Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23373 |
|---|---|
| ensemblid | ENSG00000105662.16 |
| hgncid | 16062 |
| symbol | CRTC1 |
| name | CREB regulated transcription coactivator 1 |
| refseq_nuc | NM_015321.3 |
| refseq_prot | NP_056136.2 |
| ensembl_nuc | ENST00000321949.13 |
| ensembl_prot | ENSP00000323332.7 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 18683680 |
| end | 18782333 |
| strand | + |
| ver | v1.2 |
| region | chr19:18683680-18782333 |
| region5000 | chr19:18678680-18787333 |
| regionname0 | CRTC1_chr19_18683680_18782333 |
| regionname5000 | CRTC1_chr19_18678680_18787333 |
| 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 | 1/1 | 634 | 224 | 78 | 58 | 51 | 6 | 29 | 33 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002 | 0/0 | 634 | 39 | 2 | 3 | 21 | 5 | 8 | 16 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0003 | 0/0 | 634 | 7 | 0 | 4 | 1 | 1 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0004 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0005 | 0/0 | 634 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0006 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0007 | 0/0 | 634 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| 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 | 1/1 | 1905 | 206 | 77 | 46 | 48 | 6 | 27 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0002 | 0/0 | 1905 | 36 | 2 | 3 | 21 | 5 | 5 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0003 | 0/0 | 1905 | 17 | 0 | 12 | 3 | 0 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0004 | 0/0 | 1905 | 7 | 0 | 4 | 1 | 1 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0005 | 0/0 | 1905 | 3 | 0 | 0 | 0 | 0 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0006 | 0/0 | 1905 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0007 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0008 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0009 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| c0010 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| 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 | 4975 | 129 | 31 | 33 | 38 | 3 | 22 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0002 | 0/0 | 4975 | 42 | 9 | 15 | 14 | 1 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0003 | 0/0 | 4975 | 37 | 4 | 1 | 20 | 5 | 7 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0004 | 0/0 | 4974 | 13 | 11 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0005 | 0/0 | 4974 | 9 | 8 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0006 | 0/0 | 4975 | 6 | 6 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0007 | 0/0 | 4975 | 5 | 0 | 2 | 0 | 1 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0008 | 0/0 | 4975 | 4 | 4 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0009 | 0/0 | 4975 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0010 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0011 | 0/0 | 4973 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0012 | 0/0 | 4975 | 2 | 0 | 1 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0013 | 0/0 | 4975 | 2 | 0 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0014 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0015 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0016 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0017 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0018 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0019 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0020 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0021 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0022 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0023 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0024 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0025 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0026 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0027 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0028 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0029 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0030 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0031 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| t0032 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| 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 | 1/1 | 1905 | 206 | 77 | 46 | 48 | 6 | 27 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0003 | 0/0 | 1905 | 17 | 0 | 12 | 3 | 0 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0007 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002 | 0/0 | 1905 | 36 | 2 | 3 | 21 | 5 | 5 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0005 | 0/0 | 1905 | 3 | 0 | 0 | 0 | 0 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0003c0004 | 0/0 | 1905 | 7 | 0 | 4 | 1 | 1 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0004c0008 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0005c0009 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0006c0010 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0007c0006 | 0/0 | 1905 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6879 | 126 | 30 | 32 | 37 | 3 | 22 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0002 | 0/0 | 6879 | 23 | 9 | 2 | 10 | 0 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0003 | 0/0 | 6879 | 3 | 2 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0004 | 0/0 | 6878 | 13 | 11 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0005 | 0/0 | 6878 | 9 | 8 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0006 | 0/0 | 6879 | 6 | 6 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0007 | 0/0 | 6879 | 5 | 0 | 2 | 0 | 1 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0008 | 0/0 | 6879 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0009 | 0/0 | 6879 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0011 | 0/0 | 6877 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0012 | 0/0 | 6879 | 2 | 0 | 1 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0013 | 0/0 | 6879 | 2 | 0 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0014 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0015 | 0/0 | 6878 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0018 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0019 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0022 | 0/0 | 6878 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0027 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0029 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0030 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0031 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0001t0032 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0003t0002 | 0/0 | 6879 | 14 | 0 | 10 | 3 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0003t0024 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0003t0025 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0003t0028 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0001c0007t0008 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0003 | 0/0 | 6879 | 30 | 1 | 1 | 19 | 5 | 4 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0010 | 0/0 | 6878 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0016 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0017 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0020 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0002t0021 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0002c0005t0003 | 0/0 | 6879 | 3 | 0 | 0 | 0 | 0 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0003c0004t0002 | 0/0 | 6879 | 5 | 0 | 3 | 1 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0003c0004t0023 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0003c0004t0026 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0004c0008t0003 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0005c0009t0001 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0006c0010t0001 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| a0007c0006t0001 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | copy fasta | chr19 | 18678680 | 18787333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0019g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0022g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0027g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0029g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0030g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0031g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0032g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0024g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0028g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0007t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0010g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0016g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0017g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0020g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0021g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0023g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0026g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0004c0008t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0005c0009t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0006c0010t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0007c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0133 | EUR | GBR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0190 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00323 | hp1 | a0003 | c0004 | t0002 | g0120 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0160 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00544 | hp2 | a0002 | c0002 | t0010 | g0263 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0162 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00733 | hp2 | a0001 | c0001 | t0029 | g0062 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0121 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01069 | hp2 | a0001 | c0001 | t0015 | g0005 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0030 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0221 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0214 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01099 | hp1 | a0002 | c0002 | t0020 | g0216 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01175 | hp2 | a0003 | c0004 | t0002 | g0243 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01192 | hp1 | a0003 | c0004 | t0002 | g0242 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0172 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0032 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01243 | hp2 | a0003 | c0004 | t0026 | g0241 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0114 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01346 | hp1 | a0001 | c0001 | t0013 | g0069 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0255 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01361 | hp1 | a0001 | c0001 | t0019 | g0139 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01361 | hp2 | a0001 | c0003 | t0028 | g0094 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01496 | hp2 | a0001 | c0003 | t0025 | g0201 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0204 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01517 | hp1 | a0001 | c0001 | t0014 | g0023 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0203 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01884 | hp2 | a0001 | c0001 | t0027 | g0004 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01928 | hp2 | a0002 | c0002 | t0017 | g0176 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0270 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01978 | hp2 | a0005 | c0009 | t0001 | g0068 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02004 | hp2 | a0001 | c0001 | t0013 | g0065 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0089 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02135 | hp2 | a0003 | c0004 | t0002 | g0240 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02145 | hp1 | a0001 | c0001 | t0031 | g0251 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0205 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CDX | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02257 | hp2 | a0002 | c0002 | t0016 | g0060 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0256 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0152 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02647 | hp2 | a0006 | c0010 | t0001 | g0141 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02735 | hp2 | a0001 | c0003 | t0024 | g0200 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02886 | hp1 | a0001 | c0001 | t0030 | g0041 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0124 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03017 | hp2 | a0002 | c0005 | t0003 | g0199 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0226 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03139 | hp1 | a0001 | c0007 | t0008 | g0025 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0027 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03492 | hp1 | a0002 | c0002 | t0021 | g0217 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0034 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0187 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0273 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0207 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03831 | hp2 | a0002 | c0005 | t0003 | g0158 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04115 | hp1 | a0001 | c0001 | t0032 | g0213 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04115 | hp2 | a0002 | c0005 | t0003 | g0254 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0224 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0218 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | CHB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18940 | hp2 | a0007 | c0006 | t0001 | g0149 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0173 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18977 | hp1 | a0002 | c0002 | t0010 | g0154 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0202 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18985 | hp2 | a0002 | c0002 | t0003 | g0261 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0272 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | LWK | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19054 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19074 | hp2 | a0002 | c0002 | t0003 | g0209 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19083 | hp2 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0136 | AFR | ASW | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ASW | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0191 | EUR | TSI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0057 | EUR | TSI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | GIH | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20905 | hp2 | a0003 | c0004 | t0023 | g0118 | SAS | GIH | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02559 | hp2 | a0004 | c0008 | t0003 | g0123 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0122 | REF | REF | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18753557
|
T | C | 1 | a0007 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.596T>C | p.Leu199Pro | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/14 | 619/6879 | 596/1905 | 199/634 | chr19 | 18753557 | ||
| chr19:18753584
|
A | G | 1 | a0006 | 1 | HG02647.hp2 | missense_variant&splice_region_variant | MODERATE | c.623A>G | p.Lys208Arg | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/14 | 646/6879 | 623/1905 | 208/634 | chr19 | 18753584 | ||
| chr19:18765448
|
G | A | 1 | a0003 | 7 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(4): Show |
missense_variant | MODERATE | c.931G>A | p.Val311Ile | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/14 | 954/6879 | 931/1905 | 311/634 | chr19 | 18765448 | ||
| chr19:18765482
|
G | A | 1 | a0004 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.965G>A | p.Arg322His | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/14 | 988/6879 | 965/1905 | 322/634 | chr19 | 18765482 | ||
| chr19:18765496
|
C | T | 1 | a0005 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.979C>T | p.Pro327Ser | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/14 | 1002/6879 | 979/1905 | 327/634 | chr19 | 18765496 | ||
| chr19:18765499
|
A | G | 2 | a0002a0004 | 40 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(37): Show |
missense_variant | MODERATE | c.982A>G | p.Thr328Ala | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/14 | 1005/6879 | 982/1905 | 328/634 | chr19 | 18765499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18759583
|
C | T | 1 | a0002c0005 | 3 | HG03017.hp2 HG03831.hp2 HG04115.hp2 |
synonymous_variant | LOW | c.657C>T | p.Pro219Pro | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/14 | 680/6879 | 657/1905 | 219/634 | chr19 | 18759583 | ||
| chr19:18760188
|
G | A | 1 | a0001c0007 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.846G>A | p.Ala282Ala | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/14 | 869/6879 | 846/1905 | 282/634 | chr19 | 18760188 | ||
| chr19:18777340
|
C | T | 1 | a0001c0003 | 17 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(14): Show |
synonymous_variant | LOW | c.1863C>T | p.Ala621Ala | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 1886/6879 | 1863/1905 | 621/634 | chr19 | 18777340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18777417
|
C | T | 1 | a0001c0001t0032 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 35 | chr19 | 18777417 | |||||
| chr19:18777520
|
C | T | 1 | a0001c0001t0031 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 138 | chr19 | 18777520 | |||||
| chr19:18778165
|
A | G | 1 | a0001c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 783 | chr19 | 18778165 | |||||
| chr19:18778365
|
T | C | 1 | a0001c0001t0014 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 983 | chr19 | 18778365 | |||||
| chr19:18778867
|
C | G | 1 | a0001c0001t0029 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1485C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 1485 | chr19 | 18778867 | |||||
| chr19:18778892
|
C | T | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(10): Show | 62 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1510C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 1510 | chr19 | 18778892 | |||||
| chr19:18779014
|
T | G | 1 | a0001c0001t0009 | 2 | HG02630.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1632T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 1632 | chr19 | 18779014 | |||||
| chr19:18779457
|
CT | C | 3 | a0001c0001t0011a0001c0001t0015a0002c0002t0010 | 5 | HG00544.hp2 HG01069.hp2 HG01167.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2089delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2089 | INFO_REALIGN_3_PRIME | chr19 | 18779457 | ||||
| chr19:18779530
|
TA | T | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(1): Show | 25 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2157delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2157 | INFO_REALIGN_3_PRIME | chr19 | 18779530 | ||||
| chr19:18779672
|
G | A | 3 | a0001c0001t0008a0001c0007t0008a0002c0002t0016 | 5 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2290G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2290 | chr19 | 18779672 | |||||
| chr19:18779704
|
C | T | 1 | a0001c0001t0006 | 6 | HG02257.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2322C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2322 | chr19 | 18779704 | |||||
| chr19:18779928
|
G | A | 1 | a0001c0001t0013 | 2 | HG01346.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2546G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2546 | chr19 | 18779928 | |||||
| chr19:18780136
|
G | A | 1 | a0002c0002t0017 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2754G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2754 | chr19 | 18780136 | |||||
| chr19:18780327
|
C | T | 1 | a0002c0002t0016 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 2945 | chr19 | 18780327 | |||||
| chr19:18780395
|
C | T | 1 | a0001c0003t0028 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3013C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3013 | chr19 | 18780395 | |||||
| chr19:18780437
|
C | A | 1 | a0001c0001t0005 | 9 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3055C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3055 | chr19 | 18780437 | |||||
| chr19:18780466
|
G | A | 1 | a0003c0004t0023 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3084 | chr19 | 18780466 | |||||
| chr19:18780538
|
G | A | 1 | a0002c0002t0017 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3156G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3156 | chr19 | 18780538 | |||||
| chr19:18780565
|
C | A | 1 | a0001c0001t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3183C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3183 | chr19 | 18780565 | |||||
| chr19:18780641
|
G | A | 1 | a0001c0001t0019 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3259G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3259 | chr19 | 18780641 | |||||
| chr19:18780658
|
G | A | 1 | a0001c0001t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3276G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3276 | chr19 | 18780658 | |||||
| chr19:18780859
|
C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3477C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3477 | chr19 | 18780859 | |||||
| chr19:18780862
|
C | T | 1 | a0001c0001t0006 | 6 | HG02257.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3480C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3480 | chr19 | 18780862 | |||||
| chr19:18781161
|
C | T | 1 | a0001c0001t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3779C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 3779 | chr19 | 18781161 | |||||
| chr19:18781414
|
T | C | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 76 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*4032T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4032 | chr19 | 18781414 | |||||
| chr19:18781417
|
C | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(1): Show | 25 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4035C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4035 | chr19 | 18781417 | |||||
| chr19:18781571
|
A | G | 1 | a0002c0002t0021 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4189A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4189 | chr19 | 18781571 | |||||
| chr19:18781710
|
C | T | 1 | a0002c0002t0020 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4328C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4328 | chr19 | 18781710 | |||||
| chr19:18781732
|
G | C | 1 | a0001c0003t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4350G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4350 | chr19 | 18781732 | |||||
| chr19:18781788
|
A | T | 1 | a0003c0004t0026 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4406A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4406 | chr19 | 18781788 | |||||
| chr19:18781842
|
G | A | 1 | a0001c0001t0012 | 2 | HG00323.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4460G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4460 | chr19 | 18781842 | |||||
| chr19:18781918
|
C | A | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(9): Show | 61 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*4536C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4536 | chr19 | 18781918 | |||||
| chr19:18782308
|
G | A | 1 | a0001c0001t0007 | 5 | HG01243.hp1 HG01496.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4926G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 14/14 | 4926 | chr19 | 18782308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18683911
|
T | TG | 61 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0222others(58): Show | 61 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.126+92dupG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18683911 | |||||
| chr19:18683919
|
GGCGCGGC others(13): Show |
G | 2 | a0001c0001t0001g0212a0001c0001t0002g0211 | 2 | HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.126+110_126+129del others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18683919 | |||||
| chr19:18684087
|
C | T | 1 | a0002c0002t0003g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+259C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18684087 | ||||||
| chr19:18684488
|
CTCTTGGA others(15): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.126+663_126+684del others(22): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18684488 | |||||
| chr19:18684678
|
CT | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+851delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18684678 | ||||||
| chr19:18684768
|
T | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.126+940T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18684768 | ||||||
| chr19:18684884
|
T | TCTTCC | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.126+1059_126+1060i others(7): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18684884 | |||||
| chr19:18685044
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+1216C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685044 | ||||||
| chr19:18685276
|
G | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+1448G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685276 | ||||||
| chr19:18685366
|
AT | A | 12 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG02056.hp2 HG02071.hp1 NA18977.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+1539delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685366 | ||||||
| chr19:18685367
|
T | A | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 116 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.126+1539T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685367 | ||||||
| chr19:18685446
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.126+1618T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685446 | ||||||
| chr19:18685512
|
C | T | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+1684C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685512 | ||||||
| chr19:18685739
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.126+1911A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685739 | ||||||
| chr19:18685841
|
T | C | 1 | a0001c0001t0032g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+2013T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685841 | ||||||
| chr19:18685845
|
G | A | 13 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0119others(10): Show | 13 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+2017G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685845 | ||||||
| chr19:18685892
|
A | C | 3 | a0002c0002t0003g0209a0002c0002t0003g0210a0002c0002t0003g0272 | 3 | NA18941.hp1 NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.126+2064A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685892 | ||||||
| chr19:18685916
|
C | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+2088C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18685916 | ||||||
| chr19:18686133
|
G | A | 1 | a0002c0002t0003g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.126+2305G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18686133 | ||||||
| chr19:18686277
|
T | C | 1 | a0001c0001t0003g0253 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.126+2449T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18686277 | ||||||
| chr19:18686700
|
CCCTGGAA others(2995): Show |
C | 1 | a0001c0001t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+2875_126+5876d others(2): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18686700 | |||||
| chr19:18686765
|
G | A | 2 | a0002c0002t0003g0155a0002c0002t0010g0154 | 2 | NA18977.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.126+2937G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18686765 | ||||||
| chr19:18686986
|
T | A | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+3158T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18686986 | ||||||
| chr19:18687011
|
C | CT | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(110): Show | 114 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.126+3205dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18687011 | |||||
| chr19:18687011
|
C | CTT | 65 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(62): Show | 65 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.126+3204_126+3205d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18687011 | |||||
| chr19:18687011
|
C | CTTT | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0239others(2): Show | 5 | HG02280.hp2 HG02300.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+3203_126+3205d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18687011 | |||||
| chr19:18687406
|
T | C | 2 | a0002c0002t0020g0216a0002c0002t0021g0217 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+3578T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18687406 | ||||||
| chr19:18687724
|
G | A | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+3896G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18687724 | ||||||
| chr19:18687746
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.126+3918G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18687746 | ||||||
| chr19:18687979
|
C | T | 2 | a0001c0003t0002g0208a0001c0003t0002g0271 | 2 | NA19011.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.126+4151C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18687979 | ||||||
| chr19:18688160
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126+4332C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688160 | ||||||
| chr19:18688225
|
G | A | 7 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG00642.hp2 HG01346.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+4397G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688225 | ||||||
| chr19:18688466
|
G | GC | 11 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0248others(8): Show | 11 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+4645dupC | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18688466 | |||||
| chr19:18688541
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+4713C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688541 | ||||||
