| geneid | 64784 |
|---|---|
| ensemblid | ENSG00000140577.17 |
| hgncid | 26148 |
| symbol | CRTC3 |
| name | CREB regulated transcription coactivator 3 |
| refseq_nuc | NM_022769.5 |
| refseq_prot | NP_073606.3 |
| ensembl_nuc | ENST00000268184.11 |
| ensembl_prot | ENSP00000268184.6 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 90529923 |
| end | 90645345 |
| strand | + |
| ver | v1.2 |
| region | chr15:90529923-90645345 |
| region5000 | chr15:90524923-90650345 |
| regionname0 | CRTC3_chr15_90529923_90645345 |
| regionname5000 | CRTC3_chr15_90524923_90650345 |
| 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 | 1/0 | 619 | 170 | 45 | 35 | 69 | 7 | 13 | 51 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002 | 0/1 | 619 | 71 | 18 | 17 | 17 | 7 | 11 | 12 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003 | 0/0 | 465 | 26 | 6 | 7 | 11 | 0 | 2 | 5 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004 | 0/0 | 465 | 5 | 3 | 1 | 1 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0005 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0006 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0007 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0008 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| 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 | 1/0 | 1860 | 157 | 44 | 35 | 61 | 5 | 11 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0002 | 0/1 | 1860 | 69 | 18 | 16 | 16 | 7 | 11 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0003 | 0/0 | 1861 | 24 | 5 | 7 | 10 | 0 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0004 | 0/0 | 1860 | 7 | 0 | 0 | 6 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0005 | 0/0 | 1861 | 5 | 3 | 1 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0006 | 0/0 | 1860 | 3 | 0 | 0 | 0 | 1 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0007 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0009 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0010 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0011 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0012 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0013 | 0/0 | 1861 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0014 | 0/0 | 1861 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0015 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| c0016 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| 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 | 1/1 | 3355 | 141 | 26 | 31 | 56 | 9 | 17 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0002 | 0/0 | 3355 | 40 | 1 | 13 | 22 | 2 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0003 | 0/0 | 3355 | 25 | 4 | 5 | 10 | 1 | 5 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0004 | 0/0 | 3355 | 6 | 1 | 4 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0005 | 0/0 | 3355 | 4 | 0 | 0 | 3 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0006 | 0/0 | 3669 | 4 | 4 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0007 | 0/0 | 3355 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0008 | 0/0 | 3355 | 3 | 0 | 0 | 3 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0009 | 0/0 | 3355 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0010 | 0/0 | 3355 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0011 | 0/0 | 3355 | 3 | 2 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0012 | 0/0 | 3355 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0013 | 0/0 | 3355 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0014 | 0/0 | 3355 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0015 | 0/0 | 3355 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0016 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0017 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0018 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0019 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0020 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0021 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0022 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0023 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0024 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0025 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0026 | 0/0 | 3408 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0027 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0028 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0029 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0030 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0031 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0032 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0033 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0034 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0035 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0036 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0037 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0038 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0039 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0040 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0041 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0042 | 0/0 | 3326 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0043 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0044 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0045 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0046 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0047 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| t0048 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| 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 | 1/0 | 1860 | 157 | 44 | 35 | 61 | 5 | 11 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0004 | 0/0 | 1860 | 7 | 0 | 0 | 6 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0006 | 0/0 | 1860 | 3 | 0 | 0 | 0 | 1 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0007 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0015 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002 | 0/1 | 1860 | 69 | 18 | 16 | 16 | 7 | 11 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0009 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0010 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003 | 0/0 | 1861 | 24 | 5 | 7 | 10 | 0 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0013 | 0/0 | 1861 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0014 | 0/0 | 1861 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004c0005 | 0/0 | 1861 | 5 | 3 | 1 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0005c0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0006c0011 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0007c0016 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0008c0012 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5214 | 89 | 21 | 19 | 38 | 3 | 7 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0002 | 0/0 | 5214 | 32 | 1 | 11 | 16 | 2 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0003 | 0/0 | 5214 | 9 | 1 | 1 | 5 | 0 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0004 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0006 | 0/0 | 5528 | 4 | 4 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0007 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0009 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0010 | 0/0 | 5214 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0011 | 0/0 | 5214 | 3 | 2 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0016 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0019 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0023 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0024 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0025 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0032 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0035 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0037 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0040 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0041 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0042 | 0/0 | 5185 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0001t0046 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0004t0005 | 0/0 | 5214 | 3 | 0 | 0 | 2 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0004t0008 | 0/0 | 5214 | 3 | 0 | 0 | 3 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0004t0034 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0006t0003 | 0/0 | 5214 | 3 | 0 | 0 | 0 | 1 | 2 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0007t0001 | 0/0 | 5214 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0001c0015t0029 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0001 | 0/1 | 5214 | 32 | 0 | 8 | 8 | 6 | 9 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0002 | 0/0 | 5214 | 6 | 0 | 1 | 5 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0003 | 0/0 | 5214 | 6 | 2 | 1 | 2 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0004 | 0/0 | 5214 | 5 | 0 | 4 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0007 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0012 | 0/0 | 5214 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0013 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0014 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0015 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0017 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0018 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0020 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0022 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0028 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0031 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0033 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0038 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0044 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0047 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0002t0048 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0009t0001 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0002c0010t0003 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0001 | 0/0 | 5215 | 13 | 3 | 3 | 6 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0002 | 0/0 | 5215 | 2 | 0 | 1 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0003 | 0/0 | 5215 | 5 | 0 | 2 | 3 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0009 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0027 | 0/0 | 5215 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0036 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0003t0039 | 0/0 | 5215 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0013t0005 | 0/0 | 5215 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0003c0014t0030 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004c0005t0001 | 0/0 | 5215 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004c0005t0003 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004c0005t0026 | 0/0 | 5268 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0004c0005t0045 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0005c0008t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0006c0011t0043 | 0/0 | 5204 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0007c0016t0001 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| a0008c0012t0021 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | copy fasta | chr15 | 90524923 | 90650345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0011g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0016g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0023g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0024g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0025g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0032g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0035g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0037g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0040g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0041g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0042g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0001t0046g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0004t0034g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0006t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0006t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0006t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0007t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0001c0015t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0012g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0014g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0014g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0015g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0017g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0020g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0022g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0028g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0031g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0033g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0038g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0044g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0047g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0002t0048g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0009t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0002c0010t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0027g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0036g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0003t0039g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0013t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0003c0014t0030g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0004c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0004c0005t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0004c0005t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0004c0005t0026g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0004c0005t0045g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0005c0008t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0006c0011t0043g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0007c0016t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| a0008c0012t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | GBR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0092 | EUR | GBR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0075 | EUR | GBR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0118 | EUR | FIN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00323 | hp2 | a0001 | c0004 | t0005 | g0004 | EUR | FIN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00408 | hp2 | a0002 | c0009 | t0001 | g0098 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00438 | hp1 | a0003 | c0013 | t0005 | g0014 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0234 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00597 | hp1 | a0001 | c0007 | t0001 | g0206 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00639 | hp2 | a0002 | c0002 | t0048 | g0089 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00735 | hp1 | a0003 | c0003 | t0039 | g0144 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00735 | hp2 | a0003 | c0003 | t0003 | g0145 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00738 | hp1 | a0004 | c0005 | t0001 | g0091 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01081 | hp2 | a0002 | c0002 | t0004 | g0115 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0266 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0162 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01192 | hp2 | a0002 | c0010 | t0003 | g0090 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0188 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0267 | AMR | PUR | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0045 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01257 | hp2 | a0002 | c0002 | t0004 | g0111 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01258 | hp2 | a0002 | c0002 | t0004 | g0112 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01346 | hp1 | a0002 | c0002 | t0012 | g0138 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01433 | hp1 | a0001 | c0001 | t0024 | g0154 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01496 | hp2 | a0001 | c0001 | t0011 | g0030 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0117 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01516 | hp2 | a0001 | c0006 | t0003 | g0055 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0113 | EUR | IBS | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0168 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01891 | hp2 | a0008 | c0012 | t0021 | g0029 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0094 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01981 | hp2 | a0001 | c0001 | t0023 | g0147 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02015 | hp1 | a0001 | c0001 | t0042 | g0191 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02055 | hp2 | a0003 | c0003 | t0009 | g0032 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02074 | hp1 | a0006 | c0011 | t0043 | g0083 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02129 | hp2 | a0001 | c0001 | t0041 | g0172 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0174 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02135 | hp2 | a0001 | c0007 | t0001 | g0205 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02257 | hp2 | a0002 | c0002 | t0047 | g0003 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02258 | hp2 | a0003 | c0014 | t0030 | g0253 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0195 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02280 | hp2 | a0002 | c0002 | t0014 | g0134 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0141 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0068 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | KHV | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02572 | hp2 | a0003 | c0003 | t0036 | g0031 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0210 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02615 | hp1 | a0002 | c0002 | t0012 | g0136 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0217 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0218 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02630 | hp2 | a0002 | c0002 | t0013 | g0194 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02717 | hp2 | a0001 | c0001 | t0032 | g0033 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02809 | hp1 | a0001 | c0001 | t0037 | g0139 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02809 | hp2 | a0004 | c0005 | t0045 | g0132 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02896 | hp1 | a0001 | c0001 | t0035 | g0061 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02896 | hp2 | a0002 | c0002 | t0013 | g0131 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02970 | hp1 | a0001 | c0015 | t0029 | g0042 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02970 | hp2 | a0002 | c0002 | t0014 | g0135 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0034 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02976 | hp2 | a0002 | c0002 | t0038 | g0085 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03098 | hp2 | a0002 | c0002 | t0033 | g0025 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03130 | hp1 | a0002 | c0002 | t0020 | g0137 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03209 | hp1 | a0002 | c0002 | t0031 | g0128 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03209 | hp2 | a0001 | c0001 | t0046 | g0020 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03225 | hp2 | a0002 | c0002 | t0017 | g0133 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03239 | hp1 | a0001 | c0006 | t0003 | g0148 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03492 | hp2 | a0001 | c0006 | t0003 | g0149 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03516 | hp2 | a0002 | c0002 | t0018 | g0119 | AFR | ESN | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03540 | hp1 | a0004 | c0005 | t0001 | g0084 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03540 | hp2 | a0001 | c0001 | t0040 | g0023 | AFR | GWD | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03579 | hp2 | a0002 | c0002 | t0015 | g0196 | AFR | MSL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | BEB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG03831 | hp2 | a0003 | c0003 | t0027 | g0022 | SAS | BEB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0109 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04204 | hp1 | a0002 | c0002 | t0022 | g0107 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | CHB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18940 | hp1 | a0001 | c0004 | t0005 | g0005 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18944 | hp1 | a0001 | c0004 | t0034 | g0156 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18944 | hp2 | a0001 | c0004 | t0005 | g0009 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18947 | hp2 | a0002 | c0002 | t0028 | g0081 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18950 | hp1 | a0001 | c0004 | t0008 | g0015 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18954 | hp1 | a0003 | c0003 | t0003 | g0247 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18982 | hp2 | a0007 | c0016 | t0001 | g0237 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18984 | hp2 | a0001 | c0004 | t0008 | g0008 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18991 | hp1 | a0001 | c0004 | t0008 | g0007 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0140 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19030 | hp2 | a0004 | c0005 | t0003 | g0086 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0220 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19083 | hp1 | a0004 | c0005 | t0026 | g0088 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19083 | hp2 | a0003 | c0003 | t0003 | g0019 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0142 | AFR | YRI | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0028 | AFR | ASW | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | ASW | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0105 | EUR | TSI | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0114 | EUR | TSI | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0129 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02559 | hp1 | a0002 | c0002 | t0015 | g0026 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG02559 | hp2 | a0002 | c0002 | t0044 | g0021 | AFR | ACB | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | USA | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA21309 | hp1 | a0002 | c0002 | t0007 | g0130 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| NA21309 | hp2 | a0005 | c0008 | t0001 | g0259 | AFR | LWK | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0027 | REF | REF | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | CRTC3_chr15_90524923_90650345 | CRTC3 | chr15 | 90524923 | 90650345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:90540067
|
G | A | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.161G>A | p.Arg54His | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/15 | 310/5214 | 161/1860 | 54/619 | chr15 | 90540067 | ||
| chr15:90540121
|
G | A | 3 | a0002a0004a0006 | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
missense_variant | MODERATE | c.215G>A | p.Ser72Asn | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/15 | 364/5214 | 215/1860 | 72/619 | chr15 | 90540121 | ||
| chr15:90638446
|
A | G | 1 | a0006 | 1 | HG02074.hp1 | missense_variant&splice_region_variant | MODERATE | c.1267A>G | p.Met423Val | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 12/15 | 1416/5214 | 1267/1860 | 423/619 | chr15 | 90638446 | ||
| chr15:90638514
|
A | AC | 2 | a0003a0004 | 31 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(28): Show |
frameshift_variant | HIGH | c.1340dupC | p.Tyr448fs | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 12/15 | 1490/5214 | 1341/1860 | 447/619 | INFO_REALIGN_3_PRIME | chr15 | 90638514 | |
| chr15:90638603
|
C | G | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1424C>G | p.Ala475Gly | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 12/15 | 1573/5214 | 1424/1860 | 475/619 | chr15 | 90638603 | ||
| chr15:90641103
|
C | G | 1 | a0007 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1555C>G | p.Leu519Val | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/15 | 1704/5214 | 1555/1860 | 519/619 | chr15 | 90641103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:90540083
|
T | C | 1 | a0002c0009 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.177T>C | p.His59His | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/15 | 326/5214 | 177/1860 | 59/619 | chr15 | 90540083 | ||
| chr15:90593683
|
G | A | 1 | a0008c0012 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.279G>A | p.Gly93Gly | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/15 | 428/5214 | 279/1860 | 93/619 | chr15 | 90593683 | ||
| chr15:90617932
|
G | A | 2 | a0001c0004a0003c0013 | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
synonymous_variant | LOW | c.663G>A | p.Pro221Pro | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/15 | 812/5214 | 663/1860 | 221/619 | chr15 | 90617932 | ||
| chr15:90629379
|
C | T | 1 | a0001c0007 | 2 | HG00597.hp1 HG02135.hp2 |
synonymous_variant | LOW | c.1113C>T | p.Asn371Asn | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/15 | 1262/5214 | 1113/1860 | 371/619 | chr15 | 90629379 | ||
| chr15:90638779
|
G | A | 2 | a0001c0015a0003c0014 | 2 | HG02258.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1512G>A | p.Gln504Gln | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/15 | 1661/5214 | 1512/1860 | 504/619 | chr15 | 90638779 | ||
| chr15:90641972
|
G | A | 2 | a0001c0004a0003c0013 | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
synonymous_variant | LOW | c.1692G>A | p.Ala564Ala | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1841/5214 | 1692/1860 | 564/619 | chr15 | 90641972 | ||
| chr15:90642059
|
C | T | 2 | a0001c0006a0002c0010 | 4 | HG01192.hp2 HG01516.hp2 HG03239.hp1 others(1): Show |
synonymous_variant | LOW | c.1779C>T | p.Asp593Asp | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1928/5214 | 1779/1860 | 593/619 | chr15 | 90642059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:90529959
|
G | T | 1 | a0002c0002t0048 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/15 | 113 | chr15 | 90529959 | |||||
| chr15:90529967
|
A | G | 4 | a0001c0001t0046a0002c0002t0044a0002c0002t0047others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02809.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-105A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/15 | 105 | chr15 | 90529967 | |||||
| chr15:90529996
|
T | G | 1 | a0001c0001t0016 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/15 | 76 | chr15 | 90529996 | |||||
| chr15:90530003
|
G | C | 8 | a0001c0001t0019a0002c0002t0012a0002c0002t0013others(5): Show | 11 | HG01346.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-69G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/15 | 69 | chr15 | 90530003 | |||||
| chr15:90642253
|
A | G | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(21): Show | 54 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*113A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 113 | chr15 | 90642253 | |||||
| chr15:90642342
|
T | A | 4 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(1): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*202T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 202 | chr15 | 90642342 | |||||
| chr15:90642362
|
A | G | 1 | a0001c0001t0010 | 3 | HG02451.hp1 HG02717.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*222A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 222 | chr15 | 90642362 | |||||
| chr15:90642369
|
A | G | 3 | a0001c0001t0009a0001c0001t0019a0003c0003t0009 | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*229A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 229 | chr15 | 90642369 | |||||
| chr15:90642434
|
A | C | 1 | a0003c0003t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 294 | chr15 | 90642434 | |||||
| chr15:90642541
|
G | A | 1 | a0002c0002t0022 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 401 | chr15 | 90642541 | |||||
| chr15:90642554
|
C | T | 1 | a0001c0001t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 414 | chr15 | 90642554 | |||||
| chr15:90642568
|
G | A | 1 | a0002c0002t0038 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 428 | chr15 | 90642568 | |||||
| chr15:90642588
|
G | A | 1 | a0001c0001t0023 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*448G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 448 | chr15 | 90642588 | |||||
| chr15:90642610
|
A | G | 46 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(43): Show | 84 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*470A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 470 | chr15 | 90642610 | |||||
| chr15:90642630
|
G | A | 20 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(17): Show | 30 | HG01346.hp1 HG01496.hp2 HG01891.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*490G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 490 | chr15 | 90642630 | |||||
| chr15:90642739
|
G | A | 7 | a0001c0001t0002a0001c0001t0023a0001c0001t0024others(4): Show | 44 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*599G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 599 | chr15 | 90642739 | |||||
| chr15:90642762
|
C | T | 50 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(47): Show | 125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 622 | chr15 | 90642762 | |||||
| chr15:90642817
|
G | A | 12 | a0001c0001t0007a0001c0001t0009a0001c0001t0019others(9): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 677 | chr15 | 90642817 | |||||
| chr15:90642920
|
G | T | 1 | a0001c0001t0006 | 4 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*780G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 780 | chr15 | 90642920 | |||||
| chr15:90642995
|
G | A | 1 | a0003c0003t0039 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 855 | chr15 | 90642995 | |||||
| chr15:90643013
|
C | G | 1 | a0002c0002t0033 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 873 | chr15 | 90643013 | |||||
| chr15:90643150
|
C | G | 2 | a0001c0001t0004a0002c0002t0004 | 6 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1010C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1010 | chr15 | 90643150 | |||||
| chr15:90643183
|
G | A | 1 | a0002c0002t0013 | 2 | HG02630.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1043G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1043 | chr15 | 90643183 | |||||
| chr15:90643207
|
G | A | 1 | a0002c0002t0047 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1067 | chr15 | 90643207 | |||||
| chr15:90643229
|
G | A | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(37): Show | 105 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1089G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1089 | chr15 | 90643229 | |||||
| chr15:90643381
|
G | C | 1 | a0001c0001t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1241 | chr15 | 90643381 | |||||
| chr15:90643397
|
T | C | 1 | a0001c0001t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1257 | chr15 | 90643397 | |||||
| chr15:90643523
|
G | A | 4 | a0001c0004t0005a0001c0004t0008a0001c0004t0034others(1): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1383 | chr15 | 90643523 | |||||
| chr15:90643585
|
T | G | 4 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(1): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1445T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1445 | chr15 | 90643585 | |||||
| chr15:90643593
|
AGGCCTAA others(51): Show |
A | 1 | a0001c0015t0029 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454_*1511delGGCC others(54): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1454 | chr15 | 90643593 | |||||
| chr15:90643634
|
T | C | 1 | a0001c0004t0008 | 3 | NA18950.hp1 NA18984.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1494T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1494 | chr15 | 90643634 | |||||
| chr15:90643637
|
T | TAAAATAG others(307): Show |
1 | a0001c0001t0006 | 4 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1513_*1514insGCCG others(310): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1514 | INFO_REALIGN_3_PRIME | chr15 | 90643637 | ||||
| chr15:90643637
|
T | TAAAATAG others(309): Show |
1 | a0008c0012t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513_*1514insGCCG others(312): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1514 | INFO_REALIGN_3_PRIME | chr15 | 90643637 | ||||
| chr15:90643788
|
C | T | 8 | a0001c0001t0007a0001c0001t0009a0001c0001t0019others(5): Show | 10 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1648 | chr15 | 90643788 | |||||
| chr15:90643872
|
C | CCCAGAGG others(46): Show |
1 | a0004c0005t0026 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733_*1785dupCCAG others(49): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1786 | INFO_REALIGN_3_PRIME | chr15 | 90643872 | ||||
| chr15:90643927
|
T | C | 4 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(1): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1787T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1787 | chr15 | 90643927 | |||||
| chr15:90643979
|
T | G | 1 | a0001c0001t0040 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 1839 | chr15 | 90643979 | |||||
| chr15:90644258
|
C | A | 7 | a0001c0001t0002a0001c0001t0023a0001c0001t0024others(4): Show | 44 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2118C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2118 | chr15 | 90644258 | |||||
| chr15:90644321
|
A | G | 4 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(1): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2181A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2181 | chr15 | 90644321 | |||||
| chr15:90644406
|
C | T | 1 | a0002c0002t0028 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2266C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2266 | chr15 | 90644406 | |||||
| chr15:90644408
|
T | C | 1 | a0001c0001t0041 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2268T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2268 | chr15 | 90644408 | |||||
| chr15:90644518
|
A | C | 16 | a0001c0001t0007a0001c0001t0009a0001c0001t0011others(13): Show | 22 | HG01346.hp1 HG01496.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2378A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2378 | chr15 | 90644518 | |||||
| chr15:90644571
|
G | T | 1 | a0003c0003t0027 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2431G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2431 | chr15 | 90644571 | |||||
| chr15:90644700
|
A | T | 1 | a0004c0005t0045 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2560A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2560 | chr15 | 90644700 | |||||
| chr15:90644779
|
T | C | 1 | a0001c0001t0037 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2639 | chr15 | 90644779 | |||||
| chr15:90644803
|
CTGCATAC others(22): Show |
C | 1 | a0001c0001t0042 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665_*2693delGCAT others(25): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2665 | INFO_REALIGN_3_PRIME | chr15 | 90644803 | ||||
| chr15:90644841
|
T | G | 2 | a0001c0001t0007a0002c0002t0007 | 3 | HG03139.hp1 HG03579.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2701T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2701 | chr15 | 90644841 | |||||
| chr15:90644852
|
A | C | 1 | a0002c0002t0020 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2712 | chr15 | 90644852 | |||||
| chr15:90644856
|
C | T | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2716C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2716 | chr15 | 90644856 | |||||
| chr15:90644974
|
AGGGGTTT others(3): Show |
A | 1 | a0006c0011t0043 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836_*2845delGGGT others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2836 | INFO_REALIGN_3_PRIME | chr15 | 90644974 | ||||
| chr15:90645037
|
C | T | 2 | a0002c0002t0044a0004c0005t0045 | 2 | HG02559.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2897C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2897 | chr15 | 90645037 | |||||
| chr15:90645038
|
G | A | 2 | a0001c0001t0035a0003c0003t0036 | 2 | HG02572.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2898G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2898 | chr15 | 90645038 | |||||
| chr15:90645085
|
G | A | 2 | a0001c0001t0006a0008c0012t0021 | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2945G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 2945 | chr15 | 90645085 | |||||
| chr15:90645310
|
T | C | 7 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(4): Show | 9 | HG01496.hp2 HG02559.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3170T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 3170 | chr15 | 90645310 | |||||
| chr15:90645324
|
T | G | 4 | a0001c0001t0011a0001c0001t0037a0001c0001t0046others(1): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3184T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 15/15 | 3184 | chr15 | 90645324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:90530214
|
G | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.132+11G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530214 | ||||||
| chr15:90530232
|
GCGGCCA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(76): Show | 82 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.132+35_132+40delAC others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90530232 | |||||
| chr15:90530256
|
C | T | 1 | a0002c0002t0015g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.132+53C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530256 | ||||||
| chr15:90530278
|
G | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+75G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530278 | ||||||
| chr15:90530438
|
G | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.132+235G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530438 | ||||||
| chr15:90530472
|
C | A | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.132+269C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530472 | ||||||
| chr15:90530481
|
G | T | 1 | a0002c0002t0013g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.132+278G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530481 | ||||||
| chr15:90530516
|
G | T | 1 | a0001c0001t0002g0273 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.132+313G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530516 | ||||||
| chr15:90530635
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(75): Show | 81 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.132+432G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530635 | ||||||
| chr15:90530661
|
G | A | 2 | a0001c0001t0040g0023a0003c0003t0027g0022 | 2 | HG03540.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.132+458G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90530661 | ||||||
| chr15:90531068
|
C | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+865C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531068 | ||||||
| chr15:90531299
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.132+1096T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531299 | ||||||
| chr15:90531469
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0254a0003c0014t0030g0253 | 3 | HG02258.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132+1266G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531469 | ||||||
| chr15:90531552
|
T | G | 3 | a0002c0002t0003g0024a0002c0002t0015g0026a0002c0002t0033g0025 | 3 | HG01109.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.132+1349T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531552 | ||||||
| chr15:90531554
|
T | G | 112 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.132+1351T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531554 | ||||||
| chr15:90531596
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.132+1393T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531596 | ||||||
