Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8549 |
| ensemblid | ENSG00000139292.13 |
| hgncid | 4504 |
| symbol | LGR5 |
| name | leucine rich repeat containing G protein-coupled receptor 5 |
| refseq_nuc | NM_003667.4 |
| refseq_prot | NP_003658.1 |
| ensembl_nuc | ENST00000266674.10 |
| ensembl_prot | ENSP00000266674.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71439798 |
| end | 71586310 |
| strand | + |
| ver | v1.2 |
| region | chr12:71439798-71586310 |
| region5000 | chr12:71434798-71591310 |
| regionname0 | LGR5_chr12_71439798_71586310 |
| regionname5000 | LGR5_chr12_71434798_71591310 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 907 | 174 | 36 | 40 | 67 | 10 | 19 | 51 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0002 | 0/0 | 907 | 13 | 8 | 2 | 2 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0003 | 0/0 | 907 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0004 | 0/0 | 907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0005 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0006 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0007 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0008 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0009 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0010 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0011 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0012 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| a0013 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | MDTSR others(902): Show |
chr12 | 71434798 | 71591310 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2721 | 153 | 24 | 37 | 65 | 9 | 17 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0001c0002 | 1/0 | 2721 | 18 | 11 | 2 | 1 | 1 | 2 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0001c0006 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0001c0009 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0001c0016 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0002c0003 | 0/0 | 2721 | 13 | 8 | 2 | 2 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0003c0004 | 0/0 | 2721 | 2 | 0 | 0 | 2 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0004c0005 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0005c0007 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0006c0011 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0007c0015 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0008c0014 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0009c0017 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0010c0012 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0011c0008 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0012c0010 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 | ||
| a0013c0013 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | ATGGA others(2716): Show |
chr12 | 71434798 | 71591310 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4583 | 47 | 7 | 11 | 16 | 3 | 9 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0002 | 0/0 | 4583 | 44 | 2 | 16 | 19 | 2 | 5 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0003 | 0/0 | 4583 | 36 | 0 | 7 | 23 | 4 | 2 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0004 | 0/0 | 4583 | 13 | 5 | 2 | 5 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0006 | 0/0 | 4583 | 4 | 4 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0007 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0008 | 0/0 | 4583 | 3 | 2 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0009 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0014 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0016 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0017 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0001t0020 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0001 | 0/0 | 4583 | 7 | 5 | 1 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0002 | 1/0 | 4583 | 3 | 0 | 0 | 1 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0007 | 0/0 | 4583 | 2 | 1 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0009 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0010 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0012 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0002t0021 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0006t0003 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0009t0009 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0001c0016t0015 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0002c0003t0001 | 0/0 | 4583 | 2 | 0 | 2 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0002c0003t0002 | 0/0 | 4583 | 3 | 0 | 0 | 2 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0002c0003t0005 | 0/0 | 4583 | 7 | 7 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0002c0003t0013 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0003c0004t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0003c0004t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0004c0005t0011 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0004c0005t0019 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0005c0007t0006 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0006c0011t0003 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0007c0015t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0008c0014t0011 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0009c0017t0018 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0010c0012t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0011c0008t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0012c0010t0003 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| a0013c0013t0004 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | GCTCC others(4578): Show |
chr12 | 71434798 | 71591310 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0001t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0002g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0002t0021g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0006t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0009t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0001c0016t0015g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0002c0003t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0003c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0003c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0004c0005t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0004c0005t0019g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0005c0007t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0006c0011t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0007c0015t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0008c0014t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0009c0017t0018g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0010c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0011c0008t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0012c0010t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| a0013c0013t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0090 | EUR | GBR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | GBR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | FIN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | FIN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0125 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0020 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0186 | AMR | PUR | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01361 | hp1 | a0005 | c0007 | t0006 | g0190 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01496 | hp2 | a0001 | c0016 | t0015 | g0056 | AMR | CLM | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0154 | EUR | IBS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01884 | hp2 | a0002 | c0003 | t0005 | g0194 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01943 | hp1 | a0006 | c0011 | t0003 | g0104 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02055 | hp2 | a0002 | c0003 | t0005 | g0175 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02080 | hp1 | a0003 | c0004 | t0002 | g0113 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02132 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0086 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0083 | EAS | KHV | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0018 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02165 | hp2 | a0001 | c0006 | t0003 | g0115 | EAS | CDX | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02257 | hp2 | a0002 | c0003 | t0005 | g0100 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02258 | hp2 | a0002 | c0003 | t0005 | g0032 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02280 | hp2 | a0001 | c0002 | t0010 | g0184 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02622 | hp1 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02630 | hp1 | a0002 | c0003 | t0005 | g0033 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02698 | hp1 | a0001 | c0002 | t0021 | g0132 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02723 | hp1 | a0008 | c0014 | t0011 | g0200 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0191 | AFR | GWD | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02965 | hp2 | a0001 | c0009 | t0009 | g0009 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02970 | hp2 | a0009 | c0017 | t0018 | g0004 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03098 | hp2 | a0002 | c0003 | t0005 | g0165 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03130 | hp2 | a0002 | c0003 | t0013 | g0010 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03139 | hp1 | a0004 | c0005 | t0011 | g0199 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0188 | AFR | ESN | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03225 | hp1 | a0001 | c0002 | t0010 | g0182 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0134 | SAS | BEB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | STU | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | STU | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | CHB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | YRI | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | YRI | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18965 | hp2 | a0001 | c0001 | t0014 | g0054 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18981 | hp2 | a0010 | c0012 | t0001 | g0040 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18987 | hp1 | a0011 | c0008 | t0002 | g0080 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0097 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19090 | hp1 | a0012 | c0010 | t0003 | g0121 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ASW | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20129 | hp2 | a0001 | c0001 | t0016 | g0071 | AFR | ASW | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20905 | hp1 | a0002 | c0003 | t0002 | g0093 | SAS | GIH | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02486 | hp1 | a0004 | c0005 | t0019 | g0181 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02486 | hp2 | a0001 | c0002 | t0012 | g0006 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| HG02559 | hp2 | a0007 | c0015 | t0001 | g0031 | AFR | ACB | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20300 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | USA | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | USA | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA21309 | hp1 | a0013 | c0013 | t0004 | g0157 | AFR | LWK | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| NA21309 | hp2 | a0002 | c0003 | t0005 | g0195 | AFR | LWK | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0118 | REF | REF | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0081 | REF | REF | LGR5_chr12_71434798_71591310 | LGR5 | chr12 | 71434798 | 71591310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71440190 | A | C | 1 | a0009 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.110A>C | p.His37Pro | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 393/4583 | 110/2724 | 37/907 | chr12 | 71440190 | |||
| chr12:71553284 | G | A | 1 | a0005 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.640G>A | p.Val214Ile | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/18 | 923/4583 | 640/2724 | 214/907 | chr12 | 71553284 | |||
| chr12:71566878 | A | C | 1 | a0013 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1036A>C | p.Thr346Pro | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/18 | 1319/4583 | 1036/2724 | 346/907 | chr12 | 71566878 | |||
| chr12:71566906 | A | G | 1 | a0003 | 2 | HG02080.hp1 HG02132.hp1 |
missense_variant | MODERATE | c.1064A>G | p.Gln355Arg | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/18 | 1347/4583 | 1064/2724 | 355/907 | chr12 | 71566906 | |||
| chr12:71578904 | T | C | 1 | a0004 | 2 | HG02486.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1381T>C | p.Ser461Pro | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/18 | 1664/4583 | 1381/2724 | 461/907 | chr12 | 71578904 | |||
| chr12:71580283 | T | C | 1 | a0011 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.1412T>C | p.Ile471Thr | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/18 | 1695/4583 | 1412/2724 | 471/907 | chr12 | 71580283 | |||
| chr12:71580315 | T | C | 2 | a0004 a0008 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1444T>C | p.Phe482Leu | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/18 | 1727/4583 | 1444/2724 | 482/907 | chr12 | 71580315 | |||
| chr12:71584007 | T | C | 2 | a0002 a0009 |
14 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(11): Show |
missense_variant | MODERATE | c.1997T>C | p.Val666Ala | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2280/4583 | 1997/2724 | 666/907 | chr12 | 71584007 | |||
| chr12:71584265 | A | G | 1 | a0010 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.2255A>G | p.Asp752Gly | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2538/4583 | 2255/2724 | 752/907 | chr12 | 71584265 | |||
| chr12:71584481 | A | G | 1 | a0006 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.2471A>G | p.Asn824Ser | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2754/4583 | 2471/2724 | 824/907 | chr12 | 71584481 | |||
| chr12:71584528 | G | A | 1 | a0012 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.2518G>A | p.Val840Ile | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2801/4583 | 2518/2724 | 840/907 | chr12 | 71584528 | |||
| chr12:71584663 | G | A | 1 | a0007 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.2653G>A | p.Val885Met | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2936/4583 | 2653/2724 | 885/907 | chr12 | 71584663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71440167 | G | A | 1 | a0001c0006 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.87G>A | p.Val29Val | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 370/4583 | 87/2724 | 29/907 | chr12 | 71440167 | |||
| chr12:71566428 | G | A | 11 | a0001c0001 a0001c0006 a0001c0009 others(8): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
synonymous_variant | LOW | c.882G>A | p.Gln294Gln | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 9/18 | 1165/4583 | 882/2724 | 294/907 | chr12 | 71566428 | |||
| chr12:71578813 | G | T | 1 | a0001c0016 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1290G>T | p.Ser430Ser | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/18 | 1573/4583 | 1290/2724 | 430/907 | chr12 | 71578813 | |||
| chr12:71584395 | T | C | 2 | a0004c0005 a0008c0014 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.2385T>C | p.Phe795Phe | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2668/4583 | 2385/2724 | 795/907 | chr12 | 71584395 | |||
