T | 7 | a0001c0001t0002g0030a0001c0001t0004g0054a0001c0005t0001g0019others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+5024C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268863 | ||||||
| chr12:111268865
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(18): Show | 21 | HG01099.hp1 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.301+5026T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268865 | ||||||
| chr12:111268925
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+5086G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268925 | ||||||
| chr12:111268986
|
A | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+5147A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111268986 | ||||||
| chr12:111269073
|
C | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(72): Show | 75 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.301+5234C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269073 | ||||||
| chr12:111269158
|
G | T | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.301+5319G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269158 | ||||||
| chr12:111269205
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG01099.hp1 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.301+5366A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269205 | ||||||
| chr12:111269322
|
G | A | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+5483G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269322 | ||||||
| chr12:111269347
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.301+5508A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269347 | ||||||
| chr12:111269412
|
T | C | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+5573T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269412 | ||||||
| chr12:111269433
|
G | A | 6 | a0001c0001t0002g0062a0001c0002t0001g0018a0001c0002t0001g0051others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+5594G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269433 | ||||||
| chr12:111269485
|
G | A | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+5646G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269485 | ||||||
| chr12:111269571
|
A | G | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301+5732A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269571 | ||||||
| chr12:111269752
|
G | A | 20 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(17): Show | 20 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.301+5913G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269752 | ||||||
| chr12:111269823
|
G | T | 7 | a0001c0001t0002g0030a0001c0001t0004g0054a0001c0005t0001g0019others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+5984G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269823 | ||||||
| chr12:111269950
|
A | T | 20 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(17): Show | 20 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.301+6111A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269950 | ||||||
| chr12:111269993
|
C | T | 4 | a0001c0002t0001g0061a0001c0007t0001g0098a0001c0010t0001g0049others(1): Show | 4 | HG00597.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+6154C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111269993 | ||||||
| chr12:111270114
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.301+6275C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270114 | ||||||
| chr12:111270115
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301+6276G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270115 | ||||||
| chr12:111270234
|
A | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+6395A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270234 | ||||||
| chr12:111270587
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.301+6748A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270587 | ||||||
| chr12:111270643
|
G | GA | 10 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+6820dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111270643 | |||||
| chr12:111270654
|
A | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0056 | 2 | HG01099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.301+6815A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270654 | ||||||
| chr12:111270822
|
G | C | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.301+6983G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270822 | ||||||
| chr12:111270823
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.301+6984G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111270823 | ||||||
| chr12:111271045
|
G | C | 2 | a0001c0003t0001g0017a0001c0013t0001g0063 | 2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.301+7206G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111271045 | ||||||
| chr12:111271079
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+7240C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111271079 | ||||||
| chr12:111271234
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.301+7395G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111271234 | ||||||
| chr12:111271249
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(13): Show | 16 | HG01099.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.301+7410A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111271249 | ||||||
| chr12:111272335
|
C | T | 1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.301+8496C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111272335 | ||||||
| chr12:111272662
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.301+8823C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111272662 | ||||||
| chr12:111272710
|
T | C | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+8871T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111272710 | ||||||
| chr12:111272994
|
C | T | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.301+9155C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111272994 | ||||||
| chr12:111273175
|
G | A | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+9336G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111273175 | ||||||
| chr12:111273275
|
G | A | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.301+9436G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111273275 | ||||||
| chr12:111273590
|
C | A | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.301+9751C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111273590 | ||||||
| chr12:111273794
|
C | T | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.301+9955C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111273794 | ||||||
| chr12:111273814
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.301+9975G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111273814 | ||||||
| chr12:111274798
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.301+10959C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111274798 | ||||||
| chr12:111274951
|
CA | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(44): Show | 47 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.301+11124delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111274951 | |||||
| chr12:111275452
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.301+11613C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111275452 | ||||||
| chr12:111275867
|
G | C | 20 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0002t0001g0018others(17): Show | 20 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.301+12028G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111275867 | ||||||
| chr12:111276101
|
A | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.301+12262A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276101 | ||||||
| chr12:111276123
|
C | T | 2 | a0001c0003t0001g0046a0001c0004t0006g0075 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.301+12284C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276123 | ||||||
| chr12:111276207
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.301+12368G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276207 | ||||||
| chr12:111276627
|
TTTTG | T | 2 | a0001c0001t0002g0083a0001c0014t0001g0042 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+12808_301+1281 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111276627 | |||||
| chr12:111276643
|
G | GT | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+12807dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111276643 | |||||
| chr12:111276643
|
G | GTTTGT | 27 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(24): Show | 27 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.301+12829_301+1283 others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111276643 | |||||
| chr12:111276808
|
C | T | 15 | a0001c0001t0003g0045a0001c0002t0001g0004a0001c0002t0001g0023others(12): Show | 15 | HG00597.hp2 HG01099.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+12969C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276808 | ||||||
| chr12:111276837
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.301+12998G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276837 | ||||||
| chr12:111276926
|
C | T | 24 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0079others(21): Show | 24 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.301+13087C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111276926 | ||||||
| chr12:111277041
|
T | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301+13202T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111277041 | ||||||
| chr12:111277393
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0056 | 2 | HG01099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.301+13554C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111277393 | ||||||
| chr12:111277400
|
T | G | 10 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.301+13561T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111277400 | ||||||
| chr12:111277700
|
A | G | 2 | a0001c0001t0003g0045a0001c0002t0001g0090 | 2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.302-13718A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111277700 | ||||||
| chr12:111277763
|
C | A | 21 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0083others(18): Show | 21 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.302-13655C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111277763 | ||||||
| chr12:111278509
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.302-12909A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111278509 | ||||||
| chr12:111278554
|
G | A | 10 | a0001c0001t0003g0045a0001c0004t0001g0002a0001c0004t0001g0005others(7): Show | 10 | HG01081.hp1 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-12864G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111278554 | ||||||
| chr12:111278572
|
C | T | 67 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(64): Show | 67 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.302-12846C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111278572 | ||||||
| chr12:111278597
|
C | T | 3 | a0001c0003t0001g0017a0001c0004t0004g0041a0001c0013t0001g0063 | 3 | HG02486.hp1 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.302-12821C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111278597 | ||||||
| chr12:111278914
|
G | A | 60 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0059others(57): Show | 60 | HG00597.hp1 HG01081.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.302-12504G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111278914 | ||||||
| chr12:111279022
|
A | G | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0014t0001g0042 | 3 | HG01081.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.302-12396A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279022 | ||||||
| chr12:111279080
|
A | G | 1 | a0001c0018t0004g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.302-12338A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279080 | ||||||
| chr12:111279385
|
G | T | 2 | a0001c0002t0001g0061a0001c0007t0001g0098 | 2 | HG00597.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.302-12033G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279385 | ||||||
| chr12:111279585
|
G | A | 17 | a0001c0001t0002g0030a0001c0002t0001g0095a0001c0003t0001g0008others(14): Show | 17 | HG01891.hp1 HG02280.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.302-11833G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279585 | ||||||
| chr12:111279655
|
T | C | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.302-11763T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279655 | ||||||
| chr12:111279811
|
T | C | 22 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0086others(19): Show | 22 | HG00597.hp1 HG01069.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.302-11607T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279811 | ||||||
| chr12:111279875
|
G | A | 2 | a0001c0002t0001g0061a0001c0007t0001g0098 | 2 | HG00597.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.302-11543G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279875 | ||||||
| chr12:111279907
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.302-11511G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111279907 | ||||||
| chr12:111280062
|
T | A | 1 | a0001c0001t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-11356T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280062 | ||||||
| chr12:111280095
|
C | T | 34 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0086others(31): Show | 34 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.302-11323C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280095 | ||||||
| chr12:111280105
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.302-11313G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280105 | ||||||
| chr12:111280258
|
C | T | 3 | a0001c0001t0002g0067a0001c0002t0001g0061a0001c0007t0001g0098 | 3 | HG00597.hp2 HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.302-11160C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280258 | ||||||
| chr12:111280344
|
G | T | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.302-11074G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280344 | ||||||
| chr12:111280427
|
C | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.302-10991C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280427 | ||||||
| chr12:111280506
|
A | T | 3 | a0001c0001t0002g0083a0001c0003t0001g0014a0001c0003t0001g0040 | 3 | HG02970.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-10912A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280506 | ||||||
| chr12:111280518
|
G | A | 4 | a0001c0003t0001g0033a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02698.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-10900G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280518 | ||||||
| chr12:111280613
|
G | A | 27 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0086others(24): Show | 27 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.302-10805G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280613 | ||||||
| chr12:111280617
|
G | A | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-10801G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111280617 | ||||||
| chr12:111281056
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302-10362T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111281056 | ||||||
| chr12:111281256
|
T | A | 80 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(77): Show | 80 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.302-10162T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111281256 | ||||||
| chr12:111281523
|
G | A | 8 | a0001c0001t0003g0045a0001c0003t0001g0017a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.302-9895G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111281523 | ||||||
| chr12:111281789
|
G | T | 4 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-9629G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111281789 | ||||||
| chr12:111282106
|
G | A | 2 | a0001c0004t0001g0005a0001c0014t0001g0042 | 2 | HG01081.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.302-9312G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111282106 | ||||||
| chr12:111282321
|
C | CA | 6 | a0001c0001t0001g0013a0001c0002t0001g0025a0001c0003t0001g0033others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-9081dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111282321 | |||||
| chr12:111282321
|
CA | C | 43 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0016others(40): Show | 43 | HG01081.hp1 HG01099.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.302-9081delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111282321 | |||||
| chr12:111282328
|
A | G | 26 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0083others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.302-9090A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111282328 | ||||||
| chr12:111282349
|
G | A | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.302-9069G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111282349 | ||||||
| chr12:111282402
|
A | G | 7 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.302-9016A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111282402 | ||||||
| chr12:111282557
|
C | T | 1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-8861C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111282557 | ||||||
| chr12:111282625
|
TAA | T | 35 | a0001c0001t0002g0016a0001c0001t0002g0059a0001c0001t0002g0062others(32): Show | 35 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.302-8770_302-8769d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111282625 | |||||
| chr12:111282625
|
TAAA | T | 37 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0083others(34): Show | 37 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.302-8771_302-8769d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111282625 | |||||
| chr12:111282625
|
TAAAA | T | 6 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-8772_302-8769d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111282625 | |||||
| chr12:111283086
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0085 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.302-8332C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283086 | ||||||
| chr12:111283218
|
T | TA | 31 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0030others(28): Show | 31 | HG01169.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.302-8188dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111283218 | |||||
| chr12:111283340
|
G | A | 4 | a0001c0003t0001g0033a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02698.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-8078G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283340 | ||||||
| chr12:111283522
|
G | A | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302-7896G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283522 | ||||||
| chr12:111283700
|
C | T | 4 | a0001c0003t0001g0033a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02698.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-7718C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283700 | ||||||
| chr12:111283940
|
C | T | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.302-7478C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283940 | ||||||
| chr12:111283971
|
A | T | 51 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(48): Show | 51 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.302-7447A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111283971 | ||||||
| chr12:111284329
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.302-7089C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111284329 | ||||||
| chr12:111284392
|
G | A | 22 | a0001c0001t0001g0091a0001c0001t0002g0030a0001c0001t0002g0083others(19): Show | 22 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.302-7026G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111284392 | ||||||
| chr12:111284425
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.302-6993G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111284425 | ||||||
| chr12:111284452
|
C | T | 5 | a0001c0003t0001g0033a0001c0003t0001g0088a0002c0006t0001g0053others(2): Show | 5 | HG01884.hp2 HG02698.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-6966C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111284452 | ||||||
| chr12:111285135
|
G | A | 99 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(96): Show | 99 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.302-6283G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285135 | ||||||
| chr12:111285445
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0085 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.302-5973G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285445 | ||||||
| chr12:111285565
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.302-5853C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285565 | ||||||
| chr12:111285716
|
C | T | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-5702C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285716 | ||||||
| chr12:111285740
|
G | A | 5 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-5678G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285740 | ||||||
| chr12:111285810
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302-5608C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285810 | ||||||
| chr12:111285935
|
G | A | 15 | a0001c0001t0003g0045a0001c0002t0001g0037a0001c0003t0001g0017others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.302-5483G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285935 | ||||||
| chr12:111285973
|
G | A | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.302-5445G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285973 | ||||||
| chr12:111285978
|
A | C | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.302-5440A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111285978 | ||||||
| chr12:111286574
|
A | G | 6 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-4844A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111286574 | ||||||
| chr12:111286638
|
C | T | 26 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0086others(23): Show | 26 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.302-4780C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111286638 | ||||||
| chr12:111286689
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0007t0001g0021 | 3 | HG02257.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.302-4729A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111286689 | ||||||
| chr12:111286895
|
T | C | 30 | a0001c0001t0002g0016a0001c0001t0002g0059a0001c0001t0002g0062others(27): Show | 30 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.302-4523T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111286895 | ||||||
| chr12:111287147
|
C | A | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.302-4271C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287147 | ||||||
| chr12:111287269
|
C | A | 10 | a0001c0001t0003g0045a0001c0004t0001g0002a0001c0004t0001g0027others(7): Show | 10 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-4149C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287269 | ||||||
| chr12:111287302
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0083a0001c0002t0001g0061others(6): Show | 9 | HG00597.hp2 HG02717.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-4116C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287302 | ||||||
| chr12:111287381
|
C | A | 30 | a0001c0001t0002g0030a0001c0001t0002g0062a0001c0001t0002g0086others(27): Show | 30 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.302-4037C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287381 | ||||||
| chr12:111287587
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302-3831G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287587 | ||||||
| chr12:111287810
|
G | A | 3 | a0001c0001t0002g0083a0001c0003t0001g0014a0001c0003t0001g0040 | 3 | HG02970.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-3608G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111287810 | ||||||
| chr12:111288657
|
A | C | 1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.302-2761A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111288657 | ||||||
