Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0002 | 0/0 | 634 | 39 | 2 | 3 | 21 | 5 | 8 | 16 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0003 | 0/0 | 634 | 7 | 0 | 4 | 1 | 1 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0004 | 0/0 | 634 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0005 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0006 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| a0007 | 0/0 | 634 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | MATSN others(629): Show |
chr19 | 18678680 | 18787333 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1902 | 206 | 77 | 46 | 48 | 6 | 27 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0001c0003 | 0/0 | 1902 | 17 | 0 | 12 | 3 | 0 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0001c0007 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0002c0002 | 0/0 | 1902 | 36 | 2 | 3 | 21 | 5 | 5 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0002c0005 | 0/0 | 1902 | 3 | 0 | 0 | 0 | 0 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0003c0004 | 0/0 | 1902 | 7 | 0 | 4 | 1 | 1 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0004c0009 | 0/0 | 1902 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0005c0008 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0006c0010 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
chr19 | 18678680 | 18787333 | ||
| a0007c0006 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | ATGGC others(1897): Show |
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 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0002 | 0/0 | 6879 | 23 | 9 | 2 | 10 | 0 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0003 | 0/0 | 6879 | 3 | 2 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0004 | 0/0 | 6878 | 13 | 11 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6873): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0005 | 0/0 | 6878 | 9 | 8 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6873): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0006 | 0/0 | 6879 | 6 | 6 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0007 | 0/0 | 6879 | 5 | 0 | 2 | 0 | 1 | 2 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0008 | 0/0 | 6879 | 3 | 3 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0009 | 0/0 | 6879 | 2 | 2 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0011 | 0/0 | 6877 | 2 | 1 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6872): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0012 | 0/0 | 6879 | 2 | 0 | 1 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0013 | 0/0 | 6879 | 2 | 0 | 2 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0014 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0015 | 0/0 | 6878 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6873): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0018 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0019 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0022 | 0/0 | 6878 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6873): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0027 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0029 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0030 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0031 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0001t0032 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0003t0002 | 0/0 | 6879 | 14 | 0 | 10 | 3 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0003t0024 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0003t0025 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0003t0028 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0001c0007t0008 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0003 | 0/0 | 6879 | 30 | 1 | 1 | 19 | 5 | 4 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0010 | 0/0 | 6878 | 2 | 0 | 0 | 2 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6873): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0016 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0017 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0020 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0002t0021 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0002c0005t0003 | 0/0 | 6879 | 3 | 0 | 0 | 0 | 0 | 3 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0003c0004t0002 | 0/0 | 6879 | 5 | 0 | 3 | 1 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0003c0004t0023 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0003c0004t0026 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0004c0009t0001 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0005c0008t0003 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0006c0010t0001 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| a0007c0006t0001 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | GAGGA others(6874): Show |
chr19 | 18678680 | 18787333 |
| actghapid | grch38/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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0139 | 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 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0208 | 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 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0144 | 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 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0003g0143 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0009g0249 | 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 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0013g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0014g0091 | 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 |
| a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0019g0035 | 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 |
| a0001c0001t0029g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0030g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0031g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0001t0032g0218 | 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 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0024g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0025g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0003t0028g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0001c0007t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0171 | 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 |
| a0002c0002t0003g0185 | 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 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0010g0172 | 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 |
| a0002c0002t0016g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0017g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0020g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0002t0021g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0002c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0023g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0003c0004t0026g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0004c0009t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0005c0008t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0006c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| a0007c0006t0001g0148 | 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 | g0136 | 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 | g0208 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00323 | hp1 | a0003 | c0004 | t0002 | g0028 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0188 | EUR | FIN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0239 | 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 | g0177 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0154 | 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 | g0233 | 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 | g0092 | 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 | g0051 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0030 | 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 | g0071 | 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 | g0126 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | 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 | g0072 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0228 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0223 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01099 | hp1 | a0002 | c0002 | t0020 | g0245 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0070 | 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 | g0184 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0250 | 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 | g0069 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01175 | hp2 | a0003 | c0004 | t0002 | g0222 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01192 | hp1 | a0003 | c0004 | t0002 | g0221 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0167 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01243 | hp2 | a0003 | c0004 | t0026 | g0220 | AMR | PUR | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0026 | 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 | g0110 | 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 | g0042 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01361 | hp1 | a0001 | c0001 | t0019 | g0035 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01361 | hp2 | a0001 | c0003 | t0028 | g0116 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0056 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01496 | hp2 | a0001 | c0003 | t0025 | g0203 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0206 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01517 | hp1 | a0001 | c0001 | t0014 | g0091 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0205 | EUR | IBS | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0099 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01928 | hp2 | a0002 | c0002 | t0017 | g0173 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0271 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | 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 | a0004 | c0009 | t0001 | g0093 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02004 | hp2 | a0001 | c0001 | t0013 | g0050 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0102 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0243 | 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 | g0217 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02135 | hp2 | a0003 | c0004 | t0002 | g0219 | EAS | KHV | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02145 | hp1 | a0001 | c0001 | t0031 | g0247 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0207 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0114 | 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 | g0100 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02257 | hp2 | a0002 | c0002 | t0016 | g0103 | 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 | g0134 | 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 | g0180 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0230 | 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 | g0183 | AMR | PEL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0249 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02647 | hp2 | a0006 | c0010 | t0001 | g0150 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0165 | 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 | g0128 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0036 | 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 | g0201 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02886 | hp1 | a0001 | c0001 | t0030 | g0076 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03017 | hp2 | a0002 | c0005 | t0003 | g0200 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0225 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03139 | hp1 | a0001 | c0007 | t0008 | g0041 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0244 | 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 | g0121 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03492 | hp1 | a0002 | c0002 | t0021 | g0246 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0181 | 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 | g0040 | AFR | ESN | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0185 | 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 | g0048 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0169 | 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 | g0047 | SAS | PJL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03831 | hp2 | a0002 | c0005 | t0003 | g0156 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04115 | hp1 | a0001 | c0001 | t0032 | g0218 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04115 | hp2 | a0002 | c0005 | t0003 | g0270 | 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 | g0235 | SAS | BEB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0238 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0229 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0170 | EAS | CHB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18940 | hp2 | a0007 | c0006 | t0001 | g0148 | 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 | g0090 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0032 | 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 | g0060 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18977 | hp1 | a0002 | c0002 | t0010 | g0172 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0204 | 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 | g0022 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | 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 | g0018 | 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 | g0231 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19054 | hp2 | a0002 | c0002 | t0003 | g0199 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0213 | 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 | g0216 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19083 | hp2 | a0001 | c0003 | t0002 | g0260 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0020 | 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 | g0214 | EAS | JPT | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0145 | AFR | ASW | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0013 | 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 | g0054 | EUR | TSI | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20905 | hp2 | a0003 | c0004 | t0023 | g0029 | SAS | GIH | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0142 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG02559 | hp2 | a0005 | c0008 | t0003 | g0146 | AFR | ACB | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0232 | 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 | g0182 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0033 | REF | REF | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0179 | REF | REF | CRTC1_chr19_18678680_18787333 | CRTC1 | chr19 | 18678680 | 18787333 |
| view | 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 | a0005 | 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 | a0004 | 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 | a0002 a0005 |
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 |
| view | 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 |
| view | 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0011 a0001c0001t0015 a0002c0002t0010 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(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 | a0001c0001t0008 a0001c0007t0008 a0002c0002t0016 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(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 |
| view | 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 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0212 a0001c0001t0002g0211 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.126+940T>G | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18684768 | |||||||
| chr19:18684884 | T | TCTTCC | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0042 others(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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0032g0218 | 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 | 12 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0031 others(9): Show |
12 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(9): 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 | a0002c0002t0003g0209 a0002c0002t0003g0210 a0002c0002t0003g0272 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0002c0002t0003g0223 | 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 | a0001c0001t0004g0224 | 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 | a0002c0002t0003g0199 a0002c0002t0010g0172 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | 64 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(61): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(61): 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 | a0001c0001t0001g0039 a0001c0001t0001g0105 a0001c0001t0001g0214 others(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 | a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0008g0252 | 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 | a0001c0001t0001g0131 | 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 | a0001c0003t0002g0161 a0001c0003t0002g0260 |