| chr12:71584458 | T | C | 1 | a0001c0009 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2448T>C | p.Asn816Asn | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 2731/4583 | 2448/2724 | 816/907 | chr12 | 71584458 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71439893 | G | A | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0002t0007 others(1): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 188 | chr12 | 71439893 | ||||||
| chr12:71439901 | T | A | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(25): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-180T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 180 | chr12 | 71439901 | ||||||
| chr12:71439905 | C | T | 2 | a0001c0002t0010 a0004c0005t0019 |
4 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-176C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 176 | chr12 | 71439905 | ||||||
| chr12:71439921 | T | C | 1 | a0001c0001t0020 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-160T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 160 | chr12 | 71439921 | ||||||
| chr12:71439932 | G | A | 6 | a0001c0001t0008 a0001c0001t0009 a0001c0002t0009 others(3): Show |
8 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 149 | chr12 | 71439932 | ||||||
| chr12:71440002 | G | A | 1 | a0001c0001t0014 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | 79 | chr12 | 71440002 | ||||||
| chr12:71440043 | C | T | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0002t0007 others(1): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/18 | chr12 | 71440043 | |||||||
| chr12:71584836 | G | C | 1 | a0001c0002t0012 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 102 | chr12 | 71584836 | ||||||
| chr12:71584948 | G | A | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(7): Show |
62 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 214 | chr12 | 71584948 | ||||||
| chr12:71585132 | T | C | 1 | a0001c0016t0015 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 398 | chr12 | 71585132 | ||||||
| chr12:71585426 | A | G | 4 | a0004c0005t0011 a0004c0005t0019 a0008c0014t0011 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*692A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 692 | chr12 | 71585426 | ||||||
| chr12:71585554 | A | T | 1 | a0001c0001t0017 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 820 | chr12 | 71585554 | ||||||
| chr12:71585766 | G | A | 6 | a0002c0003t0005 a0002c0003t0013 a0004c0005t0011 others(3): Show |
12 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1032 | chr12 | 71585766 | ||||||
| chr12:71586062 | A | G | 1 | a0001c0001t0016 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1328 | chr12 | 71586062 | ||||||
| chr12:71586142 | C | T | 1 | a0009c0017t0018 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1408 | chr12 | 71586142 | ||||||
| chr12:71586211 | T | C | 3 | a0004c0005t0011 a0004c0005t0019 a0008c0014t0011 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1477T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1477 | chr12 | 71586211 | ||||||
| chr12:71586214 | A | T | 1 | a0001c0002t0021 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1480A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1480 | chr12 | 71586214 | ||||||
| chr12:71586243 | A | G | 3 | a0004c0005t0011 a0004c0005t0019 a0008c0014t0011 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1509A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 18/18 | 1509 | chr12 | 71586243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71440505 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(18): Show |
21 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.212+213T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71440505 | |||||||
| chr12:71440945 | C | T | 7 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(4): Show |
7 | HG01069.hp2 HG01884.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.212+653C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71440945 | |||||||
| chr12:71440984 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.212+692G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71440984 | |||||||
| chr12:71441277 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+985C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441277 | |||||||
| chr12:71441294 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.212+1002C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441294 | |||||||
| chr12:71441467 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.212+1175C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441467 | |||||||
| chr12:71441551 | C | T | 4 | a0001c0002t0010g0182 a0001c0002t0010g0183 a0001c0002t0010g0184 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+1259C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441551 | |||||||
| chr12:71441581 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212+1289T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441581 | |||||||
| chr12:71441608 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.212+1316A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441608 | |||||||
| chr12:71441760 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.212+1468G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441760 | |||||||
| chr12:71441769 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG01175.hp2 HG01192.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1477C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441769 | |||||||
| chr12:71441841 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.212+1549G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71441841 | |||||||
| chr12:71442115 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.212+1823T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71442115 | |||||||
| chr12:71442331 | A | G | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+2039A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71442331 | |||||||
| chr12:71442446 | T | C | 2 | a0001c0001t0003g0025 a0001c0001t0003g0026 |
2 | HG01361.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.212+2154T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71442446 | |||||||
| chr12:71442700 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.212+2408G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71442700 | |||||||
| chr12:71442854 | A | G | 4 | a0001c0002t0010g0182 a0001c0002t0010g0183 a0001c0002t0010g0184 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+2562A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71442854 | |||||||
| chr12:71443109 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.212+2817A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443109 | |||||||
| chr12:71443127 | TCAAA | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+2838_212+2841d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71443127 | ||||||
| chr12:71443141 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.212+2849G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443141 | |||||||
| chr12:71443146 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+2854C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443146 | |||||||
| chr12:71443160 | A | T | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+2868A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443160 | |||||||
| chr12:71443519 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.212+3227A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443519 | |||||||
| chr12:71443530 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.212+3238G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443530 | |||||||
| chr12:71443539 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.212+3247T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443539 | |||||||
| chr12:71443743 | T | C | 29 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(26): Show |
29 | HG00423.hp2 HG00438.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.212+3451T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443743 | |||||||
| chr12:71443812 | T | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+3520T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443812 | |||||||
| chr12:71443859 | C | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.212+3567C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71443859 | |||||||
| chr12:71443914 | A | AT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.212+3633dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71443914 | ||||||
| chr12:71444007 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0004g0168 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.212+3715T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444007 | |||||||
| chr12:71444197 | A | G | 1 | a0001c0001t0004g0014 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.212+3905A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444197 | |||||||
| chr12:71444213 | T | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+3921T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444213 | |||||||
| chr12:71444588 | C | T | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212+4296C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444588 | |||||||
| chr12:71444617 | A | T | 1 | a0001c0002t0010g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.212+4325A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444617 | |||||||
| chr12:71444900 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+4608T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444900 | |||||||
| chr12:71444932 | C | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG00280.hp2 HG00741.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.212+4640C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71444932 | |||||||
| chr12:71445179 | T | C | 2 | a0001c0016t0015g0056 a0002c0003t0005g0175 |
2 | HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.212+4887T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445179 | |||||||
| chr12:71445212 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.212+4920C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445212 | |||||||
| chr12:71445310 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.212+5018C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445310 | |||||||
| chr12:71445343 | G | A | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.212+5051G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445343 | |||||||
| chr12:71445499 | A | G | 3 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0014g0054 |
3 | HG00423.hp2 NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.212+5207A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445499 | |||||||
| chr12:71445706 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+5414G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445706 | |||||||
| chr12:71445715 | CG | C | 7 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(4): Show |
7 | HG01069.hp2 HG01884.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.212+5424delG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445715 | |||||||
| chr12:71445738 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0017g0018 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.212+5446A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445738 | |||||||
| chr12:71445837 | C | G | 7 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.212+5545C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445837 | |||||||
| chr12:71445921 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.212+5629G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71445921 | |||||||
| chr12:71446139 | T | C | 1 | a0001c0002t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.212+5847T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446139 | |||||||
| chr12:71446169 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.212+5877G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446169 | |||||||
| chr12:71446449 | A | G | 4 | a0001c0002t0010g0182 a0001c0002t0010g0183 a0001c0002t0010g0184 others(1): Show |
4 | HG02280.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+6157A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446449 | |||||||
| chr12:71446478 | C | G | 4 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0004g0007 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+6186C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446478 | |||||||
| chr12:71446478 | C | T | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG01109.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.212+6186C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446478 | |||||||
| chr12:71446509 | A | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+6217A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446509 | |||||||
| chr12:71446976 | G | T | 1 | a0001c0001t0003g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.212+6684G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71446976 | |||||||
| chr12:71447079 | C | G | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+6787C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447079 | |||||||
| chr12:71447084 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.212+6792T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447084 | |||||||
| chr12:71447376 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0002t0012g0006 |
3 | HG01243.hp1 HG01993.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.212+7084T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447376 | |||||||
| chr12:71447479 | A | G | 4 | a0001c0002t0010g0182 a0001c0002t0010g0183 a0001c0002t0010g0184 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+7187A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447479 | |||||||
| chr12:71447583 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(64): Show |
67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.212+7291C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447583 | |||||||
| chr12:71447595 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+7303C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447595 | |||||||
| chr12:71447608 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0004g0173 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.212+7316G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447608 | |||||||
| chr12:71447653 | G | A | 39 | a0001c0001t0001g0030 a0001c0001t0001g0150 a0001c0001t0002g0029 others(36): Show |
39 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.212+7361G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447653 | |||||||
| chr12:71447811 | A | G | 4 | a0001c0002t0010g0182 a0001c0002t0010g0183 a0001c0002t0010g0184 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+7519A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447811 | |||||||
| chr12:71447828 | G | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0009c0017t0018g0004 |
3 | HG01243.hp1 HG01993.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.212+7536G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71447828 | |||||||
| chr12:71448076 | C | T | 2 | a0001c0001t0002g0159 a0001c0001t0003g0160 |
2 | NA18612.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.212+7784C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448076 | |||||||
| chr12:71448084 | A | AAC | 56 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
56 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.212+7820_212+7821d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACAC | 3 | a0002c0003t0013g0010 a0004c0005t0011g0199 a0008c0014t0011g0200 |
3 | HG02723.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.212+7816_212+7821d others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACACA others(7): Show |
1 | a0001c0002t0010g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212+7808_212+7821d others(16): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACACA others(9): Show |