| chr12:111289016
|
G | A | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.302-2402G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111289016 | ||||||
| chr12:111289046
|
A | T | 53 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0030others(50): Show | 53 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.302-2372A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111289046 | ||||||
| chr12:111289446
|
G | A | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.302-1972G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111289446 | ||||||
| chr12:111290069
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-1349G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290069 | ||||||
| chr12:111290275
|
T | C | 3 | a0001c0002t0001g0037a0001c0004t0001g0015a0001c0004t0001g0027 | 3 | HG01884.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.302-1143T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290275 | ||||||
| chr12:111290483
|
A | C | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.302-935A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290483 | ||||||
| chr12:111290543
|
T | A | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.302-875T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290543 | ||||||
| chr12:111290544
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.302-874C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290544 | ||||||
| chr12:111290545
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.302-873A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290545 | ||||||
| chr12:111290867
|
CT | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(39): Show | 42 | HG00597.hp2 HG01081.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-538delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111290867 | |||||
| chr12:111290867
|
CTT | C | 4 | a0001c0003t0001g0033a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02698.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-539_302-538del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 111290867 | |||||
| chr12:111290896
|
T | G | 3 | a0001c0002t0001g0037a0001c0004t0001g0015a0001c0004t0001g0027 | 3 | HG01884.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.302-522T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111290896 | ||||||
| chr12:111291364
|
G | A | 1 | a0001c0003t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.302-54G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111291364 | ||||||
| chr12:111291402
|
T | C | 9 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0066others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-16T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | chr12 | 111291402 | ||||||
| chr12:111292074
|
A | G | 20 | a0001c0001t0001g0091a0001c0001t0002g0016a0001c0001t0002g0062others(17): Show | 20 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.436+522A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111292074 | ||||||
| chr12:111292352
|
GA | G | 30 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(27): Show | 30 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.436+801delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111292352 | ||||||
| chr12:111292939
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437-507A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111292939 | ||||||
| chr12:111292989
|
G | T | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.437-457G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111292989 | ||||||
| chr12:111293128
|
C | CA | 38 | a0001c0001t0002g0067a0001c0001t0004g0054a0001c0002t0001g0004others(35): Show | 38 | HG00597.hp1 HG00597.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.437-308dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 111293128 | |||||
| chr12:111293300
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.437-146C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111293300 | ||||||
| chr12:111293360
|
A | G | 5 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-86A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 5/21 | chr12 | 111293360 | ||||||
| chr12:111293646
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.560+77C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111293646 | ||||||
| chr12:111293751
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02109.hp1 HG02698.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+182G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111293751 | ||||||
| chr12:111293827
|
G | T | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.560+258G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111293827 | ||||||
| chr12:111294048
|
A | G | 3 | a0001c0001t0001g0091a0001c0004t0004g0041a0001c0013t0001g0063 | 3 | HG02486.hp1 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.560+479A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294048 | ||||||
| chr12:111294459
|
G | A | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-874G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294459 | ||||||
| chr12:111294585
|
CA | C | 23 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(20): Show | 23 | HG01169.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.561-730delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 111294585 | |||||
| chr12:111294585
|
CAA | C | 18 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(15): Show | 18 | HG01081.hp1 HG02109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-731_561-730del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 111294585 | |||||
| chr12:111294585
|
CAAA | C | 27 | a0001c0001t0004g0054a0001c0002t0001g0004a0001c0002t0001g0023others(24): Show | 27 | HG00597.hp1 HG00597.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.561-732_561-730del others(3): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 111294585 | |||||
| chr12:111294600
|
A | G | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.561-733A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294600 | ||||||
| chr12:111294613
|
C | T | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-720C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294613 | ||||||
| chr12:111294630
|
C | T | 5 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-703C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294630 | ||||||
| chr12:111294978
|
G | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.561-355G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111294978 | ||||||
| chr12:111295020
|
G | T | 19 | a0001c0001t0001g0091a0001c0001t0002g0016a0001c0001t0002g0062others(16): Show | 19 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-313G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111295020 | ||||||
| chr12:111295026
|
G | T | 5 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-307G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111295026 | ||||||
| chr12:111295246
|
G | T | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.561-87G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 6/21 | chr12 | 111295246 | ||||||
| chr12:111295419
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.637+10G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295419 | ||||||
| chr12:111295470
|
C | T | 31 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(28): Show | 31 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.637+61C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295470 | ||||||
| chr12:111295481
|
G | A | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+72G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295481 | ||||||
| chr12:111295488
|
G | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.637+79G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295488 | ||||||
| chr12:111295751
|
C | CTAAT | 43 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0002t0001g0004others(40): Show | 43 | HG01069.hp2 HG01099.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.637+368_637+371dup others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr12 | 111295751 | |||||
| chr12:111295918
|
C | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.637+509C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295918 | ||||||
| chr12:111295995
|
G | A | 3 | a0001c0001t0002g0059a0001c0003t0001g0008a0001c0003t0001g0033 | 3 | HG02572.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.638-478G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111295995 | ||||||
| chr12:111296074
|
G | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.638-399G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111296074 | ||||||
| chr12:111296240
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.638-233C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111296240 | ||||||
| chr12:111296244
|
G | T | 5 | a0001c0001t0001g0091a0001c0004t0004g0041a0001c0004t0005g0007others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-229G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111296244 | ||||||
| chr12:111296317
|
C | T | 75 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0016others(72): Show | 75 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-156C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 7/21 | chr12 | 111296317 | ||||||
| chr12:111296648
|
ACCTCCTC others(77): Show |
A | 36 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(33): Show | 36 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.704+284_704+367del others(84): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr12 | 111296648 | |||||
| chr12:111296661
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704+122G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111296661 | ||||||
| chr12:111296733
|
C | A | 18 | a0001c0001t0002g0016a0001c0001t0002g0030a0001c0001t0002g0059others(15): Show | 18 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.704+194C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111296733 | ||||||
| chr12:111296823
|
C | A | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.704+284C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111296823 | ||||||
| chr12:111296861
|
A | G | 1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.704+322A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111296861 | ||||||
| chr12:111296877
|
C | T | 48 | a0001c0001t0001g0091a0001c0002t0001g0004a0001c0002t0001g0018others(45): Show | 48 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.704+338C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111296877 | ||||||
| chr12:111297068
|
C | T | 2 | a0001c0003t0001g0010a0001c0003t0001g0011 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.704+529C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297068 | ||||||
| chr12:111297203
|
C | T | 47 | a0001c0001t0001g0091a0001c0002t0001g0004a0001c0002t0001g0018others(44): Show | 47 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.704+664C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297203 | ||||||
| chr12:111297394
|
G | A | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.704+855G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297394 | ||||||
| chr12:111297598
|
A | G | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.705-943A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297598 | ||||||
| chr12:111297733
|
G | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.705-808G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297733 | ||||||
| chr12:111297964
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.705-577A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111297964 | ||||||
| chr12:111298043
|
T | C | 34 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0030others(31): Show | 34 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.705-498T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298043 | ||||||
| chr12:111298077
|
G | A | 1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.705-464G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298077 | ||||||
| chr12:111298110
|
A | T | 35 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(32): Show | 35 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.705-431A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298110 | ||||||
| chr12:111298134
|
C | G | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.705-407C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298134 | ||||||
| chr12:111298150
|
C | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.705-391C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298150 | ||||||
| chr12:111298210
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(4): Show | 7 | HG00597.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.705-331C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298210 | ||||||
| chr12:111298274
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(4): Show | 7 | HG00597.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.705-267C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298274 | ||||||
| chr12:111298358
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(32): Show | 35 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.705-183A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 8/21 | chr12 | 111298358 | ||||||
| chr12:111298613
|
G | A | 2 | a0001c0003t0001g0046a0001c0017t0001g0065 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.753+24G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111298613 | ||||||
| chr12:111298763
|
C | T | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.753+174C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111298763 | ||||||
| chr12:111298996
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.753+407C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111298996 | ||||||
| chr12:111299257
|
G | A | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.753+668G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299257 | ||||||
| chr12:111299311
|
T | C | 34 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0030others(31): Show | 34 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.753+722T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299311 | ||||||
| chr12:111299370
|
G | A | 13 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(10): Show | 13 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+781G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299370 | ||||||
| chr12:111299419
|
G | A | 5 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+830G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299419 | ||||||
| chr12:111299839
|
C | T | 28 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0059others(25): Show | 28 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.753+1250C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299839 | ||||||
| chr12:111299874
|
A | G | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+1285A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111299874 | ||||||
| chr12:111300012
|
A | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.753+1423A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300012 | ||||||
| chr12:111300181
|
A | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(81): Show | 84 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.753+1592A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300181 | ||||||
| chr12:111300390
|
G | A | 15 | a0001c0001t0001g0091a0001c0001t0002g0079a0001c0001t0003g0045others(12): Show | 15 | HG01169.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.753+1801G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300390 | ||||||
| chr12:111300483
|
G | A | 54 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0016others(51): Show | 54 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.753+1894G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300483 | ||||||
| chr12:111300505
|
C | T | 14 | a0001c0001t0001g0091a0001c0004t0001g0002a0001c0004t0004g0041others(11): Show | 14 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.753+1916C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300505 | ||||||
| chr12:111300560
|
A | G | 41 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(38): Show | 41 | HG00597.hp2 HG01169.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.753+1971A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300560 | ||||||
| chr12:111300589
|
G | T | 18 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0079others(15): Show | 18 | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.753+2000G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300589 | ||||||
| chr12:111300623
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.753+2034A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300623 | ||||||
| chr12:111300760
|
G | A | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.753+2171G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111300760 | ||||||
| chr12:111301020
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.753+2431C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111301020 | ||||||
| chr12:111301038
|
C | CA | 4 | a0001c0001t0001g0013a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+2468dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
C | CAA | 7 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0004g0054others(4): Show | 7 | HG00597.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+2467_753+2468d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
C | CAAA | 5 | a0001c0001t0002g0012a0001c0001t0002g0086a0002c0006t0001g0053others(2): Show | 5 | HG02109.hp1 HG02698.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+2466_753+2468d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
C | CAAAAA | 11 | a0001c0001t0002g0030a0001c0001t0002g0079a0001c0001t0002g0083others(8): Show | 11 | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+2464_753+2468d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
C | CAAAAAA | 4 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+2463_753+2468d others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
CA | C | 28 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(25): Show | 28 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.753+2468delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301038
|
CAAA | C | 21 | a0001c0001t0001g0091a0001c0003t0001g0017a0001c0004t0001g0002others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.753+2466_753+2468d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301038 | |||||
| chr12:111301432
|
T | C | 49 | a0001c0001t0001g0091a0001c0002t0001g0004a0001c0002t0001g0018others(46): Show | 49 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.754-2778T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111301432 | ||||||
| chr12:111301515
|
CT | C | 8 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG00597.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-2684delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111301515 | |||||
| chr12:111301576
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.754-2634G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111301576 | ||||||
| chr12:111301696
|
A | G | 82 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(79): Show | 82 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.754-2514A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111301696 | ||||||
| chr12:111301814
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.754-2396G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111301814 | ||||||
| chr12:111302503
|
A | G | 2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.754-1707A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111302503 | ||||||
| chr12:111302729
|
G | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.754-1481G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111302729 | ||||||
| chr12:111302899
|
TA | T | 49 | a0001c0001t0001g0091a0001c0001t0002g0060a0001c0002t0001g0004others(46): Show | 49 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.754-1292delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111302899 | |||||
| chr12:111302899
|
TAA | T | 5 | a0001c0004t0001g0002a0001c0004t0001g0096a0002c0006t0001g0053others(2): Show | 5 | HG01243.hp1 HG02698.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-1293_754-1292d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111302899 | |||||
| chr12:111302899
|
TAAA | T | 27 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(24): Show | 27 | HG00597.hp2 HG01169.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.754-1294_754-1292d others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111302899 | |||||
| chr12:111303087
|
A | G | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(9): Show | 12 | HG00597.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.754-1123A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111303087 | ||||||
| chr12:111303221
|
GA | G | 40 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0002g0079others(37): Show | 40 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.754-963delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111303221 | |||||
| chr12:111303221
|
GAA | G | 15 | a0001c0001t0001g0091a0001c0003t0001g0011a0001c0003t0001g0017others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.754-964_754-963del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111303221 | |||||
| chr12:111303221
|
GAAAA | G | 8 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-966_754-963del others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111303221 | |||||
| chr12:111303221
|
GAAAAA | G | 4 | a0001c0001t0004g0054a0001c0003t0001g0094a0001c0007t0001g0098others(1): Show | 4 | HG00597.hp2 HG02717.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-967_754-963del others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111303221 | |||||
| chr12:111303296
|
C | T | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-914C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111303296 | ||||||
| chr12:111303511
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(81): Show | 84 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.754-699T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | chr12 | 111303511 | ||||||
| chr12:111303636
|
C | CA | 16 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(13): Show | 16 | HG00597.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.754-560dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 111303636 | |||||
| chr12:111304361
|
T | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.858+47T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111304361 | ||||||
| chr12:111304404
|
TTTGTGGT others(3): Show |
T | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858+96_858+105delG others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 111304404 | |||||
| chr12:111304418
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(81): Show | 84 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.858+104T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111304418 | ||||||
| chr12:111304525
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858+211C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111304525 | ||||||
| chr12:111304761
|
G | A | 20 | a0001c0001t0001g0091a0001c0003t0001g0017a0001c0004t0001g0002others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.858+447G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111304761 | ||||||
| chr12:111305243
|
G | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0069a0001c0002t0001g0070others(3): Show | 6 | HG00597.hp1 HG01243.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+929G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305243 | ||||||
| chr12:111305570
|
C | G | 2 | a0001c0004t0001g0015a0001c0004t0001g0027 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.858+1256C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305570 | ||||||
| chr12:111305638
|
C | T | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.859-1283C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305638 | ||||||
| chr12:111305666
|
GA | G | 12 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(9): Show | 12 | HG00597.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.859-1245delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 111305666 | |||||
| chr12:111305823
|