| chr19:18688578
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.126+4750G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688578 | ||||||
| chr19:18688686
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.126+4858C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688686 | ||||||
| chr19:18688951
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.126+5123T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18688951 | ||||||
| chr19:18689039
|
G | A | 2 | a0002c0002t0020g0216a0002c0002t0021g0217 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+5211G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689039 | ||||||
| chr19:18689193
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+5365C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689193 | ||||||
| chr19:18689295
|
A | G | 1 | a0002c0002t0003g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.126+5467A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689295 | ||||||
| chr19:18689434
|
C | CT | 16 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0248others(13): Show | 16 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+5620dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689434 | |||||
| chr19:18689434
|
CT | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0135a0001c0001t0001g0156others(2): Show | 5 | HG02280.hp2 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+5620delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689434 | |||||
| chr19:18689482
|
G | GTGTAGTA others(491): Show |
1 | a0001c0001t0018g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.126+5656_126+5657i others(500): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689482 | |||||
| chr19:18689482
|
G | GTGTAGTA others(491): Show |
2 | a0002c0005t0003g0158a0002c0005t0003g0254 | 2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.126+5656_126+5657i others(500): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689482 | |||||
| chr19:18689482
|
G | GTGTAGTA others(491): Show |
264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(261): Show | 265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.126+5656_126+5657i others(500): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689482 | |||||
| chr19:18689482
|
G | GTGTAGTA others(491): Show |
4 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+5656_126+5657i others(500): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689482 | |||||
| chr19:18689564
|
C | CAT | 11 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0248others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+5757_126+5758d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATAT | 9 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0005g0130others(6): Show | 9 | HG00099.hp2 HG01099.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+5755_126+5758d others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0159a0001c0001t0002g0137a0001c0001t0004g0126others(2): Show | 5 | HG01934.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+5749_126+5758d others(12): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(5): Show |
1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+5747_126+5758d others(14): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.126+5741_126+5758d others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(13): Show |
2 | a0001c0001t0001g0144a0001c0001t0004g0016 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.126+5739_126+5758d others(22): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(15): Show |
10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0142others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+5737_126+5758d others(24): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(17): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0150a0001c0001t0001g0250others(3): Show | 6 | HG01074.hp2 HG01123.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(19): Show |
5 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(2): Show | 5 | HG02451.hp1 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(28): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(21): Show |
2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(30): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
C | CATATATA others(25): Show |
1 | a0001c0001t0001g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.126+5758_126+5759i others(34): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
CATAT | C | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+5755_126+5758d others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689564
|
CATATAT | C | 18 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0119others(15): Show | 18 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+5753_126+5758d others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689564 | |||||
| chr19:18689583
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.126+5758_126+5759i others(40): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(27): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0071 | 2 | HG02602.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(36): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(25): Show |
7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0227others(4): Show | 7 | HG00544.hp1 HG01123.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(34): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(23): Show |
10 | a0001c0001t0001g0028a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 11 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(32): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(21): Show |
14 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(30): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(19): Show |
51 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0045others(48): Show | 51 | HG00639.hp2 HG01069.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(28): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(23): Show |
1 | a0002c0002t0003g0224 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.126+5758_126+5759i others(32): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(17): Show |
12 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0056others(9): Show | 12 | HG00558.hp1 HG01517.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0002g0098a0001c0001t0002g0232 | 2 | NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(30): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(15): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+5758_126+5759i others(24): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(13): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0212a0001c0001t0006g0225 | 3 | HG02735.hp1 HG02809.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(22): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126+5758_126+5759i others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0113 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.126+5758_126+5759i others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(15): Show |
3 | a0002c0002t0003g0214a0002c0002t0003g0226a0002c0002t0016g0060 | 3 | HG01081.hp2 HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(24): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0100 | 3 | HG00408.hp1 HG02683.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.126+5758_126+5759i others(16): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.126+5758_126+5759i others(14): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689583
|
A | ATATATG | 3 | a0001c0001t0001g0235a0001c0001t0001g0238a0001c0001t0002g0234 | 3 | HG02080.hp2 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.126+5758_126+5759i others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18689583 | |||||
| chr19:18689587
|
G | A | 4 | a0001c0001t0002g0137a0001c0001t0004g0126a0001c0001t0005g0138others(1): Show | 4 | HG01361.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+5759G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689587 | ||||||
| chr19:18689636
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+5808G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689636 | ||||||
| chr19:18689709
|
T | C | 4 | a0001c0001t0002g0137a0001c0001t0004g0126a0001c0001t0005g0138others(1): Show | 4 | HG01361.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+5881T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689709 | ||||||
| chr19:18689783
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+5955A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18689783 | ||||||
| chr19:18690009
|
G | T | 3 | a0001c0001t0001g0206a0001c0003t0002g0205a0001c0003t0002g0270 | 3 | HG00280.hp2 HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.126+6181G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690009 | ||||||
| chr19:18690049
|
G | A | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.126+6221G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690049 | ||||||
| chr19:18690373
|
A | G | 2 | a0002c0002t0003g0203a0002c0002t0003g0204 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.126+6545A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690373 | ||||||
| chr19:18690632
|
G | T | 4 | a0001c0001t0002g0137a0001c0001t0004g0126a0001c0001t0005g0138others(1): Show | 4 | HG01361.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6804G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690632 | ||||||
| chr19:18690792
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.126+6964G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690792 | ||||||
| chr19:18690975
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126+7147G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690975 | ||||||
| chr19:18690980
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.126+7152C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690980 | ||||||
| chr19:18690990
|
C | T | 1 | a0002c0005t0003g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.126+7162C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18690990 | ||||||
| chr19:18691003
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(191): Show | 195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.126+7175A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691003 | ||||||
| chr19:18691025
|
CA | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0096others(14): Show | 17 | HG01070.hp1 HG01167.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+7218delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691025 | |||||
| chr19:18691046
|
A | AT | 17 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0001t0001g0145others(14): Show | 17 | HG01123.hp2 HG02055.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+7218_126+7219i others(3): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691046 | ||||||
| chr19:18691046
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 178 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.126+7218A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691046 | ||||||
| chr19:18691191
|
C | CA | 126 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(123): Show | 127 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.126+7377dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691191 | |||||
| chr19:18691191
|
CA | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+7377delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691191 | |||||
| chr19:18691237
|
C | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+7409C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691237 | ||||||
| chr19:18691249
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+7421C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691249 | ||||||
| chr19:18691259
|
T | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.126+7431T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691259 | ||||||
| chr19:18691508
|
G | A | 11 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0248others(8): Show | 11 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+7680G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691508 | ||||||
| chr19:18691522
|
CA | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 158 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.126+7716delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691522 | |||||
| chr19:18691522
|
CAA | C | 21 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0093others(18): Show | 21 | HG00408.hp1 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+7715_126+7716d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691522 | |||||
| chr19:18691522
|
CAAA | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+7714_126+7716d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18691522 | |||||
| chr19:18691605
|
G | C | 1 | a0002c0002t0003g0162 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126+7777G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691605 | ||||||
| chr19:18691631
|
T | C | 4 | a0001c0001t0002g0137a0001c0001t0004g0126a0001c0001t0005g0138others(1): Show | 4 | HG01361.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+7803T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691631 | ||||||
| chr19:18691774
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+7946C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691774 | ||||||
| chr19:18691942
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+8114G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691942 | ||||||
| chr19:18691960
|
G | A | 12 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0119others(9): Show | 12 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+8132G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691960 | ||||||
| chr19:18691965
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.126+8137G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691965 | ||||||
| chr19:18691988
|
C | T | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.126+8160C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18691988 | ||||||
| chr19:18692073
|
C | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+8245C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692073 | ||||||
| chr19:18692265
|
G | A | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+8437G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692265 | ||||||
| chr19:18692362
|
T | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(191): Show | 195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.126+8534T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692362 | ||||||
| chr19:18692407
|
C | T | 4 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0098others(1): Show | 4 | HG02165.hp1 HG03834.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+8579C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692407 | ||||||
| chr19:18692502
|
G | A | 1 | a0001c0001t0005g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.126+8674G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692502 | ||||||
| chr19:18692590
|
A | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.126+8762A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692590 | ||||||
| chr19:18692601
|
CA | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.126+8789delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18692601 | |||||
| chr19:18692650
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.126+8822C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692650 | ||||||
| chr19:18692803
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+8975C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692803 | ||||||
| chr19:18692972
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0003g0052 | 3 | HG02615.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.126+9144G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692972 | ||||||
| chr19:18692990
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.126+9162G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692990 | ||||||
| chr19:18692997
|
C | G | 1 | a0001c0001t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+9169C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18692997 | ||||||
| chr19:18693054
|
G | A | 4 | a0001c0001t0002g0137a0001c0001t0004g0126a0001c0001t0005g0138others(1): Show | 4 | HG01361.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+9226G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693054 | ||||||
| chr19:18693062
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+9234G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693062 | ||||||
| chr19:18693069
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+9241C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693069 | ||||||
| chr19:18693074
|
C | CA | 165 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 165 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+9266dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693074 | |||||
| chr19:18693074
|
C | CAA | 13 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0099others(10): Show | 13 | HG00438.hp1 HG01123.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+9265_126+9266d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693074 | |||||
| chr19:18693074
|
C | CAAA | 8 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+9264_126+9266d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693074 | |||||
| chr19:18693187
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(16): Show | 19 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+9359G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693187 | ||||||
| chr19:18693355
|
C | T | 2 | a0001c0001t0013g0065a0001c0001t0013g0069 | 2 | HG01346.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.126+9527C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693355 | ||||||
| chr19:18693387
|
T | TA | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(207): Show | 211 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.126+9572dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693387 | |||||
| chr19:18693405
|
T | A | 1 | a0001c0001t0029g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.126+9577T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693405 | ||||||
| chr19:18693479
|
G | GT | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0090others(16): Show | 19 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+9656dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693479 | |||||
| chr19:18693483
|
TTG | T | 8 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(5): Show | 8 | HG02451.hp1 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9657_126+9658d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18693483 | |||||
| chr19:18693484
|
TG | T | 27 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0122others(24): Show | 27 | HG00735.hp1 HG01123.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+9657delG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693484 | ||||||
| chr19:18693485
|
G | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 157 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.126+9657G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693485 | ||||||
| chr19:18693583
|
G | A | 1 | a0002c0002t0003g0173 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.126+9755G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693583 | ||||||
| chr19:18693760
|
G | C | 23 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0122others(20): Show | 23 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+9932G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693760 | ||||||
| chr19:18693772
|
T | C | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+9944T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693772 | ||||||
| chr19:18693772
|
T | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.126+9944T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693772 | ||||||
| chr19:18694065
|
G | A | 2 | a0002c0002t0020g0216a0002c0002t0021g0217 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+10237G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694065 | ||||||
| chr19:18694135
|
G | GA | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 178 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.126+10324dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694135 | |||||
| chr19:18694135
|
G | GAA | 16 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0116others(13): Show | 16 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+10323_126+1032 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694135 | |||||
| chr19:18694298
|
CA | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 93 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.126+10489delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694298 | |||||
| chr19:18694298
|
CAA | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(91): Show | 94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.126+10488_126+1048 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694298 | |||||
| chr19:18694314
|
AAAAG | A | 14 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0122others(11): Show | 14 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+10489_126+1049 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694314 | |||||
| chr19:18694401
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0257others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10573A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694401 | ||||||
| chr19:18694522
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0004g0039a0001c0001t0011g0040 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.126+10694T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694522 | ||||||
| chr19:18694552
|
C | T | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+10724C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694552 | ||||||
| chr19:18694698
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+10870A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694698 | ||||||
| chr19:18694762
|
G | C | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+10934G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694762 | ||||||
| chr19:18694786
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+10958G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694786 | ||||||
| chr19:18694861
|
G | A | 2 | a0001c0001t0005g0138a0001c0001t0005g0146 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.126+11033G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694861 | ||||||
| chr19:18694893
|
CT | C | 39 | a0001c0001t0001g0020a0001c0001t0001g0171a0001c0001t0001g0179others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+11080delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18694893 | |||||
| chr19:18694898
|
T | G | 29 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0122others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+11070T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694898 | ||||||
| chr19:18694899
|
T | G | 1 | a0003c0004t0002g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+11071T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18694899 | ||||||
| chr19:18695003
|
G | A | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+11175G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695003 | ||||||
| chr19:18695296
|
C | T | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(8): Show | 11 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+11468C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695296 | ||||||
| chr19:18695374
|
G | A | 1 | a0001c0001t0001g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.126+11546G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695374 | ||||||
| chr19:18695375
|
G | A | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(8): Show | 11 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+11547G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695375 | ||||||
| chr19:18695492
|
G | A | 33 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0269others(30): Show | 33 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+11664G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695492 | ||||||
| chr19:18695587
|
C | T | 1 | a0001c0001t0012g0172 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+11759C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695587 | ||||||
| chr19:18695723
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+11895G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695723 | ||||||
| chr19:18695789
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.126+11961C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695789 | ||||||
| chr19:18695821
|
C | T | 92 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(89): Show | 92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.126+11993C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695821 | ||||||
| chr19:18695858
|
T | C | 176 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(173): Show | 176 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.126+12030T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695858 | ||||||
| chr19:18695916
|
C | T | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+12088C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695916 | ||||||
| chr19:18695983
|
C | T | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+12155C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18695983 | ||||||
| chr19:18696190
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126+12362C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696190 | ||||||
| chr19:18696194
|
A | G | 2 | a0002c0002t0020g0216a0002c0002t0021g0217 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+12366A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696194 | ||||||
| chr19:18696219
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.126+12391G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696219 | ||||||
| chr19:18696255
|
C | T | 1 | a0001c0001t0006g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+12427C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696255 | ||||||
| chr19:18696294
|
A | AGGGGC | 33 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0269others(30): Show | 33 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+12467_126+1247 others(9): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18696294 | |||||
| chr19:18696878
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+13050C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696878 | ||||||
| chr19:18696889
|
G | T | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+13061G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696889 | ||||||
| chr19:18696890
|
T | C | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+13062T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18696890 | ||||||
| chr19:18697027
|
G | A | 1 | a0002c0002t0003g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+13199G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697027 | ||||||
| chr19:18697255
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.126+13427G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697255 | ||||||
| chr19:18697347
|
C | T | 1 | a0002c0002t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.126+13519C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697347 | ||||||
| chr19:18697429
|
C | T | 1 | a0006c0010t0001g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+13601C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697429 | ||||||
| chr19:18697455
|
G | A | 2 | a0002c0002t0003g0089a0002c0002t0003g0198 | 2 | HG02027.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.126+13627G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697455 | ||||||
| chr19:18697589
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+13761C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697589 | ||||||
| chr19:18697590
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+13762A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697590 | ||||||
| chr19:18697671
|
C | T | 10 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+13843C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18697671 | ||||||
| chr19:18698048
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.126+14220C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698048 | ||||||
| chr19:18698049
|
G | A | 3 | a0001c0003t0002g0086a0001c0003t0002g0255a0001c0003t0002g0256 | 3 | HG01069.hp1 HG01346.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.126+14221G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698049 | ||||||
| chr19:18698082
|
C | T | 1 | a0001c0001t0001g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.126+14254C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698082 | ||||||
| chr19:18698105
|
T | A | 181 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(178): Show | 181 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.126+14277T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698105 | ||||||
| chr19:18698144
|
C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0003g0052others(12): Show | 15 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+14316C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698144 | ||||||
| chr19:18698164
|
C | T | 13 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0004g0215others(10): Show | 13 | HG01361.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+14336C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698164 | ||||||
| chr19:18698185
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.126+14357G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698185 | ||||||
| chr19:18698207
|
G | A | 2 | a0001c0001t0004g0047a0001c0001t0018g0136 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.126+14379G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698207 | ||||||
| chr19:18698494
|
ACTCAGCA others(4): Show |
A | 2 | a0001c0001t0001g0008a0001c0001t0001g0079 | 2 | HG03654.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.126+14688_126+1469 others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18698494 | |||||
| chr19:18698504
|
C | T | 62 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0128others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.126+14676C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698504 | ||||||
| chr19:18698532
|
G | A | 6 | a0001c0001t0001g0038a0001c0001t0002g0049a0001c0001t0002g0051others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+14704G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698532 | ||||||
| chr19:18698593