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 | a0001c0001t0005g0059 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
193 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(190): 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 | a0001c0001t0002g0144 | 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 | a0001c0001t0001g0117 | 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 | a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0008g0142 | 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 | a0002c0002t0003g0169 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0001g0202 others(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 | a0001c0001t0018g0145 | 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 | a0002c0005t0003g0156 a0002c0005t0003g0270 |
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 |
263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(260): Show |
264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): 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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0189 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0005g0133 others(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 | a0001c0001t0001g0158 a0001c0001t0002g0036 a0001c0001t0004g0037 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0138 a0001c0001t0004g0011 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0242 others(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 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0016 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0015 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | 17 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0031 others(14): Show |
17 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(14): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0096 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0092 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0039 others(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 | a0002c0002t0003g0238 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0068 others(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 | a0001c0001t0002g0113 a0001c0001t0002g0241 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0212 a0001c0001t0006g0237 |
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 | a0001c0001t0005g0059 | 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 | a0001c0001t0001g0018 | 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 | a0002c0002t0003g0223 a0002c0002t0003g0225 a0002c0002t0016g0103 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0002g0236 |
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 | a0001c0001t0002g0036 a0001c0001t0004g0037 a0001c0001t0005g0034 others(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 | a0001c0001t0002g0036 | 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 | a0001c0001t0002g0036 a0001c0001t0004g0037 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0208 a0001c0003t0002g0207 a0001c0003t0002g0271 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0002c0002t0003g0205 a0002c0002t0003g0206 |
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 | a0001c0001t0002g0036 a0001c0001t0004g0037 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0038 | 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 | a0002c0005t0003g0270 | 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 | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): 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 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0128 others(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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
177 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0248 others(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 | 156 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(154): 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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 others(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 | a0002c0002t0003g0154 | 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 | a0001c0001t0002g0036 a0001c0001t0004g0037 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | 11 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0031 others(8): Show |
11 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(8): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): 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 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0118 others(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 | a0001c0001t0005g0129 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0119 a0001c0001t0003g0044 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0004g0224 | 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 | a0001c0001t0002g0036 a0001c0001t0004g0037 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0013g0050 a0001c0001t0013g0110 |
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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(206): Show |
210 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(207): 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 | a0001c0001t0029g0051 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(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 | 26 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0128 others(23): Show |
26 | HG00735.hp1 HG01123.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.126+9657delG | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18693484 | |||||||
| chr19:18693485 | G | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0002c0002t0003g0168 | 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 | 22 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0127 others(19): Show |
22 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(19): 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | |||||||
| chr19:18694065 | G | A | 2 | a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(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 | 13 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0128 others(10): Show |
13 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(10): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0230 a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0129 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0166 a0001c0001t0001g0176 others(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 | 28 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0122 others(25): Show |
28 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(25): 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 | a0003c0004t0002g0028 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | |||||||
| chr19:18695375 | G | A | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0269 others(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 | a0001c0001t0012g0167 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 175 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(172): Show |
175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): 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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0122 | 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 | a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0006g0049 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0269 others(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 | a0001c0001t0008g0142 | 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 | a0002c0002t0003g0225 | 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 | a0002c0002t0003g0102 | 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 | a0006c0010t0001g0150 | 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 | a0002c0002t0003g0102 a0002c0002t0003g0198 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0003t0002g0071 a0001c0003t0002g0255 a0001c0003t0002g0256 |
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 | |||||||
| chr19:18698105 | T | A | 180 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(177): Show |
180 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.126+14277T>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 1/13 | chr19 | 18698105 | |||||||