2 | a0001c0002t0010g0183 a0004c0005t0019g0181 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.212+7806_212+7821d others(18): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACACA others(11): Show |
1 | a0001c0002t0010g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.212+7804_212+7821d others(20): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACACA others(13): Show |
1 | a0001c0001t0004g0014 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.212+7802_212+7821d others(22): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | A | AACACACA others(15): Show |
1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.212+7800_212+7821d others(24): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | AAC | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0167 a0001c0001t0001g0169 others(11): Show |
14 | HG00280.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.212+7820_212+7821d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448084 | AACAC | A | 3 | a0001c0001t0004g0173 a0001c0001t0008g0011 a0001c0001t0008g0012 |
3 | HG01109.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.212+7818_212+7821d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448084 | ||||||
| chr12:71448176 | T | C | 3 | a0002c0003t0013g0010 a0004c0005t0011g0199 a0008c0014t0011g0200 |
3 | HG02723.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.212+7884T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448176 | |||||||
| chr12:71448464 | T | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+8172T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448464 | |||||||
| chr12:71448610 | C | G | 5 | a0001c0001t0001g0021 a0001c0001t0002g0023 a0001c0001t0003g0117 others(2): Show |
5 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+8318C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448610 | |||||||
| chr12:71448634 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(147): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.212+8342C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448634 | |||||||
| chr12:71448638 | CT | C | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+8349delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71448638 | ||||||
| chr12:71448649 | T | C | 5 | a0001c0001t0004g0168 a0001c0002t0009g0008 a0002c0003t0005g0032 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+8357T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448649 | |||||||
| chr12:71448657 | A | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+8365A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448657 | |||||||
| chr12:71448823 | G | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.212+8531G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448823 | |||||||
| chr12:71448832 | T | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0009t0009g0009 others(1): Show |
4 | HG01243.hp1 HG01993.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+8540T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448832 | |||||||
| chr12:71448861 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+8569G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448861 | |||||||
| chr12:71448883 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0002g0023 a0001c0001t0003g0117 others(2): Show |
5 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+8591C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71448883 | |||||||
| chr12:71449011 | G | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0167 a0001c0001t0004g0168 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.212+8719G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449011 | |||||||
| chr12:71449031 | C | T | 13 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.212+8739C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449031 | |||||||
| chr12:71449195 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212+8903G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449195 | |||||||
| chr12:71449275 | G | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+8983G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449275 | |||||||
| chr12:71449339 | C | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+9047C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449339 | |||||||
| chr12:71449518 | C | T | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212+9226C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449518 | |||||||
| chr12:71449576 | G | T | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212+9284G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449576 | |||||||
| chr12:71449594 | T | C | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+9302T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449594 | |||||||
| chr12:71449627 | T | C | 7 | a0001c0001t0001g0167 a0001c0001t0007g0191 a0001c0002t0010g0182 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.212+9335T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71449627 | |||||||
| chr12:71450005 | C | G | 2 | a0001c0001t0003g0025 a0002c0003t0002g0093 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.212+9713C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450005 | |||||||
| chr12:71450224 | C | G | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+9932C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450224 | |||||||
| chr12:71450360 | T | C | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+10068T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450360 | |||||||
| chr12:71450792 | G | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212+10500G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450792 | |||||||
| chr12:71450799 | G | A | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+10507G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450799 | |||||||
| chr12:71450886 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+10594A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71450886 | |||||||
| chr12:71451030 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+10738A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451030 | |||||||
| chr12:71451117 | A | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+10825A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451117 | |||||||
| chr12:71451336 | A | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.212+11044A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451336 | |||||||
| chr12:71451646 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.212+11354C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451646 | |||||||
| chr12:71451655 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0028 |
2 | HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.212+11363A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451655 | |||||||
| chr12:71451677 | G | C | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.212+11385G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71451677 | |||||||
| chr12:71452314 | A | C | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+12022A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71452314 | |||||||
| chr12:71452528 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.212+12236A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71452528 | |||||||
| chr12:71452604 | A | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+12312A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71452604 | |||||||
| chr12:71452755 | A | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+12463A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71452755 | |||||||
| chr12:71452798 | C | T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+12506C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71452798 | |||||||
| chr12:71453075 | T | A | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+12783T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453075 | |||||||
| chr12:71453189 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.212+12897C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453189 | |||||||
| chr12:71453230 | C | T | 5 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0091 others(2): Show |
5 | HG00140.hp1 HG00735.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+12938C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453230 | |||||||
| chr12:71453464 | CT | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0167 others(24): Show |
27 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.212+13189delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71453464 | ||||||
| chr12:71453706 | CT | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0167 a0001c0001t0002g0023 others(24): Show |
27 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.212+13426delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71453706 | ||||||
| chr12:71453717 | T | A | 5 | a0001c0001t0004g0168 a0001c0002t0009g0008 a0002c0003t0005g0032 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+13425T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453717 | |||||||
| chr12:71453823 | C | A | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+13531C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453823 | |||||||
| chr12:71453884 | T | G | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+13592T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453884 | |||||||
| chr12:71453893 | G | C | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212+13601G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453893 | |||||||
| chr12:71453947 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
151 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.212+13655C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71453947 | |||||||
| chr12:71454198 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.212+13906G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71454198 | |||||||
| chr12:71454207 | G | GA | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+13921dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71454207 | ||||||
| chr12:71454382 | A | T | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.212+14090A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71454382 | |||||||
| chr12:71454505 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212+14213G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71454505 | |||||||
| chr12:71454776 | A | AAC | 3 | a0001c0001t0001g0022 a0001c0001t0001g0185 a0001c0001t0002g0096 |
3 | HG03831.hp2 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.212+14508_212+1450 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71454776 | ||||||
| chr12:71454776 | A | C | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212+14484A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71454776 | |||||||
| chr12:71454776 | AAC | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(30): Show |
33 | HG00423.hp2 HG01243.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.212+14508_212+1450 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71454776 | ||||||
| chr12:71454776 | AACAC | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+14506_212+1450 others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71454776 | ||||||
| chr12:71454842 | G | GA | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+14560dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71454842 | ||||||
| chr12:71455001 | G | A | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(2): Show |
5 | NA18747.hp2 NA18948.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.212+14709G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455001 | |||||||
| chr12:71455141 | G | A | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+14849G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455141 | |||||||
| chr12:71455215 | C | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+14923C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455215 | |||||||
| chr12:71455486 | T | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+15194T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455486 | |||||||
| chr12:71455496 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(124): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.212+15204T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455496 | |||||||
| chr12:71455764 | C | T | 9 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(6): Show |
9 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+15472C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71455764 | |||||||
| chr12:71455785 | TACTC | T | 2 | a0001c0001t0002g0142 a0001c0001t0003g0141 |
2 | NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.212+15495_212+1549 others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71455785 | ||||||
| chr12:71456187 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0009t0009g0009 |
3 | HG01243.hp1 HG01993.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.212+15895T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456187 | |||||||
| chr12:71456204 | A | C | 1 | a0002c0003t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.212+15912A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456204 | |||||||
| chr12:71456207 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.212+15915C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456207 | |||||||
| chr12:71456265 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+15973A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456265 | |||||||
| chr12:71456485 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.212+16193C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456485 | |||||||
| chr12:71456678 | GAAAAT | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0009t0009g0009 others(1): Show |
4 | HG01243.hp1 HG01993.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+16391_212+1639 others(9): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71456678 | ||||||
| chr12:71456685 | A | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.212+16393A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456685 | |||||||
| chr12:71456868 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212+16576A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456868 | |||||||
| chr12:71456915 | G | A | 1 | a0001c0001t0003g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.212+16623G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71456915 | |||||||
| chr12:71457074 | A | G | 5 | a0001c0001t0004g0168 a0001c0002t0009g0008 a0002c0003t0005g0032 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+16782A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71457074 | |||||||
| chr12:71457178 | A | G | 1 | a0001c0001t0006g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.212+16886A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71457178 | |||||||
| chr12:71457313 | A | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.212+17021A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71457313 | |||||||
| chr12:71457483 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.212+17191G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71457483 | |||||||
| chr12:71458013 | G | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212+17721G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458013 | |||||||
| chr12:71458246 | C | G | 9 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(6): Show |
9 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+17954C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458246 | |||||||
| chr12:71458290 | T | C | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212+17998T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458290 | |||||||
| chr12:71458392 | A | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(119): Show |
122 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.212+18100A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458392 | |||||||
| chr12:71458437 | A | G | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212+18145A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458437 | |||||||