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+14765T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698593 | ||||||
| chr19:18698644
|
G | A | 1 | a0002c0002t0003g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.126+14816G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698644 | ||||||
| chr19:18698645
|
C | T | 11 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+14817C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698645 | ||||||
| chr19:18698741
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.126+14913G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698741 | ||||||
| chr19:18698773
|
T | A | 1 | a0003c0004t0002g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.126+14945T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698773 | ||||||
| chr19:18698792
|
C | T | 1 | a0001c0003t0025g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126+14964C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698792 | ||||||
| chr19:18698813
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.126+14985A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698813 | ||||||
| chr19:18698884
|
C | A | 28 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0128others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+15056C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698884 | ||||||
| chr19:18698901
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 56 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.126+15073G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698901 | ||||||
| chr19:18698937
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+15109C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698937 | ||||||
| chr19:18699121
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.126+15293C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699121 | ||||||
| chr19:18699252
|
G | T | 1 | a0001c0003t0002g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.126+15424G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699252 | ||||||
| chr19:18699273
|
C | T | 3 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0005g0063 | 3 | HG02615.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.126+15445C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699273 | ||||||
| chr19:18699335
|
T | G | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+15507T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699335 | ||||||
| chr19:18699372
|
G | A | 1 | a0002c0002t0003g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+15544G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699372 | ||||||
| chr19:18699917
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+16089C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699917 | ||||||
| chr19:18699985
|
A | T | 35 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0258others(32): Show | 35 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+16157A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699985 | ||||||
| chr19:18699987
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.126+16159C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18699987 | ||||||
| chr19:18700024
|
C | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0145others(13): Show | 16 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+16196C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700024 | ||||||
| chr19:18700038
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+16210A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700038 | ||||||
| chr19:18700066
|
G | A | 35 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0258others(32): Show | 35 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+16238G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700066 | ||||||
| chr19:18700238
|
C | T | 9 | a0001c0001t0001g0115a0001c0001t0001g0122a0003c0004t0002g0120others(6): Show | 9 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+16410C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700238 | ||||||
| chr19:18700259
|
A | C | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+16431A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700259 | ||||||
| chr19:18700302
|
T | C | 35 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0258others(32): Show | 35 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+16474T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700302 | ||||||
| chr19:18700442
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0004g0126 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.126+16614C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700442 | ||||||
| chr19:18700461
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.126+16633C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700461 | ||||||
| chr19:18700495
|
C | CT | 7 | a0002c0002t0003g0089a0002c0002t0003g0117a0002c0002t0003g0163others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+16679dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18700495 | |||||
| chr19:18700495
|
CT | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG00609.hp2 HG02895.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+16679delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18700495 | |||||
| chr19:18700664
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0018g0136 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.126+16836C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700664 | ||||||
| chr19:18700665
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01070.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.126+16837G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700665 | ||||||
| chr19:18700812
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+16984G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700812 | ||||||
| chr19:18700908
|
A | G | 31 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0128others(28): Show | 31 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+17080A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700908 | ||||||
| chr19:18700930
|
C | T | 91 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(88): Show | 91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.126+17102C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700930 | ||||||
| chr19:18700995
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+17167T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18700995 | ||||||
| chr19:18701054
|
T | G | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+17226T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701054 | ||||||
| chr19:18701156
|
A | G | 179 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.126+17328A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701156 | ||||||
| chr19:18701207
|
C | T | 2 | a0002c0002t0003g0203a0002c0002t0003g0204 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.126+17379C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701207 | ||||||
| chr19:18701214
|
A | G | 174 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.126+17386A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701214 | ||||||
| chr19:18701571
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+17743T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701571 | ||||||
| chr19:18701662
|
A | G | 35 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0258others(32): Show | 35 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+17834A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701662 | ||||||
| chr19:18701806
|
C | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0008g0134others(7): Show | 10 | HG01099.hp1 HG01361.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+17978C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701806 | ||||||
| chr19:18701917
|
G | GT | 4 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0009g0124others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+18093dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18701917 | |||||
| chr19:18701922
|
G | GT | 20 | a0001c0001t0001g0007a0001c0001t0001g0171a0001c0001t0001g0228others(17): Show | 20 | HG01099.hp1 HG01123.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+18112dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18701922 | |||||
| chr19:18701922
|
G | T | 6 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0009g0124others(3): Show | 6 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+18094G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701922 | ||||||
| chr19:18701922
|
GT | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0166a0001c0003t0002g0030others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+18112delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18701922 | |||||
| chr19:18701927
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0008g0151 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.126+18099T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701927 | ||||||
| chr19:18701946
|
G | A | 91 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(88): Show | 91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.126+18118G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701946 | ||||||
| chr19:18701975
|
A | G | 179 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.126+18147A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18701975 | ||||||
| chr19:18702033
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+18205C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702033 | ||||||
| chr19:18702096
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0022g0152 | 2 | HG02280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.126+18268T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702096 | ||||||
| chr19:18702150
|
C | T | 1 | a0002c0002t0003g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.126+18322C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702150 | ||||||
| chr19:18702164
|
T | G | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+18336T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702164 | ||||||
| chr19:18702222
|
A | AT | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(28): Show | 31 | HG00738.hp1 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+18409dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18702222 | |||||
| chr19:18702222
|
AT | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+18409delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18702222 | |||||
| chr19:18702395
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0004g0126 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.126+18567A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702395 | ||||||
| chr19:18702435
|
A | G | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+18607A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702435 | ||||||
| chr19:18702533
|
C | CT | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(106): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.126+18722dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18702533 | |||||
| chr19:18702533
|
CT | C | 14 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(11): Show | 14 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+18722delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18702533 | |||||
| chr19:18702595
|
A | G | 87 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 87 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.126+18767A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702595 | ||||||
| chr19:18702873
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19045C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702873 | ||||||
| chr19:18702960
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.126+19132T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702960 | ||||||
| chr19:18702977
|
C | T | 3 | a0001c0007t0008g0025a0002c0002t0020g0216a0002c0002t0021g0217 | 3 | HG01099.hp1 HG03139.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+19149C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18702977 | ||||||
| chr19:18703203
|
G | A | 4 | a0001c0003t0002g0001a0001c0003t0002g0030a0001c0003t0002g0218others(1): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+19375G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703203 | ||||||
| chr19:18703240
|
A | G | 11 | a0001c0001t0001g0115a0001c0001t0001g0122a0002c0002t0003g0117others(8): Show | 11 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+19412A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703240 | ||||||
| chr19:18703367
|
T | C | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+19539T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703367 | ||||||
| chr19:18703400
|
C | A | 1 | a0001c0001t0006g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126+19572C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703400 | ||||||
| chr19:18703520
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.126+19692A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703520 | ||||||
| chr19:18703521
|
C | T | 39 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+19693C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703521 | ||||||
| chr19:18703706
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+19878G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703706 | ||||||
| chr19:18703715
|
G | A | 1 | a0001c0001t0029g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.126+19887G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703715 | ||||||
| chr19:18703718
|
C | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+19890C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703718 | ||||||
| chr19:18703805
|
C | G | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+19977C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703805 | ||||||
| chr19:18703819
|
A | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.126+19991A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703819 | ||||||
| chr19:18703947
|
T | G | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+20119T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18703947 | ||||||
| chr19:18704057
|
T | G | 6 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0002g0058others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+20229T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704057 | ||||||
| chr19:18704119
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.126+20291A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704119 | ||||||
| chr19:18704167
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+20339C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704167 | ||||||
| chr19:18704315
|
C | G | 2 | a0001c0001t0005g0130a0001c0001t0005g0131 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.126+20487C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704315 | ||||||
| chr19:18704339
|
T | G | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+20511T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704339 | ||||||
| chr19:18704406
|
G | T | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.126+20578G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704406 | ||||||
| chr19:18704435
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+20607G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704435 | ||||||
| chr19:18704440
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.126+20612G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704440 | ||||||
| chr19:18704523
|
T | G | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+20695T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704523 | ||||||
| chr19:18704528
|
A | C | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+20700A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704528 | ||||||
| chr19:18704597
|
A | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+20769A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704597 | ||||||
| chr19:18704648
|
G | A | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+20820G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704648 | ||||||
| chr19:18704666
|
C | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+20838C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704666 | ||||||
| chr19:18704704
|
C | A | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+20876C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704704 | ||||||
| chr19:18704801
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.126+20973T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704801 | ||||||
| chr19:18704934
|
A | G | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+21106A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704934 | ||||||
| chr19:18704957
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.126+21129C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18704957 | ||||||
| chr19:18705088
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+21260C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705088 | ||||||
| chr19:18705092
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+21264C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705092 | ||||||
| chr19:18705107
|
C | CA | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+21280dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705107 | |||||
| chr19:18705220
|
C | T | 3 | a0002c0002t0003g0214a0002c0002t0003g0226a0002c0002t0016g0060 | 3 | HG01081.hp2 HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+21392C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705220 | ||||||
| chr19:18705251
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+21423T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705251 | ||||||
| chr19:18705330
|
A | AT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+21510dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705330 | |||||
| chr19:18705462
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.126+21634C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705462 | ||||||
| chr19:18705463
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.126+21635G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705463 | ||||||
| chr19:18705559
|
T | C | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0257others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+21731T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705559 | ||||||
| chr19:18705611
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126+21783G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705611 | ||||||
| chr19:18705797
|
AT | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 237 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.126+21979delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705797 | |||||
| chr19:18705819
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0228 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.126+21991T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18705819 | ||||||
| chr19:18705967
|
C | CT | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(43): Show | 46 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+22154dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705967 | |||||
| chr19:18705967
|
C | CTT | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+22153_126+2215 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705967 | |||||
| chr19:18705967
|
CT | C | 12 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0067others(9): Show | 12 | HG01168.hp2 HG01433.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+22154delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18705967 | |||||
| chr19:18706144
|
A | G | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+22316A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706144 | ||||||
| chr19:18706182
|
C | CT | 18 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0099others(15): Show | 18 | HG00438.hp1 HG00735.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+22395dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0266 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.126+22386_126+2239 others(14): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0012g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.126+22385_126+2239 others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CT | C | 47 | a0001c0001t0001g0050a0001c0001t0001g0066a0001c0001t0001g0083others(44): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+22395delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTT | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0061others(34): Show | 37 | HG00408.hp1 HG00639.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.126+22394_126+2239 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTT | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(32): Show | 35 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+22393_126+2239 others(7): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTT | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0028others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+22392_126+2239 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0031a0001c0001t0031g0251 | 2 | HG02145.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.126+22385_126+2239 others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(5): Show |
C | 23 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0128others(20): Show | 23 | HG02080.hp1 HG02109.hp1 HG02148.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+22384_126+2239 others(16): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(6): Show |
C | 29 | a0001c0001t0001g0076a0001c0001t0001g0170a0001c0001t0001g0197others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+22383_126+2239 others(17): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0010g0263 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.126+22382_126+2239 others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+22380_126+2239 others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0003g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.126+22379_126+2239 others(21): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0182a0001c0003t0002g0256 | 2 | HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.126+22378_126+2239 others(22): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+22374_126+2239 others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706182
|
CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0127a0001c0001t0027g0004 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126+22372_126+2239 others(28): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706182 | |||||
| chr19:18706231
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.126+22403G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706231 | ||||||
| chr19:18706394
|
T | TG | 12 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+22570dupG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18706394 | |||||
| chr19:18706453
|
C | G | 1 | a0001c0001t0014g0023 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.126+22625C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706453 | ||||||
| chr19:18706487
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+22659G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706487 | ||||||
| chr19:18706536
|
A | C | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+22708A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706536 | ||||||
| chr19:18706788
|
T | C | 1 | a0003c0004t0023g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+22960T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706788 | ||||||
| chr19:18706832
|
T | G | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG00642.hp2 HG01123.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+23004T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706832 | ||||||
| chr19:18706918
|
T | G | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+23090T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706918 | ||||||
| chr19:18706978
|
G | A | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+23150G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18706978 | ||||||
| chr19:18707082
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+23254C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707082 | ||||||
| chr19:18707093
|
C | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(131): Show | 134 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.126+23265C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707093 | ||||||
| chr19:18707369
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+23541C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707369 | ||||||
| chr19:18707370
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.126+23542G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707370 | ||||||
| chr19:18707414
|
T | C | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+23586T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707414 | ||||||
| chr19:18707525
|
A | G | 10 | a0001c0001t0001g0115a0001c0001t0001g0252a0003c0004t0002g0120others(7): Show | 10 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+23697A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707525 | ||||||
| chr19:18707615
|
A | AT | 10 | a0001c0001t0001g0115a0001c0001t0001g0252a0003c0004t0002g0120others(7): Show | 10 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+23794dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18707615 | |||||
| chr19:18707717
|
G | A | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+23889G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707717 | ||||||
| chr19:18707795
|
G | C | 1 | a0002c0002t0003g0202 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.126+23967G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707795 | ||||||
| chr19:18707923
|
C | G | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+24095C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707923 | ||||||
| chr19:18707949
|
G | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24121G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707949 | ||||||
| chr19:18707955
|
A | C | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24127A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707955 | ||||||
| chr19:18707956
|
C | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24128C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707956 | ||||||
| chr19:18707960
|
G | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24132G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707960 | ||||||
| chr19:18707961
|
T | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24133T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707961 | ||||||
| chr19:18707968
|
A | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24140A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707968 | ||||||
| chr19:18707969
|
T | G | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24141T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707969 | ||||||
| chr19:18707986
|
T | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24158T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707986 | ||||||
| chr19:18707988
|
T | G | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24160T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707988 | ||||||
| chr19:18707996
|
A | C | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24168A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707996 | ||||||
| chr19:18707999
|
G | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24171G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18707999 | ||||||
| chr19:18708000
|
G | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24172G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708000 | ||||||
| chr19:18708001
|
T | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24173T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708001 | ||||||
| chr19:18708002
|
A | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24174A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708002 | ||||||
| chr19:18708004
|
T | G | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24176T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708004 | ||||||
| chr19:18708027
|
T | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24199T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708027 | ||||||
| chr19:18708029
|
C | A | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24201C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708029 | ||||||
| chr19:18708031
|
G | C | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24203G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708031 | ||||||
| chr19:18708032
|
G | T | 1 | a0002c0002t0003g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+24204G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708032 | ||||||
| chr19:18708134
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+24306G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708134 | ||||||
| chr19:18708235
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(171): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.126+24407A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708235 | ||||||
| chr19:18708250
|
T | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.126+24422T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708250 | ||||||
| chr19:18708425
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+24597G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708425 | ||||||
| chr19:18708429
|
C | T | 1 | a0002c0002t0003g0198 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.126+24601C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708429 | ||||||
| chr19:18708938
|
G | A | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+25110G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708938 | ||||||
| chr19:18708952
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.126+25124T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18708952 | ||||||
| chr19:18709066
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(38): Show | 41 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.126+25238A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709066 | ||||||
| chr19:18709174
|
C | T | 94 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(91): Show | 94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.126+25346C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709174 | ||||||
| chr19:18709354
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0079others(1): Show | 4 | HG00735.hp2 HG02148.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+25526C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709354 | ||||||