| chr15:90531780
|
T | A | 1 | a0002c0002t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.132+1577T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531780 | ||||||
| chr15:90531792
|
A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+1589A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531792 | ||||||
| chr15:90531821
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(137): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.132+1618C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531821 | ||||||
| chr15:90531827
|
C | T | 16 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0257others(13): Show | 16 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+1624C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531827 | ||||||
| chr15:90531883
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(138): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.132+1680A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531883 | ||||||
| chr15:90531897
|
G | A | 63 | a0001c0001t0002g0063a0002c0002t0001g0027a0002c0002t0001g0064others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.132+1694G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90531897 | ||||||
| chr15:90532143
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(76): Show | 82 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.132+1940C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532143 | ||||||
| chr15:90532146
|
G | A | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.132+1943G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532146 | ||||||
| chr15:90532282
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.132+2079G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532282 | ||||||
| chr15:90532303
|
C | T | 62 | a0001c0001t0002g0063a0002c0002t0001g0027a0002c0002t0001g0064others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.132+2100C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532303 | ||||||
| chr15:90532356
|
C | G | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+2153C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532356 | ||||||
| chr15:90532377
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.132+2174T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532377 | ||||||
| chr15:90532570
|
A | G | 13 | a0001c0001t0046g0020a0002c0002t0012g0136a0002c0002t0012g0138others(10): Show | 13 | HG01346.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+2367A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532570 | ||||||
| chr15:90532692
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.132+2489A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532692 | ||||||
| chr15:90532707
|
G | T | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+2504G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532707 | ||||||
| chr15:90532758
|
G | A | 1 | a0002c0002t0003g0062 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.132+2555G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532758 | ||||||
| chr15:90532796
|
G | A | 78 | a0001c0001t0002g0063a0001c0001t0046g0020a0002c0002t0001g0027others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.132+2593G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532796 | ||||||
| chr15:90532977
|
C | T | 1 | a0002c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.132+2774C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90532977 | ||||||
| chr15:90533084
|
C | CA | 43 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0165others(40): Show | 43 | HG00544.hp2 HG00597.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.132+2918dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
C | CAA | 17 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(14): Show | 17 | HG00558.hp1 HG00735.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.132+2917_132+2918d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0001g0036a0001c0001t0010g0035a0001c0001t0011g0030others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.132+2909_132+2918d others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(4): Show |
C | 39 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.132+2908_132+2918d others(13): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(5): Show |
C | 56 | a0001c0001t0001g0059a0001c0001t0035g0061a0002c0002t0001g0027others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+2907_132+2918d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0046g0020a0002c0002t0001g0116a0002c0002t0001g0117others(1): Show | 4 | HG01167.hp1 HG01516.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2906_132+2918d others(15): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(7): Show |
C | 12 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0013g0131others(9): Show | 12 | HG01346.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+2905_132+2918d others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(10): Show |
C | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+2902_132+2918d others(19): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0009g0195a0003c0003t0001g0060 | 2 | HG01099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.132+2900_132+2918d others(21): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(16): Show |
C | 1 | a0002c0002t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.132+2896_132+2918d others(25): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533084
|
CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.132+2895_132+2918d others(26): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533084 | |||||
| chr15:90533169
|
C | T | 60 | a0001c0001t0002g0063a0002c0002t0001g0027a0002c0002t0001g0064others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.132+2966C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533169 | ||||||
| chr15:90533172
|
G | A | 3 | a0002c0002t0013g0131a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.132+2969G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533172 | ||||||
| chr15:90533397
|
G | A | 1 | a0001c0001t0016g0168 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.132+3194G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533397 | ||||||
| chr15:90533420
|
A | AG | 76 | a0001c0001t0002g0063a0001c0001t0046g0020a0002c0002t0001g0027others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.132+3219dupG | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533420 | |||||
| chr15:90533421
|
G | GA | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(93): Show | 99 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.132+3218_132+3219i others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533421 | ||||||
| chr15:90533422
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(94): Show | 100 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.132+3219G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533422 | ||||||
| chr15:90533422
|
GA | G | 43 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.132+3234delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90533422 | |||||
| chr15:90533423
|
A | G | 1 | a0004c0005t0045g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.132+3220A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533423 | ||||||
| chr15:90533461
|
G | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+3258G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533461 | ||||||
| chr15:90533496
|
A | G | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.132+3293A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533496 | ||||||
| chr15:90533523
|
C | T | 7 | a0002c0002t0001g0027a0002c0002t0001g0113a0002c0002t0001g0117others(4): Show | 7 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+3320C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533523 | ||||||
| chr15:90533574
|
A | T | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132+3371A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533574 | ||||||
| chr15:90533688
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.132+3485C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533688 | ||||||
| chr15:90533874
|
T | G | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132+3671T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533874 | ||||||
| chr15:90533889
|
G | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+3686G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533889 | ||||||
| chr15:90533914
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0223 | 4 | HG01106.hp2 HG01123.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+3711C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90533914 | ||||||
| chr15:90534104
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.132+3901G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534104 | ||||||
| chr15:90534398
|
G | A | 1 | a0003c0003t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.132+4195G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534398 | ||||||
| chr15:90534402
|
G | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+4199G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534402 | ||||||
| chr15:90534428
|
A | G | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.132+4225A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534428 | ||||||
| chr15:90534503
|
G | C | 3 | a0001c0001t0001g0121a0001c0001t0007g0120a0002c0002t0003g0024 | 3 | HG01109.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.132+4300G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534503 | ||||||
| chr15:90534561
|
A | AGTTGGTT others(1): Show |
77 | a0001c0001t0002g0063a0001c0001t0046g0020a0002c0002t0001g0027others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.132+4370_132+4377d others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90534561 | |||||
| chr15:90534561
|
A | AGTTGGTT others(5): Show |
1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+4366_132+4377d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90534561 | |||||
| chr15:90534577
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(96): Show | 102 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.132+4374G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534577 | ||||||
| chr15:90534590
|
G | A | 123 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.132+4387G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534590 | ||||||
| chr15:90534597
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.132+4394A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534597 | ||||||
| chr15:90534682
|
T | C | 1 | a0002c0002t0003g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.132+4479T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534682 | ||||||
| chr15:90534894
|
T | C | 2 | a0002c0002t0007g0130a0002c0002t0015g0026 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.132+4691T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534894 | ||||||
| chr15:90534895
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.132+4692C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534895 | ||||||
| chr15:90534895
|
C | G | 1 | a0001c0001t0002g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.132+4692C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534895 | ||||||
| chr15:90534941
|
C | T | 3 | a0001c0001t0010g0141a0001c0001t0010g0142a0001c0001t0040g0023 | 3 | HG02451.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+4738C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90534941 | ||||||
| chr15:90535161
|
CA | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.133-4859delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90535161 | |||||
| chr15:90535173
|
A | T | 78 | a0001c0001t0002g0063a0001c0001t0046g0020a0002c0002t0001g0027others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-4866A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535173 | ||||||
| chr15:90535434
|
C | T | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133-4605C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535434 | ||||||
| chr15:90535571
|
A | C | 59 | a0001c0001t0002g0063a0002c0002t0001g0027a0002c0002t0001g0064others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.133-4468A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535571 | ||||||
| chr15:90535583
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.133-4456A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535583 | ||||||
| chr15:90535674
|
C | CA | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.133-4364dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90535674 | |||||
| chr15:90535695
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.133-4344C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535695 | ||||||
| chr15:90535892
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.133-4147T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535892 | ||||||
| chr15:90535906
|
G | C | 1 | a0001c0001t0002g0169 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.133-4133G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90535906 | ||||||
| chr15:90536060
|
A | C | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133-3979A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536060 | ||||||
| chr15:90536233
|
G | C | 121 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.133-3806G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536233 | ||||||
| chr15:90536352
|
A | G | 11 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(8): Show | 11 | HG00099.hp1 HG00544.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-3687A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536352 | ||||||
| chr15:90536369
|
T | TA | 8 | a0001c0001t0001g0123a0001c0001t0001g0170a0001c0001t0001g0226others(5): Show | 8 | HG01261.hp2 HG01433.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-3658dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90536369 | |||||
| chr15:90536405
|
C | T | 78 | a0001c0001t0002g0063a0001c0001t0046g0020a0002c0002t0001g0027others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-3634C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536405 | ||||||
| chr15:90536490
|
C | CA | 12 | a0001c0001t0001g0001a0001c0001t0001g0223a0001c0001t0019g0028others(9): Show | 14 | HG01106.hp2 HG01123.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.133-3534dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90536490 | |||||
| chr15:90536490
|
C | CAA | 70 | a0001c0001t0002g0063a0002c0002t0001g0027a0002c0002t0001g0064others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.133-3535_133-3534d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90536490 | |||||
| chr15:90536631
|
A | C | 124 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.133-3408A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536631 | ||||||
| chr15:90536688
|
A | G | 124 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.133-3351A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536688 | ||||||
| chr15:90536690
|
G | C | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133-3349G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536690 | ||||||
| chr15:90536769
|
G | A | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.133-3270G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536769 | ||||||
| chr15:90536876
|
G | A | 43 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.133-3163G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536876 | ||||||
| chr15:90536892
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.133-3147A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90536892 | ||||||
| chr15:90537071
|
G | A | 43 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.133-2968G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537071 | ||||||
| chr15:90537151
|
C | A | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133-2888C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537151 | ||||||
| chr15:90537155
|
A | G | 78 | a0001c0001t0046g0020a0002c0002t0001g0027a0002c0002t0001g0064others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-2884A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537155 | ||||||
| chr15:90537240
|
T | TAAG | 123 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.133-2798_133-2796d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90537240 | |||||
| chr15:90537280
|
G | A | 59 | a0002c0002t0001g0027a0002c0002t0001g0064a0002c0002t0001g0066others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.133-2759G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537280 | ||||||
| chr15:90537319
|
G | A | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133-2720G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537319 | ||||||
| chr15:90537321
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.133-2718G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537321 | ||||||
| chr15:90537377
|
G | C | 2 | a0002c0002t0004g0111a0002c0002t0004g0112 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.133-2662G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537377 | ||||||
| chr15:90537397
|
T | C | 1 | a0002c0002t0001g0064 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.133-2642T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537397 | ||||||
| chr15:90537414
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133-2625C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537414 | ||||||
| chr15:90537452
|
C | T | 3 | a0001c0001t0010g0141a0001c0001t0010g0142a0001c0001t0040g0023 | 3 | HG02451.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.133-2587C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537452 | ||||||
| chr15:90537519
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0152others(79): Show | 85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.133-2520G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537519 | ||||||
| chr15:90537544
|
T | C | 123 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.133-2495T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537544 | ||||||
| chr15:90537588
|
C | G | 124 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.133-2451C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537588 | ||||||
| chr15:90537605
|
C | T | 1 | a0001c0001t0042g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.133-2434C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537605 | ||||||
| chr15:90537613
|
T | C | 4 | a0001c0001t0046g0020a0002c0002t0013g0131a0002c0002t0044g0021others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-2426T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537613 | ||||||
| chr15:90537654
|
G | A | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.133-2385G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537654 | ||||||
| chr15:90537740
|
T | A | 1 | a0001c0015t0029g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133-2299T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537740 | ||||||
| chr15:90537789
|
T | C | 123 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.133-2250T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537789 | ||||||
| chr15:90537964
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133-2075G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537964 | ||||||
| chr15:90537984
|
G | A | 1 | a0003c0003t0003g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.133-2055G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90537984 | ||||||
| chr15:90538312
|
C | T | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133-1727C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538312 | ||||||
| chr15:90538314
|
C | G | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0261others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-1725C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538314 | ||||||
| chr15:90538333
|
A | ACT | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.133-1705_133-1704i others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90538333 | |||||
| chr15:90538559
|
G | T | 123 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.133-1480G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538559 | ||||||
| chr15:90538645
|
A | AGAT | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 103 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.133-1392_133-1390d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90538645 | |||||
| chr15:90538660
|
A | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133-1379A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538660 | ||||||
| chr15:90538767
|
C | G | 1 | a0004c0005t0045g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.133-1272C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538767 | ||||||
| chr15:90538773
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(113): Show | 119 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.133-1252dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90538773 | |||||
| chr15:90538773
|
C | CTT | 19 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(16): Show | 19 | HG00099.hp1 HG00544.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.133-1253_133-1252d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90538773 | |||||
| chr15:90538773
|
C | CTTT | 67 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.133-1254_133-1252d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr15 | 90538773 | |||||
| chr15:90538986
|
G | A | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133-1053G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90538986 | ||||||
| chr15:90539300
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.133-739A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539300 | ||||||
| chr15:90539321
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.133-718G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539321 | ||||||
| chr15:90539415
|
T | A | 3 | a0002c0002t0013g0131a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.133-624T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539415 | ||||||
| chr15:90539423
|
A | AG | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.133-616_133-615ins others(1): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539423 | ||||||
| chr15:90539499
|
C | T | 1 | a0002c0002t0022g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133-540C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539499 | ||||||
| chr15:90539607
|
G | C | 1 | a0004c0005t0045g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.133-432G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539607 | ||||||
| chr15:90539637
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.133-402T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539637 | ||||||
| chr15:90539773
|
C | A | 2 | a0002c0002t0014g0134a0002c0002t0014g0135 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.133-266C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539773 | ||||||
| chr15:90539954
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(77): Show | 83 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.133-85C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539954 | ||||||
| chr15:90539973
|
A | G | 1 | a0001c0001t0003g0167 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.133-66A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 1/14 | chr15 | 90539973 | ||||||
| chr15:90540430
|
C | G | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+293C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90540430 | ||||||
| chr15:90540477
|
TTAAA | T | 42 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.231+346_231+349del others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90540477 | |||||
| chr15:90540571
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18960.hp2 NA18966.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.231+434G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90540571 | ||||||
| chr15:90540849
|
A | T | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.231+712A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90540849 | ||||||
| chr15:90541264
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231+1127G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541264 | ||||||
| chr15:90541277
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.231+1140C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541277 | ||||||
| chr15:90541358
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+1221A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541358 | ||||||
| chr15:90541400
|
A | G | 64 | a0002c0002t0001g0027a0002c0002t0001g0064a0002c0002t0001g0066others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.231+1263A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541400 | ||||||
| chr15:90541459
|
T | C | 1 | a0003c0003t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.231+1322T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541459 | ||||||
| chr15:90541767
|
G | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0004t0005g0004others(4): Show | 7 | HG00323.hp2 NA18940.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+1630G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541767 | ||||||
| chr15:90541782
|
C | CT | 127 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.231+1652dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90541782 | |||||
| chr15:90541782
|
C | CTT | 8 | a0001c0001t0006g0051a0001c0001t0010g0035a0001c0001t0011g0030others(5): Show | 8 | HG01496.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+1651_231+1652d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90541782 | |||||
| chr15:90541789
|
TC | T | 20 | a0001c0001t0001g0229a0001c0001t0001g0257a0001c0001t0001g0258others(17): Show | 20 | HG01074.hp2 HG01346.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.231+1653delC | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541789 | ||||||
| chr15:90541790
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.231+1653C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541790 | ||||||
| chr15:90541846
|
T | C | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.231+1709T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90541846 | ||||||
| chr15:90542181
|
A | AT | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0170others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.231+2059dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90542181 | |||||
| chr15:90542181
|
AT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(88): Show | 94 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.231+2059delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90542181 | |||||
| chr15:90542324
|
G | A | 2 | a0001c0001t0006g0260a0003c0003t0001g0266 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.231+2187G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542324 | ||||||
| chr15:90542409
|
C | T | 2 | a0002c0002t0001g0075a0002c0002t0001g0105 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.231+2272C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542409 | ||||||
| chr15:90542426
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.231+2289A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542426 | ||||||
| chr15:90542435
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0171 | 2 | NA18955.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.231+2298T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542435 | ||||||
| chr15:90542719
|
T | C | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+2582T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542719 | ||||||
| chr15:90542792
|
C | T | 2 | a0002c0002t0007g0130a0002c0002t0015g0026 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.231+2655C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542792 | ||||||
| chr15:90542855
|
T | C | 3 | a0001c0001t0046g0020a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+2718T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542855 | ||||||
| chr15:90542966
|
A | T | 1 | a0001c0001t0006g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.231+2829A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90542966 | ||||||
| chr15:90543072
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.231+2935A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543072 | ||||||
| chr15:90543074
|
A | C | 40 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.231+2937A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543074 | ||||||
| chr15:90543081
|
G | A | 2 | a0002c0002t0044g0021a0004c0005t0045g0132 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.231+2944G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543081 | ||||||
| chr15:90543132
|
C | T | 2 | a0001c0001t0019g0028a0008c0012t0021g0029 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.231+2995C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543132 | ||||||
| chr15:90543134
|
G | GA | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(122): Show | 128 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.231+3012dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90543134 | |||||
| chr15:90543134
|
G | GAA | 73 | a0001c0001t0001g0197a0001c0001t0037g0139a0002c0002t0001g0027others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.231+3011_231+3012d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90543134 | |||||
| chr15:90543197
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.231+3060C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543197 | ||||||
| chr15:90543252
|
C | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.231+3115C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543252 | ||||||
| chr15:90543300
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0043others(78): Show | 84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.231+3182dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90543300 | |||||
| chr15:90543300
|
C | CAA | 116 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.231+3181_231+3182d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90543300 | |||||
| chr15:90543332
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.231+3195G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543332 | ||||||
| chr15:90543452
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.231+3315C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543452 | ||||||
| chr15:90543486
|
A | G | 1 | a0002c0002t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.231+3349A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543486 | ||||||
| chr15:90543508
|
A | G | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+3371A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543508 | ||||||
| chr15:90543589
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.231+3452G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543589 | ||||||
| chr15:90543636
|
T | G | 43 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.231+3499T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543636 | ||||||
| chr15:90543833
|
A | T | 1 | a0002c0002t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.231+3696A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90543833 | ||||||
| chr15:90544003
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.231+3866G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544003 | ||||||
| chr15:90544140
|
T | C | 81 | a0001c0001t0011g0140a0001c0001t0019g0028a0001c0001t0037g0139others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.231+4003T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544140 | ||||||
| chr15:90544180
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231+4043C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544180 | ||||||
| chr15:90544242
|
C | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+4105C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544242 | ||||||
| chr15:90544295
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0254a0002c0002t0007g0130others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+4158C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544295 | ||||||
| chr15:90544713
|
C | G | 1 | a0002c0002t0018g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.231+4576C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544713 | ||||||
| chr15:90544755
|
A | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+4618A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544755 | ||||||
| chr15:90544771
|
T | C | 2 | a0002c0002t0013g0194a0002c0002t0018g0119 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.231+4634T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90544771 | ||||||
| chr15:90545079
|
T | C | 5 | a0001c0001t0046g0020a0002c0002t0013g0131a0002c0002t0044g0021others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+4942T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545079 | ||||||
| chr15:90545123
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0254a0002c0002t0015g0026others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+4986G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545123 | ||||||
| chr15:90545192
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.231+5055G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545192 | ||||||
| chr15:90545364
|
G | A | 6 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(3): Show | 6 | HG00140.hp2 HG00323.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+5227G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545364 | ||||||
| chr15:90545400
|
A | AT | 102 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.231+5280dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90545400 | |||||
| chr15:90545400
|
A | ATT | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0197others(78): Show | 84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.231+5279_231+5280d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90545400 | |||||
| chr15:90545400
|
AT | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 17 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.231+5280delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90545400 | |||||
| chr15:90545420
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.231+5283G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545420 | ||||||
| chr15:90545430
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.231+5293C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545430 | ||||||
| chr15:90545447
|
T | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.231+5310T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545447 | ||||||
| chr15:90545479
|
T | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.231+5342T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545479 | ||||||
| chr15:90545536
|
T | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.231+5399T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545536 | ||||||
| chr15:90545546
|
C | T | 2 | a0001c0001t0001g0248a0003c0003t0003g0247 | 2 | NA18954.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.231+5409C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545546 | ||||||
| chr15:90545547
|
G | A | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.231+5410G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545547 | ||||||
| chr15:90545576
|
G | GC | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+5439_231+5440i others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545576 | ||||||
| chr15:90545576
|
G | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+5439G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545576 | ||||||
| chr15:90545629
|
T | C | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.231+5492T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545629 | ||||||
| chr15:90545652
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0044others(84): Show | 90 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.231+5515C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545652 | ||||||
| chr15:90545669
|
T | G | 1 | a0001c0001t0002g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231+5532T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545669 | ||||||
| chr15:90545708
|
C | G | 2 | a0001c0001t0001g0252a0003c0014t0030g0253 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.231+5571C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545708 | ||||||
| chr15:90545722
|
A | G | 1 | a0001c0007t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.231+5585A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545722 | ||||||
| chr15:90545725
|
T | C | 1 | a0001c0007t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.231+5588T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545725 | ||||||
| chr15:90545734
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0016g0168 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.231+5597G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545734 | ||||||
| chr15:90545743
|
AT | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.231+5614delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90545743 | |||||
| chr15:90545763
|
A | G | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.231+5626A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545763 | ||||||
| chr15:90545768
|
C | T | 13 | a0001c0001t0001g0049a0001c0001t0001g0254a0001c0001t0003g0255others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+5631C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545768 | ||||||
| chr15:90545779
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.231+5642T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545779 | ||||||
| chr15:90545780
|
G | A | 1 | a0001c0007t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.231+5643G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545780 | ||||||
| chr15:90545785
|
A | C | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+5648A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545785 | ||||||
| chr15:90545786
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.231+5649G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545786 | ||||||
| chr15:90545790
|
G | A | 1 | a0003c0003t0027g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.231+5653G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545790 | ||||||
| chr15:90545793
|
T | G | 1 | a0002c0002t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.231+5656T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545793 | ||||||
| chr15:90545799
|
C | T | 1 | a0002c0002t0004g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.231+5662C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545799 | ||||||
| chr15:90545800
|
C | A | 4 | a0002c0002t0002g0073a0002c0002t0004g0111a0002c0002t0004g0112others(1): Show | 4 | HG01257.hp2 HG01258.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+5663C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545800 | ||||||
| chr15:90545800
|
C | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0036others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.231+5663C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545800 | ||||||
| chr15:90545802
|
T | A | 1 | a0002c0002t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.231+5665T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545802 | ||||||
| chr15:90545811
|
T | C | 7 | a0001c0001t0032g0033a0002c0002t0001g0071a0002c0002t0004g0111others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+5674T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545811 | ||||||
| chr15:90545812
|
T | A | 2 | a0002c0002t0004g0111a0002c0002t0004g0112 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.231+5675T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545812 | ||||||
| chr15:90545813
|
T | C | 4 | a0001c0001t0032g0033a0002c0002t0004g0111a0002c0002t0004g0112others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+5676T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545813 | ||||||
| chr15:90545813
|
T | G | 1 | a0002c0002t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.231+5676T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545813 | ||||||
| chr15:90545820
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.231+5683C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545820 | ||||||
| chr15:90545821
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0002t0001g0080 | 3 | HG03239.hp2 NA18941.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.231+5684G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545821 | ||||||
| chr15:90545825
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(1): Show | 4 | HG01884.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+5688G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545825 | ||||||