C | T | 3 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0099 | 3 | HG02055.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.859-1098C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305823 | ||||||
| chr12:111305861
|
G | A | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.859-1060G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305861 | ||||||
| chr12:111305875
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859-1046C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111305875 | ||||||
| chr12:111306152
|
G | A | 1 | a0001c0019t0004g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.859-769G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111306152 | ||||||
| chr12:111306295
|
TG | T | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.859-622delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 111306295 | |||||
| chr12:111306326
|
G | GT | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-580dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 111306326 | |||||
| chr12:111306326
|
GT | G | 76 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(73): Show | 76 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.859-580delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 111306326 | |||||
| chr12:111306387
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.859-534C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111306387 | ||||||
| chr12:111306506
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.859-415G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111306506 | ||||||
| chr12:111306838
|
C | T | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.859-83C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111306838 | ||||||
| chr12:111306867
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.859-54C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 10/21 | chr12 | 111306867 | ||||||
| chr12:111307847
|
G | A | 8 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG00597.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110-438G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 12/21 | chr12 | 111307847 | ||||||
| chr12:111308216
|
C | T | 1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1110-69C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 12/21 | chr12 | 111308216 | ||||||
| chr12:111308564
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1258+38C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111308564 | ||||||
| chr12:111308695
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(81): Show | 84 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.1258+169A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111308695 | ||||||
| chr12:111308794
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1258+268C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111308794 | ||||||
| chr12:111308874
|
T | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.1258+348T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111308874 | ||||||
| chr12:111308931
|
G | A | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+405G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111308931 | ||||||
| chr12:111309158
|
G | A | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1258+632G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111309158 | ||||||
| chr12:111309430
|
T | C | 1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1259-611T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111309430 | ||||||
| chr12:111309581
|
C | T | 11 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0062others(8): Show | 11 | HG00597.hp2 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1259-460C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111309581 | ||||||
| chr12:111309654
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1259-387T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111309654 | ||||||
| chr12:111309741
|
A | ATCTC | 3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1259-285_1259-282d others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 111309741 | |||||
| chr12:111310005
|
C | CGTCT | 4 | a0001c0001t0001g0091a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02559.hp1 HG02698.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259-14_1259-11dup others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 111310005 | |||||
| chr12:111310035
|
T | C | 2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.1259-6T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 14/21 | chr12 | 111310035 | ||||||
| chr12:111310720
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1900+38C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111310720 | ||||||
| chr12:111310939
|
C | T | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1900+257C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111310939 | ||||||
| chr12:111311481
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1901-619G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311481 | ||||||
| chr12:111311594
|
A | AT | 16 | a0001c0002t0001g0004a0001c0002t0001g0047a0001c0002t0001g0048others(13): Show | 16 | HG01243.hp2 HG02109.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1901-504dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311594 | |||||
| chr12:111311594
|
A | ATT | 4 | a0001c0002t0001g0092a0001c0002t0001g0095a0001c0014t0001g0042others(1): Show | 4 | HG00597.hp1 HG01081.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-505_1901-504d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311594 | |||||
| chr12:111311597
|
A | ATTT | 4 | a0001c0004t0001g0096a0001c0004t0004g0041a0001c0004t0005g0007others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-501_1901-500i others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311597 | |||||
| chr12:111311597
|
A | T | 30 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(27): Show | 30 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1901-503A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311597 | ||||||
| chr12:111311600
|
A | ATT | 4 | a0001c0001t0003g0078a0001c0004t0001g0002a0001c0004t0001g0005others(1): Show | 4 | HG02055.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-499_1901-498d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311600 | |||||
| chr12:111311600
|
A | ATTT | 2 | a0001c0004t0001g0015a0001c0008t0002g0022 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1901-498_1901-497i others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311600 | |||||
| chr12:111311600
|
A | T | 36 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(33): Show | 36 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1901-500A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311600 | ||||||
| chr12:111311601
|
T | TA | 2 | a0001c0002t0001g0037a0001c0002t0001g0090 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1901-499_1901-498i others(3): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311601 | ||||||
| chr12:111311603
|
A | ATT | 13 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0079others(10): Show | 13 | HG01169.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1901-485_1901-484d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311603 | |||||
| chr12:111311603
|
A | T | 43 | a0001c0001t0003g0078a0001c0002t0001g0004a0001c0002t0001g0018others(40): Show | 43 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1901-497A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311603 | ||||||
| chr12:111311604
|
T | TTA | 16 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0030others(13): Show | 16 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1901-495_1901-494i others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 111311604 | |||||
| chr12:111311606
|
T | A | 2 | a0001c0003t0001g0017a0007c0021t0002g0064 | 2 | HG02886.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1901-494T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311606 | ||||||
| chr12:111311607
|
T | A | 14 | a0001c0001t0002g0016a0001c0001t0002g0030a0001c0001t0002g0059others(11): Show | 14 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1901-493T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311607 | ||||||
| chr12:111311859
|
G | A | 29 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(26): Show | 29 | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1901-241G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111311859 | ||||||
| chr12:111312051
|
C | T | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1901-49C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111312051 | ||||||
| chr12:111312084
|
C | T | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1901-16C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 15/21 | chr12 | 111312084 | ||||||
| chr12:111312269
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2002+68C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111312269 | ||||||
| chr12:111312543
|
ATACAAAA others(1): Show |
A | 48 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(45): Show | 48 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.2002+346_2002+353d others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111312543 | |||||
| chr12:111312825
|
G | A | 29 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(26): Show | 29 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.2002+624G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111312825 | ||||||
| chr12:111312875
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2002+674C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111312875 | ||||||
| chr12:111313228
|
A | AT | 45 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(42): Show | 45 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2002+1041dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111313228 | |||||
| chr12:111313228
|
A | ATT | 29 | a0001c0001t0002g0016a0001c0001t0002g0030a0001c0001t0002g0059others(26): Show | 29 | HG00597.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.2002+1040_2002+104 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111313228 | |||||
| chr12:111313228
|
A | ATTT | 6 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2002+1039_2002+104 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111313228 | |||||
| chr12:111313305
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2002+1104G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313305 | ||||||
| chr12:111313323
|
C | T | 48 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(45): Show | 48 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.2002+1122C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313323 | ||||||
| chr12:111313564
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2002+1363C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313564 | ||||||
| chr12:111313613
|
G | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2002+1412G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313613 | ||||||
| chr12:111313785
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2002+1584G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313785 | ||||||
| chr12:111313885
|
AGACT | A | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2002+1691_2002+169 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111313885 | |||||
| chr12:111313943
|
G | T | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2002+1742G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111313943 | ||||||
| chr12:111314037
|
GC | G | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2002+1838delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314037 | |||||
| chr12:111314125
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2002+1924G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314125 | ||||||
| chr12:111314134
|
C | T | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2002+1933C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314134 | ||||||
| chr12:111314326
|
G | GC | 77 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(74): Show | 77 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.2002+2126dupC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314326 | |||||
| chr12:111314327
|
C | CG | 5 | a0001c0001t0004g0054a0001c0003t0001g0046a0001c0003t0001g0094others(2): Show | 5 | HG00597.hp2 HG02717.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2002+2126_2002+212 others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314327 | ||||||
| chr12:111314401
|
G | A | 1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2002+2200G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314401 | ||||||
| chr12:111314407
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.2002+2206A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314407 | ||||||
| chr12:111314639
|
T | TA | 5 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0003t0001g0052others(2): Show | 5 | HG01069.hp2 HG02145.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2002+2467dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314639
|
T | TAAAAAAA others(4): Show |
1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2002+2457_2002+246 others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314639
|
T | TAAAAAAA others(15): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2002+2446_2002+246 others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314639
|
TA | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0079a0001c0001t0003g0045others(2): Show | 5 | HG01169.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2002+2467delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314639
|
TAA | T | 6 | a0001c0001t0002g0016a0001c0001t0002g0059a0001c0001t0002g0062others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002+2466_2002+246 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314639
|
TAAA | T | 9 | a0001c0001t0002g0030a0001c0001t0002g0083a0001c0003t0001g0008others(6): Show | 9 | HG01884.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2002+2465_2002+246 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111314639 | |||||
| chr12:111314654
|
AAAAAAAA others(8): Show |
A | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2002+2454_2002+246 others(19): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314654 | ||||||
| chr12:111314657
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2002+2456A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314657 | ||||||
| chr12:111314657
|
AAAAAAAA others(5): Show |
A | 4 | a0001c0001t0001g0091a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02559.hp1 HG02698.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2002+2457_2002+246 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314657 | ||||||
| chr12:111314658
|
AAAAAAAA others(4): Show |
A | 19 | a0001c0002t0001g0023a0001c0002t0001g0061a0001c0004t0001g0005others(16): Show | 19 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2002+2458_2002+246 others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314658 | ||||||
| chr12:111314659
|
AAAAAAAA others(3): Show |
A | 14 | a0001c0002t0001g0004a0001c0002t0001g0025a0001c0002t0001g0026others(11): Show | 14 | HG00597.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2002+2459_2002+246 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314659 | ||||||
| chr12:111314660
|
AAAAAAAA others(2): Show |
A | 14 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0048others(11): Show | 14 | HG01081.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2002+2460_2002+246 others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314660 | ||||||
| chr12:111314923
|
CAT | C | 6 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2002+2723_2002+272 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314923 | ||||||
| chr12:111314963
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2002+2762C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111314963 | ||||||
| chr12:111315550
|
C | T | 5 | a0001c0002t0001g0037a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG02970.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2002+3349C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111315550 | ||||||
| chr12:111315699
|
A | G | 55 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(52): Show | 55 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.2002+3498A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111315699 | ||||||
| chr12:111315731
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2002+3530A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111315731 | ||||||
| chr12:111315800
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2002+3599G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111315800 | ||||||
| chr12:111316004
|
T | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.2002+3803T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316004 | ||||||
| chr12:111316142
|
C | CT | 60 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0016others(57): Show | 60 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.2003-3854dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316142 | |||||
| chr12:111316142
|
CT | C | 17 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2003-3854delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316142 | |||||
| chr12:111316214
|
T | C | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2003-3798T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316214 | ||||||
| chr12:111316244
|
T | C | 82 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(79): Show | 82 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.2003-3768T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316244 | ||||||
| chr12:111316262
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2003-3750C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316262 | ||||||
| chr12:111316305
|
A | AT | 59 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(56): Show | 59 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.2003-3694dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316305 | |||||
| chr12:111316413
|
TG | T | 16 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2003-3596delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316413 | |||||
| chr12:111316442
|
G | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2003-3570G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316442 | ||||||
| chr12:111316448
|
T | A | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2003-3564T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316448 | ||||||
| chr12:111316449
|
C | CT | 50 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(47): Show | 50 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.2003-3545dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316449 | |||||
| chr12:111316449
|
C | CTT | 11 | a0001c0001t0002g0079a0001c0001t0003g0045a0001c0001t0003g0078others(8): Show | 11 | HG00597.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2003-3546_2003-354 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111316449 | |||||
| chr12:111316480
|
A | T | 58 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(55): Show | 58 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.2003-3532A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316480 | ||||||
| chr12:111316617
|
T | A | 4 | a0001c0001t0001g0091a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02559.hp1 HG02698.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003-3395T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316617 | ||||||
| chr12:111316793
|
T | C | 61 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(58): Show | 61 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.2003-3219T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316793 | ||||||
| chr12:111316900
|
C | T | 18 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0059others(15): Show | 18 | HG00597.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003-3112C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316900 | ||||||
| chr12:111316965
|
T | C | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003-3047T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316965 | ||||||
| chr12:111316983
|
A | G | 8 | a0001c0001t0001g0091a0001c0003t0008g0032a0001c0004t0001g0005others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2003-3029A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111316983 | ||||||
| chr12:111317259
|
G | A | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2003-2753G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317259 | ||||||
| chr12:111317374
|
T | C | 82 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(79): Show | 82 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.2003-2638T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317374 | ||||||
| chr12:111317399
|
C | T | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2003-2613C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317399 | ||||||
| chr12:111317407
|
C | CAT | 64 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0016others(61): Show | 64 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.2003-2594_2003-259 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111317407 | |||||
| chr12:111317614
|
G | A | 6 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-2398G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317614 | ||||||
| chr12:111317648
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2003-2364T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317648 | ||||||
| chr12:111317717
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003-2295C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317717 | ||||||
| chr12:111317718
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2003-2294G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317718 | ||||||
| chr12:111317889
|
A | C | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003-2123A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111317889 | ||||||
| chr12:111317997
|
CAAAAAGA | C | 20 | a0001c0001t0001g0091a0001c0004t0001g0002a0001c0004t0001g0005others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003-1997_2003-199 others(11): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111317997 | |||||
| chr12:111318097
|
A | G | 41 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0062others(38): Show | 41 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.2003-1915A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318097 | ||||||
| chr12:111318238
|
C | CT | 15 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0015others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2003-1768dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318238 | |||||
| chr12:111318238
|
C | CTT | 6 | a0001c0001t0001g0091a0001c0004t0006g0075a0001c0005t0001g0038others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-1769_2003-176 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318238 | |||||
| chr12:111318238
|
CTTTTTTC others(2): Show |
C | 6 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0062others(3): Show | 6 | HG02109.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-1767_2003-175 others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318238 | |||||
| chr12:111318242
|
TTTC | T | 12 | a0001c0001t0002g0030a0001c0001t0002g0083a0001c0003t0001g0008others(9): Show | 12 | HG01884.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2003-1767_2003-176 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318242 | |||||
| chr12:111318243
|
TTC | T | 18 | a0001c0001t0001g0013a0001c0001t0002g0059a0001c0002t0001g0061others(15): Show | 18 | HG00597.hp1 HG01081.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2003-1767_2003-176 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318243 | |||||
| chr12:111318244
|
TC | T | 21 | a0001c0001t0003g0045a0001c0001t0003g0080a0001c0001t0003g0081others(18): Show | 21 | HG00597.hp2 HG01099.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2003-1767delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318244 | ||||||
| chr12:111318245
|
C | T | 25 | a0001c0001t0001g0091a0001c0001t0003g0078a0001c0002t0001g0037others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2003-1767C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318245 | ||||||
| chr12:111318592
|
C | CT | 4 | a0001c0001t0002g0058a0001c0001t0002g0060a0001c0001t0002g0100others(1): Show | 4 | HG01069.hp1 HG01081.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003-1413dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318592 | |||||