| chr19:18698144 | C | T | 14 | a0001c0001t0001g0128 a0001c0001t0003g0044 a0001c0001t0003g0143 others(11): Show |
14 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(11): 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 | a0001c0001t0001g0122 a0001c0001t0001g0131 a0001c0001t0004g0224 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0004g0101 a0001c0001t0018g0145 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0074 |
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 | 61 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0128 others(58): Show |
61 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(58): 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 | a0001c0001t0001g0065 a0001c0001t0002g0064 a0001c0001t0002g0112 others(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 | a0001c0001t0001g0048 | 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 | a0002c0002t0003g0169 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0128 | 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 | a0003c0004t0002g0221 | 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 | a0001c0003t0025g0203 | 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 | 27 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0128 others(24): Show |
27 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(24): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | a0001c0003t0002g0260 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0005g0059 |
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 | a0002c0002t0003g0225 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0008 | 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 | 15 | a0001c0001t0001g0025 a0001c0001t0001g0128 a0001c0001t0003g0044 others(12): Show |
15 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(12): 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 | a0001c0001t0002g0244 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0257 others(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 | 8 | a0001c0001t0001g0025 a0003c0004t0002g0028 a0003c0004t0002g0030 others(5): Show |
8 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(5): 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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0257 others(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 | a0001c0001t0002g0036 a0001c0001t0004g0037 |
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 | a0002c0002t0003g0032 a0002c0002t0003g0102 a0002c0002t0003g0155 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0001t0001g0141 others(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 | a0001c0001t0004g0101 a0001c0001t0018g0145 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 |
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 | 30 | a0001c0001t0001g0025 a0001c0001t0001g0122 a0001c0001t0001g0127 others(27): Show |
30 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(27): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | 178 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
178 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(175): 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 | a0002c0002t0003g0205 a0002c0002t0003g0206 |
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 | 173 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(170): Show |
173 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(170): 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0131 a0001c0001t0008g0132 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0122 a0001c0001t0009g0147 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0166 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0122 a0001c0001t0009g0147 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0160 a0001c0003t0002g0126 others(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 | a0001c0001t0001g0128 a0001c0001t0008g0142 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 178 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
178 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(175): 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0212 a0001c0001t0022g0152 |
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 | a0002c0002t0003g0107 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0002g0036 a0001c0001t0004g0037 |
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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | 86 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(83): Show |
86 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(83): 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0001g0073 | 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 | a0001c0007t0008g0041 a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0003t0002g0001 a0001c0003t0002g0126 a0001c0003t0002g0228 others(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 | 10 | a0001c0001t0001g0025 a0002c0002t0003g0032 a0002c0002t0003g0204 others(7): Show |
10 | HG00323.hp1 HG00738.hp1 HG01175.hp2 others(7): 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0006g0081 | 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 | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0029g0051 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0112 a0001c0001t0002g0124 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0133 a0001c0001t0005g0134 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0008g0252 | 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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0002c0002t0003g0223 a0002c0002t0003g0225 a0002c0002t0016g0103 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0254 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0240 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0266 |
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 | a0001c0001t0012g0188 | 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 | 46 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0042 others(43): Show |
47 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(44): 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 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0067 others(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 | a0001c0001t0002g0052 a0001c0001t0031g0247 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0096 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0165 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0143 | 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 | a0001c0001t0003g0044 | 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 | a0001c0001t0001g0180 a0001c0003t0002g0256 |
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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0149 a0001c0001t0027g0004 |
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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0014g0091 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0019g0035 | 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 | a0003c0004t0023g0029 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0001t0004g0101 | 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 | a0001c0001t0008g0142 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0251 a0003c0004t0002g0028 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0251 a0003c0004t0002g0028 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0002c0002t0003g0204 | 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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0230 a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0002c0002t0003g0204 | 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 | a0001c0001t0001g0230 a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0008g0132 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0202 |
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 | a0001c0001t0007g0056 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0005g0059 |
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 | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG00099.hp1 HG01168.hp1 HG01978.hp1 others(3): 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 | a0001c0001t0001g0096 | 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 | a0001c0007t0008g0041 a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0005g0059 | 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 | a0007c0006t0001g0148 | 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 | a0001c0001t0001g0230 a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0048 a0002c0002t0003g0273 |