| chr15:90545829
|
T | C | 3 | a0002c0002t0001g0071a0002c0002t0001g0080a0002c0002t0007g0130 | 3 | HG01261.hp2 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.231+5692T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545829 | ||||||
| chr15:90545830
|
G | A | 2 | a0002c0002t0001g0071a0002c0002t0001g0080 | 2 | HG01261.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.231+5693G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545830 | ||||||
| chr15:90545839
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.231+5702A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545839 | ||||||
| chr15:90545839
|
A | G | 2 | a0002c0002t0001g0118a0002c0002t0007g0130 | 2 | HG00323.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.231+5702A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545839 | ||||||
| chr15:90545858
|
G | A | 1 | a0003c0003t0027g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.231+5721G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545858 | ||||||
| chr15:90545859
|
T | C | 1 | a0003c0003t0001g0234 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.231+5722T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545859 | ||||||
| chr15:90545862
|
G | A | 1 | a0002c0002t0028g0081 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.231+5725G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545862 | ||||||
| chr15:90545867
|
T | C | 5 | a0002c0002t0001g0077a0002c0002t0001g0082a0002c0002t0003g0078others(2): Show | 5 | HG01346.hp2 HG02027.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+5730T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545867 | ||||||
| chr15:90545869
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.231+5732C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545869 | ||||||
| chr15:90545870
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0152others(4): Show | 7 | HG02300.hp1 NA18940.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+5733G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545870 | ||||||
| chr15:90545873
|
T | C | 6 | a0001c0001t0009g0195a0001c0001t0010g0141a0001c0001t0010g0142others(3): Show | 6 | HG01346.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+5736T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545873 | ||||||
| chr15:90545940
|
T | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+5803T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90545940 | ||||||
| chr15:90546025
|
G | A | 34 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(31): Show | 34 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.231+5888G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546025 | ||||||
| chr15:90546174
|
G | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+6037G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546174 | ||||||
| chr15:90546199
|
T | C | 1 | a0001c0001t0025g0188 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.231+6062T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546199 | ||||||
| chr15:90546309
|
A | G | 4 | a0001c0001t0019g0028a0001c0001t0040g0023a0003c0014t0030g0253others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+6172A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546309 | ||||||
| chr15:90546379
|
T | C | 1 | a0002c0002t0022g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.231+6242T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546379 | ||||||
| chr15:90546401
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(170): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.231+6264A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546401 | ||||||
| chr15:90546584
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.231+6447G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546584 | ||||||
| chr15:90546694
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.231+6557C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546694 | ||||||
| chr15:90546713
|
C | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.231+6576C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546713 | ||||||
| chr15:90546772
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.231+6635G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546772 | ||||||
| chr15:90546807
|
T | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(70): Show | 76 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.231+6670T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546807 | ||||||
| chr15:90546870
|
G | A | 1 | a0002c0002t0003g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.231+6733G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546870 | ||||||
| chr15:90546903
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(77): Show | 83 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.231+6766G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90546903 | ||||||
| chr15:90547112
|
T | C | 2 | a0002c0002t0001g0072a0002c0002t0001g0087 | 2 | HG01433.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.231+6975T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547112 | ||||||
| chr15:90547149
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.231+7012G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547149 | ||||||
| chr15:90547153
|
C | T | 1 | a0001c0001t0007g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.231+7016C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547153 | ||||||
| chr15:90547162
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(198): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.231+7025C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547162 | ||||||
| chr15:90547277
|
A | G | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+7140A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547277 | ||||||
| chr15:90547279
|
T | C | 1 | a0001c0001t0041g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.231+7142T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547279 | ||||||
| chr15:90547536
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.231+7399G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547536 | ||||||
| chr15:90547630
|
G | A | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.231+7493G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547630 | ||||||
| chr15:90547654
|
G | T | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+7517G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547654 | ||||||
| chr15:90547655
|
C | A | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+7518C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547655 | ||||||
| chr15:90547729
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.231+7592A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547729 | ||||||
| chr15:90547790
|
A | G | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+7653A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547790 | ||||||
| chr15:90547883
|
C | T | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+7746C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547883 | ||||||
| chr15:90547889
|
CT | C | 55 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.231+7772delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90547889 | |||||
| chr15:90547889
|
CTT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.231+7771_231+7772d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90547889 | |||||
| chr15:90547918
|
G | T | 2 | a0001c0006t0003g0148a0001c0006t0003g0149 | 2 | HG03239.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.231+7781G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90547918 | ||||||
| chr15:90548050
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+7913C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548050 | ||||||
| chr15:90548112
|
C | T | 1 | a0001c0001t0024g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.231+7975C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548112 | ||||||
| chr15:90548165
|
AG | A | 53 | a0001c0001t0001g0049a0001c0001t0001g0249a0001c0001t0001g0250others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.231+8030delG | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90548165 | |||||
| chr15:90548190
|
C | T | 1 | a0002c0002t0015g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.231+8053C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548190 | ||||||
| chr15:90548390
|
G | A | 2 | a0002c0002t0003g0024a0003c0003t0001g0266 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.231+8253G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548390 | ||||||
| chr15:90548708
|
C | T | 4 | a0001c0001t0019g0028a0001c0001t0040g0023a0003c0014t0030g0253others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+8571C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548708 | ||||||
| chr15:90548761
|
A | T | 66 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0235others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231+8624A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548761 | ||||||
| chr15:90548766
|
A | G | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.231+8629A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90548766 | ||||||
| chr15:90549138
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+9001A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549138 | ||||||
| chr15:90549145
|
T | C | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+9008T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549145 | ||||||
| chr15:90549249
|
C | A | 1 | a0002c0002t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.231+9112C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549249 | ||||||
| chr15:90549285
|
GGT | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(193): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.231+9167_231+9168d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90549285 | |||||
| chr15:90549472
|
C | T | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+9335C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549472 | ||||||
| chr15:90549704
|
CT | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(196): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.231+9584delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90549704 | |||||
| chr15:90549781
|
C | T | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+9644C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549781 | ||||||
| chr15:90549830
|
G | C | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+9693G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549830 | ||||||
| chr15:90549979
|
C | T | 6 | a0001c0001t0035g0061a0001c0001t0040g0023a0001c0001t0046g0020others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+9842C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90549979 | ||||||
| chr15:90550002
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.231+9865C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90550002 | ||||||
| chr15:90550132
|
A | G | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.231+9995A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90550132 | ||||||
| chr15:90550444
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.231+10307G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90550444 | ||||||
| chr15:90550448
|
G | GTT | 110 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.231+10323_231+1032 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90550448 | |||||
| chr15:90550448
|
G | GTTT | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(88): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.231+10322_231+1032 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90550448 | |||||
| chr15:90550690
|
C | CT | 6 | a0001c0001t0001g0180a0001c0001t0006g0260a0001c0001t0010g0141others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+10563dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90550690 | |||||
| chr15:90550832
|
T | C | 66 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0228others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231+10695T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90550832 | ||||||
| chr15:90550839
|
C | G | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.231+10702C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90550839 | ||||||
| chr15:90550858
|
G | GAGCT | 11 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(8): Show | 11 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+10722_231+1072 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90550858 | |||||
| chr15:90551052
|
G | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+10915G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551052 | ||||||
| chr15:90551057
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.231+10920G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551057 | ||||||
| chr15:90551092
|
ATAAT | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+10958_231+1096 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551092 | |||||
| chr15:90551210
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.231+11073C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551210 | ||||||
| chr15:90551341
|
G | GCT | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(206): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.231+11205_231+1120 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551341 | |||||
| chr15:90551345
|
C | T | 1 | a0002c0002t0001g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.231+11208C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551345 | ||||||
| chr15:90551364
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+11227C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551364 | ||||||
| chr15:90551376
|
A | G | 13 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0011g0030others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+11239A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551376 | ||||||
| chr15:90551394
|
A | G | 2 | a0002c0002t0001g0066a0002c0002t0003g0109 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.231+11257A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551394 | ||||||
| chr15:90551558
|
A | G | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+11421A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551558 | ||||||
| chr15:90551591
|
G | A | 1 | a0002c0002t0001g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.231+11454G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551591 | ||||||
| chr15:90551629
|
C | A | 1 | a0002c0002t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.231+11492C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551629 | ||||||
| chr15:90551800
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.231+11663A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551800 | ||||||
| chr15:90551822
|
C | CCAAAATC others(151): Show |
201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(198): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.231+11740_231+1174 others(162): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551822 | |||||
| chr15:90551822
|
C | CCAAAATC others(151): Show |
1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+11740_231+1174 others(162): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551822 | |||||
| chr15:90551822
|
C | CCAAAATC others(151): Show |
1 | a0001c0001t0002g0251 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.231+11739_231+1174 others(162): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551822 | |||||
| chr15:90551878
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.231+11741T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551878 | ||||||
| chr15:90551898
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+11761C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551898 | ||||||
| chr15:90551919
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.231+11782A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551919 | ||||||
| chr15:90551932
|
ACACACAC others(5): Show |
A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+11807_231+1181 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551932 | |||||
| chr15:90551934
|
ACACACAC others(3): Show |
A | 2 | a0001c0001t0032g0033a0002c0002t0007g0130 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.231+11807_231+1181 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551934 | |||||
| chr15:90551936
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.231+11799A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551936 | ||||||
| chr15:90551936
|
ACACACAC others(1): Show |
A | 13 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0011g0030others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+11807_231+1181 others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551936 | |||||
| chr15:90551938
|
ACACACG | A | 10 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(7): Show | 10 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+11807_231+1181 others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551938 | |||||
| chr15:90551942
|
ACG | A | 3 | a0001c0001t0046g0020a0002c0002t0004g0114a0002c0002t0044g0021 | 3 | HG02559.hp2 HG03209.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.231+11807_231+1180 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551942 | |||||
| chr15:90551944
|
G | A | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+11807G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551944 | ||||||
| chr15:90551944
|
G | GCA | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(86): Show | 92 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.231+11830_231+1183 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551944
|
G | GCACA | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0248others(1): Show | 4 | HG01993.hp2 HG02109.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+11828_231+1183 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551944
|
G | GCGCACAC others(3): Show |
1 | a0001c0004t0005g0005 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.231+11808_231+1180 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551944
|
G | GCGCACAC others(5): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.231+11808_231+1180 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551944
|
G | GCGCGCAC others(5): Show |
1 | a0001c0004t0005g0009 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.231+11808_231+1180 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551944
|
GCACA | G | 50 | a0001c0001t0001g0228a0001c0001t0001g0235a0001c0001t0001g0249others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.231+11828_231+1183 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90551944 | |||||
| chr15:90551946
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0171 | 2 | NA18955.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.231+11809A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90551946 | ||||||
| chr15:90552248
|
C | T | 1 | a0001c0001t0006g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.231+12111C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552248 | ||||||
| chr15:90552262
|
G | A | 2 | a0002c0002t0044g0021a0008c0012t0021g0029 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.231+12125G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552262 | ||||||
| chr15:90552476
|
G | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+12339G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552476 | ||||||
| chr15:90552479
|
C | T | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.231+12342C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552479 | ||||||
| chr15:90552500
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.231+12363G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552500 | ||||||
| chr15:90552551
|
TC | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.231+12417delC | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90552551 | |||||
| chr15:90552638
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.231+12501A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552638 | ||||||
| chr15:90552816
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+12679C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552816 | ||||||
| chr15:90552843
|
G | T | 2 | a0001c0001t0001g0177a0001c0001t0002g0151 | 2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.231+12706G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552843 | ||||||
| chr15:90552974
|
C | T | 2 | a0001c0006t0003g0148a0001c0006t0003g0149 | 2 | HG03239.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.231+12837C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552974 | ||||||
| chr15:90552984
|
C | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+12847C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90552984 | ||||||
| chr15:90553215
|
G | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+13078G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553215 | ||||||
| chr15:90553232
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.231+13095T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553232 | ||||||
| chr15:90553482
|
C | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+13345C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553482 | ||||||
| chr15:90553555
|
A | C | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+13418A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553555 | ||||||
| chr15:90553683
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.231+13546T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553683 | ||||||
| chr15:90553695
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.231+13558A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553695 | ||||||
| chr15:90553710
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.231+13573G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553710 | ||||||
| chr15:90553886
|
G | T | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.231+13749G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553886 | ||||||
| chr15:90553923
|
G | A | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+13786G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553923 | ||||||
| chr15:90553929
|
A | G | 3 | a0002c0002t0001g0067a0002c0002t0001g0071a0002c0002t0001g0096 | 3 | HG01071.hp2 HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.231+13792A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90553929 | ||||||
| chr15:90554092
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+13955G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554092 | ||||||
| chr15:90554155
|
C | T | 2 | a0001c0001t0040g0023a0004c0005t0045g0132 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.231+14018C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554155 | ||||||
| chr15:90554157
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+14020C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554157 | ||||||
| chr15:90554169
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.231+14032T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554169 | ||||||
| chr15:90554206
|
C | CT | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0035g0061others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+14084dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90554206 | |||||
| chr15:90554279
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.231+14142C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554279 | ||||||
| chr15:90554404
|
T | C | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+14267T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554404 | ||||||
| chr15:90554569
|
G | A | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+14432G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554569 | ||||||
| chr15:90554732
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.231+14595A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554732 | ||||||
| chr15:90554754
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.231+14617G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554754 | ||||||
| chr15:90554875
|
A | G | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+14738A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90554875 | ||||||
| chr15:90555106
|
T | A | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.231+14969T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555106 | ||||||
| chr15:90555132
|
G | A | 3 | a0001c0001t0003g0167a0001c0001t0041g0172a0001c0004t0034g0156 | 3 | HG02129.hp2 NA18944.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.231+14995G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555132 | ||||||
| chr15:90555386
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.231+15249A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555386 | ||||||
| chr15:90555400
|
G | A | 3 | a0001c0001t0035g0061a0001c0001t0046g0020a0002c0002t0044g0021 | 3 | HG02559.hp2 HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.231+15263G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555400 | ||||||
| chr15:90555423
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+15286A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555423 | ||||||
| chr15:90555483
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.231+15346C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555483 | ||||||
| chr15:90555768
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.231+15631T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555768 | ||||||
| chr15:90555779
|
A | C | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.231+15642A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555779 | ||||||
| chr15:90555825
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.231+15688C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555825 | ||||||
| chr15:90555924
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.231+15787T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555924 | ||||||
| chr15:90555932
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.231+15795C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555932 | ||||||
| chr15:90555973
|
A | G | 1 | a0001c0001t0019g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.231+15836A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555973 | ||||||
| chr15:90555984
|
G | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.231+15847G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90555984 | ||||||
| chr15:90556056
|
A | G | 1 | a0002c0002t0015g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.231+15919A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556056 | ||||||
| chr15:90556103
|
A | T | 4 | a0001c0001t0019g0028a0001c0001t0040g0023a0003c0014t0030g0253others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+15966A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556103 | ||||||
| chr15:90556106
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.231+15969A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556106 | ||||||
| chr15:90556117
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+15980C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556117 | ||||||
| chr15:90556382
|
A | G | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+16245A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556382 | ||||||
| chr15:90556406
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.231+16269A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556406 | ||||||
| chr15:90556415
|
G | A | 4 | a0001c0001t0019g0028a0001c0001t0040g0023a0003c0014t0030g0253others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+16278G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556415 | ||||||
| chr15:90556578
|
G | A | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.231+16441G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556578 | ||||||
| chr15:90556958
|
C | CTA | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(21): Show | 24 | HG00438.hp1 HG00597.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+16861_231+1686 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
C | CTATA | 23 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0002g0146others(20): Show | 23 | HG00558.hp1 HG01081.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.231+16859_231+1686 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
C | CTATATAT others(1): Show |
5 | a0001c0001t0002g0230a0001c0001t0002g0238a0002c0002t0002g0065others(2): Show | 5 | HG01192.hp1 HG02300.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+16855_231+1686 others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTA | C | 17 | a0001c0001t0001g0122a0001c0001t0001g0200a0001c0001t0001g0254others(14): Show | 17 | HG00323.hp2 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.231+16861_231+1686 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATA | C | 7 | a0001c0001t0001g0121a0001c0001t0002g0183a0001c0001t0003g0173others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+16859_231+1686 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATA | C | 5 | a0001c0001t0001g0189a0001c0001t0011g0034a0001c0001t0024g0154others(2): Show | 5 | HG01433.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+16857_231+1686 others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(1): Show |
C | 4 | a0001c0001t0004g0256a0002c0002t0004g0111a0002c0002t0004g0112others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+16855_231+1686 others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(3): Show |
C | 3 | a0001c0001t0001g0187a0001c0001t0006g0051a0001c0001t0019g0028 | 3 | HG02258.hp1 HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.231+16853_231+1686 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(5): Show |
C | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0006g0050others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+16851_231+1686 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(7): Show |
C | 4 | a0001c0001t0009g0041a0001c0001t0010g0035a0003c0003t0009g0032others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+16849_231+1686 others(18): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(9): Show |
C | 11 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0127others(8): Show | 11 | HG01070.hp1 HG01255.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+16847_231+1686 others(20): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(11): Show |
C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(128): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.231+16845_231+1686 others(22): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556958
|
CTATATAT others(17): Show |
C | 3 | a0001c0006t0003g0149a0002c0002t0001g0066a0002c0002t0003g0109 | 3 | HG03492.hp2 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.231+16839_231+1686 others(28): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90556958 | |||||
| chr15:90556972
|
A | C | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.231+16835A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556972 | ||||||
| chr15:90556974
|
A | C | 1 | a0004c0005t0045g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.231+16837A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90556974 | ||||||
| chr15:90557000
|
C | A | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+16863C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557000 | ||||||
| chr15:90557000
|
C | G | 12 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0006g0260others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+16863C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557000 | ||||||
| chr15:90557222
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.231+17085T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557222 | ||||||
| chr15:90557330
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.231+17193C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557330 | ||||||
| chr15:90557505
|
G | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+17368G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557505 | ||||||
| chr15:90557621
|
A | G | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+17484A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557621 | ||||||
| chr15:90557741
|
C | T | 1 | a0003c0003t0001g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.231+17604C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557741 | ||||||
| chr15:90557883
|
G | A | 1 | a0001c0004t0005g0005 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.231+17746G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557883 | ||||||
| chr15:90557969
|
G | A | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.231+17832G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90557969 | ||||||
| chr15:90558100
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0016g0168 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.231+17963G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558100 | ||||||
| chr15:90558230
|
C | T | 1 | a0001c0001t0019g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.231+18093C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558230 | ||||||
| chr15:90558329
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+18192G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558329 | ||||||
| chr15:90558391
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+18254C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558391 | ||||||
| chr15:90558518
|
A | G | 5 | a0001c0001t0006g0260a0001c0001t0010g0141a0001c0001t0010g0142others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+18381A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558518 | ||||||
| chr15:90558545
|
C | G | 2 | a0001c0001t0003g0255a0003c0003t0003g0267 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.231+18408C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558545 | ||||||
| chr15:90558682
|
C | T | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+18545C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558682 | ||||||
| chr15:90558802
|
C | T | 2 | a0001c0001t0007g0219a0003c0003t0001g0218 | 2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.231+18665C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558802 | ||||||
| chr15:90558836
|
C | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+18699C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558836 | ||||||
| chr15:90558838
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | NA18983.hp1 NA18999.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.231+18701A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558838 | ||||||
| chr15:90558913
|
G | A | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+18776G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90558913 | ||||||
| chr15:90559034
|
G | C | 1 | a0001c0001t0003g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.231+18897G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559034 | ||||||
| chr15:90559056
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0058a0002c0009t0001g0098 | 3 | HG00408.hp2 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.231+18919A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559056 | ||||||
| chr15:90559236
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0227 | 2 | NA18960.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.231+19099A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559236 | ||||||
| chr15:90559474
|
C | G | 1 | a0002c0002t0003g0062 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.231+19337C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559474 | ||||||
| chr15:90559640
|
T | C | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+19503T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559640 | ||||||
| chr15:90559643
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.231+19506G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559643 | ||||||
| chr15:90559674
|
G | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+19537G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559674 | ||||||
| chr15:90559687
|
T | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+19550T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559687 | ||||||
| chr15:90559768
|
G | T | 3 | a0002c0002t0001g0067a0002c0002t0001g0071a0002c0002t0001g0096 | 3 | HG01071.hp2 HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.231+19631G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559768 | ||||||
| chr15:90559770
|
G | A | 2 | a0001c0007t0001g0205a0003c0003t0001g0204 | 2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.231+19633G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559770 | ||||||
| chr15:90559785
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | NA18983.hp1 NA18999.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.231+19648C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559785 | ||||||
| chr15:90559864
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.231+19727A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559864 | ||||||
| chr15:90559933
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.231+19796A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90559933 | ||||||
| chr15:90560067
|
T | G | 1 | a0002c0002t0001g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.231+19930T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560067 | ||||||
| chr15:90560129
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231+19992C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560129 | ||||||
| chr15:90560254
|
G | T | 3 | a0002c0002t0038g0085a0004c0005t0001g0084a0004c0005t0003g0086 | 3 | HG02976.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.231+20117G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560254 | ||||||
| chr15:90560284
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.231+20147G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560284 | ||||||
| chr15:90560313
|
C | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+20176C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560313 | ||||||
| chr15:90560374
|
G | T | 1 | a0002c0002t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.231+20237G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560374 | ||||||
| chr15:90560449
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.231+20312G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560449 | ||||||
| chr15:90560454
|
C | T | 2 | a0002c0002t0001g0075a0002c0002t0001g0105 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.231+20317C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560454 | ||||||
| chr15:90560538
|
G | C | 1 | a0002c0002t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.231+20401G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560538 | ||||||
| chr15:90560575
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+20438G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560575 | ||||||
| chr15:90560627
|
C | T | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.231+20490C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560627 | ||||||
| chr15:90560666
|
C | G | 5 | a0001c0001t0006g0260a0001c0001t0010g0141a0001c0001t0010g0142others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+20529C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560666 | ||||||
| chr15:90560677
|
C | A | 1 | a0002c0002t0003g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.231+20540C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560677 | ||||||
| chr15:90560920
|
A | G | 1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.231+20783A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90560920 | ||||||
| chr15:90561114
|
G | A | 24 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0004g0256others(21): Show | 24 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+20977G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561114 | ||||||
| chr15:90561438
|
C | G | 3 | a0001c0001t0006g0260a0001c0001t0010g0035a0001c0015t0029g0042 | 3 | HG02109.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.231+21301C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561438 | ||||||
| chr15:90561462
|
C | G | 2 | a0001c0001t0011g0140a0001c0001t0037g0139 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.231+21325C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561462 | ||||||
| chr15:90561500
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.231+21363G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561500 | ||||||
| chr15:90561581
|
C | G | 2 | a0001c0001t0011g0140a0001c0001t0037g0139 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.231+21444C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561581 | ||||||