| chr12:111318592
|
CT | C | 9 | a0001c0002t0001g0023a0001c0002t0001g0066a0001c0003t0001g0088others(6): Show | 9 | HG01081.hp1 HG01099.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2003-1413delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111318592 | |||||
| chr12:111318597
|
T | TA | 7 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(4): Show | 7 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003-1415_2003-141 others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318597 | ||||||
| chr12:111318598
|
T | A | 51 | a0001c0001t0001g0091a0001c0001t0003g0045a0001c0001t0003g0078others(48): Show | 51 | HG00597.hp1 HG01169.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.2003-1414T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318598 | ||||||
| chr12:111318598
|
T | TA | 7 | a0001c0001t0002g0012a0001c0001t0002g0016a0001c0001t0002g0062others(4): Show | 7 | HG02109.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2003-1414_2003-141 others(5): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318598 | ||||||
| chr12:111318599
|
T | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(83): Show | 86 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.2003-1413T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318599 | ||||||
| chr12:111318600
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2003-1412A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318600 | ||||||
| chr12:111318634
|
A | G | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(86): Show | 89 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(86): Show |
intron_variant | MODIFIER | c.2003-1378A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318634 | ||||||
| chr12:111318810
|
G | A | 2 | a0001c0001t0004g0054a0001c0007t0001g0098 | 2 | HG00597.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2003-1202G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111318810 | ||||||
| chr12:111319426
|
T | C | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2003-586T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319426 | ||||||
| chr12:111319433
|
A | G | 14 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(11): Show | 14 | HG00597.hp2 HG01884.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2003-579A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319433 | ||||||
| chr12:111319694
|
T | G | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2003-318T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319694 | ||||||
| chr12:111319730
|
T | TCAAAA | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-266_2003-262d others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | 111319730 | |||||
| chr12:111319780
|
G | A | 9 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2003-232G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319780 | ||||||
| chr12:111319843
|
A | C | 31 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(28): Show | 31 | HG00597.hp1 HG01069.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2003-169A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319843 | ||||||
| chr12:111319856
|
A | G | 14 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(11): Show | 14 | HG00597.hp2 HG01884.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2003-156A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319856 | ||||||
| chr12:111319968
|
G | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2003-44G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | chr12 | 111319968 | ||||||
| chr12:111320816
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(81): Show | 84 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.2766+41A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320816 | ||||||
| chr12:111320825
|
G | C | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2766+50G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320825 | ||||||
| chr12:111320872
|
C | T | 7 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0008t0001g0003others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2766+97C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320872 | ||||||
| chr12:111320881
|
C | G | 2 | a0001c0001t0004g0054a0001c0007t0001g0098 | 2 | HG00597.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2766+106C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320881 | ||||||
| chr12:111320922
|
G | A | 16 | a0001c0001t0001g0091a0001c0004t0001g0002a0001c0004t0001g0005others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2766+147G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320922 | ||||||
| chr12:111320987
|
A | G | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2766+212A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111320987 | ||||||
| chr12:111321312
|
T | C | 3 | a0001c0003t0001g0046a0001c0003t0001g0094a0001c0011t0001g0001 | 3 | HG02717.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2766+537T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321312 | ||||||
| chr12:111321326
|
G | A | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2766+551G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321326 | ||||||
| chr12:111321342
|
CGGTATAG others(4): Show |
C | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2766+570_2766+580d others(13): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111321342 | |||||
| chr12:111321373
|
G | T | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2766+598G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321373 | ||||||
| chr12:111321433
|
T | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.2766+658T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321433 | ||||||
| chr12:111321474
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2766+699A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321474 | ||||||
| chr12:111321732
|
T | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(86): Show | 89 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(86): Show |
intron_variant | MODIFIER | c.2767-689T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321732 | ||||||
| chr12:111321944
|
G | A | 9 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2767-477G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321944 | ||||||
| chr12:111321950
|
G | A | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2767-471G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111321950 | ||||||
| chr12:111322174
|
C | CAGACGTG others(64): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2767-180_2767-179i others(73): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111322174 | |||||
| chr12:111322242
|
T | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2767-179T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111322242 | ||||||
| chr12:111322283
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2767-138A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | chr12 | 111322283 | ||||||
| chr12:111322321
|
CA | C | 14 | a0001c0001t0001g0091a0001c0001t0004g0054a0001c0004t0001g0002others(11): Show | 14 | HG01069.hp2 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2767-77delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111322321 | |||||
| chr12:111322321
|
CAA | C | 5 | a0001c0001t0002g0059a0001c0001t0002g0083a0001c0003t0001g0008others(2): Show | 5 | HG00597.hp2 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2767-78_2767-77del others(2): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111322321 | |||||
| chr12:111322321
|
CAAA | C | 11 | a0001c0001t0001g0013a0001c0001t0002g0030a0001c0002t0001g0072others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2767-79_2767-77del others(3): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111322321 | |||||
| chr12:111322321
|
CAAAA | C | 37 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(34): Show | 37 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.2767-80_2767-77del others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 111322321 | |||||
| chr12:111322745
|
C | T | 9 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(6): Show | 9 | HG01169.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2926+165C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111322745 | ||||||
| chr12:111322918
|
G | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+338G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111322918 | ||||||
| chr12:111323010
|
A | G | 80 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(77): Show | 80 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.2926+430A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323010 | ||||||
| chr12:111323136
|
G | A | 19 | a0001c0001t0001g0091a0001c0004t0001g0002a0001c0004t0001g0005others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2926+556G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323136 | ||||||
| chr12:111323330
|
G | A | 3 | a0001c0003t0001g0046a0001c0003t0001g0094a0001c0011t0001g0001 | 3 | HG02717.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2926+750G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323330 | ||||||
| chr12:111323583
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2926+1003G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323583 | ||||||
| chr12:111323592
|
G | A | 30 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(27): Show | 30 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2926+1012G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323592 | ||||||
| chr12:111323613
|
GA | G | 8 | a0001c0001t0001g0091a0001c0004t0004g0041a0001c0004t0005g0007others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2926+1034delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323613 | ||||||
| chr12:111323650
|
G | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+1070G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323650 | ||||||
| chr12:111323681
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+1101C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323681 | ||||||
| chr12:111323694
|
C | A | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+1114C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111323694 | ||||||
| chr12:111324083
|
G | A | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2926+1503G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324083 | ||||||
| chr12:111324091
|
C | T | 1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2926+1511C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324091 | ||||||
| chr12:111324105
|
C | G | 55 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0030others(52): Show | 55 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.2926+1525C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324105 | ||||||
| chr12:111324107
|
T | G | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2926+1527T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324107 | ||||||
| chr12:111324119
|
G | A | 51 | a0001c0001t0001g0013a0001c0001t0002g0030a0001c0001t0002g0059others(48): Show | 51 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2926+1539G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324119 | ||||||
| chr12:111324121
|
C | A | 6 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+1541C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324121 | ||||||
| chr12:111324160
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2926+1580C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324160 | ||||||
| chr12:111324177
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2926+1597C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324177 | ||||||
| chr12:111324220
|
T | C | 17 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2926+1640T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324220 | ||||||
| chr12:111324225
|
A | C | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+1645A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324225 | ||||||
| chr12:111324315
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2926+1735C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324315 | ||||||
| chr12:111324350
|
CA | C | 4 | a0001c0001t0002g0016a0001c0003t0001g0094a0001c0007t0001g0021others(1): Show | 4 | HG02717.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+1786delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111324350 | |||||
| chr12:111324363
|
AAAAG | A | 52 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(49): Show | 52 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.2926+1795_2926+179 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111324363 | |||||
| chr12:111324375
|
GAA | G | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2926+1797_2926+179 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111324375 | |||||
| chr12:111324445
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2926+1865G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324445 | ||||||
| chr12:111324534
|
TC | T | 51 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(48): Show | 51 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2926+1955delC | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324534 | ||||||
| chr12:111324600
|
A | G | 6 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+2020A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324600 | ||||||
| chr12:111324625
|
C | T | 5 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0094others(2): Show | 5 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+2045C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324625 | ||||||
| chr12:111324626
|
G | A | 16 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(13): Show | 16 | HG00597.hp2 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.2926+2046G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324626 | ||||||
| chr12:111324688
|
C | T | 1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2926+2108C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324688 | ||||||
| chr12:111324719
|
T | G | 9 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2926+2139T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324719 | ||||||
| chr12:111324734
|
A | C | 5 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0094others(2): Show | 5 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+2154A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324734 | ||||||
| chr12:111324873
|
T | C | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2926+2293T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324873 | ||||||
| chr12:111324948
|
A | G | 12 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2926+2368A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324948 | ||||||
| chr12:111324982
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2926+2402G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111324982 | ||||||
| chr12:111325104
|
T | C | 15 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(12): Show | 15 | HG00597.hp2 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2926+2524T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325104 | ||||||
| chr12:111325128
|
CA | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0082a0001c0001t0002g0016others(9): Show | 12 | HG02257.hp1 HG02717.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.2926+2564delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325128 | |||||
| chr12:111325234
|
C | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+2654C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325234 | ||||||
| chr12:111325293
|
CAAAAG | C | 30 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(27): Show | 30 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2926+2718_2926+272 others(9): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325293 | |||||
| chr12:111325298
|
G | GA | 7 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(4): Show | 7 | HG02257.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2926+2730dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325298 | |||||
| chr12:111325335
|
G | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+2755G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325335 | ||||||
| chr12:111325341
|
A | G | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+2761A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325341 | ||||||
| chr12:111325560
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(4): Show | 7 | HG02257.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2926+2980G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325560 | ||||||
| chr12:111325625
|
G | C | 3 | a0001c0001t0004g0054a0001c0003t0001g0057a0001c0007t0001g0098 | 3 | HG00597.hp2 NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2926+3045G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325625 | ||||||
| chr12:111325627
|
T | TGGGGAGG others(28): Show |
1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2926+3099_2926+313 others(39): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325627 | |||||
| chr12:111325660
|
G | T | 6 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+3080G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325660 | ||||||
| chr12:111325675
|
GT | G | 2 | a0001c0002t0001g0037a0001c0002t0001g0090 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2926+3099delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325675 | |||||
| chr12:111325693
|
T | G | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3113T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325693 | ||||||
| chr12:111325695
|
G | GTGGGGGA others(60): Show |
5 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0005t0001g0019others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3133_2926+313 others(71): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325695 | |||||
| chr12:111325710
|
G | GT | 7 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(4): Show | 7 | HG01099.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2926+3133dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325710 | |||||
| chr12:111325710
|
G | GTTTTGTT others(905): Show |
1 | a0001c0002t0001g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2926+3133_2926+313 others(916): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325710 | |||||
| chr12:111325710
|
G | GTTTTGTT others(168): Show |
4 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3133_2926+313 others(179): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325710 | |||||
| chr12:111325710
|
G | GTTTTGTT others(307): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2926+3133_2926+313 others(318): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325710 | |||||
| chr12:111325710
|
G | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3130G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325710 | ||||||
| chr12:111325721
|
G | C | 2 | a0001c0003t0001g0014a0001c0003t0001g0040 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2926+3141G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325721 | ||||||
| chr12:111325721
|
GTGT | G | 4 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2926+3145_2926+314 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325721 | |||||
| chr12:111325724
|
T | TTGTGGTG others(25): Show |
1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2926+3148_2926+314 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325724 | |||||
| chr12:111325724
|
T | TTGTGGTG others(289): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2926+3148_2926+314 others(300): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325724 | |||||
| chr12:111325727
|
T | G | 5 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0005t0001g0019others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3147T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325727 | ||||||
| chr12:111325727
|
T | TGGTGGGG others(62): Show |
1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2926+3148_2926+314 others(73): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325727 | |||||
| chr12:111325729
|
T | G | 51 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0001t0002g0083others(48): Show | 51 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2926+3149T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325729 | ||||||
| chr12:111325742
|
G | GGGTTTTG others(25): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3184_2926+318 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325742 | |||||
| chr12:111325743
|
G | T | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2926+3163G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325743 | ||||||
| chr12:111325744
|
GT | G | 4 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3168delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325744 | |||||
| chr12:111325762
|
T | G | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2926+3182T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325762 | ||||||
| chr12:111325762
|
T | TGGGGGAG others(130): Show |
1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2926+3184_2926+318 others(141): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325762 | |||||
| chr12:111325762
|
T | TGGTGGGG others(158): Show |
2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2926+3215_2926+321 others(169): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325762 | |||||
| chr12:111325762
|
T | TGGTGGGG others(161): Show |
3 | a0001c0002t0001g0061a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG01243.hp2 HG03239.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2926+3215_2926+321 others(172): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325762 | |||||
| chr12:111325762
|
T | TGGTGGGG others(161): Show |
16 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0048others(13): Show | 16 | HG00597.hp1 HG01081.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2926+3215_2926+321 others(172): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325762 | |||||
| chr12:111325762
|
T | TGGTGGGG others(94): Show |
5 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3214_2926+321 others(105): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325762 | |||||
| chr12:111325764
|
G | A | 5 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0005t0001g0019others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3184G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325764 | ||||||
| chr12:111325764
|
G | GTGGGGAG others(160): Show |
1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2926+3189_2926+319 others(171): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325764 | |||||
| chr12:111325764
|
G | T | 3 | a0001c0001t0001g0013a0001c0002t0001g0037a0001c0003t0001g0017 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2926+3184G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325764 | ||||||
| chr12:111325791
|
G | GTGT | 23 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0030others(20): Show | 23 | HG00597.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2926+3212_2926+321 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325791 | |||||
| chr12:111325791
|
G | GTGTTGTG others(31): Show |
13 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(10): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2926+3214_2926+321 others(42): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325791 | |||||
| chr12:111325791
|
G | GTGTTGTG others(1160): Show |
1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2926+3214_2926+321 others(1171): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325791 | |||||
| chr12:111325791
|
G | GTGTTGTG others(95): Show |
5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3214_2926+321 others(106): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325791 | |||||
| chr12:111325795
|
G | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3215G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325795 | ||||||
| chr12:111325795
|
GGTGGGGG others(576): Show |
G | 1 | a0001c0001t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2926+3280_2926+386 others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325795 | |||||
| chr12:111325796
|
G | A | 27 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(24): Show | 27 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.2926+3216G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325796 | ||||||
| chr12:111325796
|