| chr12:71458670 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212+18378T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458670 | |||||||
| chr12:71458702 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.212+18410C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458702 | |||||||
| chr12:71458734 | ATT | A | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0059 others(34): Show |
37 | HG00423.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.212+18446_212+1844 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71458734 | ||||||
| chr12:71458808 | T | C | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.212+18516T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458808 | |||||||
| chr12:71458931 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.212+18639C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71458931 | |||||||
| chr12:71459077 | A | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0014 |
2 | HG01243.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.212+18785A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459077 | |||||||
| chr12:71459104 | T | C | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+18812T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459104 | |||||||
| chr12:71459221 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.212+18929T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459221 | |||||||
| chr12:71459387 | T | C | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+19095T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459387 | |||||||
| chr12:71459622 | A | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0004g0052 others(2): Show |
5 | HG00423.hp2 NA18959.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.212+19330A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459622 | |||||||
| chr12:71459932 | T | G | 13 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.212+19640T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71459932 | |||||||
| chr12:71460258 | G | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+19966G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460258 | |||||||
| chr12:71460259 | A | C | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.212+19967A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460259 | |||||||
| chr12:71460509 | A | T | 2 | a0001c0001t0004g0053 a0001c0001t0014g0054 |
2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.212+20217A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460509 | |||||||
| chr12:71460562 | C | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+20270C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460562 | |||||||
| chr12:71460725 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212+20433T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460725 | |||||||
| chr12:71460734 | A | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+20442A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460734 | |||||||
| chr12:71460983 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+20691C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71460983 | |||||||
| chr12:71461103 | G | T | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.212+20811G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461103 | |||||||
| chr12:71461230 | A | G | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212+20938A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461230 | |||||||
| chr12:71461411 | C | T | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212+21119C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461411 | |||||||
| chr12:71461585 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.212+21293A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461585 | |||||||
| chr12:71461646 | T | G | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+21354T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461646 | |||||||
| chr12:71461707 | A | G | 13 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.212+21415A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461707 | |||||||
| chr12:71461741 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.212+21449C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461741 | |||||||
| chr12:71461801 | C | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+21509C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461801 | |||||||
| chr12:71461861 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.212+21569G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461861 | |||||||
| chr12:71461946 | T | A | 5 | a0001c0001t0004g0168 a0001c0002t0009g0008 a0002c0003t0005g0032 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+21654T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461946 | |||||||
| chr12:71461966 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.212+21674A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71461966 | |||||||
| chr12:71462007 | T | G | 2 | a0001c0001t0002g0142 a0001c0001t0003g0141 |
2 | NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.212+21715T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462007 | |||||||
| chr12:71462127 | G | C | 13 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.212+21835G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462127 | |||||||
| chr12:71462226 | A | G | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212+21934A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462226 | |||||||
| chr12:71462317 | T | C | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+22025T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462317 | |||||||
| chr12:71462335 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+22043A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462335 | |||||||
| chr12:71462403 | C | T | 1 | a0002c0003t0005g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.212+22111C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462403 | |||||||
| chr12:71462409 | T | A | 12 | a0001c0001t0001g0167 a0001c0001t0004g0168 a0001c0001t0007g0191 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+22117T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462409 | |||||||
| chr12:71462706 | C | T | 1 | a0002c0003t0005g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212+22414C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71462706 | |||||||
| chr12:71463014 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+22722T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463014 | |||||||
| chr12:71463129 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.212+22837C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463129 | |||||||
| chr12:71463395 | A | T | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212+23103A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463395 | |||||||
| chr12:71463498 | CA | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+23207delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463498 | |||||||
| chr12:71463674 | G | A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.212+23382G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463674 | |||||||
| chr12:71463709 | G | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+23417G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71463709 | |||||||
| chr12:71464147 | T | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.212+23855T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464147 | |||||||
| chr12:71464295 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.212+24003T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464295 | |||||||
| chr12:71464386 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+24094A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464386 | |||||||
| chr12:71464457 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+24165A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464457 | |||||||
| chr12:71464656 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.212+24364G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464656 | |||||||
| chr12:71464671 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0001t0006g0187 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.212+24379G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464671 | |||||||
| chr12:71464690 | C | G | 13 | a0001c0001t0004g0007 a0001c0001t0004g0014 a0001c0001t0004g0173 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.212+24398C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464690 | |||||||
| chr12:71464803 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212+24511A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464803 | |||||||
| chr12:71464921 | G | A | 1 | a0002c0003t0001g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.212+24629G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71464921 | |||||||
| chr12:71465079 | C | A | 1 | a0001c0001t0003g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.212+24787C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465079 | |||||||
| chr12:71465360 | T | A | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.212+25068T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465360 | |||||||
| chr12:71465469 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(98): Show |
101 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.212+25177G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465469 | |||||||
| chr12:71465548 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.212+25256A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465548 | |||||||
| chr12:71465679 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.212+25387C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465679 | |||||||
| chr12:71465758 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212+25466G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465758 | |||||||
| chr12:71465772 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+25480T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465772 | |||||||
| chr12:71465940 | C | T | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+25648C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71465940 | |||||||
| chr12:71466114 | C | T | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212+25822C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466114 | |||||||
| chr12:71466350 | T | C | 33 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0059 others(30): Show |
33 | HG00423.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.212+26058T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466350 | |||||||
| chr12:71466523 | A | G | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+26231A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466523 | |||||||
| chr12:71466587 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.212+26295C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466587 | |||||||
| chr12:71466603 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.212+26311C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466603 | |||||||
| chr12:71466651 | AT | A | 6 | a0001c0001t0001g0021 a0001c0001t0002g0023 a0001c0001t0003g0117 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+26360delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466651 | |||||||
| chr12:71466654 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0002g0023 a0001c0001t0003g0117 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+26362A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466654 | |||||||
| chr12:71466672 | G | GGT | 10 | a0001c0001t0001g0059 a0001c0001t0006g0187 a0001c0001t0006g0189 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+26380_212+2638 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466672 | |||||||
| chr12:71466672 | GT | G | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(13): Show |
16 | HG00423.hp1 HG00423.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.212+26391delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71466672 | ||||||
| chr12:71466673 | T | G | 17 | a0001c0001t0001g0167 a0001c0001t0004g0007 a0001c0001t0004g0014 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.212+26381T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466673 | |||||||
| chr12:71466674 | T | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+26382T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466674 | |||||||
| chr12:71466734 | A | G | 1 | a0002c0003t0005g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.212+26442A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466734 | |||||||
| chr12:71466738 | G | T | 23 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(20): Show |
23 | HG00423.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.212+26446G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466738 | |||||||
| chr12:71466810 | A | C | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+26518A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466810 | |||||||
| chr12:71466977 | G | A | 1 | a0001c0001t0020g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.212+26685G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71466977 | |||||||
| chr12:71467008 | G | GT | 11 | a0001c0001t0001g0059 a0001c0001t0002g0096 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+26728dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71467008 | ||||||
| chr12:71467008 | GT | G | 19 | a0001c0001t0001g0167 a0001c0001t0004g0007 a0001c0001t0004g0014 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.212+26728delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71467008 | ||||||
| chr12:71467218 | G | A | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+26926G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467218 | |||||||
| chr12:71467228 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+26936C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467228 | |||||||
| chr12:71467300 | C | T | 33 | a0001c0001t0001g0150 a0001c0001t0002g0029 a0001c0001t0002g0058 others(30): Show |
33 | HG00438.hp1 HG00735.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.212+27008C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467300 | |||||||
| chr12:71467322 | T | C | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+27030T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467322 | |||||||
| chr12:71467400 | G | A | 5 | a0001c0001t0004g0168 a0001c0002t0009g0008 a0002c0003t0005g0032 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+27108G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467400 | |||||||
| chr12:71467406 | T | C | 23 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(20): Show |
23 | HG00423.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.212+27114T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467406 | |||||||
| chr12:71467448 | C | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212+27156C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467448 | |||||||
| chr12:71467644 | T | A | 1 | a0001c0001t0003g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.212+27352T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467644 | |||||||
| chr12:71467967 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.212+27675A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71467967 | |||||||
| chr12:71468209 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.212+27917G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71468209 | |||||||
| chr12:71468302 | T | C | 11 | a0001c0001t0001g0059 a0001c0001t0004g0173 a0001c0001t0006g0187 others(8): Show |
11 | HG01243.hp2 HG01361.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+28010T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71468302 | |||||||
| chr12:71468359 | C | CA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.212+28074dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71468359 | ||||||