| chr15:90561593
|
G | C | 2 | a0001c0001t0019g0028a0002c0002t0047g0003 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.231+21456G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561593 | ||||||
| chr15:90561647
|
C | T | 4 | a0001c0001t0007g0219a0002c0002t0003g0068a0003c0003t0001g0217others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+21510C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561647 | ||||||
| chr15:90561651
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.231+21514A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561651 | ||||||
| chr15:90561780
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.231+21643A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561780 | ||||||
| chr15:90561826
|
A | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+21689A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561826 | ||||||
| chr15:90561920
|
A | T | 18 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0002g0063others(15): Show | 18 | HG00735.hp1 HG02015.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.231+21783A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561920 | ||||||
| chr15:90561972
|
C | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+21835C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561972 | ||||||
| chr15:90561977
|
C | G | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.231+21840C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90561977 | ||||||
| chr15:90562637
|
G | A | 8 | a0001c0001t0001g0207a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 8 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.231+22500G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562637 | ||||||
| chr15:90562732
|
G | C | 35 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0003g0255others(32): Show | 35 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.231+22595G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562732 | ||||||
| chr15:90562789
|
A | C | 4 | a0001c0001t0019g0028a0001c0001t0040g0023a0003c0014t0030g0253others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+22652A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562789 | ||||||
| chr15:90562829
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.231+22692G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562829 | ||||||
| chr15:90562878
|
G | T | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+22741G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562878 | ||||||
| chr15:90562914
|
C | T | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.231+22777C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562914 | ||||||
| chr15:90562973
|
T | C | 1 | a0002c0002t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.231+22836T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90562973 | ||||||
| chr15:90563029
|
C | T | 1 | a0002c0002t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.231+22892C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563029 | ||||||
| chr15:90563039
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.231+22902C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563039 | ||||||
| chr15:90563180
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(204): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.231+23043T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563180 | ||||||
| chr15:90563216
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.231+23079G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563216 | ||||||
| chr15:90563352
|
G | A | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.231+23215G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563352 | ||||||
| chr15:90563497
|
G | T | 1 | a0002c0002t0004g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.231+23360G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563497 | ||||||
| chr15:90563509
|
G | A | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231+23372G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563509 | ||||||
| chr15:90563589
|
C | A | 2 | a0001c0001t0010g0141a0001c0001t0010g0142 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.231+23452C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563589 | ||||||
| chr15:90563835
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(192): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.231+23698T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90563835 | ||||||
| chr15:90564056
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+23919A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564056 | ||||||
| chr15:90564321
|
A | G | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+24184A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564321 | ||||||
| chr15:90564351
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.231+24214C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564351 | ||||||
| chr15:90564381
|
C | T | 18 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0120others(15): Show | 18 | HG01346.hp1 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.231+24244C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564381 | ||||||
| chr15:90564420
|
G | A | 2 | a0002c0002t0013g0194a0002c0002t0018g0119 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.231+24283G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564420 | ||||||
| chr15:90564527
|
C | T | 1 | a0002c0009t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.231+24390C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564527 | ||||||
| chr15:90564556
|
G | A | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0019g0028others(7): Show | 10 | HG01496.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+24419G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564556 | ||||||
| chr15:90564562
|
A | C | 2 | a0002c0002t0013g0194a0002c0002t0018g0119 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.231+24425A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564562 | ||||||
| chr15:90564904
|
A | ACCTT | 7 | a0001c0001t0002g0163a0001c0001t0004g0256a0002c0002t0003g0062others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+24820_231+2482 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
A | ACCTTCCT others(5): Show |
1 | a0004c0005t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.231+24812_231+2482 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTT | A | 42 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0186others(39): Show | 42 | HG00558.hp1 HG01192.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.231+24820_231+2482 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(1): Show |
A | 23 | a0001c0001t0001g0177a0001c0001t0002g0146a0001c0001t0002g0151others(20): Show | 23 | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.231+24816_231+2482 others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(5): Show |
A | 10 | a0001c0001t0001g0254a0001c0001t0002g0183a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.231+24812_231+2482 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(13): Show |
A | 1 | a0001c0001t0001g0012 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.231+24804_231+2482 others(24): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(17): Show |
A | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+24800_231+2482 others(28): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(21): Show |
A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.231+24796_231+2482 others(32): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564904
|
ACCTTCCT others(25): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.231+24792_231+2482 others(36): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90564904 | |||||
| chr15:90564994
|
G | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+24857G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90564994 | ||||||
| chr15:90565086
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.231+24949A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565086 | ||||||
| chr15:90565100
|
G | A | 1 | a0002c0002t0013g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.231+24963G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565100 | ||||||
| chr15:90565352
|
A | G | 1 | a0002c0002t0001g0093 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.231+25215A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565352 | ||||||
| chr15:90565442
|
A | C | 10 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(7): Show | 10 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+25305A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565442 | ||||||
| chr15:90565467
|
T | C | 14 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+25330T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565467 | ||||||
| chr15:90565601
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0151 | 2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.231+25464G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565601 | ||||||
| chr15:90565753
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0002g0151 | 2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.231+25616G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565753 | ||||||
| chr15:90565849
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.231+25712C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565849 | ||||||
| chr15:90565857
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+25720G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565857 | ||||||
| chr15:90565878
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.231+25741A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565878 | ||||||
| chr15:90565881
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+25744A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565881 | ||||||
| chr15:90565891
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.231+25754T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565891 | ||||||
| chr15:90565899
|
T | C | 15 | a0001c0001t0002g0063a0001c0001t0003g0157a0001c0001t0003g0167others(12): Show | 15 | HG00735.hp1 HG02015.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.231+25762T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90565899 | ||||||
| chr15:90566089
|
G | A | 1 | a0003c0003t0001g0204 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.231+25952G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566089 | ||||||
| chr15:90566142
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.231+26005G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566142 | ||||||
| chr15:90566342
|
G | T | 6 | a0001c0001t0003g0255a0001c0001t0009g0195a0002c0002t0013g0194others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+26205G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566342 | ||||||
| chr15:90566379
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(207): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.231+26242G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566379 | ||||||
| chr15:90566394
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.231+26257A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566394 | ||||||
| chr15:90566551
|
T | TA | 13 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+26426dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90566551 | |||||
| chr15:90566551
|
T | TAA | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.231+26425_231+2642 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90566551 | |||||
| chr15:90566551
|
TA | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.231+26426delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90566551 | |||||
| chr15:90566708
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.231+26571C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566708 | ||||||
| chr15:90566712
|
CT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.231+26591delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90566712 | |||||
| chr15:90566750
|
G | A | 3 | a0002c0002t0001g0067a0002c0002t0001g0071a0002c0002t0001g0096 | 3 | HG01071.hp2 HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.231+26613G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566750 | ||||||
| chr15:90566835
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.231+26698C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566835 | ||||||
| chr15:90566836
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0017a0003c0003t0003g0019 | 3 | NA18964.hp2 NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.231+26699G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566836 | ||||||
| chr15:90566855
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(208): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.231+26718T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90566855 | ||||||
| chr15:90567035
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.232-26601G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567035 | ||||||
| chr15:90567099
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(207): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.232-26537T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567099 | ||||||
| chr15:90567439
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.232-26197C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567439 | ||||||
| chr15:90567479
|
C | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.232-26157C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567479 | ||||||
| chr15:90567578
|
C | T | 1 | a0002c0002t0001g0093 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.232-26058C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567578 | ||||||
| chr15:90567580
|
C | T | 21 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(18): Show | 21 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.232-26056C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567580 | ||||||
| chr15:90567691
|
A | AAAAT | 3 | a0001c0001t0001g0197a0002c0002t0013g0131a0002c0002t0014g0134 | 3 | HG01106.hp1 HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.232-25921_232-2591 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAAATAAA others(1): Show |
6 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(3): Show | 6 | HG00140.hp2 HG00323.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-25925_232-2591 others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAAATAAA others(5): Show |
7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0165others(4): Show | 7 | HG02886.hp2 HG03139.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-25929_232-2591 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAAATAAA others(9): Show |
106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(103): Show | 109 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.232-25933_232-2591 others(20): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAAATAAA others(13): Show |
25 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0052others(22): Show | 25 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.232-25937_232-2591 others(24): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAAATAAA others(17): Show |
1 | a0001c0001t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232-25941_232-2591 others(28): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | AAATAAAT others(20): Show |
1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.232-25943_232-2594 others(31): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90567691 | |||||
| chr15:90567691
|
A | ATAAATAA others(10): Show |
1 | a0001c0001t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.232-25945_232-2594 others(21): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567691 | ||||||
| chr15:90567691
|
A | T | 3 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0196 | 3 | HG01346.hp1 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-25945A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567691 | ||||||
| chr15:90567695
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232-25941T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567695 | ||||||
| chr15:90567720
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.232-25916T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567720 | ||||||
| chr15:90567914
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.232-25722C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90567914 | ||||||
| chr15:90568161
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(147): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.232-25475A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568161 | ||||||
| chr15:90568229
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-25407A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568229 | ||||||
| chr15:90568252
|
A | G | 1 | a0001c0001t0023g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.232-25384A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568252 | ||||||
| chr15:90568317
|
A | C | 10 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(7): Show | 10 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-25319A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568317 | ||||||
| chr15:90568359
|
AT | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0165a0001c0001t0001g0263others(3): Show | 6 | HG02723.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-25265delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90568359 | |||||
| chr15:90568395
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-25241T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568395 | ||||||
| chr15:90568476
|
G | C | 11 | a0001c0001t0001g0197a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-25160G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568476 | ||||||
| chr15:90568491
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(147): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.232-25145C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568491 | ||||||
| chr15:90568577
|
CTGGCCTT others(3): Show |
C | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0019g0028others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-25056_232-2504 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90568577 | |||||
| chr15:90568628
|
G | GA | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.232-25007dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90568628 | |||||
| chr15:90568662
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-24974T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568662 | ||||||
| chr15:90568730
|
C | T | 1 | a0002c0009t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.232-24906C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568730 | ||||||
| chr15:90568934
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.232-24702G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568934 | ||||||
| chr15:90568959
|
G | T | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-24677G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568959 | ||||||
| chr15:90568983
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.232-24653A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568983 | ||||||
| chr15:90568988
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.232-24648G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568988 | ||||||
| chr15:90568989
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.232-24647A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90568989 | ||||||
| chr15:90568992
|
C | CT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(137): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.232-24629dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90568992 | |||||
| chr15:90568992
|
C | CTT | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0261others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-24630_232-2462 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90568992 | |||||
| chr15:90569024
|
T | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24612T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569024 | ||||||
| chr15:90569028
|
G | A | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.232-24608G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569028 | ||||||
| chr15:90569106
|
T | G | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-24530T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569106 | ||||||
| chr15:90569189
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-24447A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569189 | ||||||
| chr15:90569243
|
G | A | 1 | a0001c0001t0010g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232-24393G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569243 | ||||||
| chr15:90569282
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-24354G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569282 | ||||||
| chr15:90569316
|
CTTT | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.232-24305_232-2430 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90569316 | |||||
| chr15:90569316
|
CTTTT | C | 15 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0009g0195others(12): Show | 15 | HG00597.hp1 HG01243.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.232-24306_232-2430 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90569316 | |||||
| chr15:90569368
|
G | A | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232-24268G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569368 | ||||||
| chr15:90569438
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.232-24198G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569438 | ||||||
| chr15:90569548
|
A | ACCTCAG | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24088_232-2408 others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569548 | ||||||
| chr15:90569550
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24086A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569550 | ||||||
| chr15:90569551
|
C | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24085C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569551 | ||||||
| chr15:90569554
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24082A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569554 | ||||||
| chr15:90569555
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24081T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569555 | ||||||
| chr15:90569560
|
G | GCCTCAGC others(179): Show |
169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.232-24076_232-2407 others(190): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569560 | ||||||
| chr15:90569571
|
G | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.232-24065G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569571 | ||||||
| chr15:90569712
|
C | T | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.232-23924C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569712 | ||||||
| chr15:90569732
|
C | T | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-23904C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569732 | ||||||
| chr15:90569903
|
C | T | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-23733C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569903 | ||||||
| chr15:90569940
|
T | C | 20 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(17): Show | 20 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-23696T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90569940 | ||||||
| chr15:90570095
|
G | C | 5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0261others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-23541G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570095 | ||||||
| chr15:90570099
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-23537T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570099 | ||||||
| chr15:90570202
|
G | C | 2 | a0001c0001t0010g0141a0001c0001t0010g0142 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.232-23434G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570202 | ||||||
| chr15:90570264
|
A | G | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-23372A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570264 | ||||||
| chr15:90570454
|
T | C | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-23182T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570454 | ||||||
| chr15:90570831
|
A | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-22805A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90570831 | ||||||
| chr15:90571123
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-22513A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90571123 | ||||||
| chr15:90571144
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(139): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.232-22492A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90571144 | ||||||
| chr15:90571503
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.232-22133T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90571503 | ||||||
| chr15:90571508
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-22128G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90571508 | ||||||
| chr15:90571950
|
T | G | 1 | a0001c0001t0025g0188 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.232-21686T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90571950 | ||||||
| chr15:90572023
|
A | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0006g0260others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-21613A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572023 | ||||||
| chr15:90572161
|
C | CA | 6 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0151others(3): Show | 6 | HG00099.hp1 HG01515.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-21455dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90572161 | |||||
| chr15:90572161
|
CA | C | 30 | a0001c0001t0001g0059a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.232-21455delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90572161 | |||||
| chr15:90572161
|
CAA | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.232-21456_232-2145 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90572161 | |||||
| chr15:90572161
|
CAAA | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(131): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.232-21457_232-2145 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90572161 | |||||
| chr15:90572640
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(138): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.232-20996A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572640 | ||||||
| chr15:90572642
|
C | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-20994C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572642 | ||||||
| chr15:90572669
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0002g0273 | 3 | HG02129.hp1 NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.232-20967G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572669 | ||||||
| chr15:90572795
|
T | C | 1 | a0003c0003t0003g0174 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.232-20841T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572795 | ||||||
| chr15:90572931
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.232-20705A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572931 | ||||||
| chr15:90572941
|
T | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(141): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.232-20695T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90572941 | ||||||
| chr15:90573000
|
A | T | 34 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(31): Show | 34 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.232-20636A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573000 | ||||||
| chr15:90573121
|
C | G | 7 | a0001c0001t0003g0255a0001c0001t0009g0195a0001c0001t0019g0028others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-20515C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573121 | ||||||
| chr15:90573132
|
G | C | 1 | a0002c0002t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.232-20504G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573132 | ||||||
| chr15:90573154
|
T | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.232-20482T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573154 | ||||||
| chr15:90573210
|
G | C | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232-20426G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573210 | ||||||
| chr15:90573474
|
C | T | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-20162C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573474 | ||||||
| chr15:90573553
|
AT | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.232-20073delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90573553 | |||||
| chr15:90573755
|
A | G | 1 | a0002c0002t0013g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-19881A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573755 | ||||||
| chr15:90573769
|
A | G | 1 | a0003c0003t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.232-19867A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90573769 | ||||||
| chr15:90574041
|
A | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0006g0260others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-19595A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574041 | ||||||
| chr15:90574175
|
T | A | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-19461T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574175 | ||||||
| chr15:90574349
|
G | A | 2 | a0001c0001t0001g0236a0001c0007t0001g0206 | 2 | HG00597.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.232-19287G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574349 | ||||||
| chr15:90574412
|
A | G | 21 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(18): Show | 21 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.232-19224A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574412 | ||||||
| chr15:90574475
|
T | TCAAAACA others(3): Show |
20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-19150_232-1914 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90574475 | |||||
| chr15:90574507
|
C | T | 9 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0040g0023others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-19129C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574507 | ||||||
| chr15:90574525
|
A | G | 1 | a0001c0006t0003g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.232-19111A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574525 | ||||||
| chr15:90574647
|
G | A | 2 | a0002c0002t0001g0101a0002c0002t0001g0108 | 2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.232-18989G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574647 | ||||||
| chr15:90574807
|
G | A | 1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232-18829G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90574807 | ||||||
| chr15:90575008
|
A | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232-18628A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575008 | ||||||
| chr15:90575016
|
AT | A | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-18612delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90575016 | |||||
| chr15:90575071
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(152): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.232-18565T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575071 | ||||||
| chr15:90575147
|
C | T | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-18489C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575147 | ||||||
| chr15:90575275
|
C | T | 21 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(18): Show | 21 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.232-18361C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575275 | ||||||
| chr15:90575334
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232-18302A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575334 | ||||||
| chr15:90575402
|
T | C | 1 | a0002c0002t0001g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.232-18234T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575402 | ||||||
| chr15:90575585
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.232-18051G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575585 | ||||||
| chr15:90575613
|
A | T | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-18023A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575613 | ||||||
| chr15:90575782
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(152): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.232-17854T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575782 | ||||||
| chr15:90575865
|
A | G | 3 | a0001c0001t0046g0020a0002c0002t0044g0021a0008c0012t0021g0029 | 3 | HG01891.hp2 HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-17771A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575865 | ||||||
| chr15:90575882
|
A | G | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0003g0024others(3): Show | 6 | HG01109.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-17754A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575882 | ||||||
| chr15:90575893
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(215): Show | 221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.232-17743G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90575893 | ||||||
| chr15:90576028
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-17608C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576028 | ||||||
| chr15:90576350
|
G | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0006g0260others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-17286G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576350 | ||||||
| chr15:90576384
|
C | T | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-17252C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576384 | ||||||
| chr15:90576411
|
G | A | 2 | a0001c0001t0046g0020a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.232-17225G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576411 | ||||||
| chr15:90576440
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.232-17196G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576440 | ||||||
| chr15:90576471
|
G | A | 24 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0254others(21): Show | 24 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-17165G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576471 | ||||||
| chr15:90576630
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-17006G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576630 | ||||||
| chr15:90576789
|
C | T | 1 | a0001c0006t0003g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.232-16847C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576789 | ||||||
| chr15:90576854
|
GGGAGTTG others(7): Show |
G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(159): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.232-16771_232-1675 others(18): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90576854 | |||||
| chr15:90576931
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0006g0050others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-16705G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576931 | ||||||
| chr15:90576979
|
G | A | 8 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0003g0024others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-16657G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576979 | ||||||
| chr15:90576986
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.232-16650C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90576986 | ||||||
| chr15:90577029
|
T | TTTTTG | 53 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.232-16582_232-1657 others(9): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90577029 | |||||
| chr15:90577029
|
TTTTTGTT others(3): Show |
T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(162): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.232-16587_232-1657 others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90577029 | |||||
| chr15:90577174
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.232-16462C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577174 | ||||||
| chr15:90577629
|
C | G | 9 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0040g0023others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-16007C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577629 | ||||||
| chr15:90577668
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.232-15968T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577668 | ||||||
| chr15:90577786
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232-15850G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577786 | ||||||
| chr15:90577839
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.232-15797C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577839 | ||||||
| chr15:90577876
|
G | A | 2 | a0001c0015t0029g0042a0003c0003t0001g0266 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.232-15760G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90577876 | ||||||
| chr15:90578129
|
CTG | C | 8 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0040g0023others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-15506_232-1550 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578129 | ||||||
| chr15:90578206
|
C | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.232-15430C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578206 | ||||||
| chr15:90578207
|
G | A | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.232-15429G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578207 | ||||||
| chr15:90578375
|
C | T | 17 | a0001c0001t0001g0254a0001c0001t0003g0255a0001c0001t0016g0168others(14): Show | 17 | HG01243.hp2 HG01346.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.232-15261C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578375 | ||||||
| chr15:90578416
|
A | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 23 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.232-15220A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578416 | ||||||
| chr15:90578489
|
G | A | 2 | a0002c0002t0047g0003a0004c0005t0045g0132 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.232-15147G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578489 | ||||||
| chr15:90578636
|
A | G | 2 | a0002c0002t0013g0194a0002c0002t0018g0119 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.232-15000A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578636 | ||||||
| chr15:90578828
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-14808C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578828 | ||||||
| chr15:90578923
|
C | A | 1 | a0001c0007t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232-14713C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578923 | ||||||
| chr15:90578924
|
T | A | 1 | a0001c0007t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232-14712T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578924 | ||||||
| chr15:90578930
|
G | C | 1 | a0001c0007t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232-14706G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90578930 | ||||||
| chr15:90579172
|
T | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.232-14464T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579172 | ||||||
| chr15:90579282
|
T | C | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0003g0024others(3): Show | 6 | HG01109.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-14354T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579282 | ||||||
| chr15:90579292
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(152): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.232-14344T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579292 | ||||||
| chr15:90579633
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-14003A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579633 | ||||||
| chr15:90579634
|
C | CCTTT | 15 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 15 | HG00597.hp2 HG02523.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.232-14002_232-1400 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579634 | ||||||
| chr15:90579634
|
C | CT | 57 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0043others(54): Show | 59 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.232-13977dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
