Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 60680 |
| ensemblid | ENSG00000161082.13 |
| hgncid | 14058 |
| symbol | CELF5 |
| name | CUGBP Elav-like family member 5 |
| refseq_nuc | NM_021938.4 |
| refseq_prot | NP_068757.2 |
| ensembl_nuc | ENST00000292672.7 |
| ensembl_prot | ENSP00000292672.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 3224661 |
| end | 3297076 |
| strand | + |
| ver | v1.2 |
| region | chr19:3224661-3297076 |
| region5000 | chr19:3219661-3302076 |
| regionname0 | CELF5_chr19_3224661_3297076 |
| regionname5000 | CELF5_chr19_3219661_3302076 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 485 | 261 | 71 | 62 | 74 | 10 | 42 | 50 | CELF5_chr19_3219661_3302076 | CELF5 | MARLT others(480): Show |
chr19 | 3219661 | 3302076 |
| a0002 | 0/0 | 485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | MARLT others(480): Show |
chr19 | 3219661 | 3302076 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1455 | 204 | 57 | 46 | 64 | 5 | 30 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0002 | 0/0 | 1455 | 37 | 6 | 12 | 10 | 3 | 6 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0003 | 0/0 | 1455 | 13 | 3 | 4 | 0 | 2 | 4 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0004 | 0/0 | 1455 | 2 | 2 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0005 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0006 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0007 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0009 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0001c0010 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 | ||
| a0002c0008 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | ATGGC others(1450): Show |
chr19 | 3219661 | 3302076 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1896 | 88 | 17 | 15 | 32 | 3 | 19 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1891): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0002 | 0/0 | 1895 | 36 | 27 | 4 | 4 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1890): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0003 | 0/0 | 1894 | 30 | 3 | 15 | 9 | 0 | 3 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1889): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0004 | 0/0 | 1898 | 18 | 3 | 4 | 10 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0005 | 0/0 | 1897 | 25 | 6 | 7 | 5 | 1 | 6 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0006 | 0/0 | 1899 | 5 | 1 | 0 | 3 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1894): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0008 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0001c0001t0009 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1891): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0001 | 0/0 | 1896 | 13 | 1 | 1 | 7 | 1 | 3 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1891): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0002 | 0/0 | 1895 | 7 | 5 | 1 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1890): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0003 | 0/0 | 1894 | 7 | 0 | 7 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1889): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0004 | 0/0 | 1898 | 5 | 0 | 2 | 1 | 1 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0005 | 0/0 | 1897 | 4 | 0 | 0 | 1 | 1 | 2 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0001c0002t0010 | 0/0 | 1898 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0003t0001 | 0/0 | 1896 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1891): Show |
chr19 | 3219661 | 3302076 |
| a0001c0003t0002 | 0/0 | 1895 | 2 | 2 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1890): Show |
chr19 | 3219661 | 3302076 |
| a0001c0003t0003 | 0/0 | 1894 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1889): Show |
chr19 | 3219661 | 3302076 |
| a0001c0003t0004 | 0/0 | 1898 | 7 | 0 | 4 | 0 | 2 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0003t0005 | 0/0 | 1897 | 2 | 1 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0001c0004t0004 | 0/0 | 1898 | 2 | 2 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0005t0007 | 0/0 | 1898 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0006t0004 | 0/0 | 1898 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1893): Show |
chr19 | 3219661 | 3302076 |
| a0001c0007t0002 | 0/0 | 1895 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1890): Show |
chr19 | 3219661 | 3302076 |
| a0001c0009t0005 | 0/0 | 1897 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0001c0010t0005 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1892): Show |
chr19 | 3219661 | 3302076 |
| a0002c0008t0002 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | GGGAG others(1890): Show |
chr19 | 3219661 | 3302076 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0002t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0003t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0004t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0004t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0005t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0006t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0007t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0009t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0001c0010t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| a0002c0008t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0239 | EUR | GBR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | GBR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00609 | hp1 | a0001 | c0002 | t0005 | g0027 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00733 | hp1 | a0001 | c0003 | t0004 | g0220 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00735 | hp1 | a0001 | c0003 | t0004 | g0243 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0038 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0037 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0088 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01106 | hp2 | a0001 | c0003 | t0004 | g0131 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01346 | hp2 | a0001 | c0002 | t0010 | g0050 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0073 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01516 | hp2 | a0001 | c0003 | t0004 | g0134 | EUR | IBS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0022 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0031 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0029 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0042 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02055 | hp1 | a0001 | c0004 | t0004 | g0210 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02055 | hp2 | a0001 | c0005 | t0007 | g0045 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02148 | hp1 | a0001 | c0003 | t0004 | g0237 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0092 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | KHV | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02602 | hp1 | a0001 | c0003 | t0005 | g0099 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02738 | hp1 | a0001 | c0003 | t0004 | g0261 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02738 | hp2 | a0001 | c0009 | t0005 | g0114 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02886 | hp2 | a0001 | c0004 | t0004 | g0227 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02922 | hp2 | a0002 | c0008 | t0002 | g0192 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0248 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03225 | hp2 | a0001 | c0006 | t0004 | g0137 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03239 | hp1 | a0001 | c0007 | t0002 | g0144 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03486 | hp2 | a0001 | c0010 | t0005 | g0252 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0059 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0240 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0098 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0181 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0065 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03942 | hp2 | a0001 | c0002 | t0005 | g0048 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0047 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0203 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04184 | hp2 | a0001 | c0002 | t0005 | g0093 | SAS | BEB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | CHB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | CHB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0151 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | LWK | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | YRI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0035 | EUR | TSI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0044 | EUR | TSI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20805 | hp1 | a0001 | c0003 | t0004 | g0128 | EUR | TSI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | TSI | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0164 | SAS | GIH | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | GIH | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0043 | AMR | CLM | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0232 | AFR | ACB | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | USA | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | USA | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | USA | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | USA | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0070 | REF | REF | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0139 | REF | REF | CELF5_chr19_3219661_3302076 | CELF5 | chr19 | 3219661 | 3302076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3282486 | G | C | 1 | a0002 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1027G>C | p.Val343Leu | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/13 | 1106/1896 | 1027/1458 | 343/485 | chr19 | 3282486 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3224898 | G | C | 3 | a0001c0002 a0001c0005 a0001c0006 |
39 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(36): Show |
synonymous_variant | LOW | c.159G>C | p.Pro53Pro | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/13 | 238/1896 | 159/1458 | 53/485 | chr19 | 3224898 | |||
| chr19:3281231 | C | T | 1 | a0001c0010 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.636C>T | p.Ala212Ala | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/13 | 715/1896 | 636/1458 | 212/485 | chr19 | 3281231 | |||
| chr19:3281300 | G | A | 2 | a0001c0003 a0001c0005 |
14 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(11): Show |
synonymous_variant | LOW | c.705G>A | p.Pro235Pro | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/13 | 784/1896 | 705/1458 | 235/485 | chr19 | 3281300 | |||
| chr19:3282140 | G | A | 1 | a0001c0007 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.765G>A | p.Gln255Gln | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 7/13 | 844/1896 | 765/1458 | 255/485 | chr19 | 3282140 | |||
| chr19:3282449 | G | C | 2 | a0001c0004 a0001c0006 |
3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.990G>C | p.Gly330Gly | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/13 | 1069/1896 | 990/1458 | 330/485 | chr19 | 3282449 | |||
| chr19:3293341 | G | A | 1 | a0001c0009 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1353G>A | p.Pro451Pro | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/13 | 1432/1896 | 1353/1458 | 451/485 | chr19 | 3293341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3296884 | T | C | 1 | a0001c0005t0007 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3438 | chr19 | 3296884 | ||||||
| chr19:3296925 | C | T | 1 | a0001c0002t0010 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3479 | chr19 | 3296925 | ||||||
| chr19:3297016 | G | GA | 6 | a0001c0001t0005 a0001c0001t0008 a0001c0002t0005 others(3): Show |
34 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*320dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3592 | INFO_REALIGN_3_PRIME | chr19 | 3297016 | |||||
| chr19:3297016 | G | GAA | 7 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0010 others(4): Show |
35 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*320dupAA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3592 | INFO_REALIGN_3_PRIME | chr19 | 3297016 | |||||
| chr19:3297016 | G | GAAA | 1 | a0001c0001t0006 | 5 | HG00597.hp2 HG02622.hp1 HG02683.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*318_*320dupAAA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3592 | INFO_REALIGN_3_PRIME | chr19 | 3297016 | |||||
| chr19:3297016 | GA | G | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(2): Show |
47 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*320delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3591 | INFO_REALIGN_3_PRIME | chr19 | 3297016 | |||||
| chr19:3297016 | GAA | G | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 |
38 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*320delAA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3590 | INFO_REALIGN_3_PRIME | chr19 | 3297016 | |||||
| chr19:3297037 | A | C | 1 | a0001c0001t0009 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3591 | chr19 | 3297037 | ||||||
| chr19:3297038 | C | A | 1 | a0001c0001t0008 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 13/13 | 3592 | chr19 | 3297038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3225010 | G | T | 1 | a0001c0003t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.259+12G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225010 | |||||||
| chr19:3225016 | T | TC | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
8 | HG01175.hp1 HG01261.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+24dupC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3225016 | ||||||
| chr19:3225038 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0005g0009 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.259+40G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225038 | |||||||
| chr19:3225058 | G | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.259+60G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225058 | |||||||
| chr19:3225130 | G | T | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+132G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225130 | |||||||
| chr19:3225131 | T | G | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+133T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225131 | |||||||
| chr19:3225132 | T | C | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+134T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225132 | |||||||
| chr19:3225136 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+138A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225136 | |||||||
| chr19:3225139 | C | G | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+141C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225139 | |||||||
| chr19:3225141 | C | A | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+143C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225141 | |||||||
| chr19:3225145 | C | G | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+147C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225145 | |||||||
| chr19:3225172 | G | GCAGCTCA others(14): Show |
1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+174_259+175ins others(21): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225172 | |||||||
| chr19:3225173 | G | T | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+175G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225173 | |||||||
| chr19:3225185 | ACAGATCC others(3): Show |
A | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.259+189_259+198del others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3225185 | ||||||
| chr19:3225272 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259+274C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225272 | |||||||
| chr19:3225294 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18964.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.259+296C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225294 | |||||||
| chr19:3225320 | C | T | 8 | a0001c0001t0002g0247 a0001c0001t0002g0251 a0001c0001t0002g0253 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+322C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225320 | |||||||
| chr19:3225341 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.259+343C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225341 | |||||||
| chr19:3225475 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.259+477A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225475 | |||||||
| chr19:3225670 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+672C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225670 | |||||||
| chr19:3225683 | T | G | 47 | a0001c0001t0001g0024 a0001c0001t0001g0245 a0001c0001t0001g0255 others(44): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.259+685T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225683 | |||||||
| chr19:3225697 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+699G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225697 | |||||||
| chr19:3225816 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+818G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225816 | |||||||
| chr19:3225899 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(71): Show |
75 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.259+901G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225899 | |||||||
| chr19:3225982 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.259+984C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3225982 | |||||||
| chr19:3226001 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.259+1003A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226001 | |||||||
| chr19:3226267 | T | TTGAA | 15 | a0001c0001t0001g0236 a0001c0001t0002g0051 a0001c0001t0002g0242 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.259+1302_259+1305d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226267 | ||||||
| chr19:3226267 | TTGAA | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
137 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.259+1302_259+1305d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226267 | ||||||
| chr19:3226267 | TTGAATGA others(5): Show |
T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.259+1294_259+1305d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226267 | ||||||
| chr19:3226325 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(69): Show |
73 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.259+1327G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226325 | |||||||
| chr19:3226363 | G | T | 4 | a0001c0001t0002g0247 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02895.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1365G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226363 | |||||||
| chr19:3226405 | C | T | 1 | a0001c0002t0005g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.259+1407C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226405 | |||||||
| chr19:3226440 | T | TCA | 4 | a0001c0001t0001g0143 a0001c0001t0002g0251 a0001c0001t0005g0125 others(1): Show |
4 | HG01934.hp1 HG01934.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1477_259+1478d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACA | 25 | a0001c0001t0001g0024 a0001c0001t0005g0020 a0001c0001t0006g0015 others(22): Show |
25 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.259+1473_259+1478d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(1): Show |
15 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0255 others(12): Show |
15 | HG00738.hp2 HG01069.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+1471_259+1478d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(3): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0146 others(14): Show |
17 | HG02148.hp1 HG02300.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.259+1469_259+1478d others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(5): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0066 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.259+1467_259+1478d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(7): Show |
57 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0097 others(54): Show |
57 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.259+1465_259+1478d others(16): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(9): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0196 others(25): Show |
28 | HG00597.hp1 HG01069.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+1463_259+1478d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(11): Show |
23 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0116 others(20): Show |
23 | HG00733.hp1 HG00741.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.259+1461_259+1478d others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(13): Show |
8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0228 others(5): Show |
8 | HG01106.hp2 HG01516.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+1459_259+1478d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | T | TCACACAC others(15): Show |
4 | a0001c0001t0002g0012 a0001c0001t0003g0233 a0001c0003t0002g0232 others(1): Show |
4 | HG01516.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1457_259+1478d others(24): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226440 | TCACACAC others(3): Show |
T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
10 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1469_259+1478d others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226440 | ||||||
| chr19:3226466 | A | ACACACAC others(5): Show |
1 | a0001c0001t0002g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.259+1478_259+1479i others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226466 | ||||||
| chr19:3226475 | C | CACACACA others(10): Show |
1 | a0001c0001t0001g0005 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.259+1478_259+1479i others(19): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226475 | ||||||
| chr19:3226476 | A | ACACACAC others(2): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0003g0061 others(1): Show |
4 | HG02083.hp2 NA18906.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1478_259+1479i others(11): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226476 | |||||||
| chr19:3226476 | A | ACACACAC others(6): Show |
4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0003g0111 others(1): Show |
4 | HG01261.hp1 HG01496.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1478_259+1479i others(15): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226476 | |||||||
| chr19:3226476 | A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259+1478_259+1479i others(17): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226476 | |||||||
| chr19:3226476 | A | ACACACAC others(14): Show |
1 | a0001c0001t0004g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259+1478_259+1479i others(23): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226476 | |||||||
| chr19:3226477 | A | C | 1 | a0001c0001t0004g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.259+1479A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226477 | |||||||
| chr19:3226730 | G | C | 1 | a0001c0002t0005g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.259+1732G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226730 | |||||||
| chr19:3226767 | C | CT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
70 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.259+1782dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3226767 | ||||||
| chr19:3226968 | G | A | 66 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(63): Show |
66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.259+1970G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226968 | |||||||
| chr19:3226984 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+1986C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3226984 | |||||||
| chr19:3227088 | G | T | 1 | a0001c0001t0005g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259+2090G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227088 | |||||||
| chr19:3227104 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.259+2106C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227104 | |||||||
| chr19:3227105 | G | C | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+2107G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227105 | |||||||
| chr19:3227147 | C | T | 45 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0255 others(42): Show |
45 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+2149C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227147 | |||||||
| chr19:3227320 | G | A | 24 | a0001c0001t0001g0024 a0001c0001t0001g0255 a0001c0001t0001g0256 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.259+2322G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227320 | |||||||
| chr19:3227425 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.259+2427C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227425 | |||||||
| chr19:3227565 | G | A | 8 | a0001c0001t0003g0162 a0001c0001t0004g0008 a0001c0001t0005g0007 others(5): Show |
8 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+2567G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227565 | |||||||
| chr19:3227744 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
135 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.259+2746T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227744 | |||||||
| chr19:3227792 | A | G | 4 | a0001c0001t0002g0209 a0001c0001t0003g0231 a0001c0004t0004g0210 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+2794A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227792 | |||||||
| chr19:3227917 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.259+2919C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3227917 | |||||||
| chr19:3228010 | A | T | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.259+3012A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228010 | |||||||
| chr19:3228040 | G | T | 3 | a0001c0001t0001g0245 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02630.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.259+3042G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228040 | |||||||
| chr19:3228057 | G | A | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.259+3059G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228057 | |||||||
| chr19:3228074 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02630.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.259+3076G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228074 | |||||||
| chr19:3228157 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0160 others(16): Show |
19 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.259+3159C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228157 | |||||||
| chr19:3228194 | A | G | 1 | a0001c0001t0005g0249 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+3196A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228194 | |||||||
| chr19:3228396 | C | T | 1 | a0001c0006t0004g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259+3398C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228396 | |||||||
| chr19:3228437 | C | A | 3 | a0001c0001t0005g0249 a0001c0003t0002g0248 a0001c0010t0005g0252 |