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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0004g0101 | 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 | a0001c0001t0001g0006 a0001c0001t0015g0005 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0178 a0001c0001t0004g0037 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0224 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0015g0005 |
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 | a0001c0001t0012g0188 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0005g0075 a0001c0001t0005g0077 a0001c0001t0005g0078 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0084 | 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 | a0003c0004t0002g0219 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0013g0050 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0002c0002t0003g0171 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0025 a0003c0004t0023g0029 a0003c0004t0026g0220 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0020 a0002c0002t0003g0209 a0002c0002t0003g0210 others(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 | a0001c0003t0002g0260 | 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 | a0001c0003t0002g0260 | 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 | a0003c0004t0026g0220 | 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0005g0034 a0001c0001t0005g0129 |
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 | a0001c0001t0005g0075 a0001c0001t0005g0077 a0001c0001t0005g0078 others(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 | a0001c0007t0008g0041 a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0002c0005t0003g0270 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0002c0002t0003g0032 a0002c0002t0003g0102 a0002c0002t0003g0155 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0003t0002g0161 a0001c0003t0002g0260 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
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 | a0001c0001t0001g0239 | 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 | a0001c0001t0005g0059 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0131 a0001c0001t0008g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0251 a0001c0001t0003g0044 a0001c0001t0003g0143 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0002g0243 | 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 | a0001c0001t0001g0046 a0001c0001t0014g0091 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0194 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0122 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0212 a0001c0001t0002g0241 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0004g0101 | 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 | a0002c0002t0021g0246 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG00099.hp1 HG01168.hp1 HG01978.hp1 others(3): 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0002c0002t0020g0245 a0002c0002t0021g0246 |
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 | a0001c0001t0004g0101 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0005c0008t0003g0146 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0008g0142 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0008 | 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 | a0003c0004t0002g0028 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0067 | 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 | a0003c0004t0002g0219 | 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 | a0001c0001t0001g0025 a0003c0004t0023g0029 |
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 | a0007c0006t0001g0148 | 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 | a0003c0004t0002g0030 | 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 | a0003c0004t0002g0221 | 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 | a0003c0004t0026g0220 | 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 | a0001c0001t0002g0112 a0001c0001t0004g0037 |
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 | a0001c0001t0005g0034 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0144 a0001c0001t0002g0244 |
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 | a0001c0001t0002g0124 | 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 | a0001c0001t0008g0142 | 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 | a0001c0001t0005g0129 | 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 | a0001c0001t0001g0003 | 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 | a0003c0004t0002g0222 | 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 | a0001c0001t0004g0101 | 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 | a0001c0001t0018g0145 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | a0001c0001t0004g0069 | 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 | a0001c0001t0011g0070 | 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 | a0001c0001t0029g0051 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0045 a0001c0001t0006g0081 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
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 | a0001c0001t0001g0230 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0241 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0006g0100 | 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 | a0001c0001t0006g0088 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0235 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0236 a0002c0002t0003g0273 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0234 a0001c0001t0002g0043 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0153 a0001c0001t0002g0114 others(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 | a0004c0009t0001g0093 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0006g0040 | 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 | a0001c0001t0006g0237 | 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 | a0001c0001t0004g0224 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0125 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0060 |
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 | a0001c0001t0002g0108 | 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 | a0001c0001t0006g0049 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0013g0050 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0013g0110 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0165 |
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 | a0001c0001t0004g0010 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0084 | 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 | a0001c0001t0004g0016 | 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 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 |
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 | a0001c0001t0004g0017 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0011 |
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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0149 a0001c0001t0005g0034 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0113 a0001c0001t0002g0241 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0006c0010t0001g0150 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0003t0024g0201 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0024 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0003t0025g0203 | 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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 |
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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0251 a0001c0001t0004g0037 a0001c0001t0004g0101 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0176 a0002c0002t0003g0169 a0002c0002t0003g0190 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0025 a0003c0004t0002g0028 a0003c0004t0002g0030 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0019 a0001c0001t0005g0034 a0001c0001t0005g0129 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0257 a0001c0001t0005g0059 a0001c0001t0008g0132 others(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 | a0001c0001t0001g0251 | 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 | a0002c0002t0003g0174 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0007t0008g0041 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0067 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0084 | 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 | a0001c0007t0008g0041 | 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 | a0001c0007t0008g0041 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0251 | 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 | a0001c0003t0002g0001 a0001c0003t0002g0126 |