| chr19:18709394
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0004g0039a0001c0001t0011g0040 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.126+25566G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709394 | ||||||
| chr19:18709498
|
C | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.126+25670C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709498 | ||||||
| chr19:18709515
|
G | C | 13 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(10): Show | 13 | HG01099.hp1 HG01123.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+25687G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709515 | ||||||
| chr19:18709780
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+25952C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709780 | ||||||
| chr19:18709783
|
C | T | 10 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(7): Show | 10 | HG01123.hp2 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+25955C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709783 | ||||||
| chr19:18709878
|
C | T | 1 | a0002c0002t0003g0202 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.126+26050C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709878 | ||||||
| chr19:18709981
|
A | G | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+26153A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18709981 | ||||||
| chr19:18710001
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0004g0039a0001c0001t0011g0040 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.126+26173T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710001 | ||||||
| chr19:18710176
|
C | A | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+26348C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710176 | ||||||
| chr19:18710214
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.126+26386T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710214 | ||||||
| chr19:18710264
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.126+26436C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710264 | ||||||
| chr19:18710354
|
C | T | 10 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(7): Show | 10 | HG01123.hp2 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+26526C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710354 | ||||||
| chr19:18710452
|
T | C | 1 | a0001c0001t0008g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126+26624T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710452 | ||||||
| chr19:18710462
|
G | GGGAGCCA | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+26643_126+2664 others(11): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18710462 | |||||
| chr19:18710605
|
T | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0164a0001c0001t0001g0183 | 3 | HG03491.hp2 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.126+26777T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710605 | ||||||
| chr19:18710851
|
A | G | 1 | a0001c0001t0007g0033 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.126+27023A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710851 | ||||||
| chr19:18710960
|
C | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+27132C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18710960 | ||||||
| chr19:18711034
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+27206G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711034 | ||||||
| chr19:18711066
|
A | G | 3 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0005g0063 | 3 | HG02615.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.126+27238A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711066 | ||||||
| chr19:18711141
|
C | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG00099.hp1 HG01168.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+27313C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711141 | ||||||
| chr19:18711148
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126+27320C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711148 | ||||||
| chr19:18711221
|
T | C | 3 | a0001c0007t0008g0025a0002c0002t0020g0216a0002c0002t0021g0217 | 3 | HG01099.hp1 HG03139.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+27393T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711221 | ||||||
| chr19:18711321
|
C | T | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+27493C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711321 | ||||||
| chr19:18711367
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.126+27539C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711367 | ||||||
| chr19:18711402
|
G | A | 1 | a0002c0002t0003g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+27574G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711402 | ||||||
| chr19:18711411
|
G | A | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126+27583G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711411 | ||||||
| chr19:18711530
|
G | T | 1 | a0007c0006t0001g0149 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.126+27702G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711530 | ||||||
| chr19:18711612
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0004g0039a0001c0001t0011g0040 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.126+27784C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711612 | ||||||
| chr19:18711629
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+27801C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711629 | ||||||
| chr19:18711849
|
C | A | 2 | a0001c0001t0001g0099a0002c0002t0003g0273 | 2 | HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.126+28021C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18711849 | ||||||
| chr19:18712116
|
A | T | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+28288A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712116 | ||||||
| chr19:18712221
|
G | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.126+28393G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712221 | ||||||
| chr19:18712239
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+28411C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712239 | ||||||
| chr19:18712254
|
C | CGTTT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+28443_126+2844 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18712254 | |||||
| chr19:18712258
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.126+28430T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712258 | ||||||
| chr19:18712294
|
C | T | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+28466C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712294 | ||||||
| chr19:18712310
|
G | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+28482G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712310 | ||||||
| chr19:18712425
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.126+28597T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712425 | ||||||
| chr19:18712695
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+28867C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712695 | ||||||
| chr19:18712766
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0015g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.126+28938C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712766 | ||||||
| chr19:18712855
|
G | A | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.126+29027G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712855 | ||||||
| chr19:18712859
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+29031C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18712859 | ||||||
| chr19:18712957
|
CA | C | 6 | a0001c0001t0001g0067a0001c0001t0001g0181a0001c0001t0004g0126others(3): Show | 6 | HG01515.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+29144delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18712957 | |||||
| chr19:18713228
|
C | G | 93 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(90): Show | 93 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.126+29400C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18713228 | ||||||
| chr19:18713419
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.127-29491G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18713419 | ||||||
| chr19:18713546
|
T | TGCACCCT others(21): Show |
193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.127-29363_127-2933 others(32): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18713546 | |||||
| chr19:18713719
|
T | TA | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-29190dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18713719 | |||||
| chr19:18713763
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.127-29147C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18713763 | ||||||
| chr19:18713899
|
T | C | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-29011T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18713899 | ||||||
| chr19:18714017
|
C | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-28893C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714017 | ||||||
| chr19:18714036
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-28874G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714036 | ||||||
| chr19:18714060
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.127-28850A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714060 | ||||||
| chr19:18714199
|
C | T | 1 | a0001c0001t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-28711C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714199 | ||||||
| chr19:18714262
|
AGGCG | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0085a0001c0001t0015g0005 | 3 | HG01069.hp2 HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.127-28643_127-2864 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18714262 | |||||
| chr19:18714313
|
T | A | 1 | a0001c0001t0012g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.127-28597T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714313 | ||||||
| chr19:18714469
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(170): Show | 173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.127-28441A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714469 | ||||||
| chr19:18714497
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-28413C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714497 | ||||||
| chr19:18714774
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-28136C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714774 | ||||||
| chr19:18714910
|
C | A | 14 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(11): Show | 14 | HG01099.hp1 HG01123.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-28000C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714910 | ||||||
| chr19:18714937
|
C | T | 5 | a0001c0001t0005g0026a0001c0001t0005g0036a0001c0001t0005g0042others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-27973C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18714937 | ||||||
| chr19:18715242
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.127-27668A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715242 | ||||||
| chr19:18715329
|
G | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-27581G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715329 | ||||||
| chr19:18715545
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.127-27365T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715545 | ||||||
| chr19:18715621
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-27289C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715621 | ||||||
| chr19:18715650
|
C | T | 1 | a0003c0004t0002g0240 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.127-27260C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715650 | ||||||
| chr19:18715767
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-27143A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715767 | ||||||
| chr19:18715849
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-27061G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715849 | ||||||
| chr19:18715999
|
G | T | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0004g0009others(18): Show | 21 | HG01099.hp1 HG01123.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-26911G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18715999 | ||||||
| chr19:18716000
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0013g0065others(1): Show | 4 | HG00642.hp2 HG01346.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-26910G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716000 | ||||||
| chr19:18716019
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-26891G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716019 | ||||||
| chr19:18716087
|
C | T | 1 | a0002c0002t0003g0175 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.127-26823C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716087 | ||||||
| chr19:18716165
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(118): Show | 121 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.127-26745C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716165 | ||||||
| chr19:18716257
|
C | CT | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-26640dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18716257 | |||||
| chr19:18716279
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.127-26631A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716279 | ||||||
| chr19:18716352
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-26558A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716352 | ||||||
| chr19:18716559
|
A | G | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-26351A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716559 | ||||||
| chr19:18716643
|
G | A | 13 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(10): Show | 13 | HG01099.hp1 HG01123.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-26267G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716643 | ||||||
| chr19:18716964
|
CGTGCAGG others(10): Show |
C | 3 | a0001c0001t0001g0115a0003c0004t0023g0118a0003c0004t0026g0241 | 3 | HG01243.hp2 HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.127-25925_127-2590 others(21): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18716964 | |||||
| chr19:18716965
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-25945G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18716965 | ||||||
| chr19:18717017
|
G | A | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-25893G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717017 | ||||||
| chr19:18717063
|
CTA | C | 4 | a0001c0001t0001g0108a0002c0002t0003g0209a0002c0002t0003g0210others(1): Show | 4 | NA18941.hp1 NA19000.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-25845_127-2584 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18717063 | |||||
| chr19:18717118
|
C | G | 1 | a0001c0003t0002g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.127-25792C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717118 | ||||||
| chr19:18717119
|
G | C | 1 | a0001c0003t0002g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.127-25791G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717119 | ||||||
| chr19:18717518
|
A | G | 1 | a0003c0004t0026g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.127-25392A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717518 | ||||||
| chr19:18717628
|
C | G | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-25282C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717628 | ||||||
| chr19:18717736
|
G | A | 94 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(91): Show | 94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.127-25174G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717736 | ||||||
| chr19:18717749
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-25161G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717749 | ||||||
| chr19:18717779
|
G | T | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-25131G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717779 | ||||||
| chr19:18717874
|
G | C | 2 | a0001c0001t0005g0138a0001c0001t0005g0146 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.127-25036G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717874 | ||||||
| chr19:18717961
|
G | A | 5 | a0001c0001t0005g0026a0001c0001t0005g0036a0001c0001t0005g0042others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-24949G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717961 | ||||||
| chr19:18717985
|
A | G | 3 | a0001c0007t0008g0025a0002c0002t0020g0216a0002c0002t0021g0217 | 3 | HG01099.hp1 HG03139.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.127-24925A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18717985 | ||||||
| chr19:18718050
|
A | G | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-24860A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718050 | ||||||
| chr19:18718167
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-24743C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718167 | ||||||
| chr19:18718232
|
A | T | 1 | a0002c0005t0003g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127-24678A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718232 | ||||||
| chr19:18718507
|
A | AT | 29 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-24385dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18718507 | |||||
| chr19:18718507
|
A | ATT | 6 | a0002c0002t0003g0089a0002c0002t0003g0117a0002c0002t0003g0163others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-24386_127-2438 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18718507 | |||||
| chr19:18718507
|
A | G | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-24403A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718507 | ||||||
| chr19:18718507
|
AT | A | 9 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0107others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-24385delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18718507 | |||||
| chr19:18718636
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.127-24274C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718636 | ||||||
| chr19:18718675
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-24235C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718675 | ||||||
| chr19:18718719
|
C | T | 88 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(85): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.127-24191C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718719 | ||||||
| chr19:18718792
|
G | A | 2 | a0001c0003t0002g0208a0001c0003t0002g0271 | 2 | NA19011.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.127-24118G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718792 | ||||||
| chr19:18718880
|
GT | G | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-24027delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18718880 | |||||
| chr19:18718923
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.127-23987G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718923 | ||||||
| chr19:18718960
|
A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.127-23950A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718960 | ||||||
| chr19:18718977
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-23933T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18718977 | ||||||
| chr19:18719076
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-23834G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719076 | ||||||
| chr19:18719119
|
T | A | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-23791T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719119 | ||||||
| chr19:18719167
|
T | G | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-23743T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719167 | ||||||
| chr19:18719235
|
G | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-23675G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719235 | ||||||
| chr19:18719237
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-23673G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719237 | ||||||
| chr19:18719373
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127-23537G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719373 | ||||||
| chr19:18719444
|
C | T | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-23466C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719444 | ||||||
| chr19:18719593
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18982.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.127-23317G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719593 | ||||||
| chr19:18719733
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127-23177C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719733 | ||||||
| chr19:18719894
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(186): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.127-23016A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719894 | ||||||
| chr19:18719932
|
G | A | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-22978G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18719932 | ||||||
| chr19:18720055
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.127-22855G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720055 | ||||||
| chr19:18720108
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.127-22802A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720108 | ||||||
| chr19:18720224
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-22686C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720224 | ||||||
| chr19:18720268
|
A | G | 15 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-22642A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720268 | ||||||
| chr19:18720375
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0008g0134 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-22535A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720375 | ||||||
| chr19:18720525
|
G | GT | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(40): Show | 43 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-22363dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18720525 | |||||
| chr19:18720525
|
G | GTT | 7 | a0001c0001t0001g0252a0001c0001t0003g0052a0001c0001t0003g0147others(4): Show | 7 | HG01175.hp2 HG01192.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-22364_127-2236 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18720525 | |||||
| chr19:18720525
|
GT | G | 97 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(94): Show | 97 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.127-22363delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18720525 | |||||
| chr19:18720528
|
T | G | 1 | a0001c0001t0004g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-22382T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720528 | ||||||
| chr19:18720529
|
T | G | 16 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG01099.hp1 HG01123.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-22381T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720529 | ||||||
| chr19:18720530
|
T | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-22380T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720530 | ||||||
| chr19:18720577
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127-22333A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720577 | ||||||
| chr19:18720608
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127-22302C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720608 | ||||||
| chr19:18720844
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0014g0023 | 2 | HG01123.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.127-22066A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720844 | ||||||
| chr19:18720868
|
C | CTCTG | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(238): Show | 242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.127-22041_127-2203 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18720868 | |||||
| chr19:18720887
|
C | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.127-22023C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18720887 | ||||||
| chr19:18721195
|
G | GT | 118 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0024others(115): Show | 118 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.127-21699dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721195 | |||||
| chr19:18721195
|
G | GTT | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(10): Show | 13 | HG01074.hp2 HG01167.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-21700_127-2169 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721195 | |||||
| chr19:18721375
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-21535G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721375 | ||||||
| chr19:18721411
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-21499T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721411 | ||||||
| chr19:18721492
|
C | CT | 8 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0268others(5): Show | 8 | HG01361.hp2 HG02148.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-21397dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721492 | |||||
| chr19:18721492
|
CT | C | 78 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0001g0128others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.127-21397delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721492 | |||||
| chr19:18721492
|
CTT | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.127-21398_127-2139 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721492 | |||||
| chr19:18721492
|
CTTT | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0212a0001c0001t0002g0232others(4): Show | 7 | HG00323.hp1 HG01069.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-21399_127-2139 others(7): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18721492 | |||||
| chr19:18721494
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-21416T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721494 | ||||||
| chr19:18721731
|
G | A | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-21179G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721731 | ||||||
| chr19:18721755
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-21155A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721755 | ||||||
| chr19:18721775
|
G | A | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-21135G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721775 | ||||||
| chr19:18721848
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.127-21062G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18721848 | ||||||
| chr19:18722017
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-20893G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722017 | ||||||
| chr19:18722027
|
G | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-20883G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722027 | ||||||
| chr19:18722127
|
T | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(238): Show | 242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.127-20783T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722127 | ||||||
| chr19:18722140
|
C | T | 88 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(85): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.127-20770C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722140 | ||||||
| chr19:18722394
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG00099.hp1 HG01168.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-20516T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722394 | ||||||
| chr19:18722535
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-20375C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722535 | ||||||
| chr19:18722951
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127-19959T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18722951 | ||||||
| chr19:18723018
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02145.hp2 HG02818.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-19892A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723018 | ||||||
| chr19:18723239
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.127-19671C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723239 | ||||||
| chr19:18723240
|
C | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-19670C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723240 | ||||||
| chr19:18723314
|
C | T | 88 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(85): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.127-19596C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723314 | ||||||
| chr19:18723328
|
C | T | 2 | a0002c0002t0020g0216a0002c0002t0021g0217 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.127-19582C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723328 | ||||||
| chr19:18723393
|
G | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-19517G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723393 | ||||||
| chr19:18723411
|
T | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(26): Show | 29 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-19499T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723411 | ||||||
| chr19:18723541
|
TAA | T | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-19367_127-1936 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18723541 | |||||
| chr19:18723577
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-19333C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723577 | ||||||
| chr19:18723687
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-19223G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723687 | ||||||
| chr19:18723704
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.127-19206C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723704 | ||||||
| chr19:18723706
|
G | C | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-19204G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723706 | ||||||
| chr19:18723914
|
C | T | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0004c0008t0003g0123 | 3 | HG02559.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-18996C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723914 | ||||||
| chr19:18723925
|
T | C | 20 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-18985T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723925 | ||||||
| chr19:18723936
|
G | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-18974G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18723936 | ||||||
| chr19:18724089