3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+3439C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228437 | |||||||
| chr19:3228615 | T | TG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0089 others(62): Show |
65 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.259+3627dupG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228615 | ||||||
| chr19:3228688 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0062 |
2 | NA18966.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.259+3690C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228688 | |||||||
| chr19:3228707 | G | A | 1 | a0001c0007t0002g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.259+3709G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228707 | |||||||
| chr19:3228817 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02630.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.259+3819C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228817 | |||||||
| chr19:3228875 | C | CGT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0150 others(27): Show |
30 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.259+3916_259+3917d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | C | CGTGT | 19 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0110 others(16): Show |
19 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.259+3914_259+3917d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | C | CGTGTGT | 4 | a0001c0001t0001g0160 a0001c0001t0001g0230 a0001c0001t0003g0149 others(1): Show |
4 | HG02300.hp1 HG03704.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+3912_259+3917d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0005g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.259+3908_259+3917d others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | CGT | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0115 a0001c0001t0001g0138 others(12): Show |
15 | HG01256.hp1 HG02040.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.259+3916_259+3917d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | CGTGT | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0003g0055 others(6): Show |
9 | HG01106.hp1 HG01975.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+3914_259+3917d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | CGTGTGT | C | 3 | a0001c0001t0001g0116 a0001c0001t0002g0251 a0001c0001t0006g0250 |
3 | HG02622.hp1 HG02723.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.259+3912_259+3917d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228875 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.259+3906_259+3917d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3228875 | ||||||
| chr19:3228886 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+3888G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228886 | |||||||
| chr19:3228915 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(81): Show |
85 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.259+3917T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228915 | T | TGC | 36 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(33): Show |
36 | HG00423.hp1 HG00544.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.259+3917_259+3918i others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228915 | T | TGTGC | 11 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0012 others(8): Show |
11 | HG00642.hp1 HG01261.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.259+3917_259+3918i others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228915 | T | TGTGTGC | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0122 others(4): Show |
7 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+3917_259+3918i others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228915 | T | TGTGTGTG others(1): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.259+3917_259+3918i others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228915 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0002g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259+3917_259+3918i others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228915 | |||||||
| chr19:3228994 | G | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(65): Show |
69 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.259+3996G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3228994 | |||||||
| chr19:3229060 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0133 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.259+4062C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229060 | |||||||
| chr19:3229097 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.259+4099C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229097 | |||||||
| chr19:3229154 | T | G | 4 | a0001c0001t0002g0209 a0001c0001t0003g0231 a0001c0004t0004g0210 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+4156T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229154 | |||||||
| chr19:3229226 | G | A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.259+4228G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229226 | |||||||
| chr19:3229373 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.259+4375G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229373 | |||||||
| chr19:3229398 | G | T | 1 | a0001c0002t0002g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.259+4400G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229398 | |||||||
| chr19:3229399 | C | T | 1 | a0001c0002t0002g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.259+4401C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229399 | |||||||
| chr19:3229476 | C | T | 14 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0130 others(11): Show |
14 | HG01106.hp2 HG01516.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+4478C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229476 | |||||||
| chr19:3229523 | A | G | 53 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.259+4525A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229523 | |||||||
| chr19:3229625 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+4627C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229625 | |||||||
| chr19:3229747 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
84 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.259+4749A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3229747 | |||||||
| chr19:3230053 | T | C | 52 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.259+5055T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230053 | |||||||
| chr19:3230077 | C | CTCAT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.259+5115_259+5118d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3230077 | ||||||
| chr19:3230077 | C | CTCATTCA others(1): Show |
12 | a0001c0001t0001g0104 a0001c0001t0001g0165 a0001c0001t0001g0197 others(9): Show |
12 | HG01891.hp2 HG02083.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+5111_259+5118d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3230077 | ||||||
| chr19:3230077 | CTCAT | C | 11 | a0001c0001t0001g0245 a0001c0001t0002g0251 a0001c0001t0003g0162 others(8): Show |
11 | HG01255.hp2 HG02622.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+5115_259+5118d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3230077 | ||||||
| chr19:3230137 | T | C | 61 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.259+5139T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230137 | |||||||
| chr19:3230370 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
102 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.259+5372T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230370 | |||||||
| chr19:3230420 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0003g0083 a0001c0001t0003g0105 |
3 | HG00642.hp1 HG01070.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.259+5422T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230420 | |||||||
| chr19:3230505 | G | A | 2 | a0001c0001t0004g0189 a0001c0003t0002g0232 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.259+5507G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230505 | |||||||
| chr19:3230602 | T | C | 1 | a0001c0005t0007g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259+5604T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230602 | |||||||
| chr19:3230955 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.259+5957C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3230955 | |||||||
| chr19:3231101 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259+6103G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231101 | |||||||
| chr19:3231133 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.259+6135A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231133 | |||||||
| chr19:3231447 | C | CGGAT | 5 | a0001c0001t0002g0216 a0001c0001t0003g0194 a0001c0001t0003g0219 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+6492_259+6495d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231447 | ||||||
| chr19:3231447 | CGGAT | C | 52 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0001g0121 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.259+6492_259+6495d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231447 | ||||||
| chr19:3231447 | CGGATGGA others(1): Show |
C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
72 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.259+6488_259+6495d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231447 | ||||||
| chr19:3231486 | ATGGATGG others(1): Show |
A | 11 | a0001c0001t0001g0157 a0001c0001t0001g0166 a0001c0001t0001g0167 others(8): Show |
11 | HG00735.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+6495_259+6502d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231486 | ||||||
| chr19:3231490 | ATGGG | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0176 a0001c0001t0002g0211 others(3): Show |
6 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+6496_259+6499d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231490 | ||||||
| chr19:3231522 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.259+6524G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231522 | |||||||
| chr19:3231533 | G | GTGGATGG others(25): Show |
2 | a0001c0001t0001g0057 a0001c0001t0001g0062 |
2 | NA18966.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.259+6581_259+6612d others(34): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3231533 | ||||||
| chr19:3231609 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+6611A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231609 | |||||||
| chr19:3231709 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.259+6711T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231709 | |||||||
| chr19:3231781 | A | T | 1 | a0001c0001t0001g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.259+6783A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231781 | |||||||
| chr19:3231810 | G | C | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.259+6812G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231810 | |||||||
| chr19:3231845 | G | C | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+6847G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3231845 | |||||||
| chr19:3232554 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+7556G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3232554 | |||||||
| chr19:3232622 | G | A | 4 | a0001c0001t0002g0247 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02895.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+7624G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3232622 | |||||||
| chr19:3232812 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.259+7814C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3232812 | |||||||
| chr19:3233098 | A | AAAAT | 56 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(53): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.259+8127_259+8130d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3233098 | ||||||
| chr19:3233098 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0002g0123 a0001c0001t0002g0130 a0001c0001t0004g0109 |
3 | HG02615.hp2 HG03831.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259+8119_259+8130d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3233098 | ||||||
| chr19:3233148 | G | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0217 a0001c0001t0001g0222 others(3): Show |
6 | HG01074.hp1 HG01255.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+8150G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233148 | |||||||
| chr19:3233230 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0224 a0001c0003t0004g0220 |
3 | HG00733.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.259+8232G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233230 | |||||||
| chr19:3233299 | G | C | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.259+8301G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233299 | |||||||
| chr19:3233592 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
69 | HG00423.hp1 HG00597.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.259+8594G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233592 | |||||||
| chr19:3233767 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+8769C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233767 | |||||||
| chr19:3233780 | G | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.259+8782G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233780 | |||||||
| chr19:3233807 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.259+8809A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233807 | |||||||
| chr19:3233944 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0002g0053 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+8946C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3233944 | |||||||
| chr19:3234106 | A | G | 13 | a0001c0001t0001g0052 a0001c0001t0002g0011 a0001c0001t0002g0053 others(10): Show |
13 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.259+9108A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234106 | |||||||
| chr19:3234108 | G | C | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+9110G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234108 | |||||||
| chr19:3234264 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259+9266T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234264 | |||||||
| chr19:3234266 | T | C | 10 | a0001c0001t0002g0011 a0001c0001t0002g0247 a0001c0001t0002g0251 others(7): Show |
10 | HG02622.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+9268T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234266 | |||||||
| chr19:3234346 | G | T | 4 | a0001c0001t0002g0213 a0001c0001t0002g0216 a0001c0001t0004g0234 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+9348G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234346 | |||||||
| chr19:3234388 | C | T | 2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.259+9390C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234388 | |||||||
| chr19:3234490 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+9492C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234490 | |||||||
| chr19:3234958 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0002g0053 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+9960C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234958 | |||||||
| chr19:3234961 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259+9963C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234961 | |||||||
| chr19:3234966 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259+9968C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3234966 | |||||||
| chr19:3235061 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 |
3 | HG02717.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259+10063C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235061 | |||||||
| chr19:3235088 | C | T | 2 | a0001c0001t0001g0117 a0001c0003t0004g0261 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.259+10090C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235088 | |||||||
| chr19:3235190 | A | G | 53 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0215 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.259+10192A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235190 | |||||||
| chr19:3235313 | C | CT | 7 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+10325dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235313 | ||||||
| chr19:3235321 | T | C | 1 | a0001c0002t0003g0017 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259+10323T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235321 | |||||||
| chr19:3235369 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(58): Show |
62 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.259+10371A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235369 | |||||||
| chr19:3235404 | A | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0004g0109 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+10406A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235404 | |||||||
| chr19:3235486 | G | A | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+10488G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235486 | |||||||
| chr19:3235492 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
133 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.259+10494A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235492 | |||||||
| chr19:3235509 | G | GATGGATG others(453): Show |
2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18964.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(464): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235509 | ||||||
| chr19:3235509 | G | GATGGATG others(409): Show |
1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+10525_259+1052 others(420): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235509 | ||||||
| chr19:3235509 | G | GATGGATG others(409): Show |
124 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0063 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.259+10525_259+1052 others(420): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235509 | ||||||
| chr19:3235518 | A | ATGGATTG others(533): Show |
2 | a0001c0002t0001g0026 a0001c0002t0001g0046 |
2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(544): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(533): Show |
41 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0002g0103 others(38): Show |
41 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.259+10525_259+1052 others(544): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(533): Show |
11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+10525_259+1052 others(544): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(537): Show |
1 | a0001c0001t0001g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.259+10525_259+1052 others(548): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(537): Show |
3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(548): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(497): Show |
1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+10525_259+1052 others(508): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(545): Show |
1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.259+10525_259+1052 others(556): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(501): Show |
3 | a0001c0001t0002g0002 a0001c0001t0002g0130 a0001c0001t0005g0009 |
3 | HG02615.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(512): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(505): Show |
2 | a0001c0001t0004g0189 a0001c0003t0002g0232 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(516): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(489): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(15): Show |
18 | HG01106.hp1 HG01123.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+10525_259+1052 others(500): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(493): Show |
2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(504): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(497): Show |
44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0056 others(41): Show |
45 | HG00423.hp1 HG00597.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.259+10525_259+1052 others(508): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(501): Show |
1 | a0001c0001t0004g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.259+10525_259+1052 others(512): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235518 | A | ATGGATTG others(453): Show |
2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.259+10525_259+1052 others(464): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235518 | ||||||
| chr19:3235538 | G | T | 50 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0215 others(47): Show |
50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.259+10540G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235538 | |||||||
| chr19:3235634 | A | ATGAG | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+10638_259+1063 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235634 | ||||||
| chr19:3235638 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+10640G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235638 | |||||||
| chr19:3235645 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+10647A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235645 | |||||||
| chr19:3235646 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+10648G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235646 | |||||||
| chr19:3235646 | G | GTGGATGG others(1): Show |
16 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0003g0127 others(13): Show |
16 | HG00544.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+10675_259+1068 others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235646 | ||||||
| chr19:3235646 | G | GTGGATGG others(5): Show |
32 | a0001c0001t0001g0024 a0001c0001t0001g0215 a0001c0001t0002g0103 others(29): Show |
32 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+10671_259+1068 others(16): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235646 | ||||||
| chr19:3235646 | G | GTGGATGG others(9): Show |
1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+10667_259+1068 others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235646 | ||||||
| chr19:3235646 | GTGGA | G | 3 | a0001c0001t0002g0169 a0001c0002t0002g0049 a0001c0003t0005g0151 |
3 | HG02922.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.259+10679_259+1068 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235646 | ||||||
| chr19:3235654 | A | ATGGATGG others(45): Show |
2 | a0001c0001t0002g0247 a0001c0001t0004g0109 |
2 | HG02895.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.259+10682_259+1068 others(56): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235654 | ||||||
| chr19:3235654 | A | ATGGATGG others(41): Show |
10 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
10 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+10682_259+1068 others(52): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235654 | ||||||
| chr19:3235680 | G | A | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+10682G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235680 | |||||||
| chr19:3235689 | G | T | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.259+10691G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235689 | |||||||
| chr19:3235690 | G | GTGGA | 3 | a0001c0001t0005g0249 a0001c0003t0002g0248 a0001c0010t0005g0252 |
3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+10715_259+1071 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235690 | ||||||
| chr19:3235698 | A | G | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.259+10700A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235698 | |||||||
| chr19:3235717 | T | G | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.259+10719T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235717 | |||||||
| chr19:3235718 | G | A | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.259+10720G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235718 | |||||||
| chr19:3235725 | G | T | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.259+10727G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235725 | |||||||
| chr19:3235726 | GTGGA | G | 53 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0132 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.259+10755_259+1075 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235726 | ||||||
| chr19:3235732 | G | A | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(9): Show |
12 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+10734G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235732 | |||||||
| chr19:3235789 | A | AATGGATG others(9): Show |
1 | a0001c0002t0005g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.259+10803_259+1081 others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235789 | ||||||
| chr19:3235789 | A | AATGGATG others(13): Show |
1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.259+10799_259+1081 others(24): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3235789 | ||||||
| chr19:3235810 | A | G | 14 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0123 others(11): Show |
14 | HG01106.hp2 HG01175.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+10812A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235810 | |||||||
| chr19:3235826 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
134 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.259+10828A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235826 | |||||||
| chr19:3235866 | G | A | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+10868G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3235866 | |||||||
| chr19:3236006 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.259+11008G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236006 | |||||||
| chr19:3236193 | A | G | 70 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0120 others(67): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.259+11195A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236193 | |||||||
| chr19:3236238 | T | C | 2 | a0001c0001t0002g0251 a0001c0001t0006g0250 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.259+11240T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236238 | |||||||
| chr19:3236295 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0002g0198 |
2 | HG01175.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.259+11297A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236295 | |||||||
| chr19:3236363 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259+11365T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236363 | |||||||
| chr19:3236378 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0006g0250 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.259+11380G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236378 | |||||||
| chr19:3236844 | G | T | 1 | a0001c0002t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+11846G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236844 | |||||||
| chr19:3236887 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259+11889G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236887 | |||||||
| chr19:3236925 | A | G | 59 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0084 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.259+11927A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3236925 | |||||||