C | CTT | 10 | a0001c0001t0001g0127a0001c0001t0001g0152a0001c0001t0001g0170others(7): Show | 10 | HG00558.hp1 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-13978_232-1397 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
C | CTTTTTT | 6 | a0002c0002t0003g0024a0002c0002t0004g0111a0002c0002t0004g0115others(3): Show | 6 | HG01081.hp2 HG01109.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-13982_232-1397 others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
C | CTTTTTTT | 10 | a0001c0001t0004g0256a0001c0001t0019g0028a0001c0001t0040g0023others(7): Show | 10 | HG01258.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-13983_232-1397 others(11): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
CT | C | 5 | a0001c0001t0002g0171a0001c0001t0025g0188a0002c0002t0001g0113others(2): Show | 5 | HG01243.hp1 HG01517.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-13977delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
CTTTTTTT | C | 11 | a0001c0001t0003g0255a0001c0001t0016g0168a0001c0001t0046g0020others(8): Show | 11 | HG01243.hp2 HG01346.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.232-13983_232-1397 others(11): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579634
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.232-13987_232-1397 others(15): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90579634 | |||||
| chr15:90579681
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(215): Show | 221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.232-13955A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579681 | ||||||
| chr15:90579712
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232-13924G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579712 | ||||||
| chr15:90579739
|
T | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.232-13897T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579739 | ||||||
| chr15:90579804
|
G | A | 10 | a0001c0001t0009g0195a0001c0001t0011g0030a0001c0001t0011g0034others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-13832G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579804 | ||||||
| chr15:90579857
|
G | T | 1 | a0001c0004t0005g0004 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.232-13779G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579857 | ||||||
| chr15:90579888
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.232-13748C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579888 | ||||||
| chr15:90579894
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.232-13742G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579894 | ||||||
| chr15:90579974
|
A | G | 1 | a0001c0006t0003g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.232-13662A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579974 | ||||||
| chr15:90579999
|
A | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.232-13637A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90579999 | ||||||
| chr15:90580406
|
C | T | 13 | a0001c0001t0003g0255a0001c0001t0016g0168a0001c0001t0035g0061others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.232-13230C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90580406 | ||||||
| chr15:90580426
|
C | CT | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-13196dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90580426 | |||||
| chr15:90580490
|
G | A | 1 | a0001c0001t0006g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.232-13146G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90580490 | ||||||
| chr15:90580490
|
G | T | 1 | a0001c0006t0003g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.232-13146G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90580490 | ||||||
| chr15:90580559
|
T | C | 56 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 56 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.232-13077T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90580559 | ||||||
| chr15:90580909
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.232-12727A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90580909 | ||||||
| chr15:90581041
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.232-12595A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581041 | ||||||
| chr15:90581153
|
G | A | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.232-12483G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581153 | ||||||
| chr15:90581174
|
C | T | 10 | a0001c0001t0035g0061a0001c0001t0046g0020a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-12462C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581174 | ||||||
| chr15:90581302
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.232-12334G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581302 | ||||||
| chr15:90581309
|
A | G | 2 | a0002c0002t0047g0003a0004c0005t0045g0132 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.232-12327A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581309 | ||||||
| chr15:90581417
|
C | G | 2 | a0002c0002t0047g0003a0004c0005t0045g0132 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.232-12219C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581417 | ||||||
| chr15:90581433
|
C | T | 1 | a0003c0003t0003g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232-12203C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581433 | ||||||
| chr15:90581439
|
A | G | 11 | a0001c0001t0001g0254a0001c0001t0009g0195a0001c0001t0011g0030others(8): Show | 11 | HG01109.hp2 HG01496.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-12197A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581439 | ||||||
| chr15:90581537
|
G | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-12099G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581537 | ||||||
| chr15:90581602
|
C | T | 56 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 56 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.232-12034C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581602 | ||||||
| chr15:90581906
|
G | A | 8 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(5): Show | 8 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-11730G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90581906 | ||||||
| chr15:90582255
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(195): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.232-11381A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582255 | ||||||
| chr15:90582432
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0033g0025a0002c0002t0044g0021 | 3 | HG02559.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.232-11204C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582432 | ||||||
| chr15:90582470
|
A | G | 3 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051 | 3 | HG02258.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.232-11166A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582470 | ||||||
| chr15:90582721
|
G | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-10915G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582721 | ||||||
| chr15:90582843
|
T | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232-10793T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582843 | ||||||
| chr15:90582888
|
G | C | 14 | a0001c0001t0001g0254a0001c0001t0011g0030a0001c0001t0011g0034others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.232-10748G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582888 | ||||||
| chr15:90582906
|
G | A | 1 | a0001c0006t0003g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.232-10730G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582906 | ||||||
| chr15:90582914
|
C | G | 1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232-10722C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90582914 | ||||||
| chr15:90583076
|
G | A | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.232-10560G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583076 | ||||||
| chr15:90583436
|
C | T | 3 | a0001c0001t0040g0023a0002c0002t0003g0024a0002c0002t0047g0003 | 3 | HG01109.hp2 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.232-10200C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583436 | ||||||
| chr15:90583476
|
G | A | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-10160G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583476 | ||||||
| chr15:90583495
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 41 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.232-10141G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583495 | ||||||
| chr15:90583516
|
A | T | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-10120A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583516 | ||||||
| chr15:90583799
|
C | T | 2 | a0001c0015t0029g0042a0003c0014t0030g0253 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.232-9837C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90583799 | ||||||
| chr15:90583848
|
CT | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 41 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.232-9778delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90583848 | |||||
| chr15:90584000
|
C | T | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-9636C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584000 | ||||||
| chr15:90584082
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 41 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.232-9554C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584082 | ||||||
| chr15:90584237
|
C | CT | 6 | a0001c0001t0001g0010a0001c0001t0040g0023a0002c0002t0003g0024others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-9382dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90584237 | |||||
| chr15:90584237
|
CT | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(170): Show | 176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.232-9382delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90584237 | |||||
| chr15:90584237
|
CTT | C | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-9383_232-9382d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90584237 | |||||
| chr15:90584319
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0046a0003c0003t0001g0045others(1): Show | 4 | HG01255.hp2 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-9317C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584319 | ||||||
| chr15:90584483
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.232-9153C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584483 | ||||||
| chr15:90584579
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.232-9057G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584579 | ||||||
| chr15:90584714
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0017a0003c0003t0003g0019 | 3 | NA18964.hp2 NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.232-8922T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584714 | ||||||
| chr15:90584762
|
GTAGA | G | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-8869_232-8866d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90584762 | |||||
| chr15:90584957
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(208): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.232-8679G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90584957 | ||||||
| chr15:90585005
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0043others(58): Show | 62 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.232-8631A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585005 | ||||||
| chr15:90585086
|
T | A | 16 | a0001c0001t0001g0254a0001c0001t0011g0030a0001c0001t0011g0034others(13): Show | 16 | HG01109.hp2 HG01346.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.232-8550T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585086 | ||||||
| chr15:90585171
|
G | T | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.232-8465G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585171 | ||||||
| chr15:90585175
|
C | T | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.232-8461C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585175 | ||||||
| chr15:90585221
|
T | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.232-8415T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585221 | ||||||
| chr15:90585233
|
C | G | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.232-8403C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585233 | ||||||
| chr15:90585454
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.232-8182C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585454 | ||||||
| chr15:90585461
|
AT | A | 98 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0048others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.232-8164delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90585461 | |||||
| chr15:90585463
|
T | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0201a0002c0002t0047g0003 | 3 | HG02257.hp2 NA18949.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.232-8173T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585463 | ||||||
| chr15:90585464
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232-8172T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585464 | ||||||
| chr15:90585612
|
G | A | 1 | a0001c0001t0024g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.232-8024G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585612 | ||||||
| chr15:90585641
|
A | G | 4 | a0001c0001t0001g0010a0001c0004t0008g0007a0001c0004t0008g0008others(1): Show | 4 | NA18950.hp1 NA18955.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-7995A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585641 | ||||||
| chr15:90585656
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(66): Show | 72 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.232-7980G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585656 | ||||||
| chr15:90585716
|
C | G | 5 | a0001c0001t0040g0023a0002c0002t0003g0024a0002c0002t0013g0131others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-7920C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585716 | ||||||
| chr15:90585851
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.232-7785C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585851 | ||||||
| chr15:90585859
|
G | T | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.232-7777G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585859 | ||||||
| chr15:90585876
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(162): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.232-7760C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585876 | ||||||
| chr15:90585889
|
G | A | 16 | a0001c0001t0001g0254a0001c0001t0011g0030a0001c0001t0011g0034others(13): Show | 16 | HG01109.hp2 HG01346.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.232-7747G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585889 | ||||||
| chr15:90585998
|
C | T | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-7638C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90585998 | ||||||
| chr15:90586063
|
T | G | 1 | a0002c0002t0018g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.232-7573T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586063 | ||||||
| chr15:90586072
|
C | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 46 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.232-7564C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586072 | ||||||
| chr15:90586140
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.232-7496T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586140 | ||||||
| chr15:90586337
|
T | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-7299T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586337 | ||||||
| chr15:90586362
|
C | CT | 10 | a0001c0001t0001g0010a0001c0001t0004g0256a0002c0002t0003g0129others(7): Show | 10 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-7252dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90586362 | |||||
| chr15:90586362
|
CT | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(160): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.232-7252delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90586362 | |||||
| chr15:90586398
|
G | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.232-7238G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586398 | ||||||
| chr15:90586761
|
T | C | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-6875T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586761 | ||||||
| chr15:90586953
|
C | G | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.232-6683C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90586953 | ||||||
| chr15:90587364
|
T | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.232-6272T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587364 | ||||||
| chr15:90587367
|
C | T | 1 | a0003c0003t0003g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232-6269C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587367 | ||||||
| chr15:90587397
|
A | G | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-6239A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587397 | ||||||
| chr15:90587417
|
C | T | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-6219C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587417 | ||||||
| chr15:90587423
|
A | G | 1 | a0001c0001t0006g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.232-6213A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587423 | ||||||
| chr15:90587722
|
T | G | 1 | a0002c0002t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.232-5914T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587722 | ||||||
| chr15:90587749
|
G | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.232-5887G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587749 | ||||||
| chr15:90587758
|
C | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.232-5878C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587758 | ||||||
| chr15:90587760
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.232-5876T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587760 | ||||||
| chr15:90587889
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.232-5747C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90587889 | ||||||
| chr15:90588017
|
G | C | 1 | a0002c0002t0004g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.232-5619G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588017 | ||||||
| chr15:90588104
|
T | A | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232-5532T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588104 | ||||||
| chr15:90588186
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-5450G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588186 | ||||||
| chr15:90588259
|
C | CA | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(157): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.232-5363dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90588259 | |||||
| chr15:90588355
|
T | C | 10 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(7): Show | 10 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-5281T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588355 | ||||||
| chr15:90588384
|
TATTTTTC others(55): Show |
T | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.232-5251_232-5190d others(64): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588384 | ||||||
| chr15:90588447
|
T | G | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.232-5189T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588447 | ||||||
| chr15:90588600
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.232-5036A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588600 | ||||||
| chr15:90588606
|
C | CT | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.232-5023dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90588606 | |||||
| chr15:90588684
|
C | CT | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.232-4951dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90588684 | |||||
| chr15:90588740
|
T | G | 6 | a0001c0001t0001g0121a0001c0001t0006g0260a0001c0001t0011g0140others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-4896T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588740 | ||||||
| chr15:90588765
|
G | A | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.232-4871G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588765 | ||||||
| chr15:90588828
|
C | T | 1 | a0002c0002t0004g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.232-4808C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588828 | ||||||
| chr15:90588879
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.232-4757T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90588879 | ||||||
| chr15:90589243
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.232-4393G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589243 | ||||||
| chr15:90589346
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.232-4290C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589346 | ||||||
| chr15:90589419
|
A | G | 6 | a0001c0001t0001g0121a0001c0001t0006g0260a0001c0001t0011g0140others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-4217A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589419 | ||||||
| chr15:90589638
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232-3998C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589638 | ||||||
| chr15:90589706
|
G | A | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.232-3930G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589706 | ||||||
| chr15:90589752
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02129.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.232-3884C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589752 | ||||||
| chr15:90589753
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.232-3883G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589753 | ||||||
| chr15:90589856
|
T | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.232-3780T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589856 | ||||||
| chr15:90589884
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232-3752A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589884 | ||||||
| chr15:90589885
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232-3751A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589885 | ||||||
| chr15:90589888
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232-3748A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589888 | ||||||
| chr15:90589914
|
G | C | 1 | a0001c0001t0019g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.232-3722G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589914 | ||||||
| chr15:90589973
|
G | A | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.232-3663G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90589973 | ||||||
| chr15:90590129
|
A | G | 1 | a0002c0002t0048g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.232-3507A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590129 | ||||||
| chr15:90590147
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.232-3489G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590147 | ||||||
| chr15:90590361
|
C | T | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.232-3275C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590361 | ||||||
| chr15:90590629
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.232-3007G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590629 | ||||||
| chr15:90590831
|
G | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.232-2805G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590831 | ||||||
| chr15:90590876
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.232-2760C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90590876 | ||||||
| chr15:90591120
|
A | AT | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(188): Show | 194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.232-2503dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | 90591120 | |||||
| chr15:90591135
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.232-2501A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90591135 | ||||||
| chr15:90591227
|
G | T | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.232-2409G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90591227 | ||||||
| chr15:90591311
|
G | C | 1 | a0001c0001t0002g0225 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.232-2325G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90591311 | ||||||
| chr15:90592100
|
C | G | 6 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(3): Show | 6 | HG00140.hp2 HG00323.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1536C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592100 | ||||||
| chr15:90592176
|
T | C | 1 | a0001c0001t0016g0168 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.232-1460T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592176 | ||||||
| chr15:90592179
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.232-1457C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592179 | ||||||
| chr15:90592211
|
A | G | 17 | a0001c0001t0001g0254a0001c0001t0011g0030a0001c0001t0011g0034others(14): Show | 17 | HG01109.hp2 HG01346.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.232-1425A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592211 | ||||||
| chr15:90592326
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.232-1310A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592326 | ||||||
| chr15:90592354
|
A | G | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.232-1282A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592354 | ||||||
| chr15:90592442
|
A | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-1194A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592442 | ||||||
| chr15:90592451
|
C | A | 2 | a0001c0001t0003g0255a0003c0003t0003g0267 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.232-1185C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592451 | ||||||
| chr15:90592787
|
T | A | 4 | a0001c0001t0040g0023a0001c0001t0046g0020a0002c0002t0003g0024others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-849T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592787 | ||||||
| chr15:90592837
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.232-799C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592837 | ||||||
| chr15:90592843
|
A | G | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232-793A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592843 | ||||||
| chr15:90592981
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232-655C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592981 | ||||||
| chr15:90592998
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.232-638C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90592998 | ||||||
| chr15:90593022
|
G | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.232-614G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90593022 | ||||||
| chr15:90593385
|
A | G | 11 | a0001c0001t0001g0254a0001c0001t0011g0030a0001c0001t0011g0034others(8): Show | 11 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-251A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90593385 | ||||||
| chr15:90593475
|
G | C | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.232-161G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90593475 | ||||||
| chr15:90593478
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-158C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2/14 | chr15 | 90593478 | ||||||
| chr15:90593861
|
A | G | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.351+106A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90593861 | ||||||
| chr15:90593915
|
G | T | 2 | a0001c0015t0029g0042a0003c0014t0030g0253 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.351+160G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90593915 | ||||||
| chr15:90594551
|
C | T | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+796C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90594551 | ||||||
| chr15:90594599
|
A | G | 10 | a0001c0001t0001g0043a0001c0001t0001g0197a0001c0001t0001g0207others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+844A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90594599 | ||||||
| chr15:90594750
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.351+995A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90594750 | ||||||
| chr15:90594869
|
G | T | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.351+1114G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90594869 | ||||||
| chr15:90594902
|
C | T | 1 | a0003c0003t0002g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.351+1147C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90594902 | ||||||
| chr15:90595025
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.351+1270C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595025 | ||||||
| chr15:90595058
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.351+1303T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595058 | ||||||
| chr15:90595097
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.351+1342T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595097 | ||||||
| chr15:90595434
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(226): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.351+1679C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595434 | ||||||
| chr15:90595449
|
A | G | 1 | a0001c0001t0042g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.351+1694A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595449 | ||||||
| chr15:90595485
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.351+1730C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595485 | ||||||
| chr15:90595486
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.351+1731G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595486 | ||||||
| chr15:90595497
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.351+1742C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595497 | ||||||
| chr15:90595560
|
C | CA | 25 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0058others(22): Show | 25 | HG00558.hp1 HG01891.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.351+1823dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90595560 | |||||
| chr15:90595577
|
A | AC | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1822_351+1823i others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595577 | ||||||
| chr15:90595622
|
C | T | 1 | a0004c0005t0045g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.351+1867C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595622 | ||||||
| chr15:90595666
|
A | G | 9 | a0001c0001t0004g0256a0002c0002t0003g0129a0002c0002t0004g0111others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+1911A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595666 | ||||||
| chr15:90595759
|
A | G | 2 | a0002c0002t0001g0113a0002c0002t0001g0117 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.351+2004A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595759 | ||||||
| chr15:90595814
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.351+2059G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595814 | ||||||
| chr15:90595851
|
A | G | 56 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 56 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.351+2096A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595851 | ||||||
| chr15:90595866
|
A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.351+2111A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595866 | ||||||
| chr15:90595995
|
G | A | 3 | a0001c0001t0003g0255a0001c0001t0016g0168a0003c0003t0003g0267 | 3 | HG01243.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.351+2240G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595995 | ||||||
| chr15:90595999
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+2244G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90595999 | ||||||
| chr15:90596012
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(204): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.351+2257T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596012 | ||||||
| chr15:90596235
|
G | A | 4 | a0001c0001t0040g0023a0001c0001t0046g0020a0002c0002t0003g0024others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2480G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596235 | ||||||
| chr15:90596333
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG02129.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.351+2578A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596333 | ||||||
| chr15:90596566
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.351+2811T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596566 | ||||||
| chr15:90596583
|
C | T | 1 | a0002c0002t0004g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.351+2828C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596583 | ||||||
| chr15:90596703
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+2948G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596703 | ||||||
| chr15:90596716
|
C | T | 1 | a0002c0002t0002g0079 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.351+2961C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596716 | ||||||
| chr15:90596819
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.351+3064C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596819 | ||||||
| chr15:90596954
|
A | C | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0002c0002t0012g0136others(7): Show | 10 | HG01346.hp1 HG01496.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+3199A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90596954 | ||||||
| chr15:90597131
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.351+3376G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597131 | ||||||
| chr15:90597176
|
T | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.351+3421T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597176 | ||||||
| chr15:90597177
|
C | T | 1 | a0002c0002t0001g0093 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.351+3422C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597177 | ||||||
| chr15:90597358
|
G | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.351+3603G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597358 | ||||||
| chr15:90597361
|
C | CAGAA | 87 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.351+3607_351+3610d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90597361 | |||||
| chr15:90597374
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.351+3619G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597374 | ||||||
| chr15:90597528
|
T | C | 3 | a0002c0002t0015g0026a0002c0002t0018g0119a0002c0002t0047g0003 | 3 | HG02257.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.351+3773T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597528 | ||||||
| chr15:90597704
|
A | C | 3 | a0001c0001t0007g0219a0004c0005t0045g0132a0008c0012t0021g0029 | 3 | HG01891.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.351+3949A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597704 | ||||||
| chr15:90597858
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.351+4103C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597858 | ||||||
| chr15:90597943
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(224): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.351+4188A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90597943 | ||||||
| chr15:90598008
|
A | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.351+4253A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598008 | ||||||
| chr15:90598070
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.352-4254C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598070 | ||||||
| chr15:90598382
|
CAGA | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.352-3932_352-3930d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90598382 | |||||
| chr15:90598538
|
G | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.352-3786G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598538 | ||||||
| chr15:90598578
|
A | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.352-3746A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598578 | ||||||
| chr15:90598657
|
G | A | 1 | a0001c0001t0006g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.352-3667G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598657 | ||||||
| chr15:90598752
|
C | G | 5 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(2): Show | 5 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-3572C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598752 | ||||||
| chr15:90598785
|
A | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.352-3539A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598785 | ||||||
| chr15:90598823
|
C | T | 2 | a0001c0015t0029g0042a0003c0014t0030g0253 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.352-3501C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90598823 | ||||||
| chr15:90599057
|
T | A | 2 | a0001c0001t0046g0020a0003c0003t0036g0031 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.352-3267T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599057 | ||||||
| chr15:90599127
|
A | AT | 5 | a0001c0001t0002g0146a0001c0001t0006g0047a0001c0001t0006g0050others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-3186dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90599127 | |||||
| chr15:90599138
|
T | A | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-3186T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599138 | ||||||
| chr15:90599139
|
A | G | 1 | a0002c0002t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.352-3185A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599139 | ||||||
| chr15:90599177
|
T | C | 3 | a0001c0001t0007g0120a0001c0001t0007g0219a0003c0003t0001g0262 | 3 | HG03098.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.352-3147T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599177 | ||||||
| chr15:90599309
|
C | T | 2 | a0001c0001t0002g0159a0001c0001t0002g0164 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.352-3015C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599309 | ||||||
| chr15:90599336
|
G | A | 11 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.352-2988G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599336 | ||||||
| chr15:90599653
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.352-2671A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599653 | ||||||
| chr15:90599775
|
A | G | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-2549A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599775 | ||||||
| chr15:90599816
|
G | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.352-2508G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599816 | ||||||
| chr15:90599840
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.352-2484T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90599840 | ||||||
| chr15:90599969
|
C | CT | 1 | a0001c0001t0001g0001 | 3 | HG01123.hp1 HG01258.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.352-2354dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90599969 | |||||
| chr15:90600021
|
A | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(152): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.352-2303A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600021 | ||||||
| chr15:90600074
|
T | C | 1 | a0001c0001t0011g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.352-2250T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600074 | ||||||
| chr15:90600206
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.352-2118A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600206 | ||||||
| chr15:90600209
|
G | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.352-2115G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600209 | ||||||
| chr15:90600306
|
A | T | 1 | a0001c0007t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352-2018A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600306 | ||||||
| chr15:90600362
|
C | T | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(19): Show | 22 | HG00735.hp1 HG01192.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.352-1962C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600362 | ||||||
| chr15:90600423
|
C | CCTT | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.352-1899_352-1897d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90600423 | |||||
| chr15:90600471
|