|
G | A | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-18821G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724089 | ||||||
| chr19:18724130
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.127-18780C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724130 | ||||||
| chr19:18724172
|
G | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-18738G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724172 | ||||||
| chr19:18724226
|
T | TGTGGGGT others(15): Show |
1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127-18675_127-1865 others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724226 | |||||
| chr19:18724250
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-18660T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724250 | ||||||
| chr19:18724305
|
G | A | 160 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-18605G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724305 | ||||||
| chr19:18724307
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.127-18603T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724307 | ||||||
| chr19:18724338
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-18572G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724338 | ||||||
| chr19:18724418
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0170 | 3 | HG00735.hp2 HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.127-18492T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724418 | ||||||
| chr19:18724431
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0179 | 2 | HG02080.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.127-18479G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724431 | ||||||
| chr19:18724528
|
G | A | 38 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0197others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-18382G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724528 | ||||||
| chr19:18724621
|
G | C | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-18289G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724621 | ||||||
| chr19:18724733
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.127-18177C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724733 | ||||||
| chr19:18724780
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-18130A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724780 | ||||||
| chr19:18724789
|
A | AAGACTGT others(2790): Show |
1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2801): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2771): Show |
1 | a0001c0001t0001g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2782): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2791): Show |
1 | a0001c0001t0015g0005 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2802): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2831): Show |
1 | a0003c0004t0002g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2842): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2791): Show |
1 | a0001c0001t0001g0097 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2802): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2790): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0007 | 2 | HG01167.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2801): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2792): Show |
1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2803): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2791): Show |
1 | a0001c0001t0001g0006 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2802): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2835): Show |
1 | a0003c0004t0002g0240 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2846): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2832): Show |
2 | a0001c0001t0001g0115a0003c0004t0023g0118 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2843): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2747): Show |
1 | a0007c0006t0001g0149 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2758): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2834): Show |
1 | a0003c0004t0002g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2845): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2835): Show |
1 | a0003c0004t0002g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2846): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2841): Show |
1 | a0003c0004t0026g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2852): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2792): Show |
2 | a0001c0001t0002g0049a0001c0001t0004g0126 | 2 | HG02896.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2803): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2824): Show |
1 | a0001c0001t0005g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2835): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2791): Show |
3 | a0001c0001t0002g0058a0001c0001t0002g0148a0001c0001t0002g0247 | 3 | HG02809.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2802): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2790): Show |
1 | a0001c0001t0002g0051 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2801): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2810): Show |
1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2821): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2824): Show |
1 | a0001c0001t0005g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2835): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2164): Show |
1 | a0001c0001t0002g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2175): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2793): Show |
1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2804): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2835): Show |
1 | a0003c0004t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2846): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2929): Show |
1 | a0001c0001t0018g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2940): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2891): Show |
1 | a0001c0001t0001g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2902): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2890): Show |
1 | a0001c0001t0001g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2901): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2845): Show |
1 | a0001c0001t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2856): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2895): Show |
1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2906): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2903): Show |
1 | a0001c0001t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2914): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2904): Show |
1 | a0001c0001t0001g0159 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2915): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2905): Show |
1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2916): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2903): Show |
1 | a0001c0001t0001g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2914): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2904): Show |
1 | a0001c0001t0001g0235 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2915): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2906): Show |
1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2917): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2905): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG01891.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2916): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2906): Show |
1 | a0001c0001t0004g0039 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2917): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
1 | a0001c0001t0011g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2905): Show |
1 | a0001c0001t0029g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2916): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2908): Show |
1 | a0001c0001t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2919): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2906): Show |
1 | a0001c0001t0001g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2917): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
1 | a0001c0001t0002g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2908): Show |
1 | a0001c0001t0002g0043 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2919): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
2 | a0001c0001t0001g0024a0001c0001t0006g0035 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0222 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
2 | a0001c0001t0002g0110a0001c0001t0002g0232 | 2 | HG02071.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
6 | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0095others(3): Show | 6 | HG01517.hp1 HG03688.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
1 | a0001c0001t0001g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2911): Show |
1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2922): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2908): Show |
1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2919): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0006g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2907): Show |
1 | a0001c0001t0006g0029 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2918): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
2 | a0001c0001t0001g0116a0001c0001t0001g0231 | 2 | HG00438.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
3 | a0001c0001t0001g0101a0001c0001t0002g0234a0002c0002t0003g0273 | 3 | HG00609.hp1 HG02080.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0113 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
2 | a0001c0001t0001g0233a0001c0001t0002g0082 | 2 | HG03834.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2908): Show |
1 | a0001c0001t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2919): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2908): Show |
4 | a0001c0001t0001g0107a0001c0001t0001g0153a0001c0001t0002g0077others(1): Show | 4 | HG00558.hp1 HG02165.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2919): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
1 | a0005c0009t0001g0068 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2861): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01074.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2872): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2860): Show |
1 | a0001c0001t0001g0230 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2871): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2911): Show |
1 | a0001c0001t0006g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2922): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2928): Show |
1 | a0001c0001t0006g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2939): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2861): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0106 | 3 | HG01433.hp2 HG02004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2872): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0083 | 2 | HG01123.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2909): Show |
1 | a0001c0001t0002g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2920): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2911): Show |
1 | a0001c0001t0006g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2922): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2910): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0102 | 2 | HG01515.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2921): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2863): Show |
1 | a0001c0001t0001g0236 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2874): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2862): Show |
1 | a0001c0001t0001g0229 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2873): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2864): Show |
1 | a0001c0001t0001g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2875): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2913): Show |
1 | a0001c0001t0001g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2924): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2912): Show |
1 | a0001c0001t0013g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2923): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2912): Show |
1 | a0001c0001t0001g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2923): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2911): Show |
1 | a0001c0001t0013g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2922): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2864): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0109 | 2 | NA18985.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2875): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2864): Show |
1 | a0001c0001t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2875): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2865): Show |
1 | a0001c0001t0001g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2876): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2912): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0170 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2923): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2934): Show |
1 | a0001c0001t0004g0015 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2945): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2915): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0079 | 2 | HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2926): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2913): Show |
1 | a0001c0001t0001g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2924): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2936): Show |
1 | a0001c0001t0004g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2947): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2935): Show |
3 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0012 | 3 | HG02451.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2946): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2937): Show |
1 | a0001c0001t0004g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2948): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2936): Show |
1 | a0001c0001t0011g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2947): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724789
|
A | AAGACTGT others(2938): Show |
2 | a0001c0001t0004g0009a0001c0001t0004g0016 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-18108_127-1810 others(2949): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18724789 | |||||
| chr19:18724802
|
C | CTTTTCTT others(2878): Show |
1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-18108_127-1810 others(2889): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724802 | ||||||
| chr19:18724805
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-18105A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18724805 | ||||||
| chr19:18725028
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127-17882C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725028 | ||||||
| chr19:18725090
|
A | T | 59 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(56): Show | 60 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.127-17820A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725090 | ||||||
| chr19:18725122
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0005g0138 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.127-17788A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725122 | ||||||
| chr19:18725207
|
T | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0128others(6): Show | 9 | HG02717.hp2 HG02965.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-17703T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725207 | ||||||
| chr19:18725276
|
C | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0232 | 2 | NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.127-17634C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725276 | ||||||
| chr19:18725302
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.127-17608C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725302 | ||||||
| chr19:18725319
|
A | G | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-17591A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725319 | ||||||
| chr19:18725529
|
GT | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.127-17379delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18725529 | |||||
| chr19:18725572
|
C | T | 1 | a0006c0010t0001g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-17338C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725572 | ||||||
| chr19:18725793
|
C | G | 1 | a0001c0001t0002g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127-17117C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725793 | ||||||
| chr19:18725796
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-17114C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725796 | ||||||
| chr19:18725804
|
G | A | 1 | a0001c0003t0024g0200 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.127-17106G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725804 | ||||||
| chr19:18725864
|
C | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.127-17046C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725864 | ||||||
| chr19:18725867
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.127-17043G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725867 | ||||||
| chr19:18725924
|
T | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-16986T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725924 | ||||||
| chr19:18725931
|
G | A | 81 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0024others(78): Show | 81 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.127-16979G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18725931 | ||||||
| chr19:18726550
|
T | C | 1 | a0001c0003t0025g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.127-16360T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726550 | ||||||
| chr19:18726553
|
G | A | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-16357G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726553 | ||||||
| chr19:18726649
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.127-16261T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726649 | ||||||
| chr19:18726653
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01070.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.127-16257C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726653 | ||||||
| chr19:18726703
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-16207G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726703 | ||||||
| chr19:18726913
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127-15997A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726913 | ||||||
| chr19:18726925
|
T | TG | 7 | a0001c0001t0001g0252a0001c0001t0004g0047a0001c0001t0004g0126others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-15981dupG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18726925 | |||||
| chr19:18726929
|
G | GA | 88 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0038others(85): Show | 88 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.127-15958dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18726929 | |||||
| chr19:18726929
|
G | GAA | 11 | a0001c0001t0001g0024a0001c0001t0001g0070a0001c0001t0001g0103others(8): Show | 11 | HG00408.hp1 HG00733.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-15959_127-1595 others(6): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18726929 | |||||
| chr19:18726929
|
GA | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG00280.hp1 HG01070.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-15958delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18726929 | |||||
| chr19:18726930
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.127-15980A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726930 | ||||||
| chr19:18726931
|
A | G | 4 | a0001c0001t0001g0179a0002c0002t0003g0190a0002c0002t0003g0198others(1): Show | 4 | HG00280.hp1 HG03704.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-15979A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726931 | ||||||
| chr19:18726933
|
A | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15977A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726933 | ||||||
| chr19:18726995
|
C | A | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-15915C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726995 | ||||||
| chr19:18726996
|
T | C | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15914T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18726996 | ||||||
| chr19:18727013
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.127-15897G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727013 | ||||||
| chr19:18727183
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(177): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.127-15727A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727183 | ||||||
| chr19:18727204
|
T | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-15706T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727204 | ||||||
| chr19:18727248
|
TCAAA | T | 8 | a0001c0001t0001g0115a0003c0004t0002g0120a0003c0004t0002g0121others(5): Show | 8 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-15654_127-1565 others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727248 | |||||
| chr19:18727331
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15579G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727331 | ||||||
| chr19:18727412
|
T | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-15498T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727412 | ||||||
| chr19:18727423
|
T | C | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15487T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727423 | ||||||
| chr19:18727494
|
T | A | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(8): Show | 11 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-15416T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727494 | ||||||
| chr19:18727580
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0107others(4): Show | 7 | HG01515.hp1 HG01517.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-15321_127-1531 others(13): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(3): Show |
66 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(63): Show | 66 | HG00438.hp1 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.127-15322_127-1531 others(14): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(4): Show |
23 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(20): Show | 23 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-15323_127-1531 others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(5): Show |
14 | a0001c0001t0001g0111a0001c0001t0005g0138a0001c0001t0005g0146others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-15324_127-1531 others(16): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(6): Show |
48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.127-15325_127-1531 others(17): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(7): Show |
10 | a0001c0001t0001g0258a0001c0001t0005g0063a0001c0001t0008g0134others(7): Show | 10 | HG01891.hp2 HG02135.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-15326_127-1531 others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-15327_127-1531 others(19): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18727580 | |||||
| chr19:18727580
|
C | CCAAAAAA others(7): Show |
1 | a0002c0002t0003g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.127-15330_127-1532 others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727580 | ||||||
| chr19:18727595
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-15315A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727595 | ||||||
| chr19:18727598
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15312G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727598 | ||||||
| chr19:18727600
|
A | AAAAAAAA others(5): Show |
1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15310_127-1530 others(16): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727600 | ||||||
| chr19:18727604
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-15306G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727604 | ||||||
| chr19:18727617
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.127-15293A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727617 | ||||||
| chr19:18727676
|
G | C | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-15234G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18727676 | ||||||
| chr19:18728073
|
T | TTGTGTCA others(9): Show |
1 | a0001c0001t0001g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-14835_127-1482 others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728073 | |||||
| chr19:18728212
|
G | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-14698G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728212 | ||||||
| chr19:18728272
|
C | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-14638C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728272 | ||||||
| chr19:18728383
|
A | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-14527A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728383 | ||||||
| chr19:18728614
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-14296T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728614 | ||||||
| chr19:18728615
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-14295C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728615 | ||||||
| chr19:18728693
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0002g0030 | 3 | HG00738.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.127-14217C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728693 | ||||||
| chr19:18728784
|
G | A | 1 | a0003c0004t0002g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.127-14126G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728784 | ||||||
| chr19:18728815
|
C | CTTTTTTT others(1): Show |
68 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.127-14087_127-1408 others(12): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0135a0001c0001t0005g0146a0001c0001t0009g0124others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-14088_127-1408 others(13): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0011g0014 | 3 | HG02451.hp1 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.127-14090_127-1408 others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0004g0009a0001c0001t0004g0012a0001c0001t0004g0013others(4): Show | 7 | HG01123.hp2 HG03098.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-14091_127-1408 others(16): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-14092_127-1408 others(17): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-14093_127-1408 others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127-14094_127-1408 others(19): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(22): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0219others(1): Show | 4 | HG02886.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(23): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0220 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.127-14080_127-1407 others(24): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0100others(2): Show | 5 | HG02602.hp1 HG02683.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(26): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(16): Show |
30 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0038others(27): Show | 30 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(27): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(17): Show |
26 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0056others(23): Show | 26 | HG00408.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(28): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0116others(2): Show | 5 | HG00438.hp1 HG00735.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-14080_127-1407 others(29): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-14080_127-1407 others(30): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728815
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127-14080_127-1407 others(31): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18728815 | |||||
| chr19:18728851
|
C | T | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-14059C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728851 | ||||||
| chr19:18728853
|
C | T | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-14057C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728853 | ||||||
| chr19:18728871
|
A | G | 3 | a0002c0002t0003g0187a0002c0002t0003g0203a0002c0002t0003g0204 | 3 | HG01515.hp2 HG01517.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.127-14039A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728871 | ||||||
| chr19:18728873
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-14037C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728873 | ||||||
| chr19:18728916
|
G | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-13994G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18728916 | ||||||
| chr19:18729004
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-13906G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729004 | ||||||
| chr19:18729074
|
A | G | 4 | a0001c0001t0002g0051a0001c0001t0002g0058a0001c0001t0002g0148others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-13836A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729074 | ||||||
| chr19:18729093
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-13817G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729093 | ||||||
| chr19:18729094
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-13816T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729094 | ||||||
| chr19:18729147
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127-13763C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729147 | ||||||
| chr19:18729200
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-13710C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729200 | ||||||
| chr19:18729287
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-13623G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729287 | ||||||