| chr19:3236988 | C | CA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(58): Show |
62 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.259+12006dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3236988 | ||||||
| chr19:3236988 | CA | C | 9 | a0001c0001t0002g0169 a0001c0001t0002g0251 a0001c0001t0003g0175 others(6): Show |
9 | HG01975.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+12006delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3236988 | ||||||
| chr19:3236988 | CAA | C | 53 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0084 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.259+12005_259+1200 others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3236988 | ||||||
| chr19:3237048 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+12050C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237048 | |||||||
| chr19:3237079 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.259+12081G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237079 | |||||||
| chr19:3237109 | G | C | 58 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0084 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.259+12111G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237109 | |||||||
| chr19:3237140 | A | G | 58 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0084 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.259+12142A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237140 | |||||||
| chr19:3237311 | C | CA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0161 others(11): Show |
14 | HG00544.hp2 HG01261.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+12338dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3237311 | ||||||
| chr19:3237311 | CA | C | 28 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0117 others(25): Show |
28 | HG01175.hp2 HG01255.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+12338delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3237311 | ||||||
| chr19:3237311 | CAA | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(47): Show |
50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.259+12337_259+1233 others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3237311 | ||||||
| chr19:3237329 | A | G | 1 | a0001c0001t0004g0085 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259+12331A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237329 | |||||||
| chr19:3237394 | G | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(71): Show |
74 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.259+12396G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237394 | |||||||
| chr19:3237400 | A | C | 6 | a0001c0002t0002g0039 a0001c0002t0003g0016 a0001c0002t0003g0022 others(3): Show |
6 | HG00738.hp2 HG01069.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+12402A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237400 | |||||||
| chr19:3237491 | C | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.259+12493C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237491 | |||||||
| chr19:3237692 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0004g0155 |
2 | HG01496.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.259+12694T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237692 | |||||||
| chr19:3237941 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.259+12943C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3237941 | |||||||
| chr19:3238026 | G | A | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.260-12959G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238026 | |||||||
| chr19:3238044 | G | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(51): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.260-12941G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238044 | |||||||
| chr19:3238057 | G | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(51): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.260-12928G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238057 | |||||||
| chr19:3238108 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12877C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238108 | |||||||
| chr19:3238151 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12834C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238151 | |||||||
| chr19:3238210 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12775T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238210 | |||||||
| chr19:3238291 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.260-12694C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238291 | |||||||
| chr19:3238344 | AG | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12638delG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3238344 | ||||||
| chr19:3238556 | C | T | 3 | a0001c0001t0002g0251 a0001c0001t0004g0129 a0001c0001t0006g0250 |
3 | HG02083.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.260-12429C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238556 | |||||||
| chr19:3238850 | A | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12135A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238850 | |||||||
| chr19:3238980 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-12005T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3238980 | |||||||
| chr19:3239052 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.260-11933C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239052 | |||||||
| chr19:3239134 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
135 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.260-11851T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239134 | |||||||
| chr19:3239171 | C | T | 2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.260-11814C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239171 | |||||||
| chr19:3239185 | G | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.260-11800G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239185 | |||||||
| chr19:3239221 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.260-11764C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239221 | |||||||
| chr19:3239222 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.260-11763G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239222 | |||||||
| chr19:3239267 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.260-11718T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239267 | |||||||
| chr19:3239451 | G | T | 2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.260-11534G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239451 | |||||||
| chr19:3239538 | CT | C | 20 | a0001c0001t0001g0157 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
20 | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.260-11434delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3239538 | ||||||
| chr19:3239690 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.260-11295C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239690 | |||||||
| chr19:3239701 | C | A | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.260-11284C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239701 | |||||||
| chr19:3239744 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(57): Show |
60 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.260-11241T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239744 | |||||||
| chr19:3239812 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-11173T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3239812 | |||||||
| chr19:3240009 | CT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(76): Show |
80 | HG00423.hp1 HG00597.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.260-10960delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3240009 | ||||||
| chr19:3240009 | CTT | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(53): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.260-10961_260-1096 others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3240009 | ||||||
| chr19:3240087 | C | G | 1 | a0001c0001t0002g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.260-10898C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240087 | |||||||
| chr19:3240129 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0084 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.260-10856C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240129 | |||||||
| chr19:3240131 | CCTGAGTA others(1): Show |
C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-10842_260-1083 others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3240131 | ||||||
| chr19:3240161 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.260-10824T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240161 | |||||||
| chr19:3240165 | C | T | 1 | a0001c0001t0003g0233 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.260-10820C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240165 | |||||||
| chr19:3240400 | A | C | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.260-10585A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240400 | |||||||
| chr19:3240454 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.260-10531C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240454 | |||||||
| chr19:3240516 | G | A | 1 | a0001c0001t0005g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.260-10469G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240516 | |||||||
| chr19:3240642 | T | C | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.260-10343T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240642 | |||||||
| chr19:3240655 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-10330T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240655 | |||||||
| chr19:3240765 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-10220T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240765 | |||||||
| chr19:3240918 | C | T | 1 | a0001c0002t0001g0023 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.260-10067C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3240918 | |||||||
| chr19:3241018 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.260-9967C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241018 | |||||||
| chr19:3241065 | C | CT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0201 others(6): Show |
9 | HG01123.hp2 HG01255.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.260-9905dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3241065 | ||||||
| chr19:3241065 | C | CTT | 15 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0003g0127 others(12): Show |
15 | HG01106.hp2 HG01175.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-9906_260-9905d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3241065 | ||||||
| chr19:3241178 | C | G | 2 | a0001c0001t0002g0251 a0001c0001t0006g0250 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.260-9807C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241178 | |||||||
| chr19:3241293 | G | C | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.260-9692G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241293 | |||||||
| chr19:3241360 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.260-9625T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241360 | |||||||
| chr19:3241377 | G | A | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(9): Show |
12 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-9608G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241377 | |||||||
| chr19:3241485 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-9500C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241485 | |||||||
| chr19:3241495 | C | A | 8 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(5): Show |
8 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-9490C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241495 | |||||||
| chr19:3241609 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0002g0198 |
2 | HG01175.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.260-9376C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241609 | |||||||
| chr19:3241699 | C | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-9286C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241699 | |||||||
| chr19:3241728 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.260-9257C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241728 | |||||||
| chr19:3241747 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.260-9238G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241747 | |||||||
| chr19:3241877 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.260-9108C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241877 | |||||||
| chr19:3241900 | G | A | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-9085G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241900 | |||||||
| chr19:3241923 | C | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-9062C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3241923 | |||||||
| chr19:3242033 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0006g0250 a0001c0003t0002g0248 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-8952G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242033 | |||||||
| chr19:3242105 | G | A | 1 | a0001c0001t0005g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.260-8880G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242105 | |||||||
| chr19:3242126 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(55): Show |
59 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-8859G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242126 | |||||||
| chr19:3242303 | G | GCGGGCAG others(12): Show |
1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.260-8680_260-8662d others(21): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3242303 | ||||||
| chr19:3242305 | G | A | 13 | a0001c0001t0001g0084 a0001c0001t0003g0083 a0001c0001t0003g0105 others(10): Show |
13 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.260-8680G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242305 | |||||||
| chr19:3242305 | G | T | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.260-8680G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242305 | |||||||
| chr19:3242386 | A | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(37): Show |
40 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.260-8599A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242386 | |||||||
| chr19:3242523 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.260-8462A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242523 | |||||||
| chr19:3242529 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260-8456G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242529 | |||||||
| chr19:3242595 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.260-8390G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242595 | |||||||
| chr19:3242631 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.260-8354T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242631 | |||||||
| chr19:3242710 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260-8275G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242710 | |||||||
| chr19:3242804 | T | TA | 9 | a0001c0001t0002g0235 a0001c0001t0002g0251 a0001c0001t0003g0175 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-8171dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3242804 | ||||||
| chr19:3242813 | A | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.260-8172A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242813 | |||||||
| chr19:3242834 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.260-8151G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242834 | |||||||
| chr19:3242847 | C | T | 1 | a0001c0001t0004g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.260-8138C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3242847 | |||||||
| chr19:3242964 | AAAT | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
130 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.260-7997_260-7995d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3242964 | ||||||
| chr19:3243024 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(38): Show |
41 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.260-7961T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243024 | |||||||
| chr19:3243153 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0005g0208 |
2 | HG00597.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.260-7832T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243153 | |||||||
| chr19:3243229 | T | A | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.260-7756T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243229 | |||||||
| chr19:3243287 | C | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0084 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.260-7698C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243287 | |||||||
| chr19:3243368 | C | T | 1 | a0001c0004t0004g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.260-7617C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243368 | |||||||
| chr19:3243485 | TTGCCTAG others(12): Show |
T | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.260-7499_260-7481d others(21): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243485 | |||||||
| chr19:3243533 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.260-7452C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243533 | |||||||
| chr19:3243609 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0224 a0001c0003t0004g0220 |
3 | HG00733.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.260-7376G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243609 | |||||||
| chr19:3243835 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.260-7150C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243835 | |||||||
| chr19:3243849 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0006g0250 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.260-7136C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3243849 | |||||||
| chr19:3244165 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.260-6820A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244165 | |||||||
| chr19:3244218 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(39): Show |
42 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.260-6767C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244218 | |||||||
| chr19:3244341 | T | TG | 3 | a0001c0002t0002g0135 a0001c0002t0002g0136 a0001c0006t0004g0137 |
3 | HG03225.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.260-6643dupG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3244341 | ||||||
| chr19:3244411 | T | C | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260-6574T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244411 | |||||||
| chr19:3244549 | G | C | 1 | a0001c0001t0005g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.260-6436G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244549 | |||||||
| chr19:3244577 | T | G | 1 | a0001c0001t0005g0240 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.260-6408T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244577 | |||||||
| chr19:3244688 | AGT | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(56): Show |
60 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.260-6291_260-6290d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3244688 | ||||||
| chr19:3244983 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.260-6002T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3244983 | |||||||
| chr19:3245054 | G | A | 14 | a0001c0001t0001g0132 a0001c0001t0002g0251 a0001c0001t0003g0127 others(11): Show |
14 | HG01106.hp2 HG01175.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-5931G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245054 | |||||||
| chr19:3245178 | G | A | 1 | a0001c0001t0003g0233 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.260-5807G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245178 | |||||||
| chr19:3245230 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.260-5755G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245230 | |||||||
| chr19:3245368 | G | T | 3 | a0001c0001t0003g0067 a0001c0001t0005g0065 a0001c0002t0004g0040 |
3 | HG02071.hp2 HG03834.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.260-5617G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245368 | |||||||
| chr19:3245372 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.260-5613G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245372 | |||||||
| chr19:3245411 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.260-5574T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245411 | |||||||
| chr19:3245426 | G | A | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.260-5559G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245426 | |||||||
| chr19:3245502 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(54): Show |
58 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.260-5483G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245502 | |||||||
| chr19:3245570 | C | CA | 42 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0084 others(39): Show |
42 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.260-5401dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3245570 | ||||||
| chr19:3245637 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(61): Show |
65 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.260-5348A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245637 | |||||||
| chr19:3245816 | G | A | 1 | a0001c0002t0003g0022 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.260-5169G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245816 | |||||||
| chr19:3245940 | A | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(39): Show |
42 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.260-5045A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245940 | |||||||
| chr19:3245965 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.260-5020A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3245965 | |||||||
| chr19:3246040 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
138 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.260-4945G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246040 | |||||||
| chr19:3246227 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.260-4758G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246227 | |||||||
| chr19:3246233 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0184 others(1): Show |
4 | HG00544.hp2 HG03195.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-4752G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246233 | |||||||
| chr19:3246359 | G | GTC | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
132 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.260-4606_260-4605d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3246359 | ||||||
| chr19:3246359 | G | GTCTC | 4 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0002g0011 others(1): Show |
4 | HG02040.hp2 HG03195.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-4608_260-4605d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3246359 | ||||||
| chr19:3246385 | C | G | 3 | a0001c0001t0004g0189 a0001c0003t0002g0232 a0001c0003t0005g0151 |
3 | HG02145.hp2 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-4600C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246385 | |||||||
| chr19:3246446 | A | G | 2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.260-4539A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246446 | |||||||
| chr19:3246618 | C | T | 1 | a0001c0001t0005g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.260-4367C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3246618 | |||||||
| chr19:3247003 | C | T | 18 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0002g0002 others(15): Show |
18 | HG01106.hp2 HG01175.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.260-3982C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247003 | |||||||
| chr19:3247152 | A | T | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260-3833A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247152 | |||||||
| chr19:3247327 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.260-3658C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247327 | |||||||
| chr19:3247329 | T | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(44): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.260-3656T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247329 | |||||||
| chr19:3247418 | G | A | 3 | a0001c0003t0002g0248 a0001c0003t0004g0237 a0001c0010t0005g0252 |
3 | HG02148.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.260-3567G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247418 | |||||||
| chr19:3247421 | C | T | 2 | a0001c0002t0002g0135 a0001c0002t0002g0136 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.260-3564C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247421 | |||||||
| chr19:3247459 | G | C | 15 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0123 others(12): Show |
15 | HG01106.hp2 HG01175.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-3526G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247459 | |||||||
| chr19:3247716 | CA | C | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.260-3267delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3247716 | ||||||
| chr19:3247766 | A | T | 1 | a0001c0001t0005g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.260-3219A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247766 | |||||||
| chr19:3247767 | T | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.260-3218T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247767 | |||||||
| chr19:3247768 | T | A | 1 | a0001c0006t0004g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260-3217T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247768 | |||||||
| chr19:3247777 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0004g0153 |
2 | HG00735.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.260-3208A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247777 | |||||||
| chr19:3247854 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260-3131C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3247854 | |||||||
| chr19:3248111 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG02809.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.260-2874T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248111 | |||||||
| chr19:3248243 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(109): Show |
113 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(110): Show |
intron_variant | MODIFIER | c.260-2742G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248243 | |||||||
| chr19:3248525 | G | T | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.260-2460G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248525 | |||||||
| chr19:3248588 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.260-2397G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248588 | |||||||
| chr19:3248842 | TTTTC | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0245 a0001c0002t0001g0036 others(1): Show |
4 | HG03225.hp1 HG03704.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-2132_260-2129d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248842 | ||||||
| chr19:3248849 | T | TCTTC | 4 | a0001c0001t0001g0052 a0001c0001t0001g0150 a0001c0001t0002g0053 others(1): Show |