| chr12:71468405 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.212+28113G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71468405 | |||||||
| chr12:71468469 | A | G | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212+28177A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71468469 | |||||||
| chr12:71468709 | C | CT | 10 | a0001c0001t0001g0124 a0001c0001t0002g0130 a0001c0001t0004g0034 others(7): Show |
10 | HG00423.hp1 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.212+28441dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71468709 | ||||||
| chr12:71468709 | CT | C | 22 | a0001c0001t0001g0049 a0001c0001t0001g0123 a0001c0001t0001g0131 others(19): Show |
22 | HG00423.hp2 HG01069.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.212+28441delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71468709 | ||||||
| chr12:71468709 | CTT | C | 11 | a0001c0001t0001g0048 a0001c0001t0001g0167 a0001c0001t0004g0007 others(8): Show |
11 | HG01243.hp1 HG01993.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+28440_212+2844 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71468709 | ||||||
| chr12:71469138 | A | T | 1 | a0001c0001t0002g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.212+28846A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469138 | |||||||
| chr12:71469286 | G | A | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212+28994G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469286 | |||||||
| chr12:71469382 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+29090C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469382 | |||||||
| chr12:71469457 | T | C | 5 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.212+29165T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469457 | |||||||
| chr12:71469498 | G | A | 8 | a0001c0001t0001g0167 a0001c0001t0007g0191 a0001c0002t0010g0182 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+29206G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469498 | |||||||
| chr12:71469624 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+29332A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469624 | |||||||
| chr12:71469845 | C | G | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.212+29553C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71469845 | |||||||
| chr12:71470000 | G | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
18 | HG00423.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.212+29708G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470000 | |||||||
| chr12:71470003 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(16): Show |
19 | HG00423.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.212+29711G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470003 | |||||||
| chr12:71470059 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(13): Show |
16 | HG00423.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.212+29767C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470059 | |||||||
| chr12:71470092 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(12): Show |
15 | HG00423.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.212+29800T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470092 | |||||||
| chr12:71470094 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
18 | HG00423.hp2 HG01069.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.212+29802T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470094 | |||||||
| chr12:71470412 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+30120G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470412 | |||||||
| chr12:71470560 | A | ATG | 9 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+30274_212+3027 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71470560 | ||||||
| chr12:71470569 | T | C | 1 | a0002c0003t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.212+30277T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470569 | |||||||
| chr12:71470615 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 |
3 | HG02055.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.212+30323G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470615 | |||||||
| chr12:71470797 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0004g0173 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+30505G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470797 | |||||||
| chr12:71470880 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 |
3 | HG02055.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.212+30588A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470880 | |||||||
| chr12:71470960 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 |
3 | HG02055.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.212+30668G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71470960 | |||||||
| chr12:71471065 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 |
3 | HG02055.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.212+30773G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471065 | |||||||
| chr12:71471177 | G | C | 3 | a0001c0001t0004g0173 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.212+30885G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471177 | |||||||
| chr12:71471236 | G | A | 1 | a0001c0001t0020g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.212+30944G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471236 | |||||||
| chr12:71471641 | GT | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(7): Show |
10 | HG00423.hp2 HG01109.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+31362delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71471641 | ||||||
| chr12:71471648 | T | G | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212+31356T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471648 | |||||||
| chr12:71471649 | T | G | 3 | a0001c0001t0004g0173 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.212+31357T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471649 | |||||||
| chr12:71471880 | G | T | 3 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 |
3 | HG02055.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.212+31588G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71471880 | |||||||
| chr12:71472002 | A | C | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212+31710A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472002 | |||||||
| chr12:71472038 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+31746A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472038 | |||||||
| chr12:71472184 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+31892A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472184 | |||||||
| chr12:71472339 | T | G | 1 | a0001c0001t0003g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.212+32047T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472339 | |||||||
| chr12:71472351 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+32059G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472351 | |||||||
| chr12:71472415 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.212+32123G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472415 | |||||||
| chr12:71472471 | A | G | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213-32143A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71472471 | |||||||
| chr12:71473066 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-31548T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473066 | |||||||
| chr12:71473084 | A | G | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-31530A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473084 | |||||||
| chr12:71473122 | C | G | 3 | a0001c0001t0004g0173 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.213-31492C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473122 | |||||||
| chr12:71473159 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-31455G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473159 | |||||||
| chr12:71473198 | C | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.213-31416C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473198 | |||||||
| chr12:71473212 | A | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-31402A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473212 | |||||||
| chr12:71473340 | AT | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-31273delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473340 | |||||||
| chr12:71473771 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-30843A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473771 | |||||||
| chr12:71473789 | A | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-30825A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473789 | |||||||
| chr12:71473845 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-30769T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71473845 | |||||||
| chr12:71474026 | G | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-30588G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474026 | |||||||
| chr12:71474028 | G | T | 1 | a0001c0001t0003g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.213-30586G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474028 | |||||||
| chr12:71474146 | CA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.213-30457delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71474146 | ||||||
| chr12:71474272 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.213-30342C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474272 | |||||||
| chr12:71474303 | T | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(7): Show |
10 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-30311T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474303 | |||||||
| chr12:71474416 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-30198T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474416 | |||||||
| chr12:71474458 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-30156C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474458 | |||||||
| chr12:71474678 | T | C | 3 | a0001c0001t0004g0173 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.213-29936T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71474678 | |||||||
| chr12:71475032 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(10): Show |
13 | HG00423.hp2 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.213-29582G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475032 | |||||||
| chr12:71475040 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213-29574T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475040 | |||||||
| chr12:71475235 | A | T | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-29379A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475235 | |||||||
| chr12:71475237 | G | T | 2 | a0001c0001t0004g0164 a0002c0003t0005g0194 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.213-29377G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475237 | |||||||
| chr12:71475261 | ATAAAC | A | 2 | a0001c0001t0002g0142 a0001c0001t0003g0141 |
2 | NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.213-29348_213-2934 others(9): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71475261 | ||||||
| chr12:71475325 | T | A | 1 | a0002c0003t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.213-29289T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475325 | |||||||
| chr12:71475326 | T | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-29288T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475326 | |||||||
| chr12:71475413 | C | T | 2 | a0001c0001t0006g0193 a0001c0002t0001g0057 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213-29201C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475413 | |||||||
| chr12:71475449 | G | A | 2 | a0001c0001t0004g0164 a0002c0003t0005g0194 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.213-29165G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475449 | |||||||
| chr12:71475489 | CT | C | 4 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-29121delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71475489 | ||||||
| chr12:71475512 | G | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-29102G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475512 | |||||||
| chr12:71475556 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-29058T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475556 | |||||||
| chr12:71475594 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0092 |
2 | HG01106.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.213-29020G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475594 | |||||||
| chr12:71475605 | T | C | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-29009T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475605 | |||||||
| chr12:71475651 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0007g0191 a0002c0003t0005g0175 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-28963C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475651 | |||||||
| chr12:71475995 | G | C | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-28619G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71475995 | |||||||
| chr12:71476111 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(63): Show |
66 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.213-28503G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476111 | |||||||
| chr12:71476135 | C | T | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(7): Show |
10 | HG00423.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-28479C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476135 | |||||||
| chr12:71476136 | C | T | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(7): Show |
10 | HG00423.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-28478C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476136 | |||||||
| chr12:71476174 | G | A | 2 | a0001c0001t0008g0011 a0001c0001t0008g0012 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.213-28440G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476174 | |||||||
| chr12:71476222 | G | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-28392G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476222 | |||||||
| chr12:71476300 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-28314G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476300 | |||||||
| chr12:71476483 | G | A | 38 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0150 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.213-28131G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476483 | |||||||
| chr12:71476512 | G | T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-28102G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476512 | |||||||
| chr12:71476550 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-28064G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476550 | |||||||
| chr12:71476729 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-27885G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476729 | |||||||
| chr12:71476736 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.213-27878T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476736 | |||||||
| chr12:71476774 | G | A | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-27840G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476774 | |||||||
| chr12:71476963 | G | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(142): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.213-27651G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476963 | |||||||
| chr12:71476974 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.213-27640G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71476974 | |||||||
| chr12:71477014 | T | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-27600T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477014 | |||||||