G | A | 1 | a0001c0001t0003g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.352-1853G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600471 | ||||||
| chr15:90600488
|
C | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-1836C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600488 | ||||||
| chr15:90600569
|
C | T | 1 | a0002c0010t0003g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.352-1755C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600569 | ||||||
| chr15:90600570
|
G | A | 2 | a0001c0001t0009g0041a0003c0003t0009g0032 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.352-1754G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600570 | ||||||
| chr15:90600573
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-1751C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600573 | ||||||
| chr15:90600625
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-1699A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600625 | ||||||
| chr15:90600641
|
A | T | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352-1683A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600641 | ||||||
| chr15:90600677
|
G | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.352-1647G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600677 | ||||||
| chr15:90600816
|
C | A | 1 | a0002c0002t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.352-1508C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600816 | ||||||
| chr15:90600878
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0164 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.352-1446G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600878 | ||||||
| chr15:90600912
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.352-1412G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90600912 | ||||||
| chr15:90601060
|
G | A | 1 | a0002c0002t0001g0096 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.352-1264G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601060 | ||||||
| chr15:90601175
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.352-1149A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601175 | ||||||
| chr15:90601254
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-1070G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601254 | ||||||
| chr15:90601355
|
A | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.352-969A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601355 | ||||||
| chr15:90601369
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.352-955G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601369 | ||||||
| chr15:90601369
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-955G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601369 | ||||||
| chr15:90601371
|
C | T | 41 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(38): Show | 41 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-953C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601371 | ||||||
| chr15:90601392
|
C | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.352-932C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601392 | ||||||
| chr15:90601465
|
C | T | 36 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(33): Show | 36 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-859C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601465 | ||||||
| chr15:90601488
|
T | TA | 41 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(38): Show | 41 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-828dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr15 | 90601488 | |||||
| chr15:90601489
|
A | T | 2 | a0001c0015t0029g0042a0003c0014t0030g0253 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.352-835A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601489 | ||||||
| chr15:90601671
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.352-653G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601671 | ||||||
| chr15:90601707
|
G | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0165a0001c0001t0001g0170others(2): Show | 5 | HG02886.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-617G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601707 | ||||||
| chr15:90601754
|
A | G | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-570A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601754 | ||||||
| chr15:90601853
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.352-471C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601853 | ||||||
| chr15:90601937
|
G | A | 2 | a0001c0001t0002g0171a0004c0005t0026g0088 | 2 | NA18993.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.352-387G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90601937 | ||||||
| chr15:90602027
|
A | G | 3 | a0002c0002t0007g0130a0002c0002t0013g0131a0002c0002t0013g0194 | 3 | HG02630.hp2 HG02896.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.352-297A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90602027 | ||||||
| chr15:90602033
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.352-291G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90602033 | ||||||
| chr15:90602086
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.352-238C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90602086 | ||||||
| chr15:90602219
|
G | C | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.352-105G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 3/14 | chr15 | 90602219 | ||||||
| chr15:90602568
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.413+183C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602568 | ||||||
| chr15:90602606
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.413+221T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602606 | ||||||
| chr15:90602653
|
AAAC | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.413+295_413+297del others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr15 | 90602653 | |||||
| chr15:90602702
|
A | G | 7 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+317A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602702 | ||||||
| chr15:90602703
|
T | C | 7 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+318T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602703 | ||||||
| chr15:90602728
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.413+343C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602728 | ||||||
| chr15:90602744
|
G | T | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.413+359G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602744 | ||||||
| chr15:90602746
|
C | T | 10 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0051others(7): Show | 10 | HG01074.hp2 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+361C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602746 | ||||||
| chr15:90602747
|
G | C | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.413+362G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602747 | ||||||
| chr15:90602786
|
C | T | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+401C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602786 | ||||||
| chr15:90602803
|
G | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 68 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.413+418G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90602803 | ||||||
| chr15:90602841
|
G | GC | 35 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.413+457dupC | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr15 | 90602841 | |||||
| chr15:90603012
|
G | C | 1 | a0001c0001t0002g0146 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.413+627G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603012 | ||||||
| chr15:90603167
|
G | A | 1 | a0002c0002t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.413+782G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603167 | ||||||
| chr15:90603171
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.413+786C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603171 | ||||||
| chr15:90603181
|
T | C | 15 | a0001c0001t0001g0036a0001c0001t0003g0264a0001c0001t0006g0047others(12): Show | 15 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+796T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603181 | ||||||
| chr15:90603215
|
G | T | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+830G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603215 | ||||||
| chr15:90603219
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0166 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.413+834A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603219 | ||||||
| chr15:90603226
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0166 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.413+841A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603226 | ||||||
| chr15:90603229
|
C | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.413+844C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603229 | ||||||
| chr15:90603239
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0006g0047a0001c0001t0006g0050others(2): Show | 6 | HG02129.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+854C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603239 | ||||||
| chr15:90603251
|
C | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(116): Show | 122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.413+866C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603251 | ||||||
| chr15:90603260
|
G | A | 3 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051 | 3 | HG02258.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413+875G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603260 | ||||||
| chr15:90603271
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.413+886G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603271 | ||||||
| chr15:90603276
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(160): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.413+891C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603276 | ||||||
| chr15:90603299
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(148): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.413+914C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603299 | ||||||
| chr15:90603304
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413+919G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603304 | ||||||
| chr15:90603312
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.413+927A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603312 | ||||||
| chr15:90603315
|
C | T | 4 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0102others(1): Show | 4 | HG00323.hp1 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+930C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603315 | ||||||
| chr15:90603336
|
G | A | 7 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+951G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603336 | ||||||
| chr15:90603368
|
A | G | 1 | a0002c0002t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.413+983A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603368 | ||||||
| chr15:90603374
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+989C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603374 | ||||||
| chr15:90603375
|
G | A | 1 | a0003c0003t0001g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+990G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603375 | ||||||
| chr15:90603391
|
C | T | 2 | a0002c0002t0017g0133a0002c0002t0033g0025 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.414-994C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603391 | ||||||
| chr15:90603398
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0165others(2): Show | 5 | HG02723.hp1 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-987A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603398 | ||||||
| chr15:90603415
|
C | G | 2 | a0002c0002t0017g0133a0002c0002t0033g0025 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.414-970C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603415 | ||||||
| chr15:90603418
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.414-967G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603418 | ||||||
| chr15:90603422
|
G | C | 1 | a0001c0001t0002g0146 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.414-963G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603422 | ||||||
| chr15:90603678
|
C | T | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.414-707C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603678 | ||||||
| chr15:90603679
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(224): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.414-706A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603679 | ||||||
| chr15:90603859
|
A | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414-526A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603859 | ||||||
| chr15:90603912
|
A | T | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.414-473A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603912 | ||||||
| chr15:90603950
|
C | T | 43 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(40): Show | 43 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.414-435C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603950 | ||||||
| chr15:90603953
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414-432A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603953 | ||||||
| chr15:90603982
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.414-403G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90603982 | ||||||
| chr15:90604137
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.414-248A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90604137 | ||||||
| chr15:90604280
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0052others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.414-105A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 4/14 | chr15 | 90604280 | ||||||
| chr15:90604567
|
C | T | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.476+120C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90604567 | ||||||
| chr15:90604625
|
T | A | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.476+178T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90604625 | ||||||
| chr15:90604657
|
C | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.476+210C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90604657 | ||||||
| chr15:90604793
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.476+346A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90604793 | ||||||
| chr15:90604845
|
G | T | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.476+398G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90604845 | ||||||
| chr15:90605013
|
C | G | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.476+566C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605013 | ||||||
| chr15:90605042
|
T | C | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.476+595T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605042 | ||||||
| chr15:90605135
|
C | T | 1 | a0001c0001t0006g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.476+688C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605135 | ||||||
| chr15:90605149
|
G | A | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.476+702G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605149 | ||||||
| chr15:90605161
|
G | T | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.476+714G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605161 | ||||||
| chr15:90605181
|
G | C | 1 | a0003c0003t0001g0234 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.476+734G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605181 | ||||||
| chr15:90605351
|
T | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.476+904T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605351 | ||||||
| chr15:90605394
|
G | A | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.476+947G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605394 | ||||||
| chr15:90605398
|
C | T | 39 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(36): Show | 39 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.476+951C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605398 | ||||||
| chr15:90605610
|
TAA | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(214): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.476+1167_476+1168d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | 90605610 | |||||
| chr15:90605762
|
AAAG | A | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+1319_476+1321d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | 90605762 | |||||
| chr15:90605845
|
G | A | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.476+1398G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605845 | ||||||
| chr15:90605847
|
T | G | 43 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(40): Show | 43 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.476+1400T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605847 | ||||||
| chr15:90605862
|
A | C | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.476+1415A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605862 | ||||||
| chr15:90605945
|
G | C | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-1433G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605945 | ||||||
| chr15:90605958
|
C | T | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-1420C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90605958 | ||||||
| chr15:90606161
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.477-1217C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606161 | ||||||
| chr15:90606162
|
G | A | 3 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051 | 3 | HG02258.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.477-1216G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606162 | ||||||
| chr15:90606180
|
C | T | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.477-1198C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606180 | ||||||
| chr15:90606195
|
G | A | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477-1183G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606195 | ||||||
| chr15:90606202
|
A | G | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-1176A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606202 | ||||||
| chr15:90606360
|
G | A | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477-1018G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606360 | ||||||
| chr15:90606368
|
C | G | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-1010C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606368 | ||||||
| chr15:90606563
|
G | A | 46 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(43): Show | 46 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.477-815G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606563 | ||||||
| chr15:90606706
|
C | T | 1 | a0002c0002t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.477-672C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606706 | ||||||
| chr15:90606737
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.477-641G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606737 | ||||||
| chr15:90606769
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0166 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.477-609A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606769 | ||||||
| chr15:90606827
|
G | A | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477-551G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606827 | ||||||
| chr15:90606847
|
C | T | 43 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(40): Show | 43 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.477-531C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606847 | ||||||
| chr15:90606852
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(147): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.477-526C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606852 | ||||||
| chr15:90606858
|
G | C | 43 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(40): Show | 43 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.477-520G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606858 | ||||||
| chr15:90606879
|
A | G | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-499A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606879 | ||||||
| chr15:90606892
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.477-486G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606892 | ||||||
| chr15:90606964
|
C | G | 1 | a0003c0014t0030g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.477-414C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90606964 | ||||||
| chr15:90607030
|
AGCCACAG others(9): Show |
A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(176): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.477-340_477-325del others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | 90607030 | |||||
| chr15:90607063
|
G | A | 2 | a0003c0003t0003g0145a0003c0003t0039g0144 | 2 | HG00735.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.477-315G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90607063 | ||||||
| chr15:90607116
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.477-262C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90607116 | ||||||
| chr15:90607223
|
T | C | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-155T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 5/14 | chr15 | 90607223 | ||||||
| chr15:90607573
|
C | G | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.577+95C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90607573 | ||||||
| chr15:90607614
|
C | T | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+136C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90607614 | ||||||
| chr15:90607626
|
T | C | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577+148T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90607626 | ||||||
| chr15:90607887
|
T | G | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.577+409T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90607887 | ||||||
| chr15:90607984
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.577+506C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90607984 | ||||||
| chr15:90608044
|
C | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(168): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.577+566C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608044 | ||||||
| chr15:90608093
|
G | C | 1 | a0002c0002t0003g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.577+615G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608093 | ||||||
| chr15:90608099
|
C | T | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+621C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608099 | ||||||
| chr15:90608179
|
C | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.577+701C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608179 | ||||||
| chr15:90608230
|
C | T | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.577+752C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608230 | ||||||
| chr15:90608285
|
C | T | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+807C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608285 | ||||||
| chr15:90608377
|
C | T | 1 | a0002c0002t0001g0096 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.577+899C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608377 | ||||||
| chr15:90608463
|
A | T | 1 | a0004c0005t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.577+985A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608463 | ||||||
| chr15:90608489
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577+1011G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608489 | ||||||
| chr15:90608649
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.577+1171C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608649 | ||||||
| chr15:90608716
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.577+1238C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608716 | ||||||
| chr15:90608717
|
G | A | 7 | a0001c0001t0035g0061a0002c0002t0017g0133a0002c0002t0018g0119others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+1239G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608717 | ||||||
| chr15:90608731
|
C | G | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577+1253C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608731 | ||||||
| chr15:90608853
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.577+1375T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608853 | ||||||
| chr15:90608882
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.577+1404T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90608882 | ||||||
| chr15:90609049
|
T | C | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+1571T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609049 | ||||||
| chr15:90609113
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(220): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.577+1635C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609113 | ||||||
| chr15:90609126
|
G | T | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.577+1648G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609126 | ||||||
| chr15:90609305
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.577+1827C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609305 | ||||||
| chr15:90609358
|
T | A | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.577+1880T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609358 | ||||||
| chr15:90609380
|
A | G | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577+1902A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609380 | ||||||
| chr15:90609400
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.577+1922A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609400 | ||||||
| chr15:90609502
|
T | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.577+2024T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609502 | ||||||
| chr15:90609679
|
C | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.577+2201C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609679 | ||||||
| chr15:90609831
|
C | A | 5 | a0001c0001t0001g0208a0001c0001t0001g0223a0002c0002t0001g0074others(2): Show | 5 | HG01071.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.577+2353C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609831 | ||||||
| chr15:90609914
|
A | G | 4 | a0001c0001t0001g0228a0002c0002t0001g0064a0002c0002t0001g0070others(1): Show | 4 | NA18941.hp2 NA18947.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+2436A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90609914 | ||||||
| chr15:90610243
|
A | T | 1 | a0006c0011t0043g0083 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.577+2765A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610243 | ||||||
| chr15:90610440
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.577+2962A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610440 | ||||||
| chr15:90610649
|
A | C | 1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.577+3171A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610649 | ||||||
| chr15:90610708
|
T | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.577+3230T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610708 | ||||||
| chr15:90610792
|
A | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.577+3314A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610792 | ||||||
| chr15:90610935
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.577+3457G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610935 | ||||||
| chr15:90610951
|
C | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.577+3473C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610951 | ||||||
| chr15:90610972
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.578-3481C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90610972 | ||||||
| chr15:90611016
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.578-3437A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611016 | ||||||
| chr15:90611091
|
G | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-3362G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611091 | ||||||
| chr15:90611239
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.578-3214A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611239 | ||||||
| chr15:90611653
|
C | T | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.578-2800C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611653 | ||||||
| chr15:90611668
|
C | T | 1 | a0001c0001t0046g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.578-2785C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611668 | ||||||
| chr15:90611733
|
C | T | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-2720C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611733 | ||||||
| chr15:90611748
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0164 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.578-2705G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611748 | ||||||
| chr15:90611872
|
G | T | 8 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-2581G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611872 | ||||||
| chr15:90611874
|
C | T | 1 | a0003c0003t0001g0220 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.578-2579C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611874 | ||||||
| chr15:90611882
|
C | G | 8 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-2571C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90611882 | ||||||
| chr15:90612018
|
C | T | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-2435C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612018 | ||||||
| chr15:90612026
|
A | ACTC | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(152): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.578-2398_578-2396d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90612026 | |||||
| chr15:90612026
|
A | ACTCCTC | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0002t0001g0069others(2): Show | 5 | HG01346.hp2 HG01993.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.578-2401_578-2396d others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90612026 | |||||
| chr15:90612026
|
A | ACTCCTCC others(5): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578-2407_578-2396d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90612026 | |||||
| chr15:90612035
|
C | G | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.578-2418C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612035 | ||||||
| chr15:90612070
|
T | TCCTCCTC others(5): Show |
2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.578-2366_578-2355d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90612070 | |||||
| chr15:90612070
|
TCCTCCTC others(5): Show |
T | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.578-2366_578-2355d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90612070 | |||||
| chr15:90612082
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.578-2371G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612082 | ||||||
| chr15:90612176
|
G | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.578-2277G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612176 | ||||||
| chr15:90612222
|
C | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(89): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.578-2231C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612222 | ||||||
| chr15:90612240
|
T | G | 6 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.578-2213T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612240 | ||||||
| chr15:90612325
|
A | G | 8 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-2128A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612325 | ||||||
| chr15:90612393
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.578-2060G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612393 | ||||||
| chr15:90612528
|
A | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1925A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612528 | ||||||
| chr15:90612602
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.578-1851G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612602 | ||||||
| chr15:90612753
|
C | T | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.578-1700C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612753 | ||||||
| chr15:90612755
|
T | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1698T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612755 | ||||||
| chr15:90612807
|
T | C | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1646T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612807 | ||||||
| chr15:90612854
|
T | TG | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1599_578-1598i others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612854 | ||||||
| chr15:90612879
|
CT | C | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-1573delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612879 | ||||||
| chr15:90612900
|
C | T | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1553C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612900 | ||||||
| chr15:90612946
|
C | A | 1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.578-1507C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612946 | ||||||
| chr15:90612952
|
A | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.578-1501A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90612952 | ||||||
| chr15:90613104
|
G | GCGGGGGA others(10): Show |
4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-1348_578-1347i others(19): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613104 | |||||
| chr15:90613104
|
G | GCGGGGGA others(10): Show |
76 | a0001c0001t0001g0223a0001c0001t0003g0016a0001c0001t0003g0017others(73): Show | 76 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.578-1348_578-1347i others(19): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613104 | |||||
| chr15:90613127
|
G | C | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.578-1326G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613127 | ||||||
| chr15:90613135
|
G | A | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-1318G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613135 | ||||||
| chr15:90613185
|
G | GA | 20 | a0001c0001t0002g0063a0001c0001t0002g0146a0001c0001t0002g0160others(17): Show | 20 | HG00438.hp2 HG01192.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.578-1244dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613185 | |||||
| chr15:90613185
|
GA | G | 17 | a0001c0001t0003g0167a0001c0001t0003g0176a0001c0001t0009g0195others(14): Show | 17 | HG02027.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.578-1244delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613185 | |||||
| chr15:90613185
|
GAA | G | 19 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0056others(16): Show | 19 | HG00323.hp2 HG00438.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.578-1245_578-1244d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613185 | |||||
| chr15:90613185
|
GAAA | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0036others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.578-1246_578-1244d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613185 | |||||
| chr15:90613185
|
GAAAA | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.578-1247_578-1244d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90613185 | |||||
| chr15:90613189
|
A | G | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.578-1264A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613189 | ||||||
| chr15:90613190
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.578-1263A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613190 | ||||||
| chr15:90613191
|
A | G | 6 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(3): Show | 6 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.578-1262A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613191 | ||||||
| chr15:90613192
|
A | G | 2 | a0001c0001t0003g0264a0001c0001t0040g0023 | 2 | HG01074.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.578-1261A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613192 | ||||||
| chr15:90613193
|
A | G | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.578-1260A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613193 | ||||||
| chr15:90613402
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.578-1051G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613402 | ||||||
| chr15:90613473
|
T | C | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-980T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613473 | ||||||
| chr15:90613478
|
T | C | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-975T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613478 | ||||||
| chr15:90613491
|
C | T | 1 | a0001c0001t0019g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.578-962C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613491 | ||||||
| chr15:90613568
|
A | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-885A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613568 | ||||||
| chr15:90613577
|
G | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0246 | 2 | NA18940.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.578-876G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613577 | ||||||
| chr15:90613681
|
C | A | 1 | a0002c0002t0017g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.578-772C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90613681 | ||||||
| chr15:90614007
|
C | G | 1 | a0002c0002t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.578-446C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90614007 | ||||||
| chr15:90614096
|
A | C | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-357A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90614096 | ||||||
| chr15:90614137
|
T | C | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-316T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | chr15 | 90614137 | ||||||
| chr15:90614219
|
TCAGA | T | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.578-227_578-224del others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr15 | 90614219 | |||||
| chr15:90614637
|
A | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.613+149A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614637 | ||||||
| chr15:90614695
|
C | G | 1 | a0004c0005t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.613+207C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614695 | ||||||
| chr15:90614844
|
A | G | 10 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+356A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614844 | ||||||
| chr15:90614893
|
G | A | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.613+405G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614893 | ||||||
| chr15:90614905
|
A | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.613+417A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614905 | ||||||
| chr15:90614914
|
A | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613+426A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614914 | ||||||
| chr15:90614925
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.613+437G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614925 | ||||||
| chr15:90614935
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.613+447G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614935 | ||||||
| chr15:90614966
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+478A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614966 | ||||||
| chr15:90614988
|
C | T | 2 | a0002c0002t0001g0096a0002c0002t0033g0025 | 2 | HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.613+500C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90614988 | ||||||
| chr15:90615063
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051 | 3 | HG02258.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+592_613+603dup others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90615063 | |||||
| chr15:90615063
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0032g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613+588_613+603dup others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90615063 | |||||
| chr15:90615063
|