4 | HG03453.hp1 HG03491.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2133_260-2132i others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248849 | ||||||
| chr19:3248853 | T | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0063 others(18): Show |
21 | HG01175.hp2 HG01256.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-2132T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248853 | |||||||
| chr19:3248853 | T | TCTTC | 29 | a0001c0001t0001g0178 a0001c0001t0001g0217 a0001c0001t0001g0222 others(26): Show |
29 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.260-2080_260-2077d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | T | TCTTCCTT others(1): Show |
18 | a0001c0001t0001g0132 a0001c0001t0001g0161 a0001c0001t0001g0167 others(15): Show |
18 | HG00544.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-2084_260-2077d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | T | TCTTCCTT others(5): Show |
12 | a0001c0001t0001g0066 a0001c0001t0001g0157 a0001c0001t0001g0166 others(9): Show |
12 | HG00438.hp1 HG00733.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-2088_260-2077d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | T | TCTTCCTT others(9): Show |
1 | a0001c0001t0001g0184 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.260-2092_260-2077d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | T | TCTTCCTT others(13): Show |
1 | a0001c0001t0001g0148 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.260-2096_260-2077d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | TCTTC | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0141 others(18): Show |
21 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.260-2080_260-2077d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | TCTTCCTT others(1): Show |
T | 3 | a0001c0001t0001g0171 a0001c0001t0003g0173 a0001c0001t0005g0152 |
3 | HG00738.hp1 HG01346.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.260-2084_260-2077d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | TCTTCCTT others(5): Show |
T | 8 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0002g0172 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-2088_260-2077d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | TCTTCCTT others(9): Show |
T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0204 others(6): Show |
9 | HG00597.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-2092_260-2077d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248853 | TCTTCCTT others(13): Show |
T | 2 | a0001c0002t0004g0044 a0001c0002t0004g0047 |
2 | HG04115.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.260-2096_260-2077d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248853 | ||||||
| chr19:3248873 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260-2112C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248873 | |||||||
| chr19:3248873 | CCTTCCTT others(29): Show |
C | 1 | a0001c0002t0004g0040 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.260-2108_260-2073d others(38): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248873 | ||||||
| chr19:3248889 | CCTTCCTT others(17): Show |
C | 1 | a0001c0001t0002g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.260-2092_260-2069d others(26): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248889 | ||||||
| chr19:3248893 | CCTTCCTT others(9): Show |
C | 1 | a0001c0002t0003g0017 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.260-2088_260-2073d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248893 | ||||||
| chr19:3248893 | CCTTCCTT others(13): Show |
C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG01123.hp1 HG01261.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-2088_260-2069d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248893 | ||||||
| chr19:3248897 | CCTTCCTT others(5): Show |
C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0002t0003g0022 |
3 | HG01256.hp1 HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.260-2084_260-2073d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248897 | ||||||
| chr19:3248897 | CCTTCCTT others(9): Show |
C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0060 others(26): Show |
30 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-2084_260-2069d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248897 | ||||||
| chr19:3248897 | CCTTCCTT others(13): Show |
C | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260-2084_260-2065d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248897 | ||||||
| chr19:3248901 | C | T | 1 | a0001c0002t0005g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.260-2084C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248901 | |||||||
| chr19:3248905 | C | CCTTCCTT others(5): Show |
2 | a0001c0001t0001g0183 a0001c0001t0003g0162 |
2 | HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.260-2077_260-2076i others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248905 | ||||||
| chr19:3248905 | C | CCTTCCTT others(1): Show |
4 | a0001c0001t0001g0160 a0001c0001t0002g0158 a0001c0001t0002g0159 others(1): Show |
4 | HG00099.hp2 NA18943.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-2077_260-2076i others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248905 | ||||||
| chr19:3248905 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(16): Show |
19 | HG00609.hp2 HG02083.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.260-2080C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248905 | |||||||
| chr19:3248906 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.260-2079C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248906 | |||||||
| chr19:3248909 | T | C | 40 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0066 others(37): Show |
40 | HG00609.hp1 HG01175.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.260-2076T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248909 | |||||||
| chr19:3248910 | CTTTCTTT others(10): Show |
C | 1 | a0001c0006t0004g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260-2067_260-2051d others(19): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248910 | ||||||
| chr19:3248913 | T | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0116 a0001c0001t0001g0120 others(11): Show |
14 | HG02615.hp2 HG02717.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.260-2072T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248913 | |||||||
| chr19:3248914 | CTTTCTTT others(6): Show |
C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0107 others(7): Show |
10 | HG02083.hp2 HG02132.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-2063_260-2051d others(15): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248914 | ||||||
| chr19:3248917 | T | C | 7 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0259 others(4): Show |
7 | HG02615.hp2 HG02897.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-2068T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248917 | |||||||
| chr19:3248918 | CTTTCTTT others(2): Show |
C | 13 | a0001c0001t0001g0104 a0001c0001t0001g0119 a0001c0001t0002g0122 others(10): Show |
13 | HG01975.hp2 HG02132.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.260-2059_260-2051d others(11): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248918 | ||||||
| chr19:3248921 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0124 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.260-2064T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3248921 | |||||||
| chr19:3248922 | C | CTTTCT | 3 | a0001c0001t0002g0209 a0001c0001t0003g0231 a0001c0004t0004g0210 |
3 | HG02055.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.260-2040_260-2036d others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248922 | ||||||
| chr19:3248922 | CTTTCT | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0260 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-2040_260-2036d others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248922 | ||||||
| chr19:3248926 | CT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0057 others(54): Show |
58 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.260-2055delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248926 | ||||||
| chr19:3248927 | T | TTTC | 11 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0121 others(8): Show |
11 | HG01256.hp2 HG02040.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-2056_260-2055i others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 3248927 | ||||||
| chr19:3249380 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.260-1605G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3249380 | |||||||
| chr19:3249681 | C | A | 2 | a0001c0001t0001g0191 a0001c0002t0004g0043 |
2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.260-1304C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3249681 | |||||||
| chr19:3249687 | C | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0229 |
3 | HG02486.hp2 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.260-1298C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3249687 | |||||||
| chr19:3250061 | C | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
97 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(94): Show |
intron_variant | MODIFIER | c.260-924C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250061 | |||||||
| chr19:3250214 | T | G | 1 | a0001c0001t0003g0174 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.260-771T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250214 | |||||||
| chr19:3250292 | T | G | 1 | a0001c0001t0004g0085 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.260-693T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250292 | |||||||
| chr19:3250319 | T | C | 2 | a0001c0001t0001g0066 a0001c0002t0005g0093 |
2 | HG04184.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.260-666T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250319 | |||||||
| chr19:3250351 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.260-634T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250351 | |||||||
| chr19:3250480 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.260-505C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250480 | |||||||
| chr19:3250498 | A | G | 1 | a0001c0003t0004g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.260-487A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250498 | |||||||
| chr19:3250566 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.260-419C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250566 | |||||||
| chr19:3250619 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(92): Show |
96 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(93): Show |
intron_variant | MODIFIER | c.260-366T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 1/12 | chr19 | 3250619 | |||||||
| chr19:3251118 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(15): Show |
18 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+51C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251118 | |||||||
| chr19:3251221 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
97 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(94): Show |
intron_variant | MODIFIER | c.342+154T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251221 | |||||||
| chr19:3251228 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(56): Show |
60 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.342+161C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251228 | |||||||
| chr19:3251407 | G | C | 2 | a0001c0003t0003g0098 a0001c0003t0005g0099 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.342+340G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251407 | |||||||
| chr19:3251426 | C | G | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(12): Show |
15 | HG02486.hp1 HG02622.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.342+359C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251426 | |||||||
| chr19:3251439 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.342+372C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251439 | |||||||
| chr19:3251446 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.342+379G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251446 | |||||||
| chr19:3251652 | C | CT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0163 others(23): Show |
26 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.342+607dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3251652 | ||||||
| chr19:3251652 | C | CTTT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(43): Show |
47 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.342+605_342+607dup others(3): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3251652 | ||||||
| chr19:3251652 | C | CTTTT | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0097 others(6): Show |
9 | HG02165.hp2 HG02602.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+604_342+607dup others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3251652 | ||||||
| chr19:3251652 | CT | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0206 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.342+607delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3251652 | ||||||
| chr19:3251654 | T | TC | 3 | a0001c0002t0002g0135 a0001c0002t0002g0136 a0001c0006t0004g0137 |
3 | HG03225.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+587_342+588ins others(1): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251654 | |||||||
| chr19:3251669 | T | G | 1 | a0001c0001t0002g0247 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.342+602T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251669 | |||||||
| chr19:3251672 | T | G | 9 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0002g0053 others(6): Show |
9 | HG02717.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+605T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251672 | |||||||
| chr19:3251672 | T | TG | 30 | a0001c0001t0001g0066 a0001c0001t0001g0121 a0001c0001t0001g0124 others(27): Show |
30 | HG01175.hp1 HG01175.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.342+605_342+606ins others(1): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251672 | |||||||
| chr19:3251674 | TG | T | 3 | a0001c0001t0005g0238 a0001c0002t0004g0040 a0001c0007t0002g0144 |
3 | HG01071.hp2 HG02071.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.342+608delG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251674 | |||||||
| chr19:3251675 | G | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0084 others(65): Show |
68 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.342+608G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251675 | |||||||
| chr19:3251678 | G | T | 3 | a0001c0001t0003g0179 a0001c0001t0004g0180 a0001c0001t0005g0203 |
3 | HG00642.hp2 HG01167.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.342+611G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251678 | |||||||
| chr19:3251709 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+642T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251709 | |||||||
| chr19:3251719 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(56): Show |
60 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.342+652C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251719 | |||||||
| chr19:3251762 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.342+695C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251762 | |||||||
| chr19:3251768 | A | G | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+701A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251768 | |||||||
| chr19:3251820 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
95 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.342+753G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251820 | |||||||
| chr19:3251821 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(55): Show |
59 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.342+754T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251821 | |||||||
| chr19:3251855 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+788A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251855 | |||||||
| chr19:3251863 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.342+796C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251863 | |||||||
| chr19:3251973 | C | A | 1 | a0001c0001t0005g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342+906C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251973 | |||||||
| chr19:3251996 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+929C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3251996 | |||||||
| chr19:3252081 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(54): Show |
58 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.342+1014T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252081 | |||||||
| chr19:3252095 | TGGAGTAC others(1): Show |
T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(54): Show |
58 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.342+1029_342+1036d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252095 | |||||||
| chr19:3252153 | C | T | 1 | a0001c0001t0004g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.342+1086C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252153 | |||||||
| chr19:3252194 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0005g0009 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.342+1127A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252194 | |||||||
| chr19:3252196 | G | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(16): Show |
19 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+1129G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252196 | |||||||
| chr19:3252287 | G | A | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+1220G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252287 | |||||||
| chr19:3252436 | C | A | 7 | a0001c0001t0001g0245 a0001c0001t0002g0012 a0001c0001t0002g0251 others(4): Show |
7 | HG01891.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+1369C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252436 | |||||||
| chr19:3252501 | G | A | 1 | a0001c0003t0004g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.342+1434G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252501 | |||||||
| chr19:3252519 | C | T | 22 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0001g0201 others(19): Show |
22 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.342+1452C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252519 | |||||||
| chr19:3252524 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342+1457T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252524 | |||||||
| chr19:3252546 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+1479C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252546 | |||||||
| chr19:3252557 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+1490C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252557 | |||||||
| chr19:3252735 | T | G | 1 | a0001c0001t0005g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.342+1668T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252735 | |||||||
| chr19:3252865 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(52): Show |
56 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.342+1798G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252865 | |||||||
| chr19:3252879 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
117 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(114): Show |
intron_variant | MODIFIER | c.342+1812G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252879 | |||||||
| chr19:3252911 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(52): Show |
56 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.342+1844G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252911 | |||||||
| chr19:3252939 | T | C | 1 | a0001c0001t0005g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.342+1872T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3252939 | |||||||
| chr19:3253041 | G | C | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.342+1974G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253041 | |||||||
| chr19:3253101 | TA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
88 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.342+2045delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3253101 | ||||||
| chr19:3253107 | A | G | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.342+2040A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253107 | |||||||
| chr19:3253109 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.342+2042A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253109 | |||||||
| chr19:3253116 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342+2049A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253116 | |||||||
| chr19:3253138 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.342+2071C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253138 | |||||||
| chr19:3253161 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0184 |
3 | HG00544.hp2 NA19074.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.342+2094C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253161 | |||||||
| chr19:3253515 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(53): Show |
57 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.342+2448G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253515 | |||||||
| chr19:3253534 | G | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(26): Show |
29 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+2467G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253534 | |||||||
| chr19:3253596 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.342+2529A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253596 | |||||||
| chr19:3253632 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
93 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.342+2565G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253632 | |||||||
| chr19:3253792 | G | GT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(15): Show |
18 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+2730dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3253792 | ||||||
| chr19:3253812 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342+2745C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253812 | |||||||
| chr19:3253817 | G | GT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+2750_342+2751i others(3): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253817 | |||||||
| chr19:3253832 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+2765T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253832 | |||||||
| chr19:3253875 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0002g0012 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342+2808C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253875 | |||||||
| chr19:3253930 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+2863C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253930 | |||||||
| chr19:3253953 | C | A | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.342+2886C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3253953 | |||||||
| chr19:3254002 | G | C | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+2935G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254002 | |||||||
| chr19:3254126 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3059C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254126 | |||||||
| chr19:3254254 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+3187T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254254 | |||||||
| chr19:3254277 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3210T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254277 | |||||||
| chr19:3254285 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3218C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254285 | |||||||
| chr19:3254309 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342+3242G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254309 | |||||||
| chr19:3254333 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.342+3266C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254333 | |||||||
| chr19:3254349 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3282T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254349 | |||||||
| chr19:3254431 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3364G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254431 | |||||||
| chr19:3254444 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0167 a0001c0001t0001g0206 |
3 | HG02280.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.342+3377C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254444 | |||||||
| chr19:3254445 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3378G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254445 | |||||||
| chr19:3254460 | TCCATCTA others(13): Show |
T | 2 | a0001c0001t0001g0215 a0001c0001t0002g0198 |
2 | HG01175.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.342+3409_342+3428d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3254460 | ||||||
| chr19:3254541 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3474G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254541 | |||||||
| chr19:3254566 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+3499C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254566 | |||||||
| chr19:3254647 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(52): Show |
56 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.342+3580T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254647 | |||||||
| chr19:3254647 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0002g0198 |
2 | HG01175.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.342+3580T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254647 | |||||||
| chr19:3254702 | C | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+3635C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254702 | |||||||
| chr19:3254817 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+3750T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3254817 | |||||||
| chr19:3255029 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+3962T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255029 | |||||||
| chr19:3255033 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+3966C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255033 | |||||||
| chr19:3255101 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+4034A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255101 | |||||||
| chr19:3255277 | C | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+4210C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255277 | |||||||
| chr19:3255357 | T | C | 1 | a0001c0001t0004g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.342+4290T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255357 | |||||||
| chr19:3255375 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.342+4308G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255375 | |||||||
| chr19:3255488 | C | T | 1 | a0001c0002t0002g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.342+4421C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255488 | |||||||
| chr19:3255566 | G | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+4499G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255566 | |||||||