G | T | 14 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(11): Show | 14 | HG01169.hp1 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2926+3216G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325796 | ||||||
| chr12:111325826
|
T | TGATGGGG others(22): Show |
5 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0005t0001g0019others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3246_2926+324 others(33): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325826 | ||||||
| chr12:111325831
|
T | G | 50 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0030others(47): Show | 50 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.2926+3251T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325831 | ||||||
| chr12:111325833
|
G | GGGGGAGG others(56): Show |
1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2926+3281_2926+328 others(67): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325833 | |||||
| chr12:111325858
|
GTGT | G | 4 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0003t0001g0014others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3282_2926+328 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325858 | |||||
| chr12:111325864
|
T | G | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2926+3284T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325864 | ||||||
| chr12:111325865
|
G | GGGGGAGG others(257): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2926+3285_2926+328 others(268): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325865 | ||||||
| chr12:111325866
|
T | G | 12 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0002t0001g0071others(9): Show | 12 | HG00597.hp2 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2926+3286T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325866 | ||||||
| chr12:111325881
|
GT | G | 2 | a0001c0001t0001g0013a0006c0020t0001g0020 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2926+3305delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325881 | |||||
| chr12:111325889
|
T | G | 3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2926+3309T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325889 | ||||||
| chr12:111325893
|
G | GTGT | 15 | a0001c0001t0001g0013a0001c0001t0002g0083a0001c0001t0003g0045others(12): Show | 15 | HG00597.hp2 HG01169.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2926+3314_2926+331 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325893 | |||||
| chr12:111325893
|
G | GTGTTGGG others(31): Show |
3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3316_2926+331 others(42): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325893 | |||||
| chr12:111325898
|
T | A | 8 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0004t0001g0002others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2926+3318T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325898 | ||||||
| chr12:111325898
|
T | G | 13 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(10): Show | 13 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2926+3318T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325898 | ||||||
| chr12:111325898
|
T | TTGGGGGA others(901): Show |
1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2926+3355_2926+335 others(912): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325898 | |||||
| chr12:111325899
|
TG | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0003t0001g0014others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+3324delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325899 | |||||
| chr12:111325911
|
G | T | 2 | a0001c0011t0001g0001a0006c0020t0001g0020 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2926+3331G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325911 | ||||||
| chr12:111325925
|
G | GTGT | 17 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0030others(14): Show | 17 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2926+3346_2926+334 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325925 | |||||
| chr12:111325925
|
G | GTGTGTTG others(27): Show |
1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2926+3355_2926+335 others(38): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325925 | |||||
| chr12:111325925
|
G | GTGTGTTG others(28): Show |
1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2926+3350_2926+338 others(39): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325925 | |||||
| chr12:111325925
|
G | GTGTGTTG others(95): Show |
1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(106): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325925 | |||||
| chr12:111325928
|
T | TTGG | 2 | a0001c0003t0001g0046a0006c0020t0001g0020 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2926+3348_2926+334 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325928 | ||||||
| chr12:111325930
|
T | G | 9 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(6): Show | 9 | HG02257.hp1 HG02717.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2926+3350T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325930 | ||||||
| chr12:111325930
|
T | TTGGGGAG others(1142): Show |
3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2926+3355_2926+335 others(1153): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGAG others(3146): Show |
1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2926+3355_2926+335 others(3157): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(1004): Show |
3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+3380_2926+338 others(1015): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(1795): Show |
2 | a0001c0004t0001g0015a0001c0004t0001g0027 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2926+3380_2926+338 others(1806): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(1799): Show |
1 | a0001c0001t0002g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(1810): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(1798): Show |
2 | a0001c0004t0001g0005a0001c0005t0001g0039 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2926+3380_2926+338 others(1809): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(1802): Show |
1 | a0001c0005t0001g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(1813): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(892): Show |
1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(903): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(822): Show |
1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(833): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(857): Show |
1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(868): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325930
|
T | TTGGGGGA others(857): Show |
10 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0002g0043others(7): Show | 10 | HG01081.hp2 HG01099.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2926+3380_2926+338 others(868): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325930 | |||||
| chr12:111325943
|
G | T | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3363G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325943 | ||||||
| chr12:111325944
|
G | T | 1 | a0001c0002t0001g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2926+3364G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325944 | ||||||
| chr12:111325946
|
T | TTTGTTTA others(865): Show |
1 | a0005c0012t0009g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2926+3368_2926+336 others(876): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325946 | |||||
| chr12:111325946
|
T | TTTTGTTT others(1202): Show |
1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2926+3380_2926+338 others(1213): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325946 | |||||
| chr12:111325960
|
T | TGTTGGGG others(91): Show |
5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3380_2926+338 others(102): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325960 | ||||||
| chr12:111325963
|
T | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(12): Show | 15 | HG00597.hp2 HG01069.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.2926+3383T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325963 | ||||||
| chr12:111325963
|
T | TGGGGGAG others(297): Show |
5 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0090others(2): Show | 5 | HG02630.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3385_2926+338 others(308): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325963 | |||||
| chr12:111325963
|
T | TGGGGGAG others(738): Show |
7 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0066others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2926+3385_2926+338 others(749): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325963 | |||||
| chr12:111325963
|
T | TGGGGGAG others(436): Show |
2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2926+3385_2926+338 others(447): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325963 | |||||
| chr12:111325965
|
G | GGGGAGGG others(57): Show |
12 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(9): Show | 12 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2926+3385_2926+338 others(68): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325965 | ||||||
| chr12:111325965
|
G | T | 27 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(24): Show | 27 | HG01169.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2926+3385G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325965 | ||||||
| chr12:111325967
|
G | GGGGGAGG others(91): Show |
1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2926+3398_2926+339 others(102): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325967 | |||||
| chr12:111325978
|
G | GGGTTTTG others(163): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2926+3417_2926+341 others(174): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325978 | |||||
| chr12:111325978
|
G | GGGTTTTG others(968): Show |
1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2926+3417_2926+341 others(979): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325978 | |||||
| chr12:111325978
|
G | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(25): Show | 28 | HG00597.hp2 HG01069.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.2926+3398G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325978 | ||||||
| chr12:111325979
|
G | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3399G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325979 | ||||||
| chr12:111325980
|
GT | G | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3404delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325980 | |||||
| chr12:111325981
|
T | TTTTGTTT others(132): Show |
4 | a0001c0008t0001g0003a0001c0008t0002g0022a0001c0009t0001g0031others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3417_2926+341 others(143): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325981 | |||||
| chr12:111325995
|
T | TGA | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3415_2926+341 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325995 | ||||||
| chr12:111325995
|
T | TTGTGTTG others(832): Show |
1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2926+3417_2926+341 others(843): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111325995 | |||||
| chr12:111325995
|
TTGG | T | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3416_2926+341 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325995 | ||||||
| chr12:111325998
|
G | T | 45 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(42): Show | 45 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2926+3418G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111325998 | ||||||
| chr12:111326000
|
G | A | 3 | a0001c0003t0001g0033a0001c0004t0001g0002a0001c0004t0001g0096 | 3 | HG01243.hp1 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2926+3420G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326000 | ||||||
| chr12:111326000
|
G | GGAGGGGT others(20): Show |
3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3420_2926+342 others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326000 | ||||||
| chr12:111326000
|
G | T | 15 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2926+3420G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326000 | ||||||
| chr12:111326013
|
G | T | 6 | a0001c0003t0001g0094a0001c0004t0001g0005a0001c0004t0001g0015others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+3433G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326013 | ||||||
| chr12:111326014
|
G | T | 1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2926+3434G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326014 | ||||||
| chr12:111326015
|
GT | G | 4 | a0001c0011t0001g0001a0002c0006t0001g0053a0002c0006t0001g0084others(1): Show | 4 | HG02698.hp2 HG06807.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2926+3439delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326015 | |||||
| chr12:111326027
|
GTGT | G | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3451_2926+345 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326027 | |||||
| chr12:111326031
|
T | C | 1 | a0001c0003t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2926+3451T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326031 | ||||||
| chr12:111326033
|
T | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(18): Show | 21 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2926+3453T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326033 | ||||||
| chr12:111326034
|
G | GTTGGGGG others(25): Show |
1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2926+3454_2926+345 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326034 | ||||||
| chr12:111326035
|
G | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2926+3455G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326035 | ||||||
| chr12:111326035
|
G | GTGGGGGA others(139): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3468_2926+346 others(150): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326035 | |||||
| chr12:111326035
|
G | T | 16 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(13): Show | 16 | HG01069.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2926+3455G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326035 | ||||||
| chr12:111326037
|
G | GGGGGAGG others(22): Show |
2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3462_2926+349 others(33): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326037 | |||||
| chr12:111326048
|
G | GGGTTTTG others(864): Show |
1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2926+3487_2926+348 others(875): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326048 | |||||
| chr12:111326048
|
G | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(16): Show | 19 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.2926+3468G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326048 | ||||||
| chr12:111326050
|
GT | G | 2 | a0001c0001t0002g0062a0001c0003t0001g0033 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2926+3474delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326050 | |||||
| chr12:111326051
|
T | TTTTGTTT others(997): Show |
1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2926+3487_2926+348 others(1008): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326051 | |||||
| chr12:111326051
|
T | TTTTGTTT others(864): Show |
4 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0003t0001g0014others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3487_2926+348 others(875): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326051 | |||||
| chr12:111326051
|
T | TTTTGTTT others(730): Show |
1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2926+3487_2926+348 others(741): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326051 | |||||
| chr12:111326064
|
G | A | 5 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3484G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326064 | ||||||
| chr12:111326065
|
T | TGA | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3485_2926+348 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326065 | ||||||
| chr12:111326066
|
TGGG | T | 3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2926+3488_2926+349 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326066 | |||||
| chr12:111326068
|
G | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(45): Show | 48 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.2926+3488G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326068 | ||||||
| chr12:111326070
|
G | A | 10 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(7): Show | 10 | HG01081.hp1 HG01099.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2926+3490G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326070 | ||||||
| chr12:111326070
|
G | GGAGGGGT others(20): Show |
3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3490_2926+349 others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326070 | ||||||
| chr12:111326070
|
G | GTGGGGGA others(25): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2926+3515_2926+351 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326070 | |||||
| chr12:111326070
|
G | T | 9 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2926+3490G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326070 | ||||||
| chr12:111326083
|
G | T | 2 | a0001c0002t0001g0037a0001c0008t0001g0003 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2926+3503G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326083 | ||||||
| chr12:111326100
|
TTGG | T | 8 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(5): Show | 8 | HG01081.hp1 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2926+3521_2926+352 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326100 | ||||||
| chr12:111326103
|
G | T | 63 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0016others(60): Show | 63 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.2926+3523G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326103 | ||||||
| chr12:111326104
|
G | GGAGGGGT others(1348): Show |
1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2926+3525_2926+352 others(1359): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326104 | |||||
| chr12:111326105
|
G | A | 7 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0005g0007others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2926+3525G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326105 | ||||||
| chr12:111326105
|
G | T | 36 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0083others(33): Show | 36 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.2926+3525G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326105 | ||||||
| chr12:111326117
|
T | TGTGTTTG others(1453): Show |
1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2926+3538_2926+353 others(1464): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326117 | |||||
| chr12:111326120
|
G | GT | 44 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0083others(41): Show | 44 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.2926+3543dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326120 | |||||
| chr12:111326120
|
G | GTTTGTTT others(1321): Show |
2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2926+3556_2926+355 others(1332): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326120 | |||||
| chr12:111326120
|
G | GTTTTGTT others(1005): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2926+3543_2926+354 others(1016): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326120 | |||||
| chr12:111326120
|
G | GTTTTGTT others(497): Show |
1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2926+3543_2926+354 others(508): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326120 | |||||
| chr12:111326120
|
G | GTTTTGTT others(29): Show |
1 | a0001c0002t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2926+3543_2926+354 others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326120 | |||||
| chr12:111326120
|
G | T | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2926+3540G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326120 | ||||||
| chr12:111326135
|
T | G | 3 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075 | 3 | HG01243.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3555T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326135 | ||||||
| chr12:111326136
|
G | T | 3 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075 | 3 | HG01243.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3556G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326136 | ||||||
| chr12:111326137
|
T | G | 5 | a0001c0001t0001g0013a0001c0003t0001g0057a0001c0008t0002g0022others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3557T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326137 | ||||||
| chr12:111326138
|
GAT | G | 23 | a0001c0001t0002g0083a0001c0002t0001g0018a0001c0002t0001g0047others(20): Show | 23 | HG00597.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2926+3559_2926+356 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326138 | ||||||
| chr12:111326139
|
A | G | 30 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0030others(27): Show | 30 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.2926+3559A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326139 | ||||||
| chr12:111326139
|
A | T | 11 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0085others(8): Show | 11 | HG02109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2926+3559A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326139 | ||||||
| chr12:111326140
|
T | TG | 43 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(40): Show | 43 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.2926+3564dupG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326140 | |||||
| chr12:111326140
|
T | TGGGGGAG others(334): Show |
3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3564_2926+356 others(345): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326140 | |||||
| chr12:111326140
|
T | TGGGGGAG others(869): Show |
2 | a0001c0008t0002g0022a0001c0009t0001g0035 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2926+3564_2926+356 others(880): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326140 | |||||
| chr12:111326140
|
T | TGGGGGAG others(904): Show |
1 | a0001c0009t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2926+3564_2926+356 others(915): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326140 | |||||
| chr12:111326151
|
T | G | 66 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0012others(63): Show | 66 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.2926+3571T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326151 | ||||||
| chr12:111326168
|
T | TTGTGGTG others(263): Show |
1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2926+3606_2926+360 others(274): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326168 | |||||
| chr12:111326171
|
T | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0003t0001g0014others(4): Show | 7 | HG01069.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2926+3591T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326171 | ||||||
| chr12:111326173
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2926+3593G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326173 | ||||||
| chr12:111326173
|
G | T | 31 | a0001c0001t0002g0083a0001c0001t0004g0054a0001c0002t0001g0004others(28): Show | 31 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.2926+3593G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326173 | ||||||
| chr12:111326188
|
G | GT | 33 | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(30): Show | 33 | HG00597.hp1 HG00597.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2926+3611dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTGTTT others(301): Show |
1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2926+3624_2926+362 others(312): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(472): Show |
1 | a0001c0002t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2926+3611_2926+361 others(483): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(28): Show |
2 | a0001c0002t0001g0061a0006c0020t0001g0020 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2926+3611_2926+361 others(39): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(1022): Show |
1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2926+3611_2926+361 others(1033): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(197): Show |