| chr19:18729307
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-13603T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729307 | ||||||
| chr19:18729370
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-13540G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729370 | ||||||
| chr19:18729380
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0140others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-13530C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729380 | ||||||
| chr19:18729402
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-13508G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729402 | ||||||
| chr19:18729450
|
A | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.127-13460A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729450 | ||||||
| chr19:18729496
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-13414G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729496 | ||||||
| chr19:18729514
|
T | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.127-13396T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729514 | ||||||
| chr19:18729535
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-13375C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729535 | ||||||
| chr19:18729600
|
G | A | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(8): Show | 11 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-13310G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729600 | ||||||
| chr19:18729648
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.127-13262A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729648 | ||||||
| chr19:18729766
|
A | G | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-13144A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729766 | ||||||
| chr19:18729818
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127-13092C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729818 | ||||||
| chr19:18729832
|
C | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-13078C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729832 | ||||||
| chr19:18729847
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-13063A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729847 | ||||||
| chr19:18729859
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.127-13051C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729859 | ||||||
| chr19:18729905
|
C | G | 1 | a0004c0008t0003g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-13005C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18729905 | ||||||
| chr19:18730092
|
C | A | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-12818C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730092 | ||||||
| chr19:18730131
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-12779G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730131 | ||||||
| chr19:18730135
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-12775A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730135 | ||||||
| chr19:18730213
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-12697C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730213 | ||||||
| chr19:18730347
|
C | G | 83 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.127-12563C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730347 | ||||||
| chr19:18730420
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-12490G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730420 | ||||||
| chr19:18730474
|
C | G | 6 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0002g0058others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-12436C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730474 | ||||||
| chr19:18730481
|
C | T | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(8): Show | 11 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-12429C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730481 | ||||||
| chr19:18730551
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-12359C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730551 | ||||||
| chr19:18730598
|
C | T | 2 | a0001c0001t0012g0160a0001c0001t0012g0172 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.127-12312C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730598 | ||||||
| chr19:18730683
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-12227C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730683 | ||||||
| chr19:18730685
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-12225G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730685 | ||||||
| chr19:18730857
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-12053C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730857 | ||||||
| chr19:18730858
|
G | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0140others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-12052G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730858 | ||||||
| chr19:18730862
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.127-12048C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730862 | ||||||
| chr19:18730947
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-11963A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730947 | ||||||
| chr19:18730959
|
CTCCCTCC others(1): Show |
C | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-11929_127-1192 others(12): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18730959 | |||||
| chr19:18730971
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-11939C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730971 | ||||||
| chr19:18730972
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-11938T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18730972 | ||||||
| chr19:18731119
|
G | A | 1 | a0001c0001t0008g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127-11791G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731119 | ||||||
| chr19:18731697
|
G | A | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-11213G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731697 | ||||||
| chr19:18731742
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0018g0136 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.127-11168C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731742 | ||||||
| chr19:18731783
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-11127C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731783 | ||||||
| chr19:18731810
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127-11100C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731810 | ||||||
| chr19:18731930
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01361.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-10980G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731930 | ||||||
| chr19:18731940
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-10970C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18731940 | ||||||
| chr19:18732019
|
C | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01361.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-10891C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732019 | ||||||
| chr19:18732274
|
G | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.127-10636G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732274 | ||||||
| chr19:18732279
|
G | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG00642.hp2 HG01123.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-10631G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732279 | ||||||
| chr19:18732284
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-10626G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732284 | ||||||
| chr19:18732396
|
C | T | 6 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0002g0058others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-10514C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732396 | ||||||
| chr19:18732397
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-10513G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732397 | ||||||
| chr19:18732496
|
T | C | 1 | a0002c0002t0003g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-10414T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732496 | ||||||
| chr19:18732498
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01361.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-10412T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732498 | ||||||
| chr19:18732526
|
A | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01361.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-10384A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732526 | ||||||
| chr19:18732565
|
T | G | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-10345T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732565 | ||||||
| chr19:18732775
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127-10135G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732775 | ||||||
| chr19:18732812
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-10098C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732812 | ||||||
| chr19:18732834
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-10076T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732834 | ||||||
| chr19:18732914
|
A | T | 12 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-9996A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732914 | ||||||
| chr19:18732942
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.127-9968T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18732942 | ||||||
| chr19:18733087
|
T | TA | 11 | a0001c0001t0001g0135a0001c0001t0001g0252a0001c0001t0003g0052others(8): Show | 11 | HG01361.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-9809dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18733087 | |||||
| chr19:18733087
|
T | TAA | 11 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0012others(8): Show | 11 | HG01123.hp2 HG01884.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-9810_127-9809d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18733087 | |||||
| chr19:18733124
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-9786C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733124 | ||||||
| chr19:18733222
|
C | T | 1 | a0002c0002t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-9688C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733222 | ||||||
| chr19:18733366
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127-9544C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733366 | ||||||
| chr19:18733378
|
G | C | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-9532G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733378 | ||||||
| chr19:18733554
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.127-9356G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733554 | ||||||
| chr19:18733581
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-9329C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733581 | ||||||
| chr19:18733582
|
C | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-9328C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733582 | ||||||
| chr19:18733606
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0246 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-9304A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733606 | ||||||
| chr19:18733722
|
T | C | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-9188T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733722 | ||||||
| chr19:18733923
|
A | G | 8 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-8987A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18733923 | ||||||
| chr19:18734027
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0246 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-8883G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734027 | ||||||
| chr19:18734051
|
A | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG01361.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-8859A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734051 | ||||||
| chr19:18734056
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-8854C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734056 | ||||||
| chr19:18734102
|
CA | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG01361.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-8797delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18734102 | |||||
| chr19:18734110
|
A | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-8800A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734110 | ||||||
| chr19:18734170
|
G | C | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-8740G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734170 | ||||||
| chr19:18734373
|
A | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.127-8537A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734373 | ||||||
| chr19:18734394
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-8516G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734394 | ||||||
| chr19:18734526
|
G | GA | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.127-8370dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18734526 | |||||
| chr19:18734526
|
G | GAA | 6 | a0001c0001t0001g0252a0002c0002t0003g0155a0002c0002t0003g0214others(3): Show | 6 | HG01081.hp2 HG02257.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-8371_127-8370d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18734526 | |||||
| chr19:18734530
|
A | G | 1 | a0001c0001t0032g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-8380A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734530 | ||||||
| chr19:18734590
|
G | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-8320G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734590 | ||||||
| chr19:18734629
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-8281G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734629 | ||||||
| chr19:18734733
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-8177G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734733 | ||||||
| chr19:18734752
|
CCA | C | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-8149_127-8148d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18734752 | |||||
| chr19:18734866
|
C | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.127-8044C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734866 | ||||||
| chr19:18734975
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7935T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18734975 | ||||||
| chr19:18735007
|
G | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-7903G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735007 | ||||||
| chr19:18735009
|
C | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7901C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735009 | ||||||
| chr19:18735042
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.127-7868G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735042 | ||||||
| chr19:18735053
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-7857C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735053 | ||||||
| chr19:18735208
|
G | T | 12 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-7702G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735208 | ||||||
| chr19:18735243
|
G | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.127-7667G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735243 | ||||||
| chr19:18735295
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.127-7615G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735295 | ||||||
| chr19:18735313
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-7597G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735313 | ||||||
| chr19:18735314
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-7596A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735314 | ||||||
| chr19:18735405
|
C | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.127-7505C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735405 | ||||||
| chr19:18735433
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-7477T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735433 | ||||||
| chr19:18735666
|
G | A | 1 | a0001c0003t0002g0218 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.127-7244G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735666 | ||||||
| chr19:18735714
|
A | G | 4 | a0001c0001t0005g0146a0001c0001t0022g0152a0002c0002t0003g0190others(1): Show | 4 | HG00280.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7196A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735714 | ||||||
| chr19:18735865
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG00438.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.127-7045C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735865 | ||||||
| chr19:18735883
|
C | T | 2 | a0002c0002t0003g0190a0002c0002t0003g0191 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.127-7027C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735883 | ||||||
| chr19:18735974
|
G | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-6936G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18735974 | ||||||
| chr19:18736027
|
C | T | 1 | a0001c0001t0029g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.127-6883C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736027 | ||||||
| chr19:18736055
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-6855T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736055 | ||||||
| chr19:18736082
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.127-6828C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736082 | ||||||
| chr19:18736135
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-6775C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736135 | ||||||
| chr19:18736291
|
TG | T | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-6615delG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18736291 | |||||
| chr19:18736297
|
TGCAGGGT others(483): Show |
T | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-6612_127-6123d others(2): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736297 | ||||||
| chr19:18736314
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-6596C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736314 | ||||||
| chr19:18736356
|
A | G | 3 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0007t0008g0025 | 3 | HG02615.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-6554A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736356 | ||||||
| chr19:18736548
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.127-6362C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736548 | ||||||
| chr19:18736617
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-6293G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736617 | ||||||
| chr19:18736647
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-6263C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736647 | ||||||
| chr19:18736676
|
A | G | 3 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0007t0008g0025 | 3 | HG02615.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-6234A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736676 | ||||||
| chr19:18736698
|
C | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-6212C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736698 | ||||||
| chr19:18736746
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.127-6164A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736746 | ||||||
| chr19:18736765
|
C | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01070.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.127-6145C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736765 | ||||||
| chr19:18736798
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.127-6112C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736798 | ||||||
| chr19:18736878
|
T | C | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-6032T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736878 | ||||||
| chr19:18736902
|
C | T | 4 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0022g0152others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6008C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736902 | ||||||
| chr19:18736927
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-5983T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18736927 | ||||||
| chr19:18737022
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-5888C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737022 | ||||||
| chr19:18737029
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-5881T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737029 | ||||||
| chr19:18737042
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.127-5868C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737042 | ||||||
| chr19:18737111
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-5799G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737111 | ||||||
| chr19:18737168
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-5742T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737168 | ||||||
| chr19:18737197
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-5713G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737197 | ||||||
| chr19:18737199
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-5711T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737199 | ||||||
| chr19:18737234
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-5676G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737234 | ||||||
| chr19:18737245
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-5665T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737245 | ||||||
| chr19:18737259
|
G | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.127-5651G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737259 | ||||||
| chr19:18737477
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-5433T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737477 | ||||||
| chr19:18737586
|
T | C | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-5324T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737586 | ||||||
| chr19:18737736
|
G | GCTGCTCC others(11): Show |
2 | a0001c0001t0005g0138a0001c0001t0008g0245 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.127-5171_127-5154d others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737736 | |||||
| chr19:18737739
|
G | GCTCCTCC others(14): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.127-5154_127-5153i others(23): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737739 | |||||
| chr19:18737739
|
G | GCTCCTCC others(29): Show |
1 | a0002c0005t0003g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-5154_127-5153i others(38): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737739 | |||||
| chr19:18737739
|
GCTC | G | 3 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0007t0008g0025 | 3 | HG02615.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-5145_127-5143d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737739 | |||||
| chr19:18737742
|
C | CCTCCTCC others(8): Show |
2 | a0001c0001t0001g0085a0001c0001t0008g0134 | 2 | HG01993.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-5154_127-5153i others(17): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737742 | |||||
| chr19:18737742
|
C | G | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-5168C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737742 | ||||||
| chr19:18737751
|
C | CCTCCTGC others(19): Show |
1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.127-5154_127-5153i others(28): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18737751 | |||||
| chr19:18737759
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-5151T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737759 | ||||||
| chr19:18737970
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-4940T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737970 | ||||||
| chr19:18737993
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127-4917A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18737993 | ||||||
| chr19:18738019
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-4891G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738019 | ||||||
| chr19:18738402
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-4508A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738402 | ||||||
| chr19:18738411
|
A | G | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-4499A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738411 | ||||||
| chr19:18738658
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-4252T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738658 | ||||||
| chr19:18738744
|
G | C | 1 | a0002c0002t0003g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.127-4166G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738744 | ||||||
| chr19:18738757
|
G | A | 1 | a0006c0010t0001g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-4153G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738757 | ||||||
| chr19:18738763
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-4147A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738763 | ||||||
| chr19:18738796
|
G | T | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-4114G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738796 | ||||||
| chr19:18738802
|
A | AAAC | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-4087_127-4085d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18738802 | |||||
| chr19:18738802
|
AAAC | A | 12 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-4087_127-4085d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 18738802 | |||||
| chr19:18738906
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.127-4004G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18738906 | ||||||
| chr19:18739050
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244 | 3 | HG02630.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-3860C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739050 | ||||||
| chr19:18739151
|
G | A | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-3759G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739151 | ||||||
| chr19:18739186
|
C | T | 1 | a0003c0004t0023g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-3724C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739186 | ||||||
| chr19:18739300
|
C | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG00733.hp1 HG01175.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3610C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739300 | ||||||
| chr19:18739377
|
G | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.127-3533G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739377 | ||||||
| chr19:18739388
|
A | G | 5 | a0001c0001t0001g0135a0001c0001t0005g0146a0001c0001t0009g0124others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3522A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739388 | ||||||
| chr19:18739444
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-3466C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739444 | ||||||
| chr19:18739535
|
C | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.127-3375C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739535 | ||||||
| chr19:18739576
|
T | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01361.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-3334T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739576 | ||||||
| chr19:18739610
|
A | C | 1 | a0001c0001t0005g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-3300A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739610 | ||||||
| chr19:18739680
|
T | C | 2 | a0001c0001t0004g0039a0001c0001t0011g0040 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.127-3230T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739680 | ||||||
| chr19:18739714
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-3196G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739714 | ||||||
| chr19:18739762
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0250 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.127-3148C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739762 | ||||||
| chr19:18739876
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0013g0065others(1): Show | 4 | HG00642.hp2 HG01346.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-3034G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739876 | ||||||
| chr19:18739897
|
G | T | 68 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.127-3013G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739897 | ||||||
| chr19:18739898
|
A | T | 68 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.127-3012A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18739898 | ||||||
| chr19:18740177
|
C | G | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-2733C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740177 | ||||||
| chr19:18740229
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-2681G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740229 | ||||||
| chr19:18740244
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-2666C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740244 | ||||||
| chr19:18740335
|
C | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-2575C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740335 | ||||||
| chr19:18740394
|
G | A | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-2516G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740394 | ||||||
| chr19:18740553
|
C | G | 1 | a0002c0002t0003g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.127-2357C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740553 | ||||||
| chr19:18740780
|
G | A | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-2130G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740780 | ||||||
| chr19:18740937
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.127-1973G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740937 | ||||||
| chr19:18740961
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-1949C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18740961 | ||||||
| chr19:18741135
|
T | C | 2 | a0002c0002t0003g0203a0002c0002t0003g0204 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.127-1775T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18741135 | ||||||
| chr19:18741392
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.127-1518C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18741392 | ||||||