| chr19:3255636 | G | C | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.342+4569G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255636 | |||||||
| chr19:3255645 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+4578C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255645 | |||||||
| chr19:3255774 | G | A | 1 | a0001c0004t0004g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.342+4707G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255774 | |||||||
| chr19:3255791 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(15): Show |
18 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+4724G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255791 | |||||||
| chr19:3255793 | G | A | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+4726G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255793 | |||||||
| chr19:3255802 | T | G | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.342+4735T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255802 | |||||||
| chr19:3255898 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+4831C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255898 | |||||||
| chr19:3255955 | C | T | 2 | a0001c0003t0002g0248 a0001c0010t0005g0252 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.342+4888C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255955 | |||||||
| chr19:3255969 | G | T | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+4902G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255969 | |||||||
| chr19:3255970 | C | T | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+4903C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3255970 | |||||||
| chr19:3256064 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.342+5006_342+5007i others(16): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(8): Show |
2 | a0001c0003t0002g0248 a0001c0010t0005g0252 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.342+5006_342+5007i others(17): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0005g0249 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.342+5006_342+5007i others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342+5006_342+5007i others(19): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.342+5006_342+5007i others(21): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0245 a0001c0001t0002g0251 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.342+5006_342+5007i others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0006g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342+5006_342+5007i others(23): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAGAAAAA others(11): Show |
50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0056 others(47): Show |
51 | HG00597.hp2 HG01106.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.342+4998_342+4999i others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAGAAAAA others(12): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0100 others(27): Show |
30 | HG00423.hp1 HG01175.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.342+4998_342+4999i others(21): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256064 | C | CAGAAAAA others(13): Show |
5 | a0001c0001t0001g0063 a0001c0001t0001g0110 a0001c0001t0004g0109 others(2): Show |
5 | HG02055.hp2 HG03579.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+4998_342+4999i others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256064 | ||||||
| chr19:3256083 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(3): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+5016C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256083 | |||||||
| chr19:3256106 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5039G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256106 | |||||||
| chr19:3256208 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(115): Show |
119 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(116): Show |
intron_variant | MODIFIER | c.342+5141T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256208 | |||||||
| chr19:3256320 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5253T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256320 | |||||||
| chr19:3256341 | G | C | 3 | a0001c0001t0001g0245 a0001c0001t0002g0012 a0001c0001t0002g0130 |
3 | HG01891.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342+5274G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256341 | |||||||
| chr19:3256486 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5419C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256486 | |||||||
| chr19:3256496 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5429G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256496 | |||||||
| chr19:3256521 | G | T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+5454G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256521 | |||||||
| chr19:3256523 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5456C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256523 | |||||||
| chr19:3256534 | T | TTTA | 16 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0001g0228 others(13): Show |
16 | HG00738.hp2 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.342+5507_342+5509d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTA | T | 92 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0052 others(89): Show |
92 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.342+5507_342+5509d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTATTA | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0218 a0001c0001t0001g0236 others(6): Show |
9 | HG00741.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.342+5504_342+5509d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTATTAT others(2): Show |
T | 3 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 |
3 | HG02622.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342+5501_342+5509d others(11): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTATTAT others(5): Show |
T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0165 a0001c0001t0005g0073 others(2): Show |
5 | HG01358.hp2 HG01517.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+5498_342+5509d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTATTAT others(8): Show |
T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
73 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.342+5495_342+5509d others(17): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256534 | TTTATTAT others(11): Show |
T | 15 | a0001c0001t0001g0090 a0001c0001t0001g0120 a0001c0001t0001g0121 others(12): Show |
15 | HG02165.hp2 HG02486.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+5492_342+5509d others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3256534 | ||||||
| chr19:3256692 | C | G | 1 | a0001c0001t0005g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342+5625C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256692 | |||||||
| chr19:3256694 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(15): Show |
18 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+5627G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256694 | |||||||
| chr19:3256723 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
89 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+5656G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256723 | |||||||
| chr19:3256900 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.342+5833G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256900 | |||||||
| chr19:3256904 | C | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0003g0140 |
3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.342+5837C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256904 | |||||||
| chr19:3256945 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+5878A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256945 | |||||||
| chr19:3256964 | C | T | 2 | a0001c0001t0002g0235 a0001c0001t0004g0153 |
2 | HG00735.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.342+5897C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256964 | |||||||
| chr19:3256965 | G | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0105 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.342+5898G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256965 | |||||||
| chr19:3256982 | A | G | 1 | a0001c0002t0003g0029 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.342+5915A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3256982 | |||||||
| chr19:3257022 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
94 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+5955C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257022 | |||||||
| chr19:3257095 | T | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6028T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257095 | |||||||
| chr19:3257160 | G | A | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+6093G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257160 | |||||||
| chr19:3257165 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6098C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257165 | |||||||
| chr19:3257169 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.342+6102G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257169 | |||||||
| chr19:3257183 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6116G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257183 | |||||||
| chr19:3257417 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
95 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.342+6350C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257417 | |||||||
| chr19:3257419 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6352G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257419 | |||||||
| chr19:3257426 | C | G | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6359C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257426 | |||||||
| chr19:3257447 | T | A | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+6380T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257447 | |||||||
| chr19:3257451 | T | G | 23 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0001g0157 others(20): Show |
23 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.342+6384T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257451 | |||||||
| chr19:3257483 | TA | T | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+6417delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257483 | |||||||
| chr19:3257484 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+6417A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257484 | |||||||
| chr19:3257487 | T | A | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342+6420T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257487 | |||||||
| chr19:3257632 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.342+6565T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257632 | |||||||
| chr19:3257636 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.342+6569C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257636 | |||||||
| chr19:3257664 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0002g0012 a0001c0001t0002g0130 |
3 | HG01891.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342+6597C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257664 | |||||||
| chr19:3257687 | G | A | 1 | a0001c0001t0006g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.342+6620G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257687 | |||||||
| chr19:3257779 | ATTTT | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0084 others(68): Show |
72 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.342+6718_342+6721d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257779 | ||||||
| chr19:3257781 | T | TTTTA | 14 | a0001c0001t0001g0094 a0001c0001t0001g0146 a0001c0001t0001g0170 others(11): Show |
14 | HG00597.hp1 HG02040.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+6717_342+6718i others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257781 | ||||||
| chr19:3257781 | TTTTTTTT others(1): Show |
T | 20 | a0001c0001t0001g0104 a0001c0001t0001g0160 a0001c0001t0001g0171 others(17): Show |
20 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.342+6718_342+6725d others(10): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257781 | ||||||
| chr19:3257781 | TTTTTTTT others(5): Show |
T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(21): Show |
24 | HG00438.hp1 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.342+6718_342+6729d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257781 | ||||||
| chr19:3257781 | TTTTTTTT others(9): Show |
T | 21 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0132 others(18): Show |
21 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.342+6718_342+6733d others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257781 | ||||||
| chr19:3257781 | TTTTTTTT others(13): Show |
T | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+6718_342+6737d others(22): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257781 | ||||||
| chr19:3257785 | T | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0052 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.342+6718T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3257785 | |||||||
| chr19:3257785 | TTTTA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0236 others(2): Show |
5 | HG00741.hp2 HG01081.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+6766_342+6769d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257785 | ||||||
| chr19:3257966 | A | AT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(39): Show |
42 | HG01074.hp1 HG01175.hp2 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.342+6912dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3257966 | ||||||
| chr19:3258053 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.342+6986C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258053 | |||||||
| chr19:3258073 | G | T | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.342+7006G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258073 | |||||||
| chr19:3258106 | T | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+7039T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258106 | |||||||
| chr19:3258119 | G | A | 1 | a0001c0001t0005g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342+7052G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258119 | |||||||
| chr19:3258137 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(26): Show |
29 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+7070T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258137 | |||||||
| chr19:3258150 | G | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(16): Show |
19 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+7083G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258150 | |||||||
| chr19:3258220 | T | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+7153T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258220 | |||||||
| chr19:3258238 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0002g0012 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342+7171A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258238 | |||||||
| chr19:3258290 | A | ATT | 5 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+7233_342+7234d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3258290 | ||||||
| chr19:3258414 | G | A | 1 | a0001c0002t0001g0023 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.342+7347G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258414 | |||||||
| chr19:3258427 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0251 a0001c0001t0005g0249 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+7360C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258427 | |||||||
| chr19:3258616 | A | T | 6 | a0001c0001t0001g0170 a0001c0001t0002g0213 a0001c0001t0002g0216 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+7549A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258616 | |||||||
| chr19:3258650 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.342+7583C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258650 | |||||||
| chr19:3258715 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(36): Show |
39 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.342+7648A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258715 | |||||||
| chr19:3258769 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(35): Show |
38 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.342+7702G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258769 | |||||||
| chr19:3258848 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | HG01891.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342+7781C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258848 | |||||||
| chr19:3258858 | G | A | 5 | a0001c0001t0002g0251 a0001c0001t0005g0249 a0001c0001t0006g0250 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+7791G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258858 | |||||||
| chr19:3258863 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(28): Show |
31 | HG01256.hp2 HG01346.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.342+7796G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258863 | |||||||
| chr19:3258884 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0063 others(32): Show |
35 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.342+7817T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3258884 | |||||||
| chr19:3259056 | G | T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(20): Show |
23 | HG00544.hp2 HG01175.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.342+7989G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259056 | |||||||
| chr19:3259173 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(15): Show |
18 | HG01175.hp2 HG01256.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.342+8106C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259173 | |||||||
| chr19:3259177 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.342+8110C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259177 | |||||||
| chr19:3259372 | G | A | 5 | a0001c0001t0002g0193 a0001c0001t0002g0251 a0001c0001t0005g0249 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+8305G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259372 | |||||||
| chr19:3259445 | C | CA | 27 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0132 others(24): Show |
27 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.342+8378_342+8379i others(3): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259445 | |||||||
| chr19:3259631 | G | A | 2 | a0001c0001t0001g0245 a0001c0010t0005g0252 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.342+8564G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259631 | |||||||
| chr19:3259690 | A | T | 1 | a0001c0001t0004g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.342+8623A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259690 | |||||||
| chr19:3259848 | C | T | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+8781C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3259848 | |||||||
| chr19:3260094 | C | T | 1 | a0001c0003t0005g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.342+9027C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260094 | |||||||
| chr19:3260119 | T | C | 2 | a0001c0001t0003g0083 a0001c0001t0003g0105 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.342+9052T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260119 | |||||||
| chr19:3260211 | G | A | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.342+9144G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260211 | |||||||
| chr19:3260436 | T | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+9369T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260436 | |||||||
| chr19:3260505 | A | G | 21 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0182 others(18): Show |
21 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.342+9438A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260505 | |||||||
| chr19:3260545 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(17): Show |
20 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.342+9478C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260545 | |||||||
| chr19:3260621 | A | AT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0078 others(64): Show |
67 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.342+9573dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3260621 | ||||||
| chr19:3260621 | A | ATT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0110 a0001c0001t0002g0053 others(5): Show |
8 | HG01175.hp1 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+9572_342+9573d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3260621 | ||||||
| chr19:3260684 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342+9617G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260684 | |||||||
| chr19:3260783 | C | T | 1 | a0001c0002t0003g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.342+9716C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260783 | |||||||
| chr19:3260784 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.342+9717G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260784 | |||||||
| chr19:3260858 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0005g0009 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.342+9791G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3260858 | |||||||
| chr19:3261196 | G | A | 7 | a0001c0001t0002g0213 a0001c0001t0002g0216 a0001c0001t0004g0153 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+10129G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3261196 | |||||||
| chr19:3261967 | C | T | 1 | a0001c0001t0003g0233 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.342+10900C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3261967 | |||||||
| chr19:3261990 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+10923T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3261990 | |||||||
| chr19:3261997 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0086 others(22): Show |
25 | HG01175.hp2 HG01256.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.342+10930G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3261997 | |||||||
| chr19:3262069 | C | T | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.342+11002C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262069 | |||||||
| chr19:3262266 | G | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0063 others(50): Show |
53 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.342+11199G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262266 | |||||||
| chr19:3262272 | G | A | 2 | a0001c0001t0001g0245 a0001c0010t0005g0252 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.342+11205G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262272 | |||||||
| chr19:3262559 | G | A | 5 | a0001c0001t0002g0193 a0001c0001t0002g0251 a0001c0001t0005g0249 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-11313G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262559 | |||||||
| chr19:3262602 | G | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0226 a0001c0001t0002g0158 others(2): Show |
5 | HG00099.hp2 HG02523.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-11270G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262602 | |||||||
| chr19:3262922 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.343-10950G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262922 | |||||||
| chr19:3262988 | G | A | 4 | a0001c0001t0001g0245 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
4 | HG01891.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-10884G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3262988 | |||||||
| chr19:3263079 | C | T | 18 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0201 others(15): Show |
18 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.343-10793C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263079 | |||||||
| chr19:3263246 | C | CA | 17 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0101 others(14): Show |
17 | HG01106.hp1 HG02055.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-10606dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3263246 | ||||||
| chr19:3263460 | C | T | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.343-10412C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263460 | |||||||
| chr19:3263486 | G | A | 2 | a0001c0001t0001g0165 a0001c0002t0002g0025 |
2 | NA18951.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.343-10386G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263486 | |||||||
| chr19:3263492 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.343-10380C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263492 | |||||||
| chr19:3263571 | G | GAAAC | 53 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0121 others(50): Show |
53 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.343-10285_343-1028 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3263571 | ||||||
| chr19:3263576 | A | AAAC | 40 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0068 others(37): Show |
40 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.343-10293_343-1029 others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3263576 | ||||||
| chr19:3263617 | A | G | 1 | a0001c0004t0004g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-10255A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263617 | |||||||
| chr19:3263626 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.343-10246C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263626 | |||||||
| chr19:3263675 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0196 a0001c0001t0001g0202 others(1): Show |
4 | HG02683.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-10197C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263675 | |||||||
| chr19:3263733 | C | T | 2 | a0001c0003t0002g0232 a0001c0010t0005g0252 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.343-10139C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263733 | |||||||
| chr19:3263798 | A | G | 36 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(33): Show |
36 | HG00423.hp1 HG01255.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.343-10074A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263798 | |||||||
| chr19:3263805 | TGAA | T | 14 | a0001c0001t0001g0052 a0001c0001t0001g0204 a0001c0001t0002g0011 others(11): Show |
14 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-10062_343-1006 others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3263805 | ||||||
| chr19:3263938 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.343-9934G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3263938 | |||||||
| chr19:3264001 | G | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.343-9871G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264001 | |||||||
| chr19:3264108 | T | C | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.343-9764T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264108 | |||||||
| chr19:3264137 | A | G | 34 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0066 others(31): Show |
34 | HG00423.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.343-9735A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264137 | |||||||
| chr19:3264189 | G | A | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343-9683G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264189 | |||||||