4 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2926+3611_2926+361 others(208): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(1241): Show |
5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3611_2926+361 others(1252): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(127): Show |
1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2926+3611_2926+361 others(138): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(130): Show |
13 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0048others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2926+3611_2926+361 others(141): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(948): Show |
1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2926+3611_2926+361 others(959): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326188
|
G | GTTTTGTT others(133): Show |
2 | a0001c0001t0002g0083a0005c0012t0009g0044 | 2 | HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2926+3611_2926+361 others(144): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326188 | |||||
| chr12:111326192
|
G | A | 3 | a0001c0002t0001g0037a0001c0004t0005g0007a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2926+3612G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326192 | ||||||
| chr12:111326205
|
T | C | 3 | a0001c0010t0001g0049a0001c0010t0001g0050a0001c0018t0004g0029 | 3 | HG02809.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2926+3625T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326205 | ||||||
| chr12:111326207
|
G | T | 4 | a0001c0008t0001g0003a0001c0008t0002g0022a0001c0009t0001g0031others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3627G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326207 | ||||||
| chr12:111326213
|
GA | G | 2 | a0001c0005t0001g0038a0001c0005t0001g0039 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2926+3634delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326213 | ||||||
| chr12:111326214
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2926+3634A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326214 | ||||||
| chr12:111326220
|
G | T | 4 | a0001c0003t0001g0008a0001c0010t0001g0049a0001c0010t0001g0050others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2926+3640G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326220 | ||||||
| chr12:111326222
|
GT | G | 31 | a0001c0001t0002g0083a0001c0001t0003g0045a0001c0001t0003g0078others(28): Show | 31 | HG01069.hp2 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2926+3646delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326222 | |||||
| chr12:111326223
|
T | TTTTGTTT others(373): Show |
1 | a0001c0003t0001g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2926+3659_2926+366 others(384): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(230): Show |
1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2926+3659_2926+366 others(241): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(303): Show |
6 | a0001c0001t0002g0030a0001c0001t0002g0059a0001c0003t0001g0014others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2926+3659_2926+366 others(314): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(62): Show |
1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2926+3661_2926+366 others(73): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(61): Show |
3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2926+3661_2926+366 others(72): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(439): Show |
1 | a0001c0002t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2926+3680_2926+368 others(450): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(572): Show |
1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2926+3696_2926+369 others(583): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326223
|
T | TTTTGTTT others(575): Show |
2 | a0001c0002t0001g0069a0001c0002t0001g0092 | 2 | HG00597.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2926+3696_2926+369 others(586): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326223 | |||||
| chr12:111326227
|
G | GTTTATAG others(93): Show |
1 | a0001c0003t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2926+3657_2926+365 others(104): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326227 | |||||
| chr12:111326227
|
G | GTTTATAG others(61): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG02109.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2926+3661_2926+366 others(72): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326227 | |||||
| chr12:111326237
|
T | TTGTGATG others(265): Show |
2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3661_2926+366 others(276): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326237 | |||||
| chr12:111326240
|
T | G | 3 | a0001c0010t0001g0049a0001c0010t0001g0050a0001c0018t0004g0029 | 3 | HG02809.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2926+3660T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326240 | ||||||
| chr12:111326242
|
G | GTGGGGGA others(2568): Show |
1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2926+3680_2926+368 others(2579): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326242 | |||||
| chr12:111326242
|
G | T | 9 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0004t0006g0075others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2926+3662G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326242 | ||||||
| chr12:111326255
|
G | T | 3 | a0001c0002t0001g0037a0001c0004t0005g0007a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2926+3675G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326255 | ||||||
| chr12:111326256
|
G | T | 5 | a0001c0001t0002g0016a0001c0007t0001g0021a0001c0008t0002g0022others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+3676G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326256 | ||||||
| chr12:111326269
|
GTGT | G | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+3693_2926+369 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326269 | |||||
| chr12:111326275
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2926+3695T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326275 | ||||||
| chr12:111326277
|
T | A | 3 | a0001c0001t0001g0091a0001c0003t0001g0094a0001c0011t0001g0001 | 3 | HG02559.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2926+3697T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326277 | ||||||
| chr12:111326277
|
T | G | 61 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(58): Show | 61 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2926+3697T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326277 | ||||||
| chr12:111326278
|
TG | T | 4 | a0001c0001t0002g0016a0001c0003t0001g0094a0001c0007t0001g0021others(1): Show | 4 | HG02717.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926+3703delG | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326278 | |||||
| chr12:111326279
|
G | GGAGGGAG others(629): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3700_2926+370 others(640): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326279 | |||||
| chr12:111326290
|
T | G | 22 | a0001c0001t0002g0016a0001c0002t0001g0037a0001c0003t0001g0046others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.2926+3710T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326290 | ||||||
| chr12:111326290
|
T | GGGTTTTG others(165): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2926+3709_2926+371 others(176): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326290 | ||||||
| chr12:111326292
|
G | T | 2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3712G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326292 | ||||||
| chr12:111326304
|
GTGT | G | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2926+3728_2926+373 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326304 | |||||
| chr12:111326310
|
T | G | 5 | a0001c0001t0002g0016a0001c0007t0001g0021a0001c0010t0001g0049others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3730T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326310 | ||||||
| chr12:111326312
|
G | T | 3 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0008t0001g0003 | 3 | HG01243.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2926+3732G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326312 | ||||||
| chr12:111326326
|
G | T | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3746G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326326 | ||||||
| chr12:111326327
|
GT | G | 2 | a0001c0003t0001g0094a0001c0011t0001g0001 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2926+3751delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326327 | |||||
| chr12:111326347
|
G | T | 5 | a0001c0004t0004g0041a0001c0008t0001g0003a0001c0010t0001g0049others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2926+3767G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326347 | ||||||
| chr12:111326360
|
G | T | 55 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0030others(52): Show | 55 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.2926+3780G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326360 | ||||||
| chr12:111326378
|
T | G | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+3798T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326378 | ||||||
| chr12:111326378
|
T | TGTG | 53 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0030others(50): Show | 53 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.2926+3800_2926+380 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGATGG others(200): Show |
1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2926+3801_2926+380 others(211): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGATGG others(203): Show |
2 | a0001c0009t0001g0031a0001c0009t0001g0035 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2926+3801_2926+380 others(214): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGATGG others(748): Show |
1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2926+3801_2926+380 others(759): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGATGG others(66): Show |
3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3801_2926+380 others(77): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGGGG others(370): Show |
3 | a0001c0010t0001g0049a0001c0010t0001g0050a0001c0018t0004g0029 | 3 | HG02809.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2926+3862_2926+386 others(381): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGGGG others(340): Show |
1 | a0001c0008t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2926+3812_2926+381 others(351): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGTGG others(1085): Show |
2 | a0001c0001t0002g0016a0001c0007t0001g0021 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+3802_2926+380 others(1096): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGTGG others(405): Show |
1 | a0001c0011t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2926+3802_2926+380 others(416): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGTGG others(303): Show |
1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2926+3802_2926+380 others(314): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326378
|
T | TGTGGTGG others(1564): Show |
1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2926+3802_2926+380 others(1575): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326378 | |||||
| chr12:111326379
|
G | T | 3 | a0002c0006t0001g0053a0002c0006t0001g0084a0002c0006t0001g0089 | 3 | HG02698.hp2 HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2926+3799G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326379 | ||||||
| chr12:111326392
|
G | T | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2926+3812G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326392 | ||||||
| chr12:111326414
|
T | G | 7 | a0001c0003t0001g0046a0001c0005t0001g0019a0001c0005t0001g0028others(4): Show | 7 | HG02559.hp2 HG02698.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2926+3834T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326414 | ||||||
| chr12:111326419
|
G | A | 8 | a0001c0002t0001g0037a0001c0004t0004g0041a0001c0004t0005g0007others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2926+3839G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326419 | ||||||
| chr12:111326433
|
T | TGTTTATA others(2348): Show |
1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2926+3862_2926+386 others(2359): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111326433 | |||||
| chr12:111326445
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2926+3865T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326445 | ||||||
| chr12:111326518
|
A | G | 8 | a0001c0002t0001g0037a0001c0004t0004g0041a0001c0004t0005g0007others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2926+3938A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326518 | ||||||
| chr12:111326590
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2926+4010T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326590 | ||||||
| chr12:111326658
|
C | G | 76 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(73): Show | 76 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.2926+4078C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326658 | ||||||
| chr12:111326729
|
T | C | 78 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(75): Show | 78 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.2926+4149T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326729 | ||||||
| chr12:111326752
|
A | G | 9 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(6): Show | 9 | HG01169.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2926+4172A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326752 | ||||||
| chr12:111326797
|
G | A | 1 | a0001c0004t0001g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2926+4217G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326797 | ||||||
| chr12:111326867
|
C | T | 2 | a0001c0003t0001g0057a0001c0007t0001g0098 | 2 | HG00597.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2926+4287C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111326867 | ||||||
| chr12:111327038
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2926+4458C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327038 | ||||||
| chr12:111327061
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2926+4481C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327061 | ||||||
| chr12:111327507
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2926+4927G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327507 | ||||||
| chr12:111327660
|
C | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(85): Show | 88 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.2926+5080C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327660 | ||||||
| chr12:111327711
|
C | T | 2 | a0001c0001t0004g0054a0001c0018t0004g0029 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2926+5131C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327711 | ||||||
| chr12:111327741
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2926+5161C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327741 | ||||||
| chr12:111327764
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2926+5184T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327764 | ||||||
| chr12:111327860
|
C | T | 1 | a0001c0009t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2926+5280C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111327860 | ||||||
| chr12:111328023
|
C | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2926+5443C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328023 | ||||||
| chr12:111328056
|
T | C | 1 | a0007c0021t0002g0064 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2926+5476T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328056 | ||||||
| chr12:111328262
|
C | G | 7 | a0001c0001t0002g0083a0001c0003t0001g0017a0001c0004t0001g0002others(4): Show | 7 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2926+5682C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328262 | ||||||
| chr12:111328270
|
G | A | 1 | a0001c0022t0005g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2926+5690G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328270 | ||||||
| chr12:111328404
|
G | T | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2926+5824G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328404 | ||||||
| chr12:111328467
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2926+5887C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328467 | ||||||
| chr12:111328491
|
A | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2926+5911A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328491 | ||||||
| chr12:111328512
|
T | C | 14 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(11): Show | 14 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2927-5929T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328512 | ||||||
| chr12:111328580
|
T | TTG | 17 | a0001c0001t0002g0060a0001c0001t0003g0078a0001c0001t0003g0099others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2927-5822_2927-582 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
T | TTGTG | 14 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0100others(11): Show | 14 | HG01069.hp1 HG01081.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2927-5824_2927-582 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
T | TTGTGTG | 9 | a0001c0001t0002g0062a0001c0001t0004g0054a0001c0002t0001g0069others(6): Show | 9 | HG00597.hp1 HG01081.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2927-5826_2927-582 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0004t0005g0007 | 3 | HG02257.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2927-5828_2927-582 others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
T | TTGTGTGT others(3): Show |
3 | a0001c0002t0001g0072a0001c0004t0001g0005a0002c0006t0001g0053 | 3 | HG02698.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2927-5830_2927-582 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
TTG | T | 15 | a0001c0001t0002g0012a0001c0001t0002g0056a0001c0001t0002g0085others(12): Show | 15 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2927-5822_2927-582 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
TTGTG | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(15): Show | 18 | HG00597.hp2 HG01891.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2927-5824_2927-582 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
TTGTGTGT others(1): Show |
T | 2 | a0001c0002t0001g0071a0001c0018t0004g0029 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2927-5828_2927-582 others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328580
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2927-5834_2927-582 others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328580 | |||||
| chr12:111328619
|
T | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-5822T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328619 | ||||||
| chr12:111328642
|
C | T | 26 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(23): Show | 26 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2927-5799C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328642 | ||||||
| chr12:111328668
|
C | T | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2927-5773C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328668 | ||||||
| chr12:111328933
|
A | G | 1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2927-5508A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328933 | ||||||
| chr12:111328941
|
A | ATC | 4 | a0001c0001t0002g0043a0001c0004t0001g0015a0001c0004t0001g0027others(1): Show | 4 | HG01169.hp2 HG01884.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-5467_2927-546 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTC | 16 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0058others(13): Show | 16 | HG01081.hp2 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.2927-5469_2927-546 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCC others(5): Show |
2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-5494_2927-549 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(3): Show |
3 | a0001c0004t0005g0007a0001c0014t0001g0042a0001c0022t0005g0034 | 3 | HG01081.hp1 HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2927-5475_2927-546 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(5): Show |
1 | a0001c0001t0002g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2927-5477_2927-546 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(9): Show |
9 | a0001c0001t0002g0016a0001c0001t0003g0078a0001c0001t0003g0099others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2927-5481_2927-546 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(11): Show |
1 | a0001c0007t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2927-5483_2927-546 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(15): Show |
4 | a0001c0001t0003g0045a0001c0001t0003g0080a0001c0001t0003g0081others(1): Show | 4 | HG01169.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-5487_2927-546 others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(17): Show |
2 | a0001c0003t0001g0088a0001c0005t0001g0038 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2927-5489_2927-546 others(28): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(19): Show |
1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2927-5491_2927-546 others(30): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
A | ATCTCTCT others(25): Show |
1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2927-5497_2927-546 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328941
|
ATCTCTC | A | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-5471_2927-546 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328941 | |||||
| chr12:111328964
|
T | TCTCTCCC others(9): Show |
1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2927-5472_2927-547 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328964 | |||||
| chr12:111328972
|
T | C | 1 | a0001c0004t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2927-5469T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328972 | ||||||
| chr12:111328972
|
T | TCTCTCTC others(23): Show |
1 | a0001c0007t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(34): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(7): Show |
1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(9): Show |
3 | a0001c0002t0001g0026a0001c0003t0001g0046a0001c0003t0001g0052 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(27): Show |
2 | a0001c0001t0002g0083a0001c0003t0001g0017 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(38): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(11): Show |
4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0069others(1): Show | 4 | HG01099.hp1 HG01243.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(29): Show |
2 | a0001c0001t0001g0091a0001c0004t0001g0002 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(31): Show |
2 | a0001c0003t0001g0057a0001c0009t0001g0031 | 2 | HG02615.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(42): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(15): Show |
2 | a0001c0002t0001g0072a0001c0002t0001g0092 | 2 | HG00597.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(33): Show |
1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(44): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(35): Show |
2 | a0001c0008t0002g0022a0001c0009t0001g0035 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(46): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(19): Show |
1 | a0001c0002t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(30): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(37): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0024 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(48): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(21): Show |
1 | a0001c0002t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(32): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328972
|
T | TCTCTCTC others(39): Show |
2 | a0001c0001t0001g0082a0001c0008t0001g0003 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(50): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328972 | |||||
| chr12:111328975
|
C | CTCTCTCT others(8): Show |