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 | a0003c0004t0002g0221 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0122 a0001c0001t0005g0129 a0001c0001t0009g0147 others(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 | a0001c0001t0004g0012 a0001c0001t0004g0015 a0001c0001t0011g0014 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0004g0101 | 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 | a0001c0001t0003g0143 | 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 | a0001c0001t0003g0044 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0141 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0084 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0232 | 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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0002c0002t0003g0185 a0002c0002t0003g0205 a0002c0002t0003g0206 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0124 a0001c0001t0002g0144 others(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 | a0001c0001t0002g0064 | 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 | a0001c0001t0002g0064 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0059 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0005c0008t0003g0146 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0112 a0001c0001t0002g0124 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0004g0101 | 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 | a0001c0001t0012g0167 a0001c0001t0012g0188 |
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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0251 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0008g0132 | 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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0001c0001t0004g0101 a0001c0001t0018g0145 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0112 a0001c0001t0002g0124 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0002c0002t0003g0225 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0251 a0001c0001t0003g0044 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0002c0002t0003g0102 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0243 |
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 | a0001c0001t0008g0142 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0004g0101 | 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0251 a0002c0002t0003g0199 a0002c0002t0003g0223 others(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 | a0001c0001t0032g0218 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0073 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0251 | 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 | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0003t0002g0229 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 a0002c0002t0003g0190 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
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 | a0002c0002t0003g0190 a0002c0002t0003g0191 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0029g0051 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0004g0101 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0007t0008g0041 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0068 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0007t0008g0041 |
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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0008g0142 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0022g0152 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0019g0035 | 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 | a0001c0001t0005g0034 a0001c0001t0008g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0002c0005t0003g0156 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0007t0008g0041 |
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 | a0001c0001t0001g0067 a0001c0001t0008g0132 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0002c0002t0003g0032 | 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 | a0006c0010t0001g0150 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0003c0004t0023g0029 | 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 | a0001c0001t0001g0180 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0122 a0001c0001t0005g0129 a0001c0001t0009g0147 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0005g0129 | 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 | a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0013g0050 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0005g0059 | 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 | a0002c0002t0003g0107 | 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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0001c0001t0001g0067 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0002c0002t0003g0205 a0002c0002t0003g0206 |
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 | a0001c0001t0001g0045 | 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 | a0001c0001t0008g0132 | 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 | a0001c0001t0002g0130 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0003t0002g0163 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0008g0252 | 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 | a0001c0003t0002g0163 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0002c0002t0003g0107 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0003c0004t0023g0029 | 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 | a0001c0003t0002g0001 a0001c0003t0002g0026 a0001c0003t0002g0126 others(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 | a0001c0003t0002g0207 | 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 | a0002c0002t0003g0102 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0003t0002g0001 a0001c0003t0002g0126 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0232 | 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 | a0002c0002t0003g0185 | 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 | a0002c0002t0003g0204 | 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 | a0001c0003t0002g0228 a0001c0003t0002g0229 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0184 a0002c0002t0021g0246 |
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 | a0003c0004t0002g0028 | 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 | a0001c0001t0004g0101 | 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 | a0001c0003t0002g0271 | 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 | a0001c0001t0006g0040 a0001c0001t0006g0100 |
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 | a0001c0007t0008g0041 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0002c0002t0003g0238 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0019g0035 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0157 a0002c0002t0003g0190 a0002c0002t0003g0191 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0005g0059 | 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 | a0001c0001t0013g0110 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0002c0002t0003g0155 a0002c0002t0003g0168 a0002c0002t0003g0177 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0003g0253 others(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 | a0002c0002t0003g0204 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0005g0059 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(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 | a0005c0008t0003g0146 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | 40 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0023 others(37): Show |
40 | HG01069.hp1 HG01074.hp2 HG01175.hp1 others(37): 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(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 | a0001c0001t0008g0132 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0004g0011 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0240 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0004g0017 | 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0122 a0001c0001t0009g0147 a0001c0001t0009g0249 others(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 | a0001c0001t0007g0053 a0001c0001t0007g0054 a0001c0001t0007g0056 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0164 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0004g0224 a0001c0001t0006g0040 a0001c0001t0006g0049 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0008g0142 | 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 | a0001c0001t0005g0133 a0001c0001t0005g0134 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0003g0044 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0085 others(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 | a0003c0004t0002g0028 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0002g0043 a0001c0001t0002g0090 a0001c0001t0002g0094 others(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 | a0001c0003t0002g0001 a0001c0003t0002g0126 a0001c0003t0002g0228 others(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 | a0002c0002t0010g0172 | 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 | a0001c0001t0006g0040 a0001c0001t0006g0100 |