| chr19:3264238 | A | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.343-9634A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264238 | |||||||
| chr19:3264303 | G | GT | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
219 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.343-9556dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3264303 | ||||||
| chr19:3264303 | G | GTT | 11 | a0001c0001t0001g0110 a0001c0001t0001g0148 a0001c0001t0001g0182 others(8): Show |
11 | HG01496.hp2 HG02293.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.343-9557_343-9556d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3264303 | ||||||
| chr19:3264336 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(44): Show |
48 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.343-9536T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264336 | |||||||
| chr19:3264411 | T | G | 1 | a0001c0002t0001g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.343-9461T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264411 | |||||||
| chr19:3264418 | T | G | 8 | a0001c0001t0001g0141 a0001c0001t0003g0058 a0001c0001t0003g0075 others(5): Show |
8 | HG00642.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-9454T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264418 | |||||||
| chr19:3264450 | G | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
108 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.343-9422G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264450 | |||||||
| chr19:3264517 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.343-9355G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264517 | |||||||
| chr19:3264565 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0178 |
2 | HG01358.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.343-9307G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264565 | |||||||
| chr19:3264573 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.343-9299G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264573 | |||||||
| chr19:3264696 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(38): Show |
42 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.343-9176G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264696 | |||||||
| chr19:3264706 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(39): Show |
43 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-9166A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264706 | |||||||
| chr19:3264715 | C | CT | 13 | a0001c0001t0001g0157 a0001c0001t0001g0170 a0001c0001t0002g0156 others(10): Show |
13 | HG01261.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-9145dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3264715 | ||||||
| chr19:3264715 | CT | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(39): Show |
43 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-9145delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3264715 | ||||||
| chr19:3264725 | T | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(39): Show |
43 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-9147T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3264725 | |||||||
| chr19:3265087 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(38): Show |
42 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.343-8785G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3265087 | |||||||
| chr19:3265537 | C | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(38): Show |
42 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.343-8335C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3265537 | |||||||
| chr19:3265855 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.343-8017A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3265855 | |||||||
| chr19:3265875 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0138 others(39): Show |
42 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.343-7997C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3265875 | |||||||
| chr19:3265998 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.343-7874G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3265998 | |||||||
| chr19:3266027 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-7845G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266027 | |||||||
| chr19:3266174 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0133 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.343-7698G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266174 | |||||||
| chr19:3266350 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0117 others(38): Show |
42 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.343-7522G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266350 | |||||||
| chr19:3266426 | A | T | 1 | a0001c0002t0002g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.343-7446A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266426 | |||||||
| chr19:3266803 | G | A | 2 | a0001c0003t0002g0232 a0001c0010t0005g0252 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.343-7069G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266803 | |||||||
| chr19:3266821 | A | AC | 13 | a0001c0001t0001g0157 a0001c0001t0001g0170 a0001c0001t0002g0156 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-7045dupC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3266821 | ||||||
| chr19:3266827 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.343-7045C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266827 | |||||||
| chr19:3266855 | C | G | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343-7017C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3266855 | |||||||
| chr19:3267065 | CTGTGTGT others(27): Show |
C | 2 | a0001c0001t0004g0234 a0001c0001t0005g0214 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.343-6784_343-6751d others(36): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3267065 | ||||||
| chr19:3267074 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.343-6798C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267074 | |||||||
| chr19:3267085 | G | T | 1 | a0001c0001t0005g0249 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.343-6787G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267085 | |||||||
| chr19:3267089 | A | G | 2 | a0001c0001t0002g0247 a0001c0006t0004g0137 |
2 | HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.343-6783A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267089 | |||||||
| chr19:3267089 | ATGTGTG | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.343-6770_343-6765d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3267089 | ||||||
| chr19:3267114 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.343-6758C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267114 | |||||||
| chr19:3267135 | C | T | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343-6737C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267135 | |||||||
| chr19:3267285 | AC | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
110 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.343-6580delC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3267285 | ||||||
| chr19:3267298 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
110 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.343-6574C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267298 | |||||||
| chr19:3267306 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.343-6566G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267306 | |||||||
| chr19:3267355 | C | T | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343-6517C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267355 | |||||||
| chr19:3267531 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0078 others(45): Show |
49 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.343-6341G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267531 | |||||||
| chr19:3267597 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.343-6275T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267597 | |||||||
| chr19:3267648 | G | C | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343-6224G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267648 | |||||||
| chr19:3267756 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343-6116G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267756 | |||||||
| chr19:3267805 | A | ACACAG | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.343-6067_343-6066i others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3267805 | |||||||
| chr19:3268055 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.343-5817G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268055 | |||||||
| chr19:3268084 | G | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.343-5788G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268084 | |||||||
| chr19:3268148 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.343-5724G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268148 | |||||||
| chr19:3268190 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0178 |
2 | HG01358.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.343-5682G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268190 | |||||||
| chr19:3268206 | C | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.343-5666C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268206 | |||||||
| chr19:3268339 | G | A | 2 | a0001c0001t0001g0204 a0001c0002t0001g0026 |
2 | HG03139.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.343-5533G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268339 | |||||||
| chr19:3268496 | A | C | 1 | a0001c0001t0002g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.343-5376A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268496 | |||||||
| chr19:3268668 | C | T | 5 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0194 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-5204C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268668 | |||||||
| chr19:3268724 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.343-5148A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268724 | |||||||
| chr19:3268771 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0246 |
2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.343-5101G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268771 | |||||||
| chr19:3268787 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.343-5085A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3268787 | |||||||
| chr19:3269197 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.343-4675C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269197 | |||||||
| chr19:3269198 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.343-4674G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269198 | |||||||
| chr19:3269618 | T | C | 2 | a0001c0001t0004g0189 a0001c0003t0005g0151 |
2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.343-4254T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269618 | |||||||
| chr19:3269714 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.343-4158G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269714 | |||||||
| chr19:3269745 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0217 a0001c0001t0001g0222 others(2): Show |
5 | HG01074.hp1 HG01255.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-4127T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269745 | |||||||
| chr19:3269750 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.343-4122C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269750 | |||||||
| chr19:3269801 | G | A | 4 | a0001c0001t0003g0179 a0001c0001t0003g0194 a0001c0001t0003g0200 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-4071G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269801 | |||||||
| chr19:3269869 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-4003T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269869 | |||||||
| chr19:3269878 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.343-3994C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3269878 | |||||||
| chr19:3270491 | C | T | 7 | a0001c0001t0003g0080 a0001c0001t0003g0149 a0001c0001t0003g0162 others(4): Show |
7 | HG01255.hp2 HG02300.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-3381C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270491 | |||||||
| chr19:3270506 | C | G | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343-3366C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270506 | |||||||
| chr19:3270685 | G | C | 9 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0089 others(6): Show |
9 | HG02486.hp2 HG03239.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-3187G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270685 | |||||||
| chr19:3270720 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.343-3152C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270720 | |||||||
| chr19:3270725 | T | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0251 a0001c0001t0006g0250 |
3 | HG02622.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343-3147T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270725 | |||||||
| chr19:3270830 | G | T | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343-3042G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3270830 | |||||||
| chr19:3271069 | G | A | 10 | a0001c0001t0001g0171 a0001c0001t0001g0215 a0001c0001t0002g0123 others(7): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-2803G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271069 | |||||||
| chr19:3271189 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.343-2683G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271189 | |||||||
| chr19:3271207 | G | A | 1 | a0001c0002t0003g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.343-2665G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271207 | |||||||
| chr19:3271234 | G | GC | 55 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0078 others(52): Show |
56 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.343-2631dupC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3271234 | ||||||
| chr19:3271272 | G | A | 2 | a0001c0001t0002g0213 a0002c0008t0002g0192 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343-2600G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271272 | |||||||
| chr19:3271516 | C | T | 1 | a0001c0003t0002g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.343-2356C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271516 | |||||||
| chr19:3271586 | A | G | 3 | a0001c0001t0002g0193 a0001c0001t0002g0251 a0001c0001t0006g0250 |
3 | HG02622.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343-2286A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271586 | |||||||
| chr19:3271764 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0167 a0001c0001t0002g0053 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-2108A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271764 | |||||||
| chr19:3271795 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.343-2077A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271795 | |||||||
| chr19:3271822 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.343-2050G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271822 | |||||||
| chr19:3271861 | TG | T | 5 | a0001c0001t0001g0138 a0001c0001t0003g0055 a0001c0001t0003g0127 others(2): Show |
5 | HG01081.hp1 HG01256.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-2006delG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3271861 | ||||||
| chr19:3271885 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.343-1987G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271885 | |||||||
| chr19:3271887 | A | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.343-1985A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271887 | |||||||
| chr19:3271909 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0078 others(56): Show |
60 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.343-1963C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271909 | |||||||
| chr19:3271950 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(119): Show |
122 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.343-1922T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3271950 | |||||||
| chr19:3272090 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0057 others(23): Show |
26 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-1782G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272090 | |||||||
| chr19:3272098 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.343-1774G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272098 | |||||||
| chr19:3272105 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0245 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.343-1767C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272105 | |||||||
| chr19:3272133 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
171 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.343-1739T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272133 | |||||||
| chr19:3272134 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
151 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.343-1738G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272134 | |||||||
| chr19:3272142 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.343-1730C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272142 | |||||||
| chr19:3272152 | A | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
126 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.343-1720A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272152 | |||||||
| chr19:3272171 | T | G | 4 | a0001c0001t0002g0145 a0001c0001t0003g0174 a0001c0001t0003g0175 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1701T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272171 | |||||||
| chr19:3272241 | T | C | 1 | a0001c0001t0004g0102 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.343-1631T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272241 | |||||||
| chr19:3272367 | C | CA | 3 | a0001c0001t0004g0189 a0001c0003t0002g0248 a0001c0003t0005g0151 |
3 | HG02145.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.343-1503dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3272367 | ||||||
| chr19:3272367 | CA | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0001t0002g0253 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-1503delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 3272367 | ||||||
| chr19:3272368 | A | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.343-1504A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272368 | |||||||
| chr19:3272369 | A | C | 6 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0001t0002g0253 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-1503A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272369 | |||||||
| chr19:3272370 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.343-1502G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272370 | |||||||
| chr19:3272370 | G | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0001t0002g0253 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-1502G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272370 | |||||||
| chr19:3272424 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0116 others(36): Show |
39 | HG00733.hp2 HG00735.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.343-1448C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272424 | |||||||
| chr19:3272481 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.343-1391T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272481 | |||||||
| chr19:3272666 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0002g0211 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.343-1206C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272666 | |||||||
| chr19:3272668 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343-1204G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272668 | |||||||
| chr19:3272746 | G | T | 1 | a0001c0001t0006g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.343-1126G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272746 | |||||||
| chr19:3272771 | G | A | 1 | a0001c0003t0002g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.343-1101G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272771 | |||||||
| chr19:3272779 | G | T | 1 | a0001c0001t0006g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.343-1093G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3272779 | |||||||
| chr19:3273190 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0056 others(107): Show |
110 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.343-682T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273190 | |||||||
| chr19:3273383 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0211 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.343-489C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273383 | |||||||
| chr19:3273390 | C | T | 1 | a0001c0001t0006g0071 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.343-482C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273390 | |||||||
| chr19:3273431 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-441A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273431 | |||||||
| chr19:3273470 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0218 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.343-402G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273470 | |||||||
| chr19:3273557 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.343-315C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273557 | |||||||
| chr19:3273586 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0211 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.343-286G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273586 | |||||||
| chr19:3273683 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343-189C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273683 | |||||||
| chr19:3273698 | G | A | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.343-174G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273698 | |||||||
| chr19:3273709 | G | A | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.343-163G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273709 | |||||||
| chr19:3273791 | C | T | 3 | a0001c0003t0004g0220 a0001c0003t0004g0237 a0001c0003t0004g0243 |
3 | HG00733.hp1 HG00735.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.343-81C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273791 | |||||||
| chr19:3273820 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
225 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.343-52T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 2/12 | chr19 | 3273820 | |||||||
| chr19:3273962 | G | A | 2 | a0001c0001t0002g0209 a0001c0004t0004g0210 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.394+39G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3273962 | |||||||
| chr19:3274161 | T | TG | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(120): Show |
123 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.394+244dupG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 3274161 | ||||||
| chr19:3274606 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0066 others(68): Show |
71 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.394+683G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3274606 | |||||||
| chr19:3274772 | G | A | 20 | a0001c0001t0001g0119 a0001c0001t0002g0147 a0001c0001t0002g0169 others(17): Show |
20 | HG00733.hp1 HG00735.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.394+849G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3274772 | |||||||
| chr19:3274787 | C | T | 5 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0004g0189 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+864C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3274787 | |||||||
| chr19:3275317 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0052 others(106): Show |
109 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.395-539C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3275317 | |||||||
| chr19:3275432 | C | G | 2 | a0001c0001t0001g0226 a0001c0002t0001g0014 |
2 | HG00544.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.395-424C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3275432 | |||||||
| chr19:3275442 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0201 others(24): Show |
27 | HG00597.hp2 HG00642.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.395-414A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3275442 | |||||||
| chr19:3275617 | C | G | 1 | a0001c0001t0004g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.395-239C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3275617 | |||||||
| chr19:3275626 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0211 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.395-230G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | chr19 | 3275626 | |||||||
| chr19:3275670 | GGA | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0121 others(12): Show |
15 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-181_395-180del others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 3275670 | ||||||
| chr19:3276274 | T | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(152): Show |
155 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.523+290T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276274 | |||||||
| chr19:3276341 | G | C | 1 | a0001c0001t0004g0085 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.523+357G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276341 | |||||||
| chr19:3276344 | G | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0211 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.523+360G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276344 | |||||||
| chr19:3276451 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523+467C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276451 | |||||||
| chr19:3276664 | C | CGGGCCCT others(27): Show |
5 | a0001c0001t0004g0212 a0001c0002t0004g0031 a0001c0002t0004g0043 others(2): Show |
5 | HG01123.hp2 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+683_523+716dup others(34): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 3276664 | ||||||
| chr19:3276817 | G | T | 5 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0004g0189 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+833G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276817 | |||||||
| chr19:3276844 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.523+860G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276844 | |||||||
| chr19:3276993 | C | G | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.523+1009C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3276993 | |||||||
| chr19:3277096 | T | C | 57 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0157 others(54): Show |
57 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.524-935T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277096 | |||||||
| chr19:3277112 | CTCTGGTC others(5): Show |
C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0007t0002g0144 |
3 | HG03098.hp2 HG03239.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.524-917_524-906del others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 3277112 | ||||||