AAAAT | A | 13 | a0001c0001t0001g0250a0001c0001t0003g0264a0001c0001t0009g0041others(10): Show | 13 | HG01074.hp2 HG02055.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.613+600_613+603del others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90615063 | |||||
| chr15:90615076
|
A | AAATT | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+591_613+592ins others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90615076 | |||||
| chr15:90615080
|
A | T | 13 | a0001c0001t0001g0223a0001c0001t0003g0198a0002c0002t0003g0129others(10): Show | 13 | HG00639.hp2 HG00735.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+592A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615080 | ||||||
| chr15:90615084
|
A | T | 71 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0197others(68): Show | 71 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.613+596A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615084 | ||||||
| chr15:90615088
|
A | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(223): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.613+600A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615088 | ||||||
| chr15:90615092
|
T | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+604T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615092 | ||||||
| chr15:90615096
|
T | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+608T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615096 | ||||||
| chr15:90615126
|
A | G | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.613+638A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615126 | ||||||
| chr15:90615146
|
C | T | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+658C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615146 | ||||||
| chr15:90615152
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.613+664C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615152 | ||||||
| chr15:90615209
|
C | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+721C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615209 | ||||||
| chr15:90615269
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+781A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615269 | ||||||
| chr15:90615437
|
G | C | 13 | a0001c0001t0003g0264a0001c0001t0009g0041a0001c0001t0009g0195others(10): Show | 13 | HG00597.hp1 HG01074.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+949G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615437 | ||||||
| chr15:90615446
|
G | C | 1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.613+958G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615446 | ||||||
| chr15:90615481
|
T | C | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+993T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615481 | ||||||
| chr15:90615554
|
C | G | 1 | a0002c0002t0014g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.613+1066C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615554 | ||||||
| chr15:90615610
|
C | T | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+1122C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615610 | ||||||
| chr15:90615837
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.613+1349T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615837 | ||||||
| chr15:90615866
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.613+1378A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615866 | ||||||
| chr15:90615891
|
G | A | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.613+1403G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90615891 | ||||||
| chr15:90616018
|
C | T | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613+1530C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616018 | ||||||
| chr15:90616021
|
A | G | 7 | a0001c0001t0003g0264a0001c0001t0006g0047a0001c0001t0006g0050others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.613+1533A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616021 | ||||||
| chr15:90616026
|
A | AT | 14 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+1549dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90616026 | |||||
| chr15:90616068
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+1580A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616068 | ||||||
| chr15:90616118
|
G | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+1630G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616118 | ||||||
| chr15:90616214
|
G | A | 1 | a0007c0016t0001g0237 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.614-1669G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616214 | ||||||
| chr15:90616215
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-1668A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616215 | ||||||
| chr15:90616273
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-1610A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616273 | ||||||
| chr15:90616331
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-1552C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616331 | ||||||
| chr15:90616342
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.614-1541C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616342 | ||||||
| chr15:90616420
|
T | C | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-1463T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616420 | ||||||
| chr15:90616435
|
T | C | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.614-1448T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616435 | ||||||
| chr15:90616457
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.614-1426G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616457 | ||||||
| chr15:90616546
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0192 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.614-1337T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616546 | ||||||
| chr15:90616812
|
A | C | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.614-1071A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616812 | ||||||
| chr15:90616834
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-1049C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616834 | ||||||
| chr15:90616867
|
T | G | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-1016T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616867 | ||||||
| chr15:90616968
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(87): Show | 93 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.614-915A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616968 | ||||||
| chr15:90616999
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0165others(2): Show | 5 | HG02723.hp1 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-884T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90616999 | ||||||
| chr15:90617034
|
C | T | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-849C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617034 | ||||||
| chr15:90617059
|
A | G | 1 | a0003c0003t0001g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.614-824A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617059 | ||||||
| chr15:90617085
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.614-798A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617085 | ||||||
| chr15:90617275
|
T | A | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.614-608T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617275 | ||||||
| chr15:90617289
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.614-594C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617289 | ||||||
| chr15:90617440
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.614-443A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617440 | ||||||
| chr15:90617536
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(177): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.614-347C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617536 | ||||||
| chr15:90617652
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.614-231C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617652 | ||||||
| chr15:90617681
|
C | T | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.614-202C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617681 | ||||||
| chr15:90617731
|
A | G | 1 | a0002c0002t0015g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.614-152A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617731 | ||||||
| chr15:90617764
|
C | CA | 4 | a0002c0002t0007g0130a0002c0002t0018g0119a0002c0002t0044g0021others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-117dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr15 | 90617764 | |||||
| chr15:90617769
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.614-114G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617769 | ||||||
| chr15:90617821
|
G | A | 12 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(9): Show | 12 | HG00323.hp2 HG00438.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.614-62G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 7/14 | chr15 | 90617821 | ||||||
| chr15:90618075
|
G | A | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.699+107G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618075 | ||||||
| chr15:90618206
|
T | TA | 54 | a0001c0001t0001g0250a0001c0001t0001g0265a0001c0001t0003g0016others(51): Show | 54 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.699+254dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr15 | 90618206 | |||||
| chr15:90618206
|
T | TAA | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(124): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.699+253_699+254dup others(2): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr15 | 90618206 | |||||
| chr15:90618206
|
T | TAAA | 23 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 23 | HG01993.hp2 HG02015.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.699+252_699+254dup others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr15 | 90618206 | |||||
| chr15:90618316
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.699+348A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618316 | ||||||
| chr15:90618433
|
C | T | 1 | a0001c0004t0005g0005 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.699+465C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618433 | ||||||
| chr15:90618449
|
C | A | 2 | a0001c0001t0001g0208a0002c0002t0001g0074 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.699+481C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618449 | ||||||
| chr15:90618554
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.699+586C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618554 | ||||||
| chr15:90618608
|
T | C | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.699+640T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90618608 | ||||||
| chr15:90619035
|
G | A | 5 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(2): Show | 5 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.700-706G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619035 | ||||||
| chr15:90619233
|
G | T | 1 | a0005c0008t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-508G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619233 | ||||||
| chr15:90619286
|
G | A | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.700-455G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619286 | ||||||
| chr15:90619417
|
C | T | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.700-324C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619417 | ||||||
| chr15:90619511
|
A | G | 1 | a0003c0003t0003g0174 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.700-230A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619511 | ||||||
| chr15:90619713
|
A | T | 1 | a0003c0003t0003g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.700-28A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 8/14 | chr15 | 90619713 | ||||||
| chr15:90619881
|
C | T | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.749+91C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90619881 | ||||||
| chr15:90619902
|
T | A | 1 | a0001c0006t0003g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.749+112T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90619902 | ||||||
| chr15:90619964
|
TTAAAC | T | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+178_749+182del others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90619964 | |||||
| chr15:90619999
|
C | G | 1 | a0002c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.749+209C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90619999 | ||||||
| chr15:90619999
|
C | T | 8 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.749+209C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90619999 | ||||||
| chr15:90620181
|
T | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+391T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620181 | ||||||
| chr15:90620265
|
A | G | 1 | a0003c0003t0036g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.749+475A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620265 | ||||||
| chr15:90620386
|
A | C | 9 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(6): Show | 9 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.749+596A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620386 | ||||||
| chr15:90620498
|
A | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.749+708A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620498 | ||||||
| chr15:90620580
|
G | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.749+790G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620580 | ||||||
| chr15:90620609
|
G | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.749+819G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620609 | ||||||
| chr15:90620739
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+949G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620739 | ||||||
| chr15:90620787
|
T | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.749+997T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620787 | ||||||
| chr15:90620915
|
C | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1125C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620915 | ||||||
| chr15:90620998
|
T | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1208T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90620998 | ||||||
| chr15:90621005
|
T | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1215T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621005 | ||||||
| chr15:90621010
|
C | T | 12 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(9): Show | 12 | HG00323.hp2 HG00438.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.749+1220C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621010 | ||||||
| chr15:90621036
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1246G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621036 | ||||||
| chr15:90621163
|
GAAACAA | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.749+1393_749+1398d others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90621163 | |||||
| chr15:90621169
|
AAAACAAA others(3): Show |
A | 2 | a0001c0007t0001g0205a0001c0007t0001g0206 | 2 | HG00597.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.749+1383_749+1392d others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90621169 | |||||
| chr15:90621314
|
A | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1524A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621314 | ||||||
| chr15:90621348
|
A | AGTATC | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.749+1560_749+1564d others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90621348 | |||||
| chr15:90621437
|
C | A | 1 | a0002c0002t0001g0093 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.749+1647C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621437 | ||||||
| chr15:90621587
|
T | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1797T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621587 | ||||||
| chr15:90621640
|
T | G | 5 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(2): Show | 5 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.749+1850T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621640 | ||||||
| chr15:90621649
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+1859C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621649 | ||||||
| chr15:90621804
|
T | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+2014T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621804 | ||||||
| chr15:90621903
|
G | A | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.749+2113G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90621903 | ||||||
| chr15:90622016
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+2226G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622016 | ||||||
| chr15:90622079
|
A | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+2289A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622079 | ||||||
| chr15:90622186
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.749+2396G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622186 | ||||||
| chr15:90622209
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.749+2419C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622209 | ||||||
| chr15:90622280
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.749+2490C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622280 | ||||||
| chr15:90622317
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.749+2527G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622317 | ||||||
| chr15:90622337
|
C | G | 6 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.749+2547C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622337 | ||||||
| chr15:90622354
|
C | T | 8 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+2564C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622354 | ||||||
| chr15:90622402
|
T | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.749+2612T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622402 | ||||||
| chr15:90622479
|
G | A | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.749+2689G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622479 | ||||||
| chr15:90622560
|
C | G | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.749+2770C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622560 | ||||||
| chr15:90622575
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.749+2785G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622575 | ||||||
| chr15:90622615
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.749+2825C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622615 | ||||||
| chr15:90622673
|
A | C | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.749+2883A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622673 | ||||||
| chr15:90622813
|
T | TCAAGGTG others(2): Show |
5 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(2): Show | 5 | HG01243.hp1 HG01496.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.750-2963_750-2962i others(11): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622813 | ||||||
| chr15:90622817
|
C | CCACAGTG others(8): Show |
5 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(2): Show | 5 | HG01243.hp1 HG01496.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.750-2959_750-2958i others(17): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622817 | ||||||
| chr15:90622826
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.750-2950G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622826 | ||||||
| chr15:90622829
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.750-2947C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622829 | ||||||
| chr15:90622850
|
C | G | 4 | a0001c0001t0001g0048a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-2926C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622850 | ||||||
| chr15:90622864
|
A | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-2912A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622864 | ||||||
| chr15:90622882
|
A | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-2894A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622882 | ||||||
| chr15:90622932
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0003g0264a0001c0001t0040g0023 | 3 | HG01074.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.750-2844C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622932 | ||||||
| chr15:90622933
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0002g0063 | 2 | HG02523.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.750-2843G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90622933 | ||||||
| chr15:90623054
|
C | G | 8 | a0001c0001t0001g0227a0001c0004t0005g0004a0001c0004t0005g0005others(5): Show | 8 | HG00323.hp2 NA18940.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.750-2722C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623054 | ||||||
| chr15:90623132
|
C | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.750-2644C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623132 | ||||||
| chr15:90623228
|
T | A | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750-2548T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623228 | ||||||
| chr15:90623229
|
T | C | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750-2547T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623229 | ||||||
| chr15:90623235
|
T | A | 1 | a0003c0003t0003g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750-2541T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623235 | ||||||
| chr15:90623262
|
A | C | 59 | a0001c0001t0001g0203a0001c0001t0001g0229a0001c0001t0001g0231others(56): Show | 59 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.750-2514A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623262 | ||||||
| chr15:90623265
|
A | G | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.750-2511A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623265 | ||||||
| chr15:90623335
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.750-2441G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623335 | ||||||
| chr15:90623376
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(149): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.750-2400G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623376 | ||||||
| chr15:90623381
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(149): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.750-2395G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623381 | ||||||
| chr15:90623405
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.750-2371C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623405 | ||||||
| chr15:90623406
|
G | A | 1 | a0002c0002t0001g0096 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.750-2370G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623406 | ||||||
| chr15:90623497
|
T | C | 10 | a0001c0015t0029g0042a0002c0002t0012g0136a0002c0002t0012g0138others(7): Show | 10 | HG01346.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.750-2279T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623497 | ||||||
| chr15:90623588
|
G | A | 2 | a0001c0001t0046g0020a0002c0002t0020g0137 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.750-2188G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623588 | ||||||
| chr15:90623604
|
T | C | 70 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(67): Show | 70 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.750-2172T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623604 | ||||||
| chr15:90623644
|
A | G | 5 | a0001c0001t0046g0020a0002c0002t0018g0119a0002c0002t0020g0137others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.750-2132A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623644 | ||||||
| chr15:90623866
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.750-1910G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623866 | ||||||
| chr15:90623906
|
T | G | 8 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0032g0033others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.750-1870T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623906 | ||||||
| chr15:90623952
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-1824G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90623952 | ||||||
| chr15:90624044
|
T | TACA | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-1731_750-1730i others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90624044 | |||||
| chr15:90624175
|
C | T | 43 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(40): Show | 43 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.750-1601C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624175 | ||||||
| chr15:90624185
|
G | A | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.750-1591G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624185 | ||||||
| chr15:90624262
|
T | G | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.750-1514T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624262 | ||||||
| chr15:90624263
|
A | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-1513A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624263 | ||||||
| chr15:90624370
|
C | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-1406C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624370 | ||||||
| chr15:90624469
|
G | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-1307G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624469 | ||||||
| chr15:90624634
|
A | C | 2 | a0002c0002t0018g0119a0002c0002t0044g0021 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-1142A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624634 | ||||||
| chr15:90624651
|
A | G | 4 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.750-1125A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624651 | ||||||
| chr15:90624678
|
C | T | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.750-1098C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624678 | ||||||
| chr15:90624783
|
TG | T | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-989delG | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90624783 | |||||
| chr15:90624857
|
G | A | 1 | a0003c0003t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.750-919G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624857 | ||||||
| chr15:90624978
|
G | C | 1 | a0001c0001t0025g0188 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.750-798G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90624978 | ||||||
| chr15:90625015
|
A | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.750-761A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90625015 | ||||||
| chr15:90625029
|
A | G | 6 | a0001c0001t0004g0256a0002c0002t0004g0094a0002c0002t0004g0111others(3): Show | 6 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.750-747A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90625029 | ||||||
| chr15:90625147
|
G | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.750-629G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90625147 | ||||||
| chr15:90625213
|
CCGG | C | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.750-559_750-557del others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90625213 | |||||
| chr15:90625326
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.750-450T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90625326 | ||||||
| chr15:90625361
|
A | AAAT | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750-413_750-411dup others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr15 | 90625361 | |||||
| chr15:90625744
|
T | C | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.750-32T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 9/14 | chr15 | 90625744 | ||||||
| chr15:90626037
|
G | T | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+44G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626037 | ||||||
| chr15:90626149
|
C | T | 2 | a0001c0001t0046g0020a0002c0002t0020g0137 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.967+156C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626149 | ||||||
| chr15:90626217
|
T | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.967+224T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626217 | ||||||
| chr15:90626286
|
C | T | 1 | a0002c0002t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.967+293C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626286 | ||||||
| chr15:90626611
|
C | CTTTTTT | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.967+631_967+636dup others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90626611 | |||||
| chr15:90626611
|
C | CTTTTTTT | 20 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(17): Show | 20 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.967+630_967+636dup others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90626611 | |||||
| chr15:90626611
|
C | CTTTTTTT others(3): Show |
1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.967+627_967+636dup others(10): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90626611 | |||||
| chr15:90626611
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+625_967+636dup others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90626611 | |||||
| chr15:90626611
|
CT | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0122a0001c0001t0001g0246others(4): Show | 7 | HG01257.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+636delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90626611 | |||||
| chr15:90626654
|
T | C | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.967+661T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626654 | ||||||
| chr15:90626686
|
G | A | 1 | a0002c0002t0001g0064 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.967+693G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626686 | ||||||
| chr15:90626893
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.967+900G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626893 | ||||||
| chr15:90626895
|
G | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.967+902G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626895 | ||||||
| chr15:90626980
|
G | A | 2 | a0002c0002t0017g0133a0003c0003t0036g0031 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.967+987G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90626980 | ||||||
| chr15:90627136
|
G | C | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.967+1143G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627136 | ||||||
| chr15:90627216
|
T | G | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.967+1223T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627216 | ||||||
| chr15:90627237
|
G | C | 1 | a0002c0002t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.967+1244G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627237 | ||||||
| chr15:90627356
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.967+1363C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627356 | ||||||
| chr15:90627361
|
G | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.967+1368G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627361 | ||||||
| chr15:90627487
|
A | G | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.967+1494A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627487 | ||||||
| chr15:90627569
|
A | G | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.967+1576A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627569 | ||||||
| chr15:90627621
|
C | CT | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.968-1601dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90627621 | |||||
| chr15:90627696
|
A | T | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.968-1538A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627696 | ||||||
| chr15:90627706
|
C | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-1528C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627706 | ||||||
| chr15:90627740
|
G | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.968-1494G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627740 | ||||||
| chr15:90627785
|
C | CTAATTTT others(5): Show |
48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.968-1439_968-1438i others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90627785 | |||||
| chr15:90627835
|
T | C | 1 | a0003c0003t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.968-1399T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627835 | ||||||
| chr15:90627857
|
A | ACC | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.968-1375_968-1374d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90627857 | |||||
| chr15:90627889
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.968-1345C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627889 | ||||||
| chr15:90627893
|
C | T | 9 | a0001c0001t0002g0146a0001c0001t0002g0171a0001c0001t0002g0251others(6): Show | 9 | HG00438.hp2 NA18939.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.968-1341C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627893 | ||||||
| chr15:90627898
|
G | GCCA | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.968-1334_968-1332d others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90627898 | |||||
| chr15:90627902
|
C | CCAT | 3 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0196 | 3 | HG01346.hp1 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.968-1332_968-1331i others(5): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627902 | ||||||
| chr15:90627988
|
C | T | 6 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(3): Show | 6 | HG00323.hp2 NA18940.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.968-1246C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90627988 | ||||||
| chr15:90628014
|
G | A | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-1220G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628014 | ||||||
| chr15:90628091
|
C | G | 79 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(76): Show | 79 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.968-1143C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628091 | ||||||
| chr15:90628199
|
A | C | 2 | a0001c0001t0002g0171a0004c0005t0026g0088 | 2 | NA18993.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.968-1035A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628199 | ||||||
| chr15:90628204
|
G | A | 45 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(42): Show | 45 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.968-1030G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628204 | ||||||
| chr15:90628222
|
A | T | 79 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(76): Show | 79 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.968-1012A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628222 | ||||||
| chr15:90628241
|
GATA | G | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.968-984_968-982del others(3): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr15 | 90628241 | |||||
| chr15:90628291
|
G | A | 11 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.968-943G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628291 | ||||||
| chr15:90628328
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(220): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.968-906G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628328 | ||||||
| chr15:90628458
|
T | C | 2 | a0001c0001t0046g0020a0002c0002t0020g0137 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.968-776T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628458 | ||||||
| chr15:90628518
|
C | T | 7 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.968-716C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628518 | ||||||
| chr15:90628682
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.968-552C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628682 | ||||||
| chr15:90628736
|
G | A | 2 | a0001c0001t0046g0020a0002c0002t0020g0137 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.968-498G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628736 | ||||||
| chr15:90628747
|
G | C | 1 | a0002c0002t0004g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.968-487G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628747 | ||||||
| chr15:90628801
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(73): Show | 77 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.968-433G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628801 | ||||||
| chr15:90628867
|
C | A | 62 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(59): Show | 62 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.968-367C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628867 | ||||||
| chr15:90628881
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.968-353G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628881 | ||||||
| chr15:90628899
|
T | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.968-335T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628899 | ||||||
| chr15:90628955
|
C | T | 15 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(12): Show | 15 | HG00323.hp2 HG00438.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.968-279C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628955 | ||||||
| chr15:90628992
|
G | A | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(39): Show | 42 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.968-242G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628992 | ||||||
| chr15:90628995
|
A | G | 17 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(14): Show | 17 | HG01346.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.968-239A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90628995 | ||||||
| chr15:90629008
|
T | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.968-226T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90629008 | ||||||
| chr15:90629091
|
A | G | 3 | a0001c0001t0007g0120a0001c0001t0007g0219a0002c0002t0007g0130 | 3 | HG03139.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.968-143A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 10/14 | chr15 | 90629091 | ||||||
| chr15:90629669
|
C | T | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(31): Show | 34 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1266+137C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90629669 | ||||||
| chr15:90629670
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1266+138G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90629670 | ||||||
| chr15:90629745
|
A | G | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1266+213A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90629745 | ||||||
| chr15:90629816
|
G | C | 1 | a0001c0007t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1266+284G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90629816 | ||||||
| chr15:90629980
|
T | TCCCAAAG others(19): Show |
1 | a0003c0003t0039g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1266+449_1266+474d others(28): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90629980 | |||||
| chr15:90630083
|
A | T | 2 | a0001c0001t0003g0264a0001c0001t0040g0023 | 2 | HG01074.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1266+551A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630083 | ||||||
| chr15:90630088
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0192 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1266+556T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630088 | ||||||
| chr15:90630208
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1266+676G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630208 | ||||||
| chr15:90630291
|
C | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1266+759C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630291 | ||||||
| chr15:90630293
|
T | C | 11 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1266+761T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630293 | ||||||
| chr15:90630334
|
T | A | 2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1266+802T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630334 | ||||||
| chr15:90630394
|
T | C | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1266+862T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630394 | ||||||
| chr15:90630441
|
C | T | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1266+909C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630441 | ||||||
| chr15:90630447
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1266+915C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630447 | ||||||
| chr15:90630469