| chr12:71477247 | C | A | 1 | a0001c0002t0010g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.213-27367C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477247 | |||||||
| chr12:71477264 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-27350T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477264 | |||||||
| chr12:71477310 | G | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-27304G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477310 | |||||||
| chr12:71477412 | TA | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.213-27195delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71477412 | ||||||
| chr12:71477420 | C | T | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-27194C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477420 | |||||||
| chr12:71477469 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-27145G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477469 | |||||||
| chr12:71477480 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-27134G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477480 | |||||||
| chr12:71477505 | GATA | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-27104_213-2710 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71477505 | ||||||
| chr12:71477691 | T | C | 1 | a0002c0003t0002g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.213-26923T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477691 | |||||||
| chr12:71477699 | A | G | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-26915A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477699 | |||||||
| chr12:71477775 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.213-26839G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477775 | |||||||
| chr12:71477908 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.213-26706C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477908 | |||||||
| chr12:71477946 | C | T | 2 | a0001c0001t0003g0084 a0001c0001t0003g0122 |
2 | HG01993.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.213-26668C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71477946 | |||||||
| chr12:71478099 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.213-26515C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478099 | |||||||
| chr12:71478300 | G | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-26314G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478300 | |||||||
| chr12:71478426 | C | T | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-26188C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478426 | |||||||
| chr12:71478512 | A | T | 1 | a0002c0003t0005g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.213-26102A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478512 | |||||||
| chr12:71478666 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.213-25948A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478666 | |||||||
| chr12:71478682 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-25932A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71478682 | |||||||
| chr12:71479095 | T | C | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-25519T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479095 | |||||||
| chr12:71479112 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-25502T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479112 | |||||||
| chr12:71479130 | C | T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-25484C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479130 | |||||||
| chr12:71479388 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-25226T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479388 | |||||||
| chr12:71479427 | C | T | 2 | a0001c0001t0004g0164 a0002c0003t0005g0194 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.213-25187C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479427 | |||||||
| chr12:71479572 | A | C | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG00438.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.213-25042A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479572 | |||||||
| chr12:71479604 | C | A | 1 | a0001c0001t0003g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.213-25010C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479604 | |||||||
| chr12:71479607 | T | C | 1 | a0001c0001t0003g0077 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.213-25007T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479607 | |||||||
| chr12:71479638 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-24976G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479638 | |||||||
| chr12:71479691 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24923C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479691 | |||||||
| chr12:71479743 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24871T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479743 | |||||||
| chr12:71479820 | A | AG | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24794_213-2479 others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71479820 | |||||||
| chr12:71480026 | T | C | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.213-24588T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480026 | |||||||
| chr12:71480052 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.213-24562A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480052 | |||||||
| chr12:71480061 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24553A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480061 | |||||||
| chr12:71480104 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24510C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480104 | |||||||
| chr12:71480111 | C | T | 1 | a0005c0007t0006g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.213-24503C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480111 | |||||||
| chr12:71480135 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.213-24479G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480135 | |||||||
| chr12:71480184 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-24430C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480184 | |||||||
| chr12:71480192 | C | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-24422C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480192 | |||||||
| chr12:71480210 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24404A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480210 | |||||||
| chr12:71480221 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.213-24393G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480221 | |||||||
| chr12:71480257 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24357G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480257 | |||||||
| chr12:71480259 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-24355G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480259 | |||||||
| chr12:71480276 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.213-24338G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480276 | |||||||
| chr12:71480298 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24316T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480298 | |||||||
| chr12:71480360 | C | CA | 5 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0002t0001g0196 others(2): Show |
5 | HG01069.hp2 HG01109.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-24235dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71480360 | ||||||
| chr12:71480360 | CA | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(34): Show |
37 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.213-24235delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71480360 | ||||||
| chr12:71480378 | A | G | 2 | a0001c0001t0003g0099 a0001c0001t0003g0112 |
2 | NA19076.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.213-24236A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480378 | |||||||
| chr12:71480441 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-24173T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480441 | |||||||
| chr12:71480576 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-24038T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480576 | |||||||
| chr12:71480700 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23914G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480700 | |||||||
| chr12:71480728 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23886A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480728 | |||||||
| chr12:71480798 | C | T | 1 | a0001c0001t0003g0077 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.213-23816C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480798 | |||||||
| chr12:71480799 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23815G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480799 | |||||||
| chr12:71480872 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-23742G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480872 | |||||||
| chr12:71480997 | G | A | 1 | a0001c0002t0021g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.213-23617G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71480997 | |||||||
| chr12:71481121 | T | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-23493T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481121 | |||||||
| chr12:71481229 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23385G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481229 | |||||||
| chr12:71481244 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-23370C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481244 | |||||||
| chr12:71481260 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23354T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481260 | |||||||
| chr12:71481417 | G | C | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.213-23197G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481417 | |||||||
| chr12:71481467 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-23147A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481467 | |||||||
| chr12:71481549 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.213-23065T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481549 | |||||||
| chr12:71481564 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.213-23050C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481564 | |||||||
| chr12:71481757 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-22857T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481757 | |||||||
| chr12:71481768 | A | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-22846A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481768 | |||||||
| chr12:71481841 | T | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-22773T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481841 | |||||||
| chr12:71481950 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-22664G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71481950 | |||||||
| chr12:71482013 | T | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-22601T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482013 | |||||||
| chr12:71482400 | C | G | 1 | a0001c0001t0006g0192 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.213-22214C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482400 | |||||||
| chr12:71482430 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-22184C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482430 | |||||||
| chr12:71482532 | CA | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-22072delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71482532 | ||||||
| chr12:71482569 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-22045G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482569 | |||||||
| chr12:71482785 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-21829C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482785 | |||||||
| chr12:71482872 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-21742T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482872 | |||||||
| chr12:71482914 | A | G | 5 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-21700A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482914 | |||||||
| chr12:71482925 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-21689A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71482925 | |||||||
| chr12:71483026 | T | G | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-21588T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71483026 | |||||||
| chr12:71483121 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-21493A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71483121 | |||||||
| chr12:71483214 | C | T | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.213-21400C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71483214 | |||||||
| chr12:71483752 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-20862A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71483752 | |||||||
| chr12:71484053 | T | A | 4 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0091 others(1): Show |
4 | HG00735.hp1 HG01496.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-20561T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484053 | |||||||
| chr12:71484142 | G | A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0014 |
2 | HG01243.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.213-20472G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484142 | |||||||
| chr12:71484269 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-20345T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484269 | |||||||
| chr12:71484404 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.213-20210A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484404 | |||||||
| chr12:71484450 | T | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-20164T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484450 | |||||||
| chr12:71484496 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-20118G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484496 | |||||||
| chr12:71484565 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-20049A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484565 | |||||||
| chr12:71484586 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-20028G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484586 | |||||||
| chr12:71484641 | A | ATTG | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19970_213-1996 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71484641 | ||||||
| chr12:71484803 | G | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-19811G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484803 | |||||||
| chr12:71484805 | G | A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0014 |
2 | HG01243.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.213-19809G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484805 | |||||||
| chr12:71484838 | A | G | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-19776A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484838 | |||||||
| chr12:71484862 | G | A | 2 | a0001c0001t0001g0101 a0002c0003t0005g0100 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.213-19752G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484862 | |||||||
| chr12:71484935 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19679T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484935 | |||||||
| chr12:71484941 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19673C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484941 | |||||||
| chr12:71484950 | C | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19664C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484950 | |||||||