| chr19:3277163 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0004g0234 others(1): Show |
4 | HG02630.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-868C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277163 | |||||||
| chr19:3277359 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.524-672A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277359 | |||||||
| chr19:3277372 | T | C | 21 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0197 others(18): Show |
21 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.524-659T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277372 | |||||||
| chr19:3277428 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.524-603C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277428 | |||||||
| chr19:3277493 | T | C | 1 | a0001c0003t0004g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.524-538T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277493 | |||||||
| chr19:3277543 | CT | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(93): Show |
96 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.524-479delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 3277543 | ||||||
| chr19:3277603 | C | T | 2 | a0001c0001t0002g0225 a0001c0001t0003g0186 |
2 | HG00438.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.524-428C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277603 | |||||||
| chr19:3277768 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0167 others(30): Show |
33 | HG00597.hp2 HG00642.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.524-263T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277768 | |||||||
| chr19:3277911 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.524-120C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277911 | |||||||
| chr19:3277973 | C | T | 3 | a0001c0001t0002g0106 a0001c0002t0001g0013 a0001c0002t0001g0018 |
3 | NA18966.hp1 NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.524-58C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 4/12 | chr19 | 3277973 | |||||||
| chr19:3278140 | G | A | 5 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0004g0189 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+30G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278140 | |||||||
| chr19:3278208 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.603+98G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278208 | |||||||
| chr19:3278439 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0060 others(46): Show |
49 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.603+329G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278439 | |||||||
| chr19:3278503 | C | T | 2 | a0001c0004t0004g0210 a0001c0006t0004g0137 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.603+393C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278503 | |||||||
| chr19:3278604 | G | A | 1 | a0001c0002t0001g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.603+494G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278604 | |||||||
| chr19:3278657 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.603+547G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278657 | |||||||
| chr19:3278679 | T | TTG | 77 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0133 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.603+589_603+590dup others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 3278679 | ||||||
| chr19:3278679 | T | TTGTG | 13 | a0001c0001t0002g0158 a0001c0001t0003g0173 a0001c0001t0003g0179 others(10): Show |
13 | HG00099.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.603+587_603+590dup others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 3278679 | ||||||
| chr19:3278679 | TTG | T | 19 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0084 others(16): Show |
19 | HG02004.hp1 HG02083.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.603+589_603+590del others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 3278679 | ||||||
| chr19:3278694 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0176 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.603+584T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278694 | |||||||
| chr19:3278695 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.603+585G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278695 | |||||||
| chr19:3278701 | T | G | 6 | a0001c0001t0001g0142 a0001c0001t0003g0064 a0001c0001t0003g0140 others(3): Show |
6 | HG00738.hp2 HG01069.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.603+591T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278701 | |||||||
| chr19:3278828 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.603+718T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278828 | |||||||
| chr19:3278850 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.603+740G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278850 | |||||||
| chr19:3278868 | C | CA | 14 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0001c0001t0001g0176 others(11): Show |
14 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.603+759dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 3278868 | ||||||
| chr19:3278886 | A | G | 19 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0168 others(16): Show |
19 | HG01175.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.603+776A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278886 | |||||||
| chr19:3278948 | G | T | 1 | a0001c0003t0002g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.603+838G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278948 | |||||||
| chr19:3278966 | G | A | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.603+856G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278966 | |||||||
| chr19:3278969 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.603+859T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3278969 | |||||||
| chr19:3279506 | G | C | 1 | a0001c0002t0001g0019 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.603+1396G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3279506 | |||||||
| chr19:3279999 | G | A | 16 | a0001c0001t0004g0010 a0001c0001t0004g0077 a0001c0001t0004g0085 others(13): Show |
16 | HG00597.hp2 HG00642.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.604-1200G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3279999 | |||||||
| chr19:3280022 | C | T | 44 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0001g0259 others(41): Show |
44 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.604-1177C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280022 | |||||||
| chr19:3280026 | A | G | 78 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0182 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.604-1173A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280026 | |||||||
| chr19:3280141 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604-1058A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280141 | |||||||
| chr19:3280200 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.604-999G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280200 | |||||||
| chr19:3280302 | G | A | 10 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0002 others(7): Show |
10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-897G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280302 | |||||||
| chr19:3280383 | C | A | 3 | a0001c0004t0004g0210 a0001c0004t0004g0227 a0001c0006t0004g0137 |
3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.604-816C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280383 | |||||||
| chr19:3280414 | T | A | 1 | a0001c0002t0002g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.604-785T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280414 | |||||||
| chr19:3280414 | T | TA | 8 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0002 others(5): Show |
8 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-774dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 3280414 | ||||||
| chr19:3280511 | G | T | 11 | a0001c0003t0001g0059 a0001c0003t0003g0098 a0001c0003t0004g0128 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.604-688G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280511 | |||||||
| chr19:3280531 | C | T | 1 | a0001c0003t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.604-668C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280531 | |||||||
| chr19:3280552 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-647G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280552 | |||||||
| chr19:3280555 | A | C | 1 | a0001c0001t0002g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.604-644A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280555 | |||||||
| chr19:3280563 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.604-636G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280563 | |||||||
| chr19:3280759 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.604-440C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280759 | |||||||
| chr19:3280897 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-302C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280897 | |||||||
| chr19:3280953 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-246T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280953 | |||||||
| chr19:3280981 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.604-218C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3280981 | |||||||
| chr19:3281151 | G | T | 5 | a0001c0001t0001g0117 a0001c0001t0001g0190 a0001c0002t0001g0033 others(2): Show |
5 | HG01256.hp2 HG01496.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-48G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 5/12 | chr19 | 3281151 | |||||||
| chr19:3281382 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0170 a0001c0001t0002g0053 others(1): Show |
4 | HG02622.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+37C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281382 | |||||||
| chr19:3281494 | G | T | 1 | a0001c0001t0005g0126 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.750+149G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281494 | |||||||
| chr19:3281503 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.750+158G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281503 | |||||||
| chr19:3281588 | G | A | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.750+243G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281588 | |||||||
| chr19:3281699 | C | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0150 |
2 | HG03491.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.750+354C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281699 | |||||||
| chr19:3281768 | C | G | 1 | a0001c0002t0001g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.751-358C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281768 | |||||||
| chr19:3281844 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.751-282G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281844 | |||||||
| chr19:3281946 | G | T | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.751-180G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3281946 | |||||||
| chr19:3282003 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.751-123C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 6/12 | chr19 | 3282003 | |||||||
| chr19:3282541 | A | C | 1 | a0001c0003t0001g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1039+43A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282541 | |||||||
| chr19:3282584 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1039+86C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282584 | |||||||
| chr19:3282609 | G | A | 8 | a0001c0001t0003g0058 a0001c0001t0003g0083 a0001c0001t0003g0105 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+111G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282609 | |||||||
| chr19:3282664 | G | A | 1 | a0001c0003t0002g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1039+166G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282664 | |||||||
| chr19:3282679 | C | T | 22 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0002 others(19): Show |
22 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039+181C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282679 | |||||||
| chr19:3282755 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1039+257C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282755 | |||||||
| chr19:3282773 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0244 |
2 | HG00735.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1039+275A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3282773 | |||||||
| chr19:3283022 | G | T | 1 | a0001c0001t0005g0240 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1039+524G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283022 | |||||||
| chr19:3283348 | A | G | 4 | a0001c0001t0002g0123 a0001c0001t0002g0145 a0001c0001t0002g0172 others(1): Show |
4 | HG02486.hp2 HG03098.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+850A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283348 | |||||||
| chr19:3283431 | G | A | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1039+933G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283431 | |||||||
| chr19:3283495 | C | T | 16 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(13): Show |
16 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039+997C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283495 | |||||||
| chr19:3283598 | A | C | 22 | a0001c0001t0001g0182 a0001c0001t0002g0002 a0001c0001t0002g0012 others(19): Show |
22 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039+1100A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283598 | |||||||
| chr19:3283600 | G | A | 1 | a0001c0003t0004g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1039+1102G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283600 | |||||||
| chr19:3283665 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1039+1167G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283665 | |||||||
| chr19:3283783 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1040-1119G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283783 | |||||||
| chr19:3283791 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
119 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1040-1111C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283791 | |||||||
| chr19:3283897 | G | A | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1040-1005G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283897 | |||||||
| chr19:3283998 | T | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0216 a0001c0001t0002g0242 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040-904T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3283998 | |||||||
| chr19:3284095 | T | G | 1 | a0001c0001t0003g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1040-807T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3284095 | |||||||
| chr19:3284128 | G | C | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1040-774G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3284128 | |||||||
| chr19:3284137 | C | CA | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1040-764dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr19 | 3284137 | ||||||
| chr19:3284502 | A | G | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1040-400A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3284502 | |||||||
| chr19:3284625 | G | C | 26 | a0001c0001t0001g0146 a0001c0001t0004g0072 a0001c0001t0004g0074 others(23): Show |
26 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1040-277G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3284625 | |||||||
| chr19:3284821 | T | C | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1040-81T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 8/12 | chr19 | 3284821 | |||||||
| chr19:3284998 | T | TGGCCCCG others(11): Show |
4 | a0001c0003t0004g0220 a0001c0003t0004g0237 a0001c0003t0004g0243 others(1): Show |
4 | HG00733.hp1 HG00735.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102+49_1102+50ins others(18): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 3284998 | ||||||
| chr19:3285012 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1102+48C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285012 | |||||||
| chr19:3285014 | T | C | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1102+50T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285014 | |||||||
| chr19:3285044 | C | T | 42 | a0001c0001t0001g0146 a0001c0001t0004g0010 a0001c0001t0004g0072 others(39): Show |
42 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1102+80C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285044 | |||||||
| chr19:3285201 | A | C | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1102+237A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285201 | |||||||
| chr19:3285401 | C | G | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1102+437C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285401 | |||||||
| chr19:3285452 | C | T | 1 | a0001c0003t0004g0220 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1102+488C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285452 | |||||||
| chr19:3285487 | C | G | 13 | a0001c0001t0004g0008 a0001c0003t0001g0059 a0001c0003t0002g0232 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1103-455C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285487 | |||||||
| chr19:3285551 | T | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-391T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285551 | |||||||
| chr19:3285669 | A | AC | 32 | a0001c0001t0001g0116 a0001c0001t0001g0132 a0001c0001t0001g0166 others(29): Show |
32 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1103-266dupC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 3285669 | ||||||
| chr19:3285669 | A | ACC | 47 | a0001c0001t0001g0146 a0001c0001t0002g0002 a0001c0001t0002g0145 others(44): Show |
47 | HG00099.hp1 HG00597.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1103-267_1103-266d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 3285669 | ||||||
| chr19:3285669 | A | ACCC | 16 | a0001c0001t0004g0153 a0001c0001t0004g0180 a0001c0001t0004g0207 others(13): Show |
16 | HG00597.hp1 HG00642.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1103-268_1103-266d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 3285669 | ||||||
| chr19:3285677 | T | A | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1103-265T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285677 | |||||||
| chr19:3285712 | A | C | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1103-230A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285712 | |||||||
| chr19:3285790 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1103-152C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285790 | |||||||
| chr19:3285797 | A | G | 2 | a0001c0003t0002g0248 a0001c0003t0005g0151 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1103-145A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285797 | |||||||
| chr19:3285891 | C | G | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1103-51C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 9/12 | chr19 | 3285891 | |||||||
| chr19:3286320 | A | G | 87 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1186+295A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286320 | |||||||
| chr19:3286321 | C | T | 1 | a0001c0001t0008g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1186+296C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286321 | |||||||
| chr19:3286452 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1186+427C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286452 | |||||||
| chr19:3286502 | C | T | 1 | a0001c0002t0002g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1186+477C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286502 | |||||||
| chr19:3286526 | C | A | 1 | a0001c0003t0004g0220 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1186+501C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286526 | |||||||
| chr19:3286563 | T | C | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1186+538T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286563 | |||||||
| chr19:3286567 | T | A | 19 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(16): Show |
19 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1186+542T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286567 | |||||||
| chr19:3286731 | C | CA | 24 | a0001c0001t0001g0119 a0001c0001t0001g0166 a0001c0001t0001g0206 others(21): Show |
24 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1186+727dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3286731 | ||||||
| chr19:3286731 | C | CAAAAA | 11 | a0001c0003t0001g0059 a0001c0003t0002g0232 a0001c0003t0002g0248 others(8): Show |
11 | HG00733.hp1 HG01106.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1186+723_1186+727d others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3286731 | ||||||
| chr19:3286731 | CA | C | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(146): Show |
149 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1186+727delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3286731 | ||||||
| chr19:3286806 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1186+781G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286806 | |||||||
| chr19:3286839 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1186+814C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286839 | |||||||
| chr19:3286893 | G | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+868G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286893 | |||||||
| chr19:3286989 | C | T | 1 | a0001c0002t0005g0027 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1186+964C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3286989 | |||||||
| chr19:3287034 | C | CA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0069 others(21): Show |
24 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1186+1028dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287034 | ||||||
| chr19:3287034 | CAA | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1027_1186+102 others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287034 | ||||||
| chr19:3287034 | CAAA | C | 42 | a0001c0001t0001g0146 a0001c0001t0004g0010 a0001c0001t0004g0072 others(39): Show |
42 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1186+1026_1186+102 others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287034 | ||||||
| chr19:3287034 | CAAAA | C | 23 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(20): Show |
23 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1186+1025_1186+102 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287034 | ||||||
| chr19:3287049 | A | AG | 16 | a0001c0001t0001g0228 a0001c0001t0004g0008 a0001c0003t0001g0059 others(13): Show |
16 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1186+1024_1186+102 others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287049 | |||||||
| chr19:3287060 | AAAAG | A | 15 | a0001c0001t0004g0008 a0001c0003t0001g0059 a0001c0003t0002g0232 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1186+1039_1186+104 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287060 | ||||||
| chr19:3287150 | A | G | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1186+1125A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287150 | |||||||
| chr19:3287285 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1186+1260C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287285 | |||||||
| chr19:3287351 | G | GGAGTTCA others(312): Show |
80 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1186+1354_1186+135 others(323): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287351 | ||||||
| chr19:3287351 | G | GGAGTTCA others(311): Show |
5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1354_1186+135 others(322): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287351 | ||||||
| chr19:3287351 | G | GGAGTTCA others(312): Show |
1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1186+1354_1186+135 others(323): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287351 | ||||||
| chr19:3287380 | T | C | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1355T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287380 | |||||||
| chr19:3287388 | C | T | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1363C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287388 | |||||||
| chr19:3287389 | A | G | 86 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1186+1364A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287389 | |||||||
| chr19:3287389 | A | T | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1364A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287389 | |||||||
| chr19:3287404 | A | T | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1379A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287404 | |||||||
| chr19:3287408 | C | A | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1383C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287408 | |||||||
| chr19:3287410 | A | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1385A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287410 | |||||||
| chr19:3287416 | C | T | 2 | a0001c0001t0005g0009 a0001c0002t0002g0136 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1186+1391C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287416 | |||||||
| chr19:3287417 | G | A | 86 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1186+1392G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287417 | |||||||
| chr19:3287421 | G | A | 86 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1186+1396G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287421 | |||||||
| chr19:3287429 | G | A | 47 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0167 others(44): Show |
47 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1186+1404G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287429 | |||||||
| chr19:3287446 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0003g0064 a0001c0001t0003g0140 others(1): Show |
4 | HG01943.hp2 HG01978.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+1421G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287446 | |||||||
| chr19:3287461 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1186+1436G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287461 | |||||||
| chr19:3287475 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1186+1450T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287475 | |||||||
| chr19:3287527 | T | C | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1186+1502T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287527 | |||||||
| chr19:3287655 | C | A | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1186+1630C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287655 | |||||||
| chr19:3287659 | A | G | 79 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1186+1634A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287659 | |||||||
| chr19:3287695 | C | G | 141 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0146 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1186+1670C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287695 | |||||||
| chr19:3287762 | A | AAAC | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1186+1746_1186+174 others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287762 | ||||||