| chr19:18741687
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.127-1223C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18741687 | ||||||
| chr19:18741730
|
C | T | 1 | a0001c0001t0008g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127-1180C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18741730 | ||||||
| chr19:18741824
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0246 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-1086G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18741824 | ||||||
| chr19:18742037
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.127-873A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742037 | ||||||
| chr19:18742071
|
A | G | 1 | a0001c0003t0002g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.127-839A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742071 | ||||||
| chr19:18742113
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.127-797G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742113 | ||||||
| chr19:18742145
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-765C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742145 | ||||||
| chr19:18742323
|
G | A | 1 | a0001c0003t0002g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.127-587G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742323 | ||||||
| chr19:18742327
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-583G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742327 | ||||||
| chr19:18742461
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-449C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742461 | ||||||
| chr19:18742562
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-348T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742562 | ||||||
| chr19:18742626
|
G | A | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.127-284G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742626 | ||||||
| chr19:18742698
|
G | A | 1 | a0002c0002t0003g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.127-212G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742698 | ||||||
| chr19:18742743
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.127-167T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742743 | ||||||
| chr19:18742743
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.127-167T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742743 | ||||||
| chr19:18742786
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-124C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742786 | ||||||
| chr19:18742903
|
C | T | 1 | a0003c0004t0023g0118 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.127-7C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18742903 | ||||||
| chr19:18743201
|
G | T | 5 | a0001c0003t0002g0001a0001c0003t0002g0030a0001c0003t0002g0114others(2): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+175G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743201 | ||||||
| chr19:18743220
|
C | T | 1 | a0001c0003t0002g0205 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.243+194C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743220 | ||||||
| chr19:18743223
|
A | G | 1 | a0002c0002t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.243+197A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743223 | ||||||
| chr19:18743449
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.243+423G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743449 | ||||||
| chr19:18743466
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+440C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743466 | ||||||
| chr19:18743480
|
T | A | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.243+454T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743480 | ||||||
| chr19:18743511
|
C | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+485C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743511 | ||||||
| chr19:18743627
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0002g0030 | 3 | HG00738.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.243+601C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743627 | ||||||
| chr19:18743629
|
TG | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.243+612delG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 18743629 | |||||
| chr19:18743672
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.243+646G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743672 | ||||||
| chr19:18743721
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02630.hp1 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+695A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743721 | ||||||
| chr19:18743757
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.243+731G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743757 | ||||||
| chr19:18743792
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.243+766C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18743792 | ||||||
| chr19:18744006
|
T | G | 1 | a0002c0002t0003g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.243+980T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744006 | ||||||
| chr19:18744221
|
T | C | 1 | a0002c0002t0003g0202 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.243+1195T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744221 | ||||||
| chr19:18744253
|
C | T | 2 | a0001c0003t0002g0218a0001c0003t0002g0221 | 2 | HG01081.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.243+1227C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744253 | ||||||
| chr19:18744491
|
AAC | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.244-1312_244-1311d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 18744491 | |||||
| chr19:18744505
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244-1318C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744505 | ||||||
| chr19:18744588
|
C | T | 2 | a0001c0001t0001g0186a0002c0002t0021g0217 | 2 | HG01168.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-1235C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744588 | ||||||
| chr19:18744592
|
T | C | 1 | a0003c0004t0002g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.244-1231T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744592 | ||||||
| chr19:18744885
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244-938A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744885 | ||||||
| chr19:18744990
|
C | G | 1 | a0001c0003t0002g0270 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.244-833C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18744990 | ||||||
| chr19:18745068
|
A | G | 2 | a0001c0001t0006g0046a0001c0001t0006g0074 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.244-755A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745068 | ||||||
| chr19:18745102
|
A | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244-721A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745102 | ||||||
| chr19:18745106
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244-717G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745106 | ||||||
| chr19:18745175
|
A | G | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244-648A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745175 | ||||||
| chr19:18745351
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.244-472C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745351 | ||||||
| chr19:18745412
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.244-411G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745412 | ||||||
| chr19:18745441
|
C | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG01123.hp2 HG02451.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.244-382C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745441 | ||||||
| chr19:18745734
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.244-89C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 2/13 | chr19 | 18745734 | ||||||
| chr19:18746023
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.381+63A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746023 | ||||||
| chr19:18746245
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.381+285C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746245 | ||||||
| chr19:18746341
|
C | T | 1 | a0001c0001t0019g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+381C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746341 | ||||||
| chr19:18746352
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.381+392C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746352 | ||||||
| chr19:18746477
|
T | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.381+517T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746477 | ||||||
| chr19:18746483
|
C | A | 12 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+523C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746483 | ||||||
| chr19:18746485
|
T | C | 5 | a0001c0001t0001g0164a0002c0002t0003g0190a0002c0002t0003g0191others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+525T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746485 | ||||||
| chr19:18746523
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.382-530C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746523 | ||||||
| chr19:18746549
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-504C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746549 | ||||||
| chr19:18746610
|
T | C | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.382-443T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746610 | ||||||
| chr19:18746797
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-256C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746797 | ||||||
| chr19:18746798
|
G | T | 1 | a0001c0001t0013g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.382-255G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746798 | ||||||
| chr19:18746816
|
C | G | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.382-237C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746816 | ||||||
| chr19:18746901
|
G | A | 4 | a0002c0002t0003g0163a0002c0002t0003g0173a0002c0002t0003g0180others(1): Show | 4 | HG00544.hp2 HG00558.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-152G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746901 | ||||||
| chr19:18746914
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.382-139C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18746914 | ||||||
| chr19:18747025
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.382-28G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 3/13 | chr19 | 18747025 | ||||||
| chr19:18747129
|
A | AC | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.443+25dupC | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18747129 | |||||
| chr19:18747129
|
A | ACC | 31 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0003g0253others(28): Show | 31 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.443+24_443+25dupCC | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18747129 | |||||
| chr19:18747140
|
G | C | 1 | a0002c0002t0003g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.443+26G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747140 | ||||||
| chr19:18747141
|
C | G | 1 | a0002c0002t0003g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.443+27C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747141 | ||||||
| chr19:18747275
|
A | AGGAGTTC others(8): Show |
1 | a0002c0002t0003g0202 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.443+166_443+180dup others(15): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18747275 | |||||
| chr19:18747328
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.443+223dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18747328 | |||||
| chr19:18747329
|
A | C | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.443+215A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747329 | ||||||
| chr19:18747466
|
G | A | 1 | a0001c0001t0005g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.443+352G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747466 | ||||||
| chr19:18747505
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.443+391G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747505 | ||||||
| chr19:18747544
|
G | A | 13 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0140others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+430G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747544 | ||||||
| chr19:18747707
|
A | C | 1 | a0004c0008t0003g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.443+593A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18747707 | ||||||
| chr19:18748213
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.443+1099A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748213 | ||||||
| chr19:18748240
|
C | T | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.443+1126C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748240 | ||||||
| chr19:18748320
|
G | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.443+1206G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748320 | ||||||
| chr19:18748374
|
A | AT | 41 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0073others(38): Show | 41 | HG01069.hp1 HG01074.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.443+1285dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18748374 | |||||
| chr19:18748374
|
AT | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01361.hp1 HG02145.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+1285delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 18748374 | |||||
| chr19:18748417
|
C | T | 12 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+1303C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748417 | ||||||
| chr19:18748435
|
T | A | 15 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+1321T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748435 | ||||||
| chr19:18748809
|
A | G | 1 | a0001c0001t0008g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.444-972A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748809 | ||||||
| chr19:18748870
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 234 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.444-911A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748870 | ||||||
| chr19:18748947
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.444-834G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18748947 | ||||||
| chr19:18749119
|
A | G | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.444-662A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18749119 | ||||||
| chr19:18749231
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.444-550A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18749231 | ||||||
| chr19:18749264
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.444-517G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18749264 | ||||||
| chr19:18749601
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.444-180G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18749601 | ||||||
| chr19:18749703
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.444-78G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 4/13 | chr19 | 18749703 | ||||||
| chr19:18750032
|
A | T | 1 | a0001c0001t0004g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.538+157A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750032 | ||||||
| chr19:18750066
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.538+191C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750066 | ||||||
| chr19:18750109
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.538+234G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750109 | ||||||
| chr19:18750198
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.538+323G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750198 | ||||||
| chr19:18750223
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.538+348A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750223 | ||||||
| chr19:18750321
|
G | T | 4 | a0001c0001t0001g0135a0001c0001t0009g0124a0001c0001t0009g0244others(1): Show | 4 | HG02630.hp1 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+446G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750321 | ||||||
| chr19:18750434
|
G | C | 5 | a0001c0001t0007g0027a0001c0001t0007g0032a0001c0001t0007g0033others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+559G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750434 | ||||||
| chr19:18750645
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.538+770T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750645 | ||||||
| chr19:18750852
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.538+977T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18750852 | ||||||
| chr19:18751026
|
C | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG00099.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.538+1151C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751026 | ||||||
| chr19:18751417
|
G | A | 41 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(38): Show | 42 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.538+1542G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751417 | ||||||
| chr19:18751602
|
C | T | 13 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(10): Show | 13 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.538+1727C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751602 | ||||||
| chr19:18751704
|
G | A | 7 | a0001c0001t0004g0215a0001c0001t0006g0029a0001c0001t0006g0035others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.539-1796G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751704 | ||||||
| chr19:18751718
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.539-1782C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751718 | ||||||
| chr19:18751911
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0238 | 2 | NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.539-1589A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751911 | ||||||
| chr19:18751949
|
A | G | 48 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(45): Show | 49 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.539-1551A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18751949 | ||||||
| chr19:18752147
|
C | CA | 75 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.539-1336dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 18752147 | |||||
| chr19:18752161
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.539-1339A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752161 | ||||||
| chr19:18752182
|
A | G | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.539-1318A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752182 | ||||||
| chr19:18752244
|
T | A | 2 | a0001c0001t0005g0130a0001c0001t0005g0131 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.539-1256T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752244 | ||||||
| chr19:18752406
|
C | T | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.539-1094C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752406 | ||||||
| chr19:18752419
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.539-1081A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752419 | ||||||
| chr19:18752437
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539-1063G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752437 | ||||||
| chr19:18752547
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-953G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752547 | ||||||
| chr19:18752615
|
A | T | 1 | a0003c0004t0002g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.539-885A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752615 | ||||||
| chr19:18752657
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.539-843T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752657 | ||||||
| chr19:18752735
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.539-765G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752735 | ||||||
| chr19:18752840
|
G | A | 9 | a0001c0001t0002g0043a0001c0001t0002g0077a0001c0001t0002g0078others(6): Show | 9 | HG02165.hp1 HG03834.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.539-660G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18752840 | ||||||
| chr19:18753005
|
C | T | 4 | a0001c0003t0002g0001a0001c0003t0002g0030a0001c0003t0002g0218others(1): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-495C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753005 | ||||||
| chr19:18753061
|
C | T | 1 | a0002c0002t0010g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.539-439C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753061 | ||||||
| chr19:18753081
|
C | T | 2 | a0001c0001t0006g0046a0001c0001t0006g0074 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.539-419C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753081 | ||||||
| chr19:18753117
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.539-383A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753117 | ||||||
| chr19:18753153
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.539-347G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753153 | ||||||
| chr19:18753231
|
G | A | 1 | a0001c0001t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.539-269G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753231 | ||||||
| chr19:18753254
|
C | T | 4 | a0001c0001t0003g0253a0002c0002t0003g0155a0002c0002t0003g0198others(1): Show | 4 | HG02056.hp1 NA18977.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-246C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753254 | ||||||
| chr19:18753255
|
G | A | 1 | a0001c0003t0002g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.539-245G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753255 | ||||||
| chr19:18753275
|
C | CTAAA | 98 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(95): Show | 99 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.539-192_539-189dup others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 18753275 | |||||
| chr19:18753275
|
C | CTAAATAA others(1): Show |
12 | a0001c0001t0001g0066a0001c0001t0001g0090a0001c0001t0001g0145others(9): Show | 12 | HG00642.hp2 HG01123.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.539-196_539-189dup others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 18753275 | |||||
| chr19:18753275
|
CTAAATAA others(1): Show |
C | 45 | a0001c0001t0001g0070a0001c0001t0001g0135a0001c0001t0001g0159others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.539-196_539-189del others(8): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 18753275 | |||||
| chr19:18753431
|
C | T | 1 | a0001c0001t0005g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539-69C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753431 | ||||||
| chr19:18753449
|
T | C | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.539-51T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753449 | ||||||
| chr19:18753490
|
A | G | 2 | a0001c0001t0004g0039a0001c0001t0011g0040 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.539-10A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 5/13 | chr19 | 18753490 | ||||||
| chr19:18753740
|
G | T | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.624+155G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18753740 | ||||||
| chr19:18753797
|
C | G | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.624+212C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18753797 | ||||||
| chr19:18753865
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.624+280C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18753865 | ||||||
| chr19:18753956
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.624+371C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18753956 | ||||||
| chr19:18753973
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.624+388C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18753973 | ||||||
| chr19:18754100
|
C | CA | 12 | a0001c0001t0001g0156a0001c0001t0001g0164a0001c0001t0001g0183others(9): Show | 12 | HG00280.hp2 HG01361.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.624+533dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18754100 | |||||
| chr19:18754100
|
CA | C | 13 | a0001c0001t0001g0193a0001c0001t0001g0212a0001c0001t0001g0235others(10): Show | 13 | HG01070.hp1 HG02258.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.624+533delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18754100 | |||||
| chr19:18754234
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0169 | 2 | HG00438.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.624+649C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18754234 | ||||||
| chr19:18754412
|
G | C | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.624+827G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18754412 | ||||||
| chr19:18754698
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.624+1113G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18754698 | ||||||
| chr19:18754750
|
C | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.624+1165C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18754750 | ||||||
| chr19:18754890
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0228 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.624+1305T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18754890 | ||||||
| chr19:18755082
|
C | T | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.624+1497C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755082 | ||||||
| chr19:18755113
|
C | T | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.624+1528C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755113 | ||||||
| chr19:18755203
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.624+1618G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755203 | ||||||
| chr19:18755456
|
A | C | 2 | a0001c0001t0008g0134a0001c0001t0008g0245 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.624+1871A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755456 | ||||||
| chr19:18755577
|
G | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.624+1992G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755577 | ||||||
| chr19:18755593
|
C | CT | 22 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0093others(19): Show | 22 | HG00438.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.624+2033dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18755593 | |||||
| chr19:18755593
|
CT | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+2033delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18755593 | |||||
| chr19:18755593
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.624+2024_624+2033d others(12): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18755593 | |||||
| chr19:18755593
|
CTTTTTTT others(4): Show |
C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.624+2023_624+2033d others(13): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18755593 | |||||
| chr19:18755624
|
A | G | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.624+2039A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755624 | ||||||
| chr19:18755764
|
G | A | 1 | a0001c0003t0002g0221 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.624+2179G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755764 | ||||||
| chr19:18755817
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.624+2232G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18755817 | ||||||
| chr19:18756128
|
G | A | 38 | a0001c0001t0003g0253a0002c0002t0003g0048a0002c0002t0003g0089others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.624+2543G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756128 | ||||||
| chr19:18756192
|
G | A | 13 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(10): Show | 13 | HG01123.hp2 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.624+2607G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756192 | ||||||
| chr19:18756257
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.624+2672C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756257 | ||||||
| chr19:18756334
|
C | CA | 173 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.624+2770dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756334 | |||||
| chr19:18756334
|
C | CAA | 61 | a0001c0001t0001g0071a0001c0001t0001g0100a0001c0001t0001g0109others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.624+2769_624+2770d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756334 | |||||
| chr19:18756334
|
C | CAAA | 21 | a0001c0001t0003g0052a0001c0001t0004g0009a0001c0001t0004g0010others(18): Show | 21 | HG01081.hp2 HG01123.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+2768_624+2770d others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756334 | |||||
| chr19:18756352
|
A | AAAG | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2769_624+2770i others(5): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756352 | |||||
| chr19:18756368
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0250 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.624+2783C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756368 | ||||||
| chr19:18756614
|
T | TA | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.625-2924dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756614 | |||||
| chr19:18756614
|
T | TAA | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.625-2925_625-2924d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18756614 | |||||
| chr19:18756721
|
G | A | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-2830G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756721 | ||||||
| chr19:18756751
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.625-2800C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756751 | ||||||
| chr19:18756937
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.625-2614A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756937 | ||||||
| chr19:18756941
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.625-2610A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18756941 | ||||||
| chr19:18757053
|
C | T | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.625-2498C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18757053 | ||||||
| chr19:18757104
|
C | T | 3 | a0001c0001t0004g0047a0001c0001t0018g0136a0001c0001t0027g0004 | 3 | HG01884.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.625-2447C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18757104 | ||||||
| chr19:18757473