| chr12:71484957 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0167 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.213-19657A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484957 | |||||||
| chr12:71484964 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-19650C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484964 | |||||||
| chr12:71484992 | T | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-19622T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71484992 | |||||||
| chr12:71485131 | T | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-19483T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485131 | |||||||
| chr12:71485188 | A | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-19426A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485188 | |||||||
| chr12:71485307 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19307C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485307 | |||||||
| chr12:71485370 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19244A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485370 | |||||||
| chr12:71485436 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19178G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485436 | |||||||
| chr12:71485543 | G | A | 1 | a0001c0001t0003g0138 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.213-19071G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485543 | |||||||
| chr12:71485543 | G | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-19071G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485543 | |||||||
| chr12:71485768 | CT | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-18830delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71485768 | ||||||
| chr12:71485872 | T | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-18742T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485872 | |||||||
| chr12:71485915 | G | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-18699G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71485915 | |||||||
| chr12:71486104 | T | G | 1 | a0001c0001t0003g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.213-18510T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486104 | |||||||
| chr12:71486163 | G | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.213-18451G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486163 | |||||||
| chr12:71486188 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-18426T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486188 | |||||||
| chr12:71486222 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0003g0154 |
2 | HG01517.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.213-18392C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486222 | |||||||
| chr12:71486223 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-18391G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486223 | |||||||
| chr12:71486327 | T | C | 1 | a0001c0001t0003g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.213-18287T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486327 | |||||||
| chr12:71486410 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-18204G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486410 | |||||||
| chr12:71486650 | T | A | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.213-17964T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486650 | |||||||
| chr12:71486654 | G | A | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.213-17960G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486654 | |||||||
| chr12:71486683 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-17931C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486683 | |||||||
| chr12:71486691 | T | A | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.213-17923T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486691 | |||||||
| chr12:71486790 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.213-17824A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486790 | |||||||
| chr12:71486865 | T | G | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-17749T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71486865 | |||||||
| chr12:71487065 | C | T | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-17549C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487065 | |||||||
| chr12:71487212 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-17402A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487212 | |||||||
| chr12:71487275 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-17339G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487275 | |||||||
| chr12:71487280 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0167 a0001c0001t0001g0169 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.213-17334T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487280 | |||||||
| chr12:71487574 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-17040C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487574 | |||||||
| chr12:71487664 | T | C | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.213-16950T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487664 | |||||||
| chr12:71487750 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.213-16864C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487750 | |||||||
| chr12:71487839 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-16775C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487839 | |||||||
| chr12:71487853 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-16761A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487853 | |||||||
| chr12:71487862 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-16752A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487862 | |||||||
| chr12:71487871 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-16743A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487871 | |||||||
| chr12:71487929 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-16685T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487929 | |||||||
| chr12:71487952 | C | CTAAAT | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-16660_213-1665 others(9): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71487952 | ||||||
| chr12:71487990 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-16624G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71487990 | |||||||
| chr12:71488025 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.213-16589A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488025 | |||||||
| chr12:71488069 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.213-16545G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488069 | |||||||
| chr12:71488216 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.213-16398A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488216 | |||||||
| chr12:71488579 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG00423.hp1 HG02135.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-16035T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488579 | |||||||
| chr12:71488587 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213-16027C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488587 | |||||||
| chr12:71488589 | A | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-16025A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488589 | |||||||
| chr12:71488616 | T | G | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-15998T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488616 | |||||||
| chr12:71488777 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-15837T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71488777 | |||||||
| chr12:71489024 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0028 others(8): Show |
11 | HG00741.hp1 HG01071.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.213-15590G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489024 | |||||||
| chr12:71489248 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-15366C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489248 | |||||||
| chr12:71489302 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0009t0009g0009 others(1): Show |
4 | HG02965.hp2 HG02970.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-15312G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489302 | |||||||
| chr12:71489612 | G | A | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-15002G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489612 | |||||||
| chr12:71489717 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14897A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489717 | |||||||
| chr12:71489881 | AG | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14732delG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489881 | |||||||
| chr12:71489883 | T | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14731T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71489883 | |||||||
| chr12:71490129 | C | CAAA | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14472_213-1447 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71490129 | ||||||
| chr12:71490129 | CA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.213-14470delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71490129 | ||||||
| chr12:71490141 | A | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-14473A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490141 | |||||||
| chr12:71490144 | A | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(104): Show |
107 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.213-14470A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490144 | |||||||
| chr12:71490145 | C | T | 1 | a0002c0003t0002g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.213-14469C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490145 | |||||||
| chr12:71490183 | T | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.213-14431T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490183 | |||||||
| chr12:71490188 | C | T | 1 | a0001c0001t0003g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.213-14426C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490188 | |||||||
| chr12:71490230 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14384C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490230 | |||||||
| chr12:71490385 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14229T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490385 | |||||||
| chr12:71490537 | T | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-14077T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490537 | |||||||
| chr12:71490564 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-14050C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490564 | |||||||
| chr12:71490579 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213-14035G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490579 | |||||||
| chr12:71490644 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-13970A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490644 | |||||||
| chr12:71490730 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-13884G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490730 | |||||||
| chr12:71490753 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.213-13861G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490753 | |||||||
| chr12:71490759 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-13855C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490759 | |||||||
| chr12:71490841 | T | C | 1 | a0002c0003t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.213-13773T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71490841 | |||||||
| chr12:71491021 | C | A | 16 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(13): Show |
16 | HG00423.hp2 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.213-13593C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491021 | |||||||
| chr12:71491028 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-13586C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491028 | |||||||
| chr12:71491138 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-13476T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491138 | |||||||
| chr12:71491162 | CTG | C | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-13447_213-1344 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71491162 | ||||||
| chr12:71491180 | C | A | 1 | a0001c0001t0003g0119 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.213-13434C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491180 | |||||||
| chr12:71491258 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-13356A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491258 | |||||||
| chr12:71491367 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.213-13247C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491367 | |||||||
| chr12:71491395 | T | A | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.213-13219T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491395 | |||||||
| chr12:71491497 | A | G | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-13117A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491497 | |||||||
| chr12:71491538 | C | G | 1 | a0006c0011t0003g0104 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.213-13076C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491538 | |||||||
| chr12:71491564 | G | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-13050G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491564 | |||||||
| chr12:71491757 | A | G | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-12857A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491757 | |||||||
| chr12:71491815 | C | T | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-12799C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491815 | |||||||
| chr12:71491898 | C | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-12716C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491898 | |||||||
| chr12:71491929 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(113): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.213-12685A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491929 | |||||||
| chr12:71491973 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-12641C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71491973 | |||||||
| chr12:71492125 | G | A | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.213-12489G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492125 | |||||||
| chr12:71492190 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-12424C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492190 | |||||||
| chr12:71492247 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-12367C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492247 | |||||||
| chr12:71492651 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-11963G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492651 | |||||||
| chr12:71492652 | A | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-11962A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492652 | |||||||
| chr12:71492757 | A | AG | 16 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(13): Show |
16 | HG00423.hp2 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.213-11855dupG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71492757 | ||||||
| chr12:71492784 | TTTGAGTT others(3082): Show |
T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-11829_213-8741 others(3): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492784 | |||||||
| chr12:71492798 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-11816T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492798 | |||||||
| chr12:71492881 | G | A | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213-11733G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71492881 | |||||||