3 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0013t0001g0063 | 3 | HG02109.hp2 HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(19): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(10): Show |
2 | a0001c0002t0001g0093a0001c0003t0001g0008 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(21): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(12): Show |
2 | a0001c0003t0001g0033a0002c0006t0001g0089 | 2 | HG03486.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(23): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(14): Show |
1 | a0001c0002t0001g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(25): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(16): Show |
2 | a0001c0003t0001g0014a0002c0006t0001g0053 | 2 | HG02698.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(27): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(18): Show |
4 | a0001c0002t0001g0074a0001c0003t0001g0040a0001c0005t0001g0039others(1): Show | 4 | HG02486.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-5466_2927-546 others(29): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(20): Show |
1 | a0001c0002t0001g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(31): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328975
|
C | CTCTCTCT others(24): Show |
1 | a0003c0016t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2927-5466_2927-546 others(35): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328975 | ||||||
| chr12:111328976
|
C | T | 5 | a0001c0002t0001g0037a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG02970.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2927-5465C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328976 | ||||||
| chr12:111328978
|
C | T | 5 | a0001c0002t0001g0037a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG02970.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2927-5463C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328978 | ||||||
| chr12:111328980
|
T | C | 21 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0066others(18): Show | 21 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2927-5461T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328980 | ||||||
| chr12:111328981
|
C | T | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0004g0054others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2927-5460C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328981 | ||||||
| chr12:111328982
|
T | C | 21 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0066others(18): Show | 21 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2927-5459T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111328982 | ||||||
| chr12:111328982
|
T | TCTCTCTC others(9): Show |
1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2927-5456_2927-545 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328982 | |||||
| chr12:111328982
|
T | TCTCTCTC others(13): Show |
1 | a0001c0002t0007g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2927-5456_2927-545 others(24): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328982 | |||||
| chr12:111328982
|
T | TCTCTCTC others(15): Show |
3 | a0001c0002t0001g0037a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2927-5456_2927-545 others(26): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328982 | |||||
| chr12:111328994
|
C | CCTCTCCC others(1): Show |
5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927-5443_2927-543 others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111328994 | |||||
| chr12:111329058
|
C | A | 1 | a0001c0004t0001g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2927-5383C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329058 | ||||||
| chr12:111329137
|
T | C | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-5304T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329137 | ||||||
| chr12:111329249
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(7): Show | 10 | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2927-5192C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329249 | ||||||
| chr12:111329276
|
C | G | 26 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(23): Show | 26 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2927-5165C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329276 | ||||||
| chr12:111329615
|
C | T | 26 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(23): Show | 26 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2927-4826C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329615 | ||||||
| chr12:111329657
|
G | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0040a0001c0005t0001g0038others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927-4784G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329657 | ||||||
| chr12:111329758
|
C | T | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-4683C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329758 | ||||||
| chr12:111329797
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-4644G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329797 | ||||||
| chr12:111329898
|
A | C | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-4543A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329898 | ||||||
| chr12:111329932
|
C | T | 3 | a0001c0004t0004g0041a0001c0004t0005g0007a0001c0022t0005g0034 | 3 | HG02486.hp1 HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2927-4509C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329932 | ||||||
| chr12:111329945
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2927-4496G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111329945 | ||||||
| chr12:111330006
|
CAG | C | 23 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(20): Show | 23 | HG01069.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2927-4433_2927-443 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330006 | |||||
| chr12:111330087
|
G | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.2927-4354G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330087 | ||||||
| chr12:111330190
|
A | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(55): Show | 58 | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.2927-4251A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330190 | ||||||
| chr12:111330375
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-4066G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330375 | ||||||
| chr12:111330456
|
A | G | 1 | a0001c0003t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2927-3985A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330456 | ||||||
| chr12:111330541
|
T | C | 12 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(9): Show | 12 | HG00597.hp1 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2927-3900T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330541 | ||||||
| chr12:111330676
|
A | AATACATA others(23): Show |
5 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2927-3750_2927-374 others(34): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330676 | |||||
| chr12:111330686
|
C | CATATACA others(25): Show |
1 | a0001c0002t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2927-3750_2927-374 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
C | CATATACA others(27): Show |
1 | a0001c0002t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2927-3750_2927-374 others(38): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
C | CATATACA others(57): Show |
1 | a0001c0003t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2927-3750_2927-374 others(68): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
C | CATATACA others(61): Show |
2 | a0001c0002t0001g0061a0001c0002t0001g0069 | 2 | HG03239.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2927-3750_2927-374 others(72): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATAT | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0079 | 2 | HG02698.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2927-3693_2927-369 others(8): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATAT | C | 2 | a0001c0001t0002g0083a0001c0003t0001g0017 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2927-3695_2927-369 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(1): Show |
C | 8 | a0001c0001t0001g0091a0001c0001t0002g0058a0001c0001t0002g0060others(5): Show | 8 | HG01081.hp2 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2927-3697_2927-369 others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(3): Show |
C | 17 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(14): Show | 17 | HG00597.hp2 HG01099.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2927-3699_2927-369 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(9): Show |
C | 1 | a0001c0004t0004g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2927-3705_2927-369 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(13): Show |
C | 1 | a0001c0001t0003g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2927-3709_2927-369 others(24): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(17): Show |
C | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0081others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927-3713_2927-369 others(28): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(21): Show |
C | 2 | a0001c0004t0005g0007a0001c0022t0005g0034 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2927-3717_2927-369 others(32): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(25): Show |
C | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2927-3721_2927-369 others(36): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(29): Show |
C | 1 | a0001c0001t0002g0100 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2927-3725_2927-369 others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(31): Show |
C | 7 | a0001c0002t0001g0066a0001c0003t0001g0014a0001c0003t0001g0088others(4): Show | 7 | HG01069.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2927-3727_2927-369 others(42): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330686
|
CATATATA others(33): Show |
C | 19 | a0001c0002t0001g0018a0001c0002t0001g0037a0001c0002t0001g0047others(16): Show | 19 | HG02109.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.2927-3729_2927-369 others(44): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330686 | |||||
| chr12:111330692
|
T | C | 15 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(12): Show | 15 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2927-3749T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330692 | ||||||
| chr12:111330694
|
T | C | 2 | a0001c0001t0002g0043a0001c0010t0001g0049 | 2 | HG01169.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-3747T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330694 | ||||||
| chr12:111330697
|
A | G | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2927-3744A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330697 | ||||||
| chr12:111330698
|
T | C | 2 | a0001c0001t0002g0058a0001c0010t0001g0050 | 2 | HG01081.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2927-3743T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330698 | ||||||
| chr12:111330700
|
T | C | 1 | a0001c0010t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2927-3741T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330700 | ||||||
| chr12:111330700
|
T | TATATATA others(37): Show |
1 | a0001c0018t0004g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2927-3732_2927-373 others(48): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330700 | |||||
| chr12:111330702
|
T | C | 2 | a0001c0004t0001g0015a0001c0004t0001g0027 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2927-3739T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330702 | ||||||
| chr12:111330702
|
T | TATATATA others(73): Show |
1 | a0001c0002t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2927-3732_2927-373 others(84): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330702 | |||||
| chr12:111330702
|
T | TATATATA others(29): Show |
1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2927-3732_2927-373 others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330702 | |||||
| chr12:111330703
|
A | G | 2 | a0001c0001t0002g0083a0001c0003t0001g0017 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2927-3738A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330703 | ||||||
| chr12:111330704
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2927-3737T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330704 | ||||||
| chr12:111330704
|
T | TATATACA others(29): Show |
1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2927-3732_2927-373 others(40): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330704 | |||||
| chr12:111330704
|
T | TATATACA others(33): Show |
1 | a0001c0019t0004g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2927-3732_2927-373 others(44): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330704 | |||||
| chr12:111330705
|
A | G | 3 | a0001c0001t0001g0091a0001c0009t0001g0031a0001c0009t0001g0035 | 3 | HG02559.hp1 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2927-3736A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330705 | ||||||
| chr12:111330706
|
T | C | 1 | a0001c0005t0001g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2927-3735T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330706 | ||||||
| chr12:111330707
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(5): Show | 8 | HG00597.hp2 HG01891.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2927-3734A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330707 | ||||||
| chr12:111330708
|
T | C | 3 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0005t0001g0019 | 3 | HG02647.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-3733T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330708 | ||||||
| chr12:111330708
|
T | TACACAC | 2 | a0001c0005t0001g0028a0001c0017t0001g0065 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2927-3732_2927-373 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330708 | |||||
| chr12:111330708
|
T | TATATATA others(37): Show |
1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2927-3720_2927-371 others(48): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330708 | |||||
| chr12:111330710
|
T | C | 6 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(3): Show | 6 | HG00597.hp1 HG01099.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2927-3731T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330710 | ||||||
| chr12:111330710
|
T | TATACATA others(3): Show |
3 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021 | 3 | HG02976.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2927-3728_2927-372 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330710 | |||||
| chr12:111330712
|
T | C | 2 | a0001c0002t0001g0061a0001c0002t0001g0069 | 2 | HG03239.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2927-3729T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330712 | ||||||
| chr12:111330712
|
T | TATACATA others(51): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2927-3726_2927-372 others(62): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330712 | |||||
| chr12:111330714
|
T | C | 3 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0004t0001g0002 | 3 | HG02647.hp2 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2927-3727T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330714 | ||||||
| chr12:111330716
|
T | C | 7 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(4): Show | 7 | HG00597.hp1 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2927-3725T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330716 | ||||||
| chr12:111330716
|
T | TATATACA others(7): Show |
1 | a0006c0020t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2927-3720_2927-371 others(18): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330716 | |||||
| chr12:111330716
|
T | TATATACA others(5): Show |
1 | a0001c0004t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2927-3720_2927-371 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111330716 | |||||
| chr12:111330718
|
T | C | 6 | a0001c0002t0001g0061a0001c0002t0001g0069a0001c0005t0001g0019others(3): Show | 6 | HG02559.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2927-3723T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330718 | ||||||
| chr12:111330720
|
T | C | 6 | a0001c0001t0002g0083a0001c0001t0004g0054a0001c0003t0001g0017others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2927-3721T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330720 | ||||||
| chr12:111330722
|
T | C | 9 | a0001c0001t0001g0091a0001c0001t0002g0083a0001c0003t0001g0017others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2927-3719T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330722 | ||||||
| chr12:111330724
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(9): Show | 12 | HG00597.hp2 HG01891.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2927-3717T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330724 | ||||||
| chr12:111330726
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(12): Show | 15 | HG00597.hp2 HG01081.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2927-3715T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330726 | ||||||
| chr12:111330728
|
T | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0004t0001g0015others(3): Show | 6 | HG01081.hp1 HG01884.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2927-3713T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330728 | ||||||
| chr12:111330730
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2927-3711T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330730 | ||||||
| chr12:111330734
|
T | C | 4 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(1): Show | 4 | HG01884.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-3707T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111330734 | ||||||
| chr12:111331050
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0002g0086others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2927-3391C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331050 | ||||||
| chr12:111331080
|
G | A | 1 | a0002c0006t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2927-3361G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331080 | ||||||
| chr12:111331169
|
A | G | 80 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(77): Show | 80 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.2927-3272A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331169 | ||||||
| chr12:111331288
|
G | T | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2927-3153G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331288 | ||||||
| chr12:111331329
|
A | G | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-3112A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331329 | ||||||
| chr12:111331359
|
C | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(27): Show | 30 | HG00597.hp2 HG01081.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2927-3082C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331359 | ||||||
| chr12:111331419
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-3022G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331419 | ||||||
| chr12:111331445
|
C | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-2996C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331445 | ||||||
| chr12:111331488
|
T | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(65): Show | 68 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.2927-2953T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331488 | ||||||
| chr12:111331657
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-2784G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331657 | ||||||
| chr12:111331761
|
T | C | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-2680T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331761 | ||||||
| chr12:111331826
|
C | G | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927-2615C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331826 | ||||||
| chr12:111331837
|
G | T | 60 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(57): Show | 60 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2927-2604G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331837 | ||||||
| chr12:111331901
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2927-2540G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111331901 | ||||||
| chr12:111332128
|
C | CT | 20 | a0001c0001t0001g0091a0001c0001t0002g0059a0001c0001t0002g0083others(17): Show | 20 | HG00597.hp2 HG01169.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.2927-2292dupT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332128 | |||||
| chr12:111332128
|
C | CTT | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0082others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2927-2293_2927-229 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332128 | |||||
| chr12:111332128
|
C | CTTT | 4 | a0001c0001t0001g0024a0001c0001t0002g0016a0001c0004t0001g0027others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-2294_2927-229 others(7): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332128 | |||||
| chr12:111332212
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0062others(10): Show | 13 | HG01169.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2927-2229G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111332212 | ||||||
| chr12:111332298
|
A | AATTTTTG others(218): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(9): Show | 12 | HG00597.hp2 HG01243.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2927-2128_2927-212 others(229): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(219): Show |
2 | a0001c0004t0001g0002a0001c0008t0002g0022 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2927-2128_2927-212 others(230): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(223): Show |
1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2927-2128_2927-212 others(234): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(229): Show |
1 | a0001c0017t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2927-2128_2927-212 others(240): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(230): Show |
2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-2128_2927-212 others(241): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(234): Show |
2 | a0001c0004t0001g0005a0006c0020t0001g0020 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2927-2128_2927-212 others(245): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(237): Show |
1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2927-2128_2927-212 others(248): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332298
|
A | AATTTTTG others(239): Show |
1 | a0001c0002t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2927-2128_2927-212 others(250): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332298 | |||||
| chr12:111332323
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2927-2118G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111332323 | ||||||
| chr12:111332630
|
TA | T | 38 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0025others(35): Show | 38 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2927-1809delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111332630 | |||||
| chr12:111332704
|
T | C | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2927-1737T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111332704 | ||||||
| chr12:111332721
|
G | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0059a0005c0012t0009g0044 | 3 | HG02572.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2927-1720G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111332721 | ||||||
| chr12:111332761
|
G | T | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2927-1680G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111332761 | ||||||
| chr12:111333029
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2927-1412G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333029 | ||||||
| chr12:111333134
|
G | A | 38 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0025others(35): Show | 38 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2927-1307G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333134 | ||||||
| chr12:111333203
|