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1266+937G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630469 | ||||||
| chr15:90630567
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1266+1035T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630567 | ||||||
| chr15:90630583
|
T | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1266+1051T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630583 | ||||||
| chr15:90630644
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0224others(1): Show | 4 | HG01993.hp2 HG02015.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+1112A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630644 | ||||||
| chr15:90630742
|
TCTATTAC others(326): Show |
T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1266+1227_1266+155 others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630742 | |||||
| chr15:90630756
|
A | AT | 12 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0063others(9): Show | 12 | HG00099.hp1 HG00438.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+1256dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTT | 9 | a0001c0001t0002g0164a0001c0001t0006g0047a0001c0001t0006g0050others(6): Show | 9 | HG01167.hp2 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+1254_1266+125 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTT | 9 | a0001c0001t0002g0159a0001c0001t0007g0219a0001c0001t0009g0195others(6): Show | 9 | HG01261.hp1 HG02015.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+1253_1266+125 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTT | 9 | a0001c0001t0009g0041a0001c0004t0005g0004a0001c0004t0005g0009others(6): Show | 9 | HG00323.hp2 HG01516.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1266+1252_1266+125 others(9): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1266+1246_1266+125 others(15): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0003g0176a0003c0003t0003g0247 | 2 | HG02027.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1266+1245_1266+125 others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(6): Show |
6 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0173others(3): Show | 6 | HG02135.hp1 NA18612.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+1244_1266+125 others(17): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(13): Show |
1 | a0002c0002t0003g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1266+1237_1266+125 others(24): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1266+1236_1266+125 others(25): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(16): Show |
2 | a0001c0006t0003g0148a0003c0003t0001g0243 | 2 | HG02080.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1266+1234_1266+125 others(27): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(19): Show |
1 | a0001c0006t0003g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1266+1231_1266+125 others(30): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0003g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1266+1227_1266+125 others(34): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
A | T | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+1224A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630756 | ||||||
| chr15:90630756
|
AT | A | 9 | a0001c0001t0002g0150a0001c0001t0002g0155a0001c0001t0004g0256others(6): Show | 9 | HG00558.hp1 HG01081.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1266+1256delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
ATT | A | 10 | a0001c0001t0003g0255a0001c0001t0016g0168a0001c0001t0041g0172others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1266+1255_1266+125 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
ATTTTTTT others(8): Show |
A | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266+1242_1266+125 others(19): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630756
|
ATTTTTTT others(9): Show |
A | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+1241_1266+125 others(20): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90630756 | |||||
| chr15:90630999
|
G | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+1467G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90630999 | ||||||
| chr15:90631056
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1266+1524C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631056 | ||||||
| chr15:90631116
|
TTAA | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1266+1586_1266+158 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90631116 | |||||
| chr15:90631151
|
C | G | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1266+1619C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631151 | ||||||
| chr15:90631183
|
C | G | 45 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(42): Show | 45 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1266+1651C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631183 | ||||||
| chr15:90631200
|
C | T | 2 | a0001c0001t0002g0171a0004c0005t0026g0088 | 2 | NA18993.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1266+1668C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631200 | ||||||
| chr15:90631213
|
T | C | 2 | a0001c0001t0001g0121a0003c0003t0001g0218 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1266+1681T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631213 | ||||||
| chr15:90631215
|
G | T | 1 | a0002c0002t0018g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1266+1683G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631215 | ||||||
| chr15:90631512
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0192 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1266+1980G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631512 | ||||||
| chr15:90631672
|
T | C | 83 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(80): Show | 83 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1266+2140T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631672 | ||||||
| chr15:90631726
|
C | CA | 62 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(59): Show | 62 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1266+2209dupA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90631726 | |||||
| chr15:90631726
|
C | CAA | 10 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(7): Show | 10 | HG01081.hp2 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1266+2208_1266+220 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90631726 | |||||
| chr15:90631726
|
C | CAAA | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+2207_1266+220 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90631726 | |||||
| chr15:90631742
|
T | A | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1266+2210T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631742 | ||||||
| chr15:90631797
|
G | T | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+2265G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631797 | ||||||
| chr15:90631799
|
C | T | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+2267C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631799 | ||||||
| chr15:90631963
|
C | T | 1 | a0002c0002t0003g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1266+2431C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90631963 | ||||||
| chr15:90632076
|
A | AT | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1266+2557dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90632076 | |||||
| chr15:90632076
|
A | ATT | 18 | a0001c0001t0001g0165a0001c0001t0003g0264a0001c0001t0004g0256others(15): Show | 18 | HG00323.hp2 HG00438.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266+2556_1266+255 others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90632076 | |||||
| chr15:90632076
|
A | ATTT | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+2555_1266+255 others(7): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90632076 | |||||
| chr15:90632142
|
C | T | 1 | a0005c0008t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1266+2610C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632142 | ||||||
| chr15:90632197
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1266+2665A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632197 | ||||||
| chr15:90632205
|
A | C | 4 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+2673A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632205 | ||||||
| chr15:90632561
|
C | CTAGA | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+3030_1266+303 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90632561 | |||||
| chr15:90632628
|
A | G | 18 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(15): Show | 18 | HG00438.hp1 HG01346.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266+3096A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632628 | ||||||
| chr15:90632667
|
C | T | 3 | a0002c0002t0001g0080a0002c0002t0001g0092a0002c0002t0001g0116 | 3 | HG00099.hp2 HG01167.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1266+3135C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632667 | ||||||
| chr15:90632672
|
T | G | 1 | a0002c0002t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1266+3140T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632672 | ||||||
| chr15:90632755
|
C | T | 1 | a0002c0002t0003g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1266+3223C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632755 | ||||||
| chr15:90632794
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1266+3262A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632794 | ||||||
| chr15:90632985
|
G | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1266+3453G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90632985 | ||||||
| chr15:90633074
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1266+3542A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633074 | ||||||
| chr15:90633085
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1266+3553T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633085 | ||||||
| chr15:90633160
|
T | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1266+3628T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633160 | ||||||
| chr15:90633225
|
GCCTGGTT others(8): Show |
G | 4 | a0001c0001t0001g0121a0001c0001t0010g0035a0003c0003t0001g0217others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+3694_1266+370 others(19): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633225 | ||||||
| chr15:90633238
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0017a0003c0003t0003g0019 | 3 | NA18964.hp2 NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1266+3706T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633238 | ||||||
| chr15:90633269
|
C | T | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1266+3737C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633269 | ||||||
| chr15:90633290
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266+3758A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633290 | ||||||
| chr15:90633413
|
T | C | 6 | a0001c0001t0004g0256a0002c0002t0004g0094a0002c0002t0004g0111others(3): Show | 6 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+3881T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633413 | ||||||
| chr15:90633558
|
T | G | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+4026T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633558 | ||||||
| chr15:90633696
|
T | G | 3 | a0001c0001t0003g0264a0001c0001t0040g0023a0003c0003t0036g0031 | 3 | HG01074.hp2 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1266+4164T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633696 | ||||||
| chr15:90633703
|
G | GTTCT | 41 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(38): Show | 41 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.1266+4176_1266+417 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90633703 | |||||
| chr15:90633766
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1266+4234C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633766 | ||||||
| chr15:90633853
|
C | G | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+4321C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633853 | ||||||
| chr15:90633861
|
A | G | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+4329A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633861 | ||||||
| chr15:90633890
|
C | A | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1266+4358C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633890 | ||||||
| chr15:90633901
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1266+4369T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633901 | ||||||
| chr15:90633956
|
T | C | 2 | a0002c0002t0014g0134a0002c0002t0014g0135 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1266+4424T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633956 | ||||||
| chr15:90633963
|
G | C | 67 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1266+4431G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633963 | ||||||
| chr15:90633999
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0166 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1267-4447G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90633999 | ||||||
| chr15:90634025
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1267-4421A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634025 | ||||||
| chr15:90634040
|
A | T | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1267-4406A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634040 | ||||||
| chr15:90634117
|
A | AT | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(131): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1267-4317dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90634117 | |||||
| chr15:90634129
|
T | TTGAGA | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0165others(3): Show | 6 | HG02723.hp1 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-4317_1267-431 others(9): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634129 | ||||||
| chr15:90634130
|
G | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0165others(3): Show | 6 | HG02723.hp1 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-4316G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634130 | ||||||
| chr15:90634237
|
C | T | 50 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(47): Show | 50 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.1267-4209C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634237 | ||||||
| chr15:90634331
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0044others(48): Show | 53 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.1267-4115T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634331 | ||||||
| chr15:90634334
|
A | C | 86 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267-4112A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634334 | ||||||
| chr15:90634402
|
C | T | 86 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267-4044C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634402 | ||||||
| chr15:90634547
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1267-3899G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634547 | ||||||
| chr15:90634550
|
C | G | 40 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1267-3896C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634550 | ||||||
| chr15:90634681
|
G | A | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1267-3765G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634681 | ||||||
| chr15:90634707
|
A | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1267-3739A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634707 | ||||||
| chr15:90634839
|
G | C | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1267-3607G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634839 | ||||||
| chr15:90634905
|
C | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1267-3541C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634905 | ||||||
| chr15:90634915
|
G | T | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-3531G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634915 | ||||||
| chr15:90634966
|
T | G | 1 | a0001c0001t0002g0159 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1267-3480T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90634966 | ||||||
| chr15:90635019
|
A | C | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267-3427A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635019 | ||||||
| chr15:90635046
|
C | T | 86 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267-3400C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635046 | ||||||
| chr15:90635078
|
C | T | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1267-3368C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635078 | ||||||
| chr15:90635119
|
T | C | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-3327T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635119 | ||||||
| chr15:90635124
|
C | CTCTT | 86 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267-3321_1267-332 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90635124 | |||||
| chr15:90635131
|
T | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-3315T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635131 | ||||||
| chr15:90635221
|
A | G | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-3225A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635221 | ||||||
| chr15:90635318
|
T | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1267-3128T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635318 | ||||||
| chr15:90635359
|
C | T | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1267-3087C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635359 | ||||||
| chr15:90635383
|
A | G | 1 | a0003c0003t0027g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1267-3063A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635383 | ||||||
| chr15:90635416
|
G | A | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(66): Show | 69 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1267-3030G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635416 | ||||||
| chr15:90635442
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1267-3004C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635442 | ||||||
| chr15:90635473
|
C | T | 2 | a0001c0001t0001g0236a0002c0002t0001g0071 | 2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1267-2973C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635473 | ||||||
| chr15:90635474
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1267-2972G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635474 | ||||||
| chr15:90635538
|
G | T | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-2908G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635538 | ||||||
| chr15:90635542
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-2904G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635542 | ||||||
| chr15:90635607
|
T | C | 85 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(82): Show | 85 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1267-2839T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635607 | ||||||
| chr15:90635652
|
A | ACTCTGTC others(10): Show |
1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-2778_1267-277 others(21): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90635652 | |||||
| chr15:90635757
|
G | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0257a0001c0001t0001g0261 | 3 | HG02257.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1267-2689G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635757 | ||||||
| chr15:90635763
|
C | CG | 63 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(60): Show | 63 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1267-2680dupG | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90635763 | |||||
| chr15:90635817
|
A | G | 85 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(82): Show | 85 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1267-2629A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635817 | ||||||
| chr15:90635896
|
G | C | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-2550G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635896 | ||||||
| chr15:90635931
|
T | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1267-2515T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90635931 | ||||||
| chr15:90636060
|
A | T | 1 | a0003c0013t0005g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1267-2386A>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636060 | ||||||
| chr15:90636068
|
T | G | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1267-2378T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636068 | ||||||
| chr15:90636077
|
G | A | 11 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(8): Show | 11 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1267-2369G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636077 | ||||||
| chr15:90636104
|
T | G | 1 | a0002c0002t0007g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1267-2342T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636104 | ||||||
| chr15:90636143
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1267-2303C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636143 | ||||||
| chr15:90636189
|
GTACTGGT others(13): Show |
G | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1267-2254_1267-223 others(24): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90636189 | |||||
| chr15:90636269
|
T | C | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1267-2177T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636269 | ||||||
| chr15:90636309
|
G | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-2137G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636309 | ||||||
| chr15:90636336
|
G | A | 3 | a0002c0002t0001g0080a0002c0002t0001g0092a0002c0002t0001g0116 | 3 | HG00099.hp2 HG01167.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1267-2110G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636336 | ||||||
| chr15:90636355
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(201): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1267-2091C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636355 | ||||||
| chr15:90636357
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1267-2089T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636357 | ||||||
| chr15:90636402
|
T | G | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-2044T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636402 | ||||||
| chr15:90636408
|
A | G | 1 | a0001c0001t0040g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1267-2038A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636408 | ||||||
| chr15:90636711
|
AAAAC | A | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-1728_1267-172 others(8): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90636711 | |||||
| chr15:90636861
|
C | T | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-1585C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636861 | ||||||
| chr15:90636881
|
A | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1267-1565A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90636881 | ||||||
| chr15:90637012
|
T | A | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1267-1434T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637012 | ||||||
| chr15:90637092
|
A | G | 7 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(4): Show | 7 | HG01496.hp2 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-1354A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637092 | ||||||
| chr15:90637169
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(42): Show | 46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1267-1277G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637169 | ||||||
| chr15:90637229
|
A | C | 24 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(21): Show | 24 | HG00323.hp2 HG00438.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1267-1217A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637229 | ||||||
| chr15:90637250
|
T | A | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1267-1196T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637250 | ||||||
| chr15:90637255
|
G | A | 3 | a0001c0001t0007g0120a0001c0001t0007g0219a0002c0002t0007g0130 | 3 | HG03139.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1267-1191G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637255 | ||||||
| chr15:90637297
|
C | T | 1 | a0002c0002t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1267-1149C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637297 | ||||||
| chr15:90637345
|
A | G | 1 | a0002c0002t0031g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1267-1101A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637345 | ||||||
| chr15:90637376
|
G | A | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1267-1070G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637376 | ||||||
| chr15:90637450
|
C | T | 47 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(44): Show | 47 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1267-996C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637450 | ||||||
| chr15:90637470
|
G | T | 2 | a0002c0002t0004g0111a0002c0002t0004g0112 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1267-976G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637470 | ||||||
| chr15:90637473
|
T | C | 86 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267-973T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637473 | ||||||
| chr15:90637553
|
A | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1267-893A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637553 | ||||||
| chr15:90637574
|
T | G | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-872T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637574 | ||||||
| chr15:90637637
|
T | G | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-809T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637637 | ||||||
| chr15:90637884
|
C | T | 1 | a0002c0002t0038g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1267-562C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90637884 | ||||||
| chr15:90638145
|
T | TAAAACAA others(3): Show |
83 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(80): Show | 83 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1267-294_1267-285d others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90638145 | |||||
| chr15:90638145
|
T | TAAAACAA others(8): Show |
2 | a0002c0002t0013g0131a0002c0002t0013g0194 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1267-299_1267-285d others(17): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr15 | 90638145 | |||||
| chr15:90638149
|
A | C | 1 | a0001c0001t0002g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1267-297A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638149 | ||||||
| chr15:90638257
|
A | C | 80 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(77): Show | 80 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1267-189A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638257 | ||||||
| chr15:90638307
|
G | A | 2 | a0001c0001t0003g0264a0001c0001t0040g0023 | 2 | HG01074.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1267-139G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638307 | ||||||
| chr15:90638335
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1267-111C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638335 | ||||||
| chr15:90638337
|
C | T | 3 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0006t0003g0148 | 3 | HG03139.hp1 HG03239.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1267-109C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638337 | ||||||
| chr15:90638397
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1267-49C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638397 | ||||||
| chr15:90638398
|
G | A | 1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1267-48G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 11/14 | chr15 | 90638398 | ||||||
| chr15:90638664
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1467+18C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 12/14 | chr15 | 90638664 | ||||||
| chr15:90639064
|
G | A | 1 | a0003c0003t0001g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1548+249G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639064 | ||||||
| chr15:90639170
|
G | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1548+355G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639170 | ||||||
| chr15:90639184
|
T | C | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1548+369T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639184 | ||||||
| chr15:90639201
|
T | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1548+386T>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639201 | ||||||
| chr15:90639328
|
T | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1548+513T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639328 | ||||||
| chr15:90639394
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1548+579C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639394 | ||||||
| chr15:90639426
|
A | AGGGTTGA others(8): Show |
1 | a0003c0003t0027g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1548+612_1548+626d others(17): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90639426 | |||||
| chr15:90639447
|
CT | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0269others(40): Show | 43 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1548+652delT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90639447 | |||||
| chr15:90639447
|
CTT | C | 20 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0264others(17): Show | 20 | HG01074.hp2 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1548+651_1548+652d others(4): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90639447 | |||||
| chr15:90639447
|
CTTTT | C | 15 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(12): Show | 15 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1548+649_1548+652d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90639447 | |||||
| chr15:90639481
|
A | C | 1 | a0002c0009t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1548+666A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639481 | ||||||
| chr15:90639511
|
G | A | 11 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1548+696G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639511 | ||||||
| chr15:90639544
|
G | A | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1548+729G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639544 | ||||||
| chr15:90639574
|
T | A | 1 | a0002c0002t0002g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1548+759T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639574 | ||||||
| chr15:90639677
|
G | T | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1548+862G>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639677 | ||||||
| chr15:90639802
|
G | C | 82 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1548+987G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639802 | ||||||
| chr15:90639832
|
G | A | 1 | a0003c0003t0001g0234 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1548+1017G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639832 | ||||||
| chr15:90639905
|
T | C | 25 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(22): Show | 25 | HG01346.hp1 HG01496.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1548+1090T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639905 | ||||||
| chr15:90639965
|
C | T | 6 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549-1132C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639965 | ||||||
| chr15:90639966
|
G | A | 1 | a0001c0001t0003g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1549-1131G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90639966 | ||||||
| chr15:90640018
|
C | T | 9 | a0001c0001t0011g0030a0001c0001t0011g0034a0001c0001t0011g0140others(6): Show | 9 | HG01496.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1549-1079C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640018 | ||||||
| chr15:90640039
|
A | G | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549-1058A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640039 | ||||||
| chr15:90640104
|
G | C | 1 | a0001c0001t0001g0001 | 3 | HG01123.hp1 HG01258.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1549-993G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640104 | ||||||
| chr15:90640207
|
A | ATGAT | 4 | a0002c0002t0012g0136a0002c0002t0012g0138a0002c0002t0015g0026others(1): Show | 4 | HG01346.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1549-889_1549-886d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90640207 | |||||
| chr15:90640341
|
C | T | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549-756C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640341 | ||||||
| chr15:90640366
|
G | GCCTT | 44 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0063others(41): Show | 44 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1549-728_1549-725d others(6): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90640366 | |||||
| chr15:90640397
|
G | A | 41 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(38): Show | 41 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1549-700G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640397 | ||||||
| chr15:90640555
|
GCATGTGG others(3): Show |
G | 1 | a0001c0001t0002g0225 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1549-539_1549-530d others(12): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90640555 | |||||
| chr15:90640629
|
C | A | 49 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(46): Show | 49 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1549-468C>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640629 | ||||||
| chr15:90640631
|
G | A | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1549-466G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640631 | ||||||
| chr15:90640634
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1549-463A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640634 | ||||||
| chr15:90640647
|
A | G | 3 | a0002c0002t0018g0119a0002c0002t0044g0021a0004c0005t0045g0132 | 3 | HG02559.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1549-450A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640647 | ||||||
| chr15:90640666
|
A | G | 1 | a0002c0002t0047g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1549-431A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640666 | ||||||
| chr15:90640678
|
TA | T | 130 | a0001c0001t0001g0211a0001c0001t0002g0040a0001c0001t0002g0054others(127): Show | 130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1549-408delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr15 | 90640678 | |||||
| chr15:90640723
|
T | A | 8 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(5): Show | 8 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1549-374T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640723 | ||||||
| chr15:90640797
|
C | G | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1549-300C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640797 | ||||||
| chr15:90640815
|
C | G | 1 | a0008c0012t0021g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1549-282C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640815 | ||||||
| chr15:90640942
|
C | T | 19 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(16): Show | 19 | HG00735.hp1 HG00735.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1549-155C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90640942 | ||||||
| chr15:90641056
|
C | T | 5 | a0001c0001t0006g0047a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1549-41C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 13/14 | chr15 | 90641056 | ||||||
| chr15:90641215
|
C | CT | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1651+17dupT | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641215 | |||||
| chr15:90641251
|
C | T | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1651+52C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641251 | ||||||
| chr15:90641304
|
T | C | 16 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(13): Show | 16 | HG01346.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1651+105T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641304 | ||||||
| chr15:90641383
|
G | A | 3 | a0001c0001t0035g0061a0002c0002t0017g0133a0003c0003t0036g0031 | 3 | HG02572.hp2 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1651+184G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641383 | ||||||
| chr15:90641391
|
A | C | 11 | a0001c0001t0007g0120a0001c0001t0007g0219a0001c0001t0009g0041others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1651+192A>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641391 | ||||||
| chr15:90641426
|
G | A | 45 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(42): Show | 45 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1651+227G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641426 | ||||||
| chr15:90641516
|
C | T | 1 | a0001c0001t0035g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1651+317C>T | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641516 | ||||||
| chr15:90641517
|
G | A | 9 | a0001c0004t0005g0004a0001c0004t0005g0005a0001c0004t0005g0009others(6): Show | 9 | HG00323.hp2 HG00438.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1651+318G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641517 | ||||||
| chr15:90641561
|
A | G | 73 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(70): Show | 73 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.1651+362A>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641561 | ||||||
| chr15:90641566
|
G | A | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(29): Show | 32 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1652-366G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641566 | ||||||
| chr15:90641641
|
G | A | 1 | a0002c0002t0004g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1652-291G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641641 | ||||||
| chr15:90641653
|
T | A | 4 | a0001c0001t0009g0041a0001c0001t0009g0195a0001c0001t0019g0028others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1652-279T>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641653 | ||||||
| chr15:90641685
|
C | CAAAAAAA others(5): Show |
8 | a0001c0001t0007g0120a0001c0001t0009g0195a0001c0001t0019g0028others(5): Show | 8 | HG01346.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1652-245_1652-234d others(14): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641685 | |||||
| chr15:90641685
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0007g0219a0001c0001t0009g0041a0001c0015t0029g0042others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1652-246_1652-234d others(15): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641685 | |||||
| chr15:90641685
|
C | CAAAAAAA others(7): Show |
2 | a0003c0003t0009g0032a0003c0014t0030g0253 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1652-234_1652-233i others(16): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641685 | |||||
| chr15:90641685
|
C | CAAAAAAA others(12): Show |
1 | a0002c0002t0033g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1652-234_1652-233i others(21): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641685 | |||||
| chr15:90641685
|
CA | C | 55 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1652-234delA | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr15 | 90641685 | |||||
| chr15:90641767
|
T | C | 48 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0157others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1652-165T>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641767 | ||||||
| chr15:90641791
|
G | C | 1 | a0001c0001t0023g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1652-141G>C | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641791 | ||||||
| chr15:90641800
|
C | G | 1 | a0002c0002t0022g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1652-132C>G | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641800 | ||||||
| chr15:90641811
|
G | A | 1 | a0002c0002t0048g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1652-121G>A | CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 14/14 | chr15 | 90641811 |