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 | a0001c0001t0004g0224 | 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 | a0001c0001t0003g0253 a0002c0002t0003g0198 a0002c0002t0003g0199 others(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 | a0001c0003t0002g0260 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0106 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0158 others(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 | a0001c0001t0005g0034 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0004g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0208 | 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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0240 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0007t0008g0041 | 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 | a0001c0001t0008g0132 a0001c0001t0008g0252 |
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 | a0001c0001t0004g0011 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0115 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0003t0002g0228 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0003g0253 a0002c0002t0003g0032 a0002c0002t0003g0102 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): 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 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0044 a0001c0001t0004g0009 a0001c0001t0004g0010 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0004g0101 a0001c0001t0018g0145 a0001c0001t0027g0004 |
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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0251 a0001c0001t0002g0064 a0001c0001t0002g0112 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0240 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0001t0003g0143 | 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 | a0001c0001t0002g0243 a0001c0001t0003g0044 a0001c0001t0003g0143 others(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 | a0001c0001t0005g0077 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0096 a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0264 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0008g0142 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0008g0142 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0003t0002g0001 a0001c0003t0002g0126 a0001c0003t0002g0228 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0243 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0003g0253 others(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 | a0001c0001t0002g0118 | 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 | a0001c0001t0008g0252 | 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 | a0001c0001t0008g0252 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0180 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0008g0252 | 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 | a0001c0001t0008g0132 | 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 | a0002c0002t0020g0245 | 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 | a0002c0002t0003g0169 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0007g0054 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0178 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 a0001c0001t0027g0004 |
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 | a0001c0001t0003g0044 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG01168.hp1 HG02300.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.887-1531G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 8/13 | chr19 | 18763873 | |||||||
| chr19:18763983 | C | T | 1 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0005g0129 a0001c0001t0022g0152 |
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 | a0001c0001t0006g0040 a0001c0001t0006g0049 a0001c0001t0006g0081 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0003g0253 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0122 a0001c0001t0005g0034 a0001c0001t0005g0059 others(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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0005g0034 | 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 | a0001c0001t0001g0180 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0002c0002t0021g0246 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0003g0253 a0001c0001t0004g0009 a0001c0001t0004g0010 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0157 a0001c0001t0001g0162 others(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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0202 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0004g0037 a0001c0001t0004g0069 a0001c0001t0004g0224 others(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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0043 a0001c0001t0002g0090 others(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 | a0003c0004t0002g0030 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0005c0008t0003g0146 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0002c0002t0003g0136 | 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 | a0001c0001t0018g0145 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0242 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0004g0017 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0008g0132 a0002c0002t0003g0170 |
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 | a0001c0001t0002g0113 a0001c0001t0002g0241 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
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 | a0001c0001t0002g0130 a0001c0001t0002g0243 a0001c0003t0002g0001 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0003g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1321-192G>A | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 10/13 | chr19 | 18771250 | |||||||
| chr19:18771310 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0162 | 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 | a0003c0004t0002g0028 a0003c0004t0002g0030 a0003c0004t0002g0221 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0018g0145 a0002c0002t0003g0238 |
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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0007t0008g0041 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0226 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0027 | 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 | a0001c0001t0003g0253 a0001c0001t0008g0132 a0002c0002t0003g0032 others(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 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0002c0002t0003g0102 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0018g0145 | 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 | a0001c0001t0001g0038 | 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 | a0002c0002t0003g0223 | 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 | a0002c0002t0017g0173 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0248 a0001c0001t0001g0250 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0003g0253 others(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 | a0001c0001t0008g0252 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0003g0253 others(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 | a0001c0003t0024g0201 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0143 a0001c0001t0003g0253 others(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 | a0001c0001t0003g0253 a0001c0001t0004g0009 a0001c0001t0004g0010 others(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 | a0002c0002t0003g0175 | 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 | a0001c0001t0009g0147 a0001c0001t0009g0249 |
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 | a0001c0001t0003g0253 a0001c0001t0004g0009 a0001c0001t0004g0010 others(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 | a0001c0001t0003g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1694-153C>T | CRTC1 | ENSG00000105662.16 | transcript | ENST00000321949.13 | protein_coding | 13/13 | chr19 | 18777018 |