| chr19:3287798 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1186+1773C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287798 | |||||||
| chr19:3287843 | T | A | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1186+1818T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287843 | |||||||
| chr19:3287844 | GT | G | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1186+1823delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3287844 | ||||||
| chr19:3287999 | A | G | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1186+1974A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3287999 | |||||||
| chr19:3288140 | T | G | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1187-2091T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288140 | |||||||
| chr19:3288203 | T | C | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1187-2028T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288203 | |||||||
| chr19:3288292 | T | C | 90 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1187-1939T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288292 | |||||||
| chr19:3288581 | C | G | 7 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0001c0001t0001g0176 others(4): Show |
7 | HG02486.hp1 HG02630.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1187-1650C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288581 | |||||||
| chr19:3288740 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1187-1491C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288740 | |||||||
| chr19:3288741 | G | A | 39 | a0001c0001t0001g0146 a0001c0001t0004g0010 a0001c0001t0004g0072 others(36): Show |
39 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1187-1490G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288741 | |||||||
| chr19:3288754 | G | A | 3 | a0001c0002t0002g0041 a0001c0002t0002g0136 a0001c0003t0002g0248 |
3 | HG02970.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1187-1477G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3288754 | |||||||
| chr19:3289075 | T | C | 3 | a0001c0004t0004g0210 a0001c0004t0004g0227 a0001c0006t0004g0137 |
3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1187-1156T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289075 | |||||||
| chr19:3289083 | G | T | 15 | a0001c0001t0004g0008 a0001c0003t0001g0059 a0001c0003t0002g0232 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1187-1148G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289083 | |||||||
| chr19:3289197 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0101 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1187-1034T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289197 | |||||||
| chr19:3289276 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1187-955C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289276 | |||||||
| chr19:3289280 | A | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0130 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1187-951A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289280 | |||||||
| chr19:3289376 | C | T | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1187-855C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289376 | |||||||
| chr19:3289401 | G | A | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1187-830G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289401 | |||||||
| chr19:3289596 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1187-635T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289596 | |||||||
| chr19:3289668 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1187-563C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289668 | |||||||
| chr19:3289681 | C | CA | 36 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0117 others(33): Show |
36 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1187-516dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAA | 17 | a0001c0001t0001g0171 a0001c0001t0001g0215 a0001c0001t0001g0230 others(14): Show |
17 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1187-517_1187-516d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAA | 21 | a0001c0001t0001g0132 a0001c0001t0002g0211 a0001c0001t0002g0216 others(18): Show |
21 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1187-518_1187-516d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAA | 8 | a0001c0001t0004g0102 a0001c0001t0004g0195 a0001c0001t0005g0087 others(5): Show |
8 | HG01070.hp1 HG01074.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187-519_1187-516d others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAAA | 10 | a0001c0001t0004g0074 a0001c0001t0004g0081 a0001c0001t0004g0109 others(7): Show |
10 | HG00099.hp1 HG00597.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187-520_1187-516d others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAAAA | 9 | a0001c0001t0001g0146 a0001c0001t0004g0072 a0001c0001t0004g0129 others(6): Show |
9 | HG01261.hp2 HG01358.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187-521_1187-516d others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1187-527_1187-516d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1187-530_1187-516d others(17): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | C | CAAAAAAA others(11): Show |
1 | a0001c0004t0004g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1187-533_1187-516d others(20): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | CA | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0024 others(57): Show |
60 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1187-516delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | CAA | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0217 others(5): Show |
8 | HG01074.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187-517_1187-516d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0204 a0001c0006t0004g0137 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1187-525_1187-516d others(12): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0170 a0001c0001t0005g0188 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1187-527_1187-516d others(14): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289681 | CAAAAAAA others(10): Show |
C | 15 | a0001c0001t0004g0008 a0001c0003t0001g0059 a0001c0003t0002g0232 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1187-532_1187-516d others(19): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 3289681 | ||||||
| chr19:3289698 | A | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0183 |
2 | HG01934.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1187-533A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289698 | |||||||
| chr19:3289702 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1187-529A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289702 | |||||||
| chr19:3289720 | C | T | 59 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0142 others(56): Show |
59 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1187-511C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289720 | |||||||
| chr19:3289769 | G | C | 1 | a0001c0001t0006g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1187-462G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289769 | |||||||
| chr19:3289986 | C | G | 34 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1187-245C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3289986 | |||||||
| chr19:3290103 | G | T | 1 | a0001c0003t0004g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1187-128G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 10/12 | chr19 | 3290103 | |||||||
| chr19:3290543 | G | C | 1 | a0001c0010t0005g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1330+169G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290543 | |||||||
| chr19:3290563 | C | CT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0120 others(7): Show |
10 | HG01358.hp1 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1330+207dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3290563 | ||||||
| chr19:3290563 | CT | C | 6 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0247 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1330+207delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3290563 | ||||||
| chr19:3290563 | CTT | C | 77 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0142 others(74): Show |
77 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1330+206_1330+207d others(4): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3290563 | ||||||
| chr19:3290563 | CTTT | C | 64 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(61): Show |
64 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1330+205_1330+207d others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3290563 | ||||||
| chr19:3290595 | G | T | 1 | a0001c0001t0006g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1330+221G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290595 | |||||||
| chr19:3290613 | G | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0004g0155 |
3 | HG02735.hp2 HG03927.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1330+239G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290613 | |||||||
| chr19:3290624 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1330+250T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290624 | |||||||
| chr19:3290657 | G | A | 43 | a0001c0001t0001g0146 a0001c0001t0004g0010 a0001c0001t0004g0072 others(40): Show |
43 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1330+283G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290657 | |||||||
| chr19:3290701 | C | A | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1330+327C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290701 | |||||||
| chr19:3290730 | AT | A | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1330+372delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3290730 | ||||||
| chr19:3290769 | T | C | 1 | a0001c0001t0004g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1330+395T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290769 | |||||||
| chr19:3290818 | G | A | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1330+444G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290818 | |||||||
| chr19:3290846 | A | G | 91 | a0001c0001t0001g0119 a0001c0001t0001g0146 a0001c0001t0001g0150 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1330+472A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290846 | |||||||
| chr19:3290934 | T | C | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1330+560T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290934 | |||||||
| chr19:3290960 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1330+586A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3290960 | |||||||
| chr19:3291106 | C | CA | 43 | a0001c0001t0001g0146 a0001c0001t0002g0213 a0001c0001t0004g0010 others(40): Show |
43 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1330+742dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291106 | ||||||
| chr19:3291231 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1330+857A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291231 | |||||||
| chr19:3291236 | A | C | 1 | a0001c0001t0005g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1330+862A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291236 | |||||||
| chr19:3291319 | C | A | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1330+945C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291319 | |||||||
| chr19:3291571 | C | CA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0063 others(5): Show |
8 | HG01261.hp2 HG02165.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1330+1215dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291571 | ||||||
| chr19:3291571 | C | CAA | 65 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1330+1214_1330+121 others(6): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291571 | ||||||
| chr19:3291571 | C | CAAA | 7 | a0001c0001t0002g0011 a0001c0001t0005g0249 a0001c0001t0006g0091 others(4): Show |
7 | HG02055.hp1 HG02071.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330+1213_1330+121 others(7): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291571 | ||||||
| chr19:3291571 | C | CAAAA | 14 | a0001c0001t0004g0008 a0001c0002t0001g0026 a0001c0003t0001g0059 others(11): Show |
14 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1330+1212_1330+121 others(8): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291571 | ||||||
| chr19:3291620 | A | G | 85 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1330+1246A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291620 | |||||||
| chr19:3291688 | G | C | 87 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0002 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1330+1314G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291688 | |||||||
| chr19:3291688 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1330+1314G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3291688 | |||||||
| chr19:3291932 | CT | C | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1331-1378delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291932 | ||||||
| chr19:3291947 | GT | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-1366delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3291947 | ||||||
| chr19:3292010 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1331-1309G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292010 | |||||||
| chr19:3292023 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1331-1296C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292023 | |||||||
| chr19:3292039 | T | C | 149 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0142 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1331-1280T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292039 | |||||||
| chr19:3292231 | A | G | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1331-1088A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292231 | |||||||
| chr19:3292303 | G | GT | 8 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0001c0001t0001g0132 others(5): Show |
8 | HG02004.hp1 HG02148.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1331-999dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3292303 | ||||||
| chr19:3292303 | GT | G | 84 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1331-999delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 3292303 | ||||||
| chr19:3292316 | T | G | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1331-1003T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292316 | |||||||
| chr19:3292472 | C | T | 1 | a0001c0002t0001g0013 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1331-847C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292472 | |||||||
| chr19:3292473 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1331-846G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292473 | |||||||
| chr19:3292550 | C | G | 1 | a0001c0001t0002g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1331-769C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292550 | |||||||
| chr19:3292601 | T | C | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1331-718T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292601 | |||||||
| chr19:3292814 | T | A | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1331-505T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292814 | |||||||
| chr19:3292845 | G | C | 1 | a0001c0001t0002g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1331-474G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292845 | |||||||
| chr19:3292987 | G | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-332G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3292987 | |||||||
| chr19:3293117 | A | G | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1331-202A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3293117 | |||||||
| chr19:3293151 | A | G | 1 | a0001c0004t0004g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1331-168A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3293151 | |||||||
| chr19:3293178 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1331-141C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3293178 | |||||||
| chr19:3293179 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1331-140A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3293179 | |||||||
| chr19:3293232 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1331-87G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 11/12 | chr19 | 3293232 | |||||||
| chr19:3293513 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*40+27G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293513 | |||||||
| chr19:3293562 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*40+76G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293562 | |||||||
| chr19:3293595 | A | G | 148 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0142 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.*40+109A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293595 | |||||||
| chr19:3293628 | C | T | 3 | a0001c0001t0002g0002 a0001c0002t0002g0136 a0001c0003t0002g0248 |
3 | HG02809.hp1 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.*40+142C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293628 | |||||||
| chr19:3293844 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*40+358C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293844 | |||||||
| chr19:3293847 | A | G | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.*40+361A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3293847 | |||||||
| chr19:3294080 | A | G | 19 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(16): Show |
19 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.*40+594A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294080 | |||||||
| chr19:3294281 | A | C | 89 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.*40+795A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294281 | |||||||
| chr19:3294313 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.*40+827G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294313 | |||||||
| chr19:3294322 | G | A | 88 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.*40+836G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294322 | |||||||
| chr19:3294361 | C | T | 19 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(16): Show |
19 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.*40+875C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294361 | |||||||
| chr19:3294400 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.*40+914C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294400 | |||||||
| chr19:3294407 | AT | A | 89 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0166 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.*40+935delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3294407 | ||||||
| chr19:3294528 | A | G | 2 | a0001c0001t0003g0185 a0001c0001t0003g0258 |
2 | HG00609.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.*40+1042A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294528 | |||||||
| chr19:3294529 | C | G | 16 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(13): Show |
16 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.*40+1043C>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3294529 | |||||||
| chr19:3295053 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.*40+1567C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295053 | |||||||
| chr19:3295113 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.*40+1627A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295113 | |||||||
| chr19:3295225 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.*41-1533C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295225 | |||||||
| chr19:3295270 | GC | G | 85 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.*41-1481delC | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3295270 | ||||||
| chr19:3295272 | C | A | 7 | a0001c0001t0002g0147 a0001c0001t0002g0177 a0001c0001t0002g0198 others(4): Show |
7 | HG00735.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.*41-1486C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295272 | |||||||
| chr19:3295416 | A | G | 1 | a0001c0001t0008g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.*41-1342A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295416 | |||||||
| chr19:3295430 | T | C | 19 | a0001c0001t0002g0002 a0001c0001t0004g0008 a0001c0002t0001g0026 others(16): Show |
19 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.*41-1328T>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295430 | |||||||
| chr19:3295526 | T | A | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.*41-1232T>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295526 | |||||||
| chr19:3295527 | A | T | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.*41-1231A>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295527 | |||||||
| chr19:3295528 | C | A | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.*41-1230C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295528 | |||||||
| chr19:3295644 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0110 |
3 | NA18944.hp2 NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.*41-1114G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295644 | |||||||
| chr19:3295843 | A | AG | 76 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0165 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.*41-906dupG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3295843 | ||||||
| chr19:3295843 | A | AGG | 15 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0168 others(12): Show |
15 | HG00597.hp1 HG00597.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.*41-907_*41-906dup others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3295843 | ||||||
| chr19:3295843 | A | G | 1 | a0001c0003t0002g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*41-915A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295843 | |||||||
| chr19:3295845 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.*41-913G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295845 | |||||||
| chr19:3295846 | G | C | 2 | a0001c0001t0003g0112 a0001c0001t0003g0162 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*41-912G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3295846 | |||||||
| chr19:3296058 | A | AT | 61 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0206 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.*41-687dupT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296058 | ||||||
| chr19:3296058 | AT | A | 61 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0157 others(58): Show |
61 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.*41-687delT | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296058 | ||||||
| chr19:3296058 | ATT | A | 12 | a0001c0001t0002g0130 a0001c0001t0004g0008 a0001c0003t0001g0059 others(9): Show |
12 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.*41-688_*41-687del others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296058 | ||||||
| chr19:3296117 | TG | T | 18 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0002g0011 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.*41-635delG | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296117 | ||||||
| chr19:3296118 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0110 |
2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.*41-640G>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296118 | |||||||
| chr19:3296164 | AGTGGG | A | 15 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0004g0008 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.*41-580_*41-576del others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296164 | ||||||
| chr19:3296181 | T | G | 15 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0004g0008 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.*41-577T>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296181 | |||||||
| chr19:3296263 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*41-495C>T | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296263 | |||||||
| chr19:3296336 | G | GA | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
137 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.*41-403dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296336 | ||||||
| chr19:3296336 | G | GAA | 6 | a0001c0001t0001g0115 a0001c0001t0001g0215 a0001c0001t0002g0002 others(3): Show |
6 | HG01175.hp2 HG01928.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*41-404_*41-403dup others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296336 | ||||||
| chr19:3296336 | GA | G | 60 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0168 others(57): Show |
60 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.*41-403delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296336 | ||||||
| chr19:3296336 | GAA | G | 5 | a0001c0001t0004g0153 a0001c0001t0004g0180 a0001c0001t0004g0195 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.*41-404_*41-403del others(2): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296336 | ||||||
| chr19:3296351 | A | C | 1 | a0001c0003t0005g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*41-407A>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296351 | |||||||
| chr19:3296356 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0223 |
2 | HG03688.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.*41-402C>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296356 | |||||||
| chr19:3296408 | G | C | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*41-350G>C | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296408 | |||||||
| chr19:3296434 | G | GA | 28 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0084 others(25): Show |
28 | HG01106.hp1 HG01123.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.*41-302dupA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296434 | ||||||
| chr19:3296434 | GA | G | 79 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0142 others(76): Show |
79 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.*41-302delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296434 | ||||||
| chr19:3296434 | GAAAAA | G | 5 | a0001c0003t0004g0128 a0001c0003t0004g0220 a0001c0003t0004g0237 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.*41-306_*41-302del others(5): Show |
CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296434 | ||||||
| chr19:3296452 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0197 a0001c0001t0001g0245 others(1): Show |
4 | HG00597.hp1 HG00738.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.*41-306A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296452 | |||||||
| chr19:3296458 | A | G | 2 | a0001c0003t0005g0151 a0001c0010t0005g0252 |
2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*41-300A>G | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296458 | |||||||
| chr19:3296486 | GA | G | 71 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0166 others(68): Show |
71 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.*41-261delA | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 3296486 | ||||||
| chr19:3296684 | G | A | 2 | a0001c0003t0004g0131 a0001c0003t0004g0134 |
2 | HG01106.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.*41-74G>A | CELF5 | ENSG00000161082.13 | transcript | ENST00000292672.7 | protein_coding | 12/12 | chr19 | 3296684 |