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.625-2078G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18757473 | ||||||
| chr19:18757708
|
T | TA | 9 | a0001c0001t0001g0252a0001c0001t0002g0049a0001c0001t0002g0051others(6): Show | 9 | HG02258.hp1 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-1834dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18757708 | |||||
| chr19:18757949
|
T | C | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-1602T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18757949 | ||||||
| chr19:18758143
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0228 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.625-1408T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758143 | ||||||
| chr19:18758157
|
G | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(177): Show | 180 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.625-1394G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758157 | ||||||
| chr19:18758164
|
C | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(177): Show | 180 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.625-1387C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758164 | ||||||
| chr19:18758177
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG00642.hp2 HG01123.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-1374C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758177 | ||||||
| chr19:18758189
|
G | T | 1 | a0001c0001t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.625-1362G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758189 | ||||||
| chr19:18758285
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.625-1266G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758285 | ||||||
| chr19:18758360
|
T | TA | 7 | a0001c0001t0002g0246a0001c0001t0003g0052a0001c0001t0003g0147others(4): Show | 7 | HG00558.hp2 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-1176dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 18758360 | |||||
| chr19:18758763
|
A | T | 1 | a0001c0001t0005g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.625-788A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758763 | ||||||
| chr19:18758788
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.625-763G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758788 | ||||||
| chr19:18758866
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0005g0146a0001c0001t0022g0152 | 3 | HG02148.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.625-685C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758866 | ||||||
| chr19:18758917
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0183a0001c0001t0001g0264 | 3 | HG01978.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.625-634T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758917 | ||||||
| chr19:18758935
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.625-616C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758935 | ||||||
| chr19:18758954
|
C | T | 12 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-597C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18758954 | ||||||
| chr19:18759121
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.625-430T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18759121 | ||||||
| chr19:18759392
|
C | A | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.625-159C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18759392 | ||||||
| chr19:18759422
|
A | T | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.625-129A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 6/13 | chr19 | 18759422 | ||||||
| chr19:18759657
|
T | G | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.665+66T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759657 | ||||||
| chr19:18759753
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.665+162C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759753 | ||||||
| chr19:18759761
|
C | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG01361.hp1 HG02145.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+170C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759761 | ||||||
| chr19:18759891
|
G | A | 4 | a0001c0003t0002g0001a0001c0003t0002g0030a0001c0003t0002g0218others(1): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-117G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759891 | ||||||
| chr19:18759914
|
T | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0246 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.666-94T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759914 | ||||||
| chr19:18759956
|
G | GCCAGCCC others(13): Show |
75 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0003g0253others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.666-44_666-43insCT others(18): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 18759956 | |||||
| chr19:18759965
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.666-43G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759965 | ||||||
| chr19:18759966
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.666-42C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 7/13 | chr19 | 18759966 | ||||||
| chr19:18760246
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.886+18C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760246 | ||||||
| chr19:18760347
|
G | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.886+119G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760347 | ||||||
| chr19:18760453
|
C | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG00733.hp1 HG01175.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+225C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760453 | ||||||
| chr19:18760557
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.886+329C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760557 | ||||||
| chr19:18760573
|
T | C | 1 | a0001c0001t0008g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.886+345T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760573 | ||||||
| chr19:18760620
|
A | C | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.886+392A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760620 | ||||||
| chr19:18760680
|
A | G | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.886+452A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760680 | ||||||
| chr19:18760946
|
C | T | 1 | a0002c0002t0020g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.886+718C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760946 | ||||||
| chr19:18760977
|
C | T | 1 | a0002c0002t0003g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.886+749C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18760977 | ||||||
| chr19:18761032
|
G | A | 1 | a0001c0003t0002g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.886+804G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761032 | ||||||
| chr19:18761094
|
ACATGTAG | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.886+867_886+873del others(7): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761094 | ||||||
| chr19:18761102
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.886+874T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761102 | ||||||
| chr19:18761197
|
G | A | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.886+969G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761197 | ||||||
| chr19:18761437
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.886+1209G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761437 | ||||||
| chr19:18761926
|
C | T | 1 | a0001c0001t0007g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.886+1698C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761926 | ||||||
| chr19:18761944
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.886+1716G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18761944 | ||||||
| chr19:18762107
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.886+1879A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762107 | ||||||
| chr19:18762222
|
A | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0164a0001c0001t0001g0181others(3): Show | 6 | HG00280.hp2 HG01978.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.886+1994A>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762222 | ||||||
| chr19:18762436
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+2208C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762436 | ||||||
| chr19:18762510
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.886+2282G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762510 | ||||||
| chr19:18762534
|
A | AC | 14 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0119others(11): Show | 14 | HG00438.hp2 HG00733.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.886+2310dupC | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 18762534 | |||||
| chr19:18762771
|
C | T | 9 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG00642.hp2 HG01123.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.886+2543C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762771 | ||||||
| chr19:18762792
|
T | G | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.886+2564T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18762792 | ||||||
| chr19:18763170
|
G | A | 3 | a0001c0001t0009g0124a0001c0001t0009g0244a0001c0001t0027g0004 | 3 | HG01884.hp2 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.887-2234G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763170 | ||||||
| chr19:18763187
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.887-2217G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763187 | ||||||
| chr19:18763225
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.887-2179C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763225 | ||||||
| chr19:18763392
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(179): Show | 182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.887-2012T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763392 | ||||||
| chr19:18763434
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.887-1970T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763434 | ||||||
| chr19:18763673
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 88 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.887-1731G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763673 | ||||||
| chr19:18763705
|
G | A | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.887-1699G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763705 | ||||||
| chr19:18763873
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG01168.hp1 HG02300.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.887-1531G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763873 | ||||||
| chr19:18763983
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.887-1421C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763983 | ||||||
| chr19:18764052
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.887-1352C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764052 | ||||||
| chr19:18764114
|
G | A | 2 | a0001c0001t0005g0146a0001c0001t0022g0152 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.887-1290G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764114 | ||||||
| chr19:18764211
|
C | T | 6 | a0001c0001t0006g0029a0001c0001t0006g0035a0001c0001t0006g0046others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.887-1193C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764211 | ||||||
| chr19:18764384
|
G | C | 42 | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0003g0253others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.887-1020G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764384 | ||||||
| chr19:18764390
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.887-1014A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764390 | ||||||
| chr19:18764491
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.887-913C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764491 | ||||||
| chr19:18764574
|
C | G | 10 | a0001c0001t0001g0135a0001c0001t0005g0026a0001c0001t0005g0036others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.887-830C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764574 | ||||||
| chr19:18764580
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.887-824C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764580 | ||||||
| chr19:18764616
|
A | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0150a0001c0001t0002g0051others(23): Show | 26 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.887-788A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764616 | ||||||
| chr19:18764758
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.887-646C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764758 | ||||||
| chr19:18764853
|
G | A | 8 | a0001c0001t0001g0161a0001c0001t0001g0189a0001c0001t0001g0193others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.887-551G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764853 | ||||||
| chr19:18764906
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.887-498C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18764906 | ||||||
| chr19:18765349
|
C | G | 1 | a0001c0001t0005g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.887-55C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18765349 | ||||||
| chr19:18765398
|
C | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG00733.hp1 HG01175.hp1 HG01258.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.887-6C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18765398 | ||||||
| chr19:18765557
|
GA | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02145.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1011+30delA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18765557 | ||||||
| chr19:18765780
|
G | A | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1011+252G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18765780 | ||||||
| chr19:18765960
|
C | CA | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1011+441dupA | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18765960 | |||||
| chr19:18765961
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1011+433A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18765961 | ||||||
| chr19:18766145
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1011+617G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766145 | ||||||
| chr19:18766269
|
T | TG | 70 | a0001c0001t0003g0253a0001c0001t0004g0009a0001c0001t0004g0010others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1011+742dupG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766269 | |||||
| chr19:18766287
|
A | AT | 14 | a0001c0001t0001g0104a0001c0001t0001g0164a0001c0001t0001g0167others(11): Show | 14 | HG01069.hp1 HG01346.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1011+781dupT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766287 | |||||
| chr19:18766287
|
A | ATT | 37 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1011+780_1011+781d others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766287 | |||||
| chr19:18766287
|
AT | A | 15 | a0001c0001t0001g0128a0001c0001t0001g0156a0001c0001t0001g0227others(12): Show | 15 | HG00323.hp1 HG00544.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1011+781delT | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766287 | |||||
| chr19:18766287
|
ATTTTTTT | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG01361.hp1 HG02145.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1011+775_1011+781d others(9): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766287 | |||||
| chr19:18766296
|
T | TTA | 22 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(19): Show | 22 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1011+769_1011+770i others(4): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 18766296 | |||||
| chr19:18766297
|
T | TA | 4 | a0001c0001t0004g0039a0001c0001t0004g0126a0001c0001t0004g0215others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+769_1011+770i others(3): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766297 | ||||||
| chr19:18766339
|
A | G | 42 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1011+811A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766339 | ||||||
| chr19:18766358
|
C | T | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1011+830C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766358 | ||||||
| chr19:18766383
|
C | A | 42 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1011+855C>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766383 | ||||||
| chr19:18766603
|
G | A | 11 | a0001c0001t0002g0043a0001c0001t0002g0077a0001c0001t0002g0078others(8): Show | 11 | HG02071.hp1 HG02080.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1011+1075G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766603 | ||||||
| chr19:18766836
|
C | T | 1 | a0003c0004t0002g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1011+1308C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766836 | ||||||
| chr19:18766914
|
T | C | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1011+1386T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18766914 | ||||||
| chr19:18767195
|
A | G | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1012-1290A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767195 | ||||||
| chr19:18767218
|
A | C | 1 | a0004c0008t0003g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1012-1267A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767218 | ||||||
| chr19:18767237
|
C | T | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1012-1248C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767237 | ||||||
| chr19:18767490
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012-995C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767490 | ||||||
| chr19:18767495
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG00642.hp2 HG01123.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012-990G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767495 | ||||||
| chr19:18767611
|
G | A | 1 | a0002c0002t0003g0133 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1012-874G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18767611 | ||||||
| chr19:18768275
|
C | T | 1 | a0001c0001t0018g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1012-210C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18768275 | ||||||
| chr19:18768425
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1012-60C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 9/13 | chr19 | 18768425 | ||||||
| chr19:18768814
|
C | T | 1 | a0001c0001t0027g0004 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1320+21C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18768814 | ||||||
| chr19:18769077
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0050 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1320+284C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769077 | ||||||
| chr19:18769219
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1320+426C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769219 | ||||||
| chr19:18769371
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1320+578G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769371 | ||||||
| chr19:18769373
|
C | T | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1320+580C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769373 | ||||||
| chr19:18769486
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0250 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1320+693G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769486 | ||||||
| chr19:18769489
|
C | T | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1320+696C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769489 | ||||||
| chr19:18769511
|
A | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1320+718A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769511 | ||||||
| chr19:18769748
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1320+955C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769748 | ||||||
| chr19:18769767
|
G | A | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1320+974G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769767 | ||||||
| chr19:18769769
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1320+976G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18769769 | ||||||
| chr19:18770004
|
A | AC | 8 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0229others(5): Show | 8 | HG02055.hp2 HG02615.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.1320+1217dupC | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 18770004 | |||||
| chr19:18770054
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1320+1261A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770054 | ||||||
| chr19:18770213
|
T | C | 42 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1321-1229T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770213 | ||||||
| chr19:18770287
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0246 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1321-1155C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770287 | ||||||
| chr19:18770781
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1321-661T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770781 | ||||||
| chr19:18770826
|
CCATGTGG others(11): Show |
C | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1321-593_1321-576d others(20): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 18770826 | |||||
| chr19:18770867
|
C | T | 2 | a0001c0001t0008g0134a0002c0002t0003g0174 | 2 | NA18747.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1321-575C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770867 | ||||||
| chr19:18770918
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0232 | 2 | NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1321-524G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18770918 | ||||||
| chr19:18771080
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0022 | 2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1321-362A>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771080 | ||||||
| chr19:18771171
|
C | T | 18 | a0001c0001t0002g0132a0001c0001t0002g0246a0001c0003t0002g0001others(15): Show | 19 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1321-271C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771171 | ||||||
| chr19:18771216
|
C | T | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1321-226C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771216 | ||||||
| chr19:18771250
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1321-192G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771250 | ||||||
| chr19:18771252
|
A | AG | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1321-188dupG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 18771252 | |||||
| chr19:18771310
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1321-132G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771310 | ||||||
| chr19:18771336
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1321-106C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771336 | ||||||
| chr19:18771394
|
G | A | 4 | a0003c0004t0002g0120a0003c0004t0002g0121a0003c0004t0002g0242others(1): Show | 4 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-48G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771394 | ||||||
| chr19:18771781
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1425+235G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18771781 | ||||||
| chr19:18771961
|
G | A | 2 | a0001c0001t0018g0136a0002c0002t0003g0224 | 2 | HG04199.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1425+415G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18771961 | ||||||
| chr19:18772670
|
C | G | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1425+1124C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18772670 | ||||||
| chr19:18772783
|
C | T | 75 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0028others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1425+1237C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18772783 | ||||||
| chr19:18772973
|
G | A | 138 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(135): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1425+1427G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18772973 | ||||||
| chr19:18773028
|
T | C | 42 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1425+1482T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773028 | ||||||
| chr19:18773322
|
C | T | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1426-1578C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773322 | ||||||
| chr19:18773389
|
C | T | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426-1511C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773389 | ||||||
| chr19:18773448
|
T | C | 1 | a0001c0001t0022g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1426-1452T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773448 | ||||||
| chr19:18773543
|
C | T | 1 | a0001c0007t0008g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1426-1357C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773543 | ||||||
| chr19:18773801
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02965.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1426-1099G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773801 | ||||||
| chr19:18773933
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1426-967A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773933 | ||||||
| chr19:18773941
|
G | C | 28 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(25): Show | 28 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1426-959G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773941 | ||||||
| chr19:18773946
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0147 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1426-954G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18773946 | ||||||
| chr19:18774024
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1426-876G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774024 | ||||||
| chr19:18774028
|
T | A | 42 | a0001c0001t0003g0253a0001c0001t0008g0134a0002c0002t0003g0048others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1426-872T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774028 | ||||||
| chr19:18774075
|
C | G | 8 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0012others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1426-825C>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774075 | ||||||
| chr19:18774198
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1426-702C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774198 | ||||||
| chr19:18774584
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1426-316G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774584 | ||||||
| chr19:18774594
|
C | T | 1 | a0002c0002t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1426-306C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774594 | ||||||
| chr19:18774887
|
C | T | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426-13C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 11/13 | chr19 | 18774887 | ||||||
| chr19:18775003
|
G | C | 1 | a0001c0001t0018g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1512+17G>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775003 | ||||||
| chr19:18775092
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1512+106G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775092 | ||||||
| chr19:18775097
|
C | T | 1 | a0002c0002t0003g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1512+111C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775097 | ||||||
| chr19:18775229
|
G | A | 1 | a0002c0002t0017g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1512+243G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775229 | ||||||
| chr19:18775283
|
G | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01070.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1512+297G>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775283 | ||||||
| chr19:18775335
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1513-306C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775335 | ||||||
| chr19:18775557
|
A | C | 75 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0003g0253others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1513-84A>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775557 | ||||||
| chr19:18775604
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1513-37C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775604 | ||||||
| chr19:18775605
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG00642.hp2 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513-36G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775605 | ||||||
| chr19:18775621
|
T | C | 75 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0003g0253others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1513-20T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 12/13 | chr19 | 18775621 | ||||||
| chr19:18775865
|
T | C | 1 | a0001c0003t0024g0200 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1693+44T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18775865 | ||||||
| chr19:18775953
|
T | C | 75 | a0001c0001t0003g0052a0001c0001t0003g0147a0001c0001t0003g0253others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1693+132T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18775953 | ||||||
| chr19:18776003
|
G | GGGCCA | 70 | a0001c0001t0003g0253a0001c0001t0004g0009a0001c0001t0004g0010others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1693+195_1693+199d others(7): Show |
CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 18776003 | |||||
| chr19:18776255
|
T | A | 1 | a0002c0002t0003g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1693+434T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18776255 | ||||||
| chr19:18776326
|
G | A | 2 | a0001c0001t0009g0124a0001c0001t0009g0244 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1693+505G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18776326 | ||||||
| chr19:18776867
|
T | C | 69 | a0001c0001t0003g0253a0001c0001t0004g0009a0001c0001t0004g0010others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1694-304T>C | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18776867 | ||||||
| chr19:18777018
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1694-153C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18777018 |