A | T | 3 | a0001c0001t0001g0091a0001c0004t0001g0005a0006c0020t0001g0020 | 3 | HG02559.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2927-1238A>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333203 | ||||||
| chr12:111333209
|
A | C | 3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2927-1232A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333209 | ||||||
| chr12:111333409
|
G | C | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2927-1032G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333409 | ||||||
| chr12:111333540
|
C | T | 3 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0017t0001g0065 | 3 | HG02559.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2927-901C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333540 | ||||||
| chr12:111333711
|
GT | G | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2927-728delT | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111333711 | |||||
| chr12:111333805
|
C | T | 38 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0025others(35): Show | 38 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2927-636C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333805 | ||||||
| chr12:111333812
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2927-629G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333812 | ||||||
| chr12:111333895
|
TA | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(17): Show | 20 | HG00597.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2927-545delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333895 | ||||||
| chr12:111333959
|
G | A | 35 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0025others(32): Show | 35 | HG00597.hp1 HG01069.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.2927-482G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333959 | ||||||
| chr12:111333983
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG00597.hp2 HG01243.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2927-458T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111333983 | ||||||
| chr12:111334136
|
G | A | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2927-305G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111334136 | ||||||
| chr12:111334174
|
G | A | 4 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0007t0001g0021others(1): Show | 4 | HG02809.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2927-267G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111334174 | ||||||
| chr12:111334181
|
C | T | 1 | a0001c0014t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2927-260C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111334181 | ||||||
| chr12:111334186
|
T | TA | 50 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(47): Show | 50 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.2927-239dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | 111334186 | |||||
| chr12:111334316
|
T | C | 2 | a0001c0002t0001g0018a0001c0002t0001g0093 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2927-125T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | chr12 | 111334316 | ||||||
| chr12:111334804
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3196+94C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111334804 | ||||||
| chr12:111334966
|
A | C | 54 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0003g0045others(51): Show | 54 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.3196+256A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111334966 | ||||||
| chr12:111335253
|
C | T | 3 | a0001c0003t0001g0014a0001c0003t0001g0040a0001c0011t0001g0001 | 3 | HG02970.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3196+543C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335253 | ||||||
| chr12:111335340
|
C | A | 9 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0004g0054others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3196+630C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335340 | ||||||
| chr12:111335341
|
C | T | 3 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3196+631C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335341 | ||||||
| chr12:111335342
|
G | A | 2 | a0001c0010t0001g0049a0001c0010t0001g0050 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3196+632G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335342 | ||||||
| chr12:111335368
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.3196+658A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335368 | ||||||
| chr12:111335453
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3196+743G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335453 | ||||||
| chr12:111335541
|
T | C | 42 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(39): Show | 42 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.3196+831T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335541 | ||||||
| chr12:111335544
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3196+834C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335544 | ||||||
| chr12:111335663
|
T | C | 83 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.3196+953T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335663 | ||||||
| chr12:111335708
|
A | G | 1 | a0001c0018t0004g0029 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3196+998A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335708 | ||||||
| chr12:111335713
|
A | C | 3 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0022t0005g0034 | 3 | HG02622.hp2 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3196+1003A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335713 | ||||||
| chr12:111335883
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.3196+1173A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335883 | ||||||
| chr12:111335920
|
TA | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.3196+1223delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111335920 | |||||
| chr12:111335928
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3196+1218A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111335928 | ||||||
| chr12:111336121
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.3196+1411G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336121 | ||||||
| chr12:111336264
|
A | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(66): Show | 69 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.3196+1554A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336264 | ||||||
| chr12:111336370
|
G | A | 9 | a0001c0004t0001g0002a0001c0007t0001g0021a0001c0007t0001g0098others(6): Show | 9 | HG00597.hp2 HG01081.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3196+1660G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336370 | ||||||
| chr12:111336404
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3196+1694G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336404 | ||||||
| chr12:111336424
|
T | TTG | 4 | a0001c0001t0002g0056a0001c0001t0002g0076a0001c0001t0002g0079others(1): Show | 4 | HG01099.hp2 HG02698.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3196+1748_3196+174 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
T | TTGTGTG | 7 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0007t0001g0021others(4): Show | 7 | HG00597.hp2 HG01081.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3196+1744_3196+174 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
T | TTGTGTGT others(3): Show |
5 | a0001c0004t0006g0075a0001c0009t0001g0031a0001c0009t0001g0035others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3196+1740_3196+174 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
T | TTGTGTGT others(5): Show |
2 | a0001c0005t0001g0019a0002c0006t0001g0089 | 2 | HG03540.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3196+1738_3196+174 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
T | TTGTGTGT others(11): Show |
1 | a0001c0005t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3196+1732_3196+174 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
TTG | T | 6 | a0001c0001t0001g0013a0001c0001t0003g0045a0001c0001t0003g0078others(3): Show | 6 | HG01169.hp1 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3196+1748_3196+174 others(6): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
TTGTGTG | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG02559.hp1 HG02615.hp1 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.3196+1744_3196+174 others(10): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
TTGTGTGT others(1): Show |
T | 35 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(32): Show | 35 | HG00597.hp1 HG01069.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.3196+1742_3196+174 others(12): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336424
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0004t0001g0002a0001c0004t0001g0096 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3196+1740_3196+174 others(14): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111336424 | |||||
| chr12:111336459
|
T | TGTGTGTG others(4): Show |
1 | a0002c0006t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3196+1749_3196+175 others(15): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336459 | ||||||
| chr12:111336460
|
T | G | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3196+1750T>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336460 | ||||||
| chr12:111336534
|
G | A | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3197-1752G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336534 | ||||||
| chr12:111336851
|
A | G | 7 | a0001c0002t0001g0095a0001c0003t0001g0008a0001c0003t0001g0009others(4): Show | 7 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3197-1435A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111336851 | ||||||
| chr12:111337067
|
C | T | 1 | a0001c0003t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3197-1219C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111337067 | ||||||
| chr12:111337200
|
A | G | 16 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0004g0054others(13): Show | 16 | HG00597.hp2 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3197-1086A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111337200 | ||||||
| chr12:111337352
|
C | CA | 35 | a0001c0001t0002g0100a0001c0001t0004g0054a0001c0002t0001g0004others(32): Show | 35 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.3197-918dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111337352 | |||||
| chr12:111337689
|
G | C | 13 | a0001c0001t0001g0013a0001c0004t0001g0002a0001c0004t0001g0096others(10): Show | 13 | HG00597.hp2 HG01081.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.3197-597G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111337689 | ||||||
| chr12:111337938
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3197-348G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111337938 | ||||||
| chr12:111338041
|
GA | G | 4 | a0001c0001t0001g0091a0001c0004t0001g0005a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3197-232delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 111338041 | |||||
| chr12:111338046
|
A | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0001t0004g0054others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3197-240A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111338046 | ||||||
| chr12:111338130
|
G | A | 4 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3197-156G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111338130 | ||||||
| chr12:111338216
|
A | G | 2 | a0001c0001t0001g0013a0001c0003t0001g0088 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3197-70A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 19/21 | chr12 | 111338216 | ||||||
| chr12:111338523
|
C | T | 4 | a0001c0001t0004g0054a0001c0004t0004g0041a0001c0018t0004g0029others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3385+49C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111338523 | ||||||
| chr12:111339004
|
G | A | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3385+530G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339004 | ||||||
| chr12:111339210
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3385+736C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339210 | ||||||
| chr12:111339241
|
G | A | 3 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075 | 3 | HG02280.hp2 HG02622.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3385+767G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339241 | ||||||
| chr12:111339255
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3385+781G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339255 | ||||||
| chr12:111339341
|
A | C | 8 | a0001c0007t0001g0021a0001c0007t0001g0098a0001c0009t0001g0031others(5): Show | 8 | HG00597.hp2 HG01081.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3385+867A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339341 | ||||||
| chr12:111339613
|
A | G | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3385+1139A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339613 | ||||||
| chr12:111339678
|
G | A | 1 | a0001c0003t0008g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3385+1204G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339678 | ||||||
| chr12:111339792
|
C | T | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3385+1318C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111339792 | ||||||
| chr12:111340153
|
C | T | 1 | a0001c0008t0002g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3386-1627C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111340153 | ||||||
| chr12:111340374
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.3386-1406T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111340374 | ||||||
| chr12:111340602
|
A | G | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3386-1178A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111340602 | ||||||
| chr12:111340839
|
T | C | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3386-941T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111340839 | ||||||
| chr12:111340885
|
T | C | 4 | a0001c0004t0001g0002a0001c0004t0001g0096a0001c0010t0001g0049others(1): Show | 4 | HG01243.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3386-895T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111340885 | ||||||
| chr12:111341414
|
C | G | 2 | a0001c0004t0004g0041a0001c0018t0004g0029 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3386-366C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111341414 | ||||||
| chr12:111341470
|
A | C | 7 | a0001c0002t0001g0095a0001c0003t0001g0008a0001c0003t0001g0009others(4): Show | 7 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3386-310A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111341470 | ||||||
| chr12:111341645
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3386-135C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111341645 | ||||||
| chr12:111341663
|
G | T | 1 | a0001c0019t0004g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3386-117G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 20/21 | chr12 | 111341663 | ||||||
| chr12:111342116
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3659+63C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342116 | ||||||
| chr12:111342127
|
G | C | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3659+74G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342127 | ||||||
| chr12:111342306
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3659+253C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342306 | ||||||
| chr12:111342317
|
A | G | 3 | a0001c0003t0001g0014a0001c0003t0001g0040a0001c0011t0001g0001 | 3 | HG02970.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3659+264A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342317 | ||||||
| chr12:111342455
|
G | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(89): Show | 92 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.3659+402G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342455 | ||||||
| chr12:111342828
|
G | A | 8 | a0001c0002t0001g0023a0001c0002t0001g0037a0001c0002t0001g0047others(5): Show | 8 | HG01099.hp1 HG02886.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3659+775G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342828 | ||||||
| chr12:111342840
|
T | C | 44 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(41): Show | 44 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.3659+787T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342840 | ||||||
| chr12:111342930
|
G | A | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3659+877G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111342930 | ||||||
| chr12:111342956
|
CA | C | 51 | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0016others(48): Show | 51 | HG00597.hp1 HG01069.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.3659+927delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111342956 | |||||
| chr12:111342956
|
CAA | C | 12 | a0001c0001t0002g0085a0001c0001t0002g0100a0001c0001t0003g0045others(9): Show | 12 | HG01069.hp1 HG01169.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3659+926_3659+927d others(4): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111342956 | |||||
| chr12:111343194
|
C | G | 12 | a0001c0005t0001g0019a0001c0005t0001g0028a0001c0007t0001g0021others(9): Show | 12 | HG00597.hp2 HG01081.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3659+1141C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111343194 | ||||||
| chr12:111343251
|
A | G | 37 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(34): Show | 37 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.3659+1198A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111343251 | ||||||
| chr12:111343514
|
G | C | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+1461G>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111343514 | ||||||
| chr12:111344124
|
G | A | 5 | a0001c0002t0001g0018a0001c0002t0001g0051a0001c0002t0001g0066others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+2071G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111344124 | ||||||
| chr12:111344218
|
C | T | 4 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0027others(1): Show | 4 | HG01884.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+2165C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111344218 | ||||||
| chr12:111344318
|
C | A | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+2265C>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111344318 | ||||||
| chr12:111344495
|
T | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3659+2442T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111344495 | ||||||
| chr12:111344982
|
T | A | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3660-2542T>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111344982 | ||||||
| chr12:111345216
|
A | G | 57 | a0001c0001t0001g0013a0001c0001t0002g0100a0001c0002t0001g0004others(54): Show | 57 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.3660-2308A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345216 | ||||||
| chr12:111345375
|
G | T | 44 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(41): Show | 44 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.3660-2149G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345375 | ||||||
| chr12:111345391
|
C | G | 1 | a0001c0010t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3660-2133C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345391 | ||||||
| chr12:111345432
|
G | T | 1 | a0001c0001t0005g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3660-2092G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345432 | ||||||
| chr12:111345444
|
C | CA | 11 | a0001c0001t0001g0013a0001c0001t0002g0016a0001c0001t0002g0059others(8): Show | 11 | HG00597.hp2 HG01169.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3660-2063dupA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111345444 | |||||
| chr12:111345444
|
CA | C | 43 | a0001c0001t0002g0100a0001c0002t0001g0004a0001c0002t0001g0018others(40): Show | 43 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.3660-2063delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111345444 | |||||
| chr12:111345465
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3660-2059C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345465 | ||||||
| chr12:111345466
|
G | A | 7 | a0001c0002t0001g0095a0001c0003t0001g0008a0001c0003t0001g0009others(4): Show | 7 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3660-2058G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345466 | ||||||
| chr12:111345539
|
C | G | 5 | a0001c0001t0003g0045a0001c0001t0003g0078a0001c0001t0003g0080others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3660-1985C>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345539 | ||||||
| chr12:111345735
|
CA | C | 6 | a0001c0001t0002g0062a0001c0003t0001g0014a0001c0003t0001g0040others(3): Show | 6 | HG01081.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3660-1772delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111345735 | |||||
| chr12:111345762
|
A | G | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3660-1762A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345762 | ||||||
| chr12:111345851
|
T | C | 4 | a0001c0001t0005g0055a0001c0004t0005g0007a0001c0004t0006g0075others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-1673T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345851 | ||||||
| chr12:111345876
|
G | A | 1 | a0001c0013t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3660-1648G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345876 | ||||||
| chr12:111345974
|
A | G | 57 | a0001c0001t0001g0013a0001c0001t0002g0100a0001c0002t0001g0004others(54): Show | 57 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.3660-1550A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345974 | ||||||
| chr12:111345998
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.3660-1526A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111345998 | ||||||
| chr12:111346027
|
C | T | 7 | a0001c0002t0001g0095a0001c0003t0001g0008a0001c0003t0001g0009others(4): Show | 7 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3660-1497C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346027 | ||||||
| chr12:111346029
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0059 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3660-1495C>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346029 | ||||||
| chr12:111346051
|
G | A | 4 | a0001c0001t0004g0054a0001c0004t0004g0041a0001c0018t0004g0029others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-1473G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346051 | ||||||
| chr12:111346475
|
CA | C | 4 | a0001c0001t0001g0013a0001c0005t0001g0019a0001c0005t0001g0028others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-1034delA | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 111346475 | |||||
| chr12:111346493
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3660-1031A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346493 | ||||||
| chr12:111346691
|
G | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0082others(72): Show | 75 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.3660-833G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346691 | ||||||
| chr12:111346850
|
A | G | 2 | a0001c0004t0001g0015a0001c0004t0001g0027 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3660-674A>G | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111346850 | ||||||
| chr12:111347204
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3660-320T>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111347204 | ||||||
| chr12:111347243
|
G | T | 4 | a0001c0001t0004g0054a0001c0004t0004g0041a0001c0018t0004g0029others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-281G>T | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111347243 | ||||||
| chr12:111347383
|
A | C | 2 | a0001c0005t0001g0019a0001c0005t0001g0028 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3660-141A>C | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111347383 | ||||||
| chr12:111347511
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3660-13G>A | CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 21/21 | chr12 | 111347511 |