| chr12:71493123 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.213-11491T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493123 | |||||||
| chr12:71493130 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-11484A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493130 | |||||||
| chr12:71493152 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-11462C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493152 | |||||||
| chr12:71493310 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-11304C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493310 | |||||||
| chr12:71493383 | G | T | 1 | a0001c0001t0003g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.213-11231G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493383 | |||||||
| chr12:71493411 | G | T | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-11203G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493411 | |||||||
| chr12:71493559 | G | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-11055G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493559 | |||||||
| chr12:71493599 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-11015C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493599 | |||||||
| chr12:71493634 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10980T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493634 | |||||||
| chr12:71493690 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.213-10924T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493690 | |||||||
| chr12:71493712 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10902T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493712 | |||||||
| chr12:71493770 | C | CT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(126): Show |
129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.213-10829dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71493770 | ||||||
| chr12:71493770 | C | CTTT | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10831_213-1082 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71493770 | ||||||
| chr12:71493808 | G | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-10806G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493808 | |||||||
| chr12:71493811 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.213-10803T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493811 | |||||||
| chr12:71493843 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10771A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493843 | |||||||
| chr12:71493861 | T | C | 4 | a0001c0001t0003g0066 a0001c0001t0003g0098 a0001c0001t0003g0103 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-10753T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71493861 | |||||||
| chr12:71493943 | A | AT | 23 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.213-10653dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71493943 | ||||||
| chr12:71494035 | C | CT | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10579_213-1057 others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494035 | |||||||
| chr12:71494036 | C | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10578C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494036 | |||||||
| chr12:71494045 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10569G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494045 | |||||||
| chr12:71494087 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.213-10527G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494087 | |||||||
| chr12:71494090 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(105): Show |
108 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.213-10524C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494090 | |||||||
| chr12:71494092 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.213-10522T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494092 | |||||||
| chr12:71494094 | C | T | 1 | a0002c0003t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.213-10520C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494094 | |||||||
| chr12:71494111 | T | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-10503T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494111 | |||||||
| chr12:71494119 | AC | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-10494delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494119 | |||||||
| chr12:71494135 | A | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-10479A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494135 | |||||||
| chr12:71494155 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10459C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494155 | |||||||
| chr12:71494193 | G | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-10421G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494193 | |||||||
| chr12:71494242 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-10372G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494242 | |||||||
| chr12:71494281 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(105): Show |
108 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.213-10333T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494281 | |||||||
| chr12:71494506 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-10108T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494506 | |||||||
| chr12:71494550 | G | A | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-10064G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494550 | |||||||
| chr12:71494609 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-10005C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494609 | |||||||
| chr12:71494691 | C | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9923C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494691 | |||||||
| chr12:71494715 | T | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-9899T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494715 | |||||||
| chr12:71494842 | C | T | 1 | a0001c0009t0009g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.213-9772C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494842 | |||||||
| chr12:71494872 | T | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9742T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494872 | |||||||
| chr12:71494977 | A | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9637A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494977 | |||||||
| chr12:71494981 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-9633G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71494981 | |||||||
| chr12:71495027 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-9587C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495027 | |||||||
| chr12:71495047 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.213-9567G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495047 | |||||||
| chr12:71495048 | G | A | 1 | a0006c0011t0003g0104 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.213-9566G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495048 | |||||||
| chr12:71495073 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213-9541G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495073 | |||||||
| chr12:71495077 | TC | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0102 a0002c0003t0013g0010 |
3 | HG03130.hp2 NA18951.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.213-9536delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495077 | |||||||
| chr12:71495077 | TCG | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9536_213-9535d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495077 | |||||||
| chr12:71495078 | C | A | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-9536C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495078 | |||||||
| chr12:71495078 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.213-9536C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495078 | |||||||
| chr12:71495080 | G | C | 2 | a0001c0001t0002g0142 a0001c0001t0003g0141 |
2 | NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.213-9534G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495080 | |||||||
| chr12:71495298 | T | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9316T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495298 | |||||||
| chr12:71495418 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-9196C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495418 | |||||||
| chr12:71495430 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG00438.hp2 HG02083.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-9184A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495430 | |||||||
| chr12:71495525 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-9089T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495525 | |||||||
| chr12:71495672 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8942C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495672 | |||||||
| chr12:71495677 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.213-8937A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495677 | |||||||
| chr12:71495757 | G | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8857G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495757 | |||||||
| chr12:71495834 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.213-8780A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495834 | |||||||
| chr12:71495851 | C | T | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.213-8763C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495851 | |||||||
| chr12:71495852 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8762T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495852 | |||||||
| chr12:71495937 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8677G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495937 | |||||||
| chr12:71495944 | T | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8670T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71495944 | |||||||
| chr12:71496038 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8576C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496038 | |||||||
| chr12:71496046 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8568C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496046 | |||||||
| chr12:71496106 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8508T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496106 | |||||||
| chr12:71496370 | C | CA | 29 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.213-8222dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71496370 | ||||||
| chr12:71496370 | C | CAAA | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8224_213-8222d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71496370 | ||||||
| chr12:71496370 | CA | C | 12 | a0001c0001t0002g0060 a0001c0001t0002g0064 a0001c0001t0002g0078 others(9): Show |
12 | HG01069.hp2 HG01928.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.213-8222delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71496370 | ||||||
| chr12:71496370 | CAA | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(104): Show |
107 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.213-8223_213-8222d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71496370 | ||||||
| chr12:71496389 | A | AG | 2 | a0001c0001t0004g0069 a0013c0013t0004g0157 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.213-8225_213-8224i others(3): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496389 | |||||||
| chr12:71496391 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(111): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.213-8223A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496391 | |||||||
| chr12:71496392 | AGAG | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-8221_213-8219d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496392 | |||||||
| chr12:71496499 | T | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-8115T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496499 | |||||||
| chr12:71496531 | A | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-8083A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496531 | |||||||
| chr12:71496560 | G | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-8054G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496560 | |||||||
| chr12:71496577 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-8037C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496577 | |||||||
| chr12:71496637 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-7977C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496637 | |||||||
| chr12:71496762 | C | T | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-7852C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496762 | |||||||
| chr12:71496878 | A | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-7736A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496878 | |||||||
| chr12:71496886 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(139): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.213-7728G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496886 | |||||||
| chr12:71496890 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.213-7724C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496890 | |||||||
| chr12:71496937 | G | T | 2 | a0001c0001t0001g0101 a0002c0003t0005g0100 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.213-7677G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496937 | |||||||
| chr12:71496949 | A | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0166 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.213-7665A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496949 | |||||||
| chr12:71496970 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-7644A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71496970 | |||||||
| chr12:71497010 | T | A | 2 | a0001c0002t0001g0197 a0005c0007t0006g0190 |
2 | HG01361.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.213-7604T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497010 | |||||||
| chr12:71497042 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-7572G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497042 | |||||||
| chr12:71497150 | C | CAA | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-7464_213-7463i others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497150 | |||||||
| chr12:71497151 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-7463G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497151 | |||||||
| chr12:71497262 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-7352C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497262 | |||||||
| chr12:71497291 | G | T | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.213-7323G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497291 | |||||||
| chr12:71497342 | GAGGAAGG others(9): Show |
G | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.213-7257_213-7242d others(18): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71497342 | ||||||
| chr12:71497345 | GAAGGAAG others(5): Show |
G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-7257_213-7246d others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71497345 | ||||||
| chr12:71497368 | G | A | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-7246G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497368 | |||||||
| chr12:71497428 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-7186C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497428 | |||||||
| chr12:71497508 | A | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-7106A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497508 | |||||||
| chr12:71497604 | G | T | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-7010G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497604 | |||||||
| chr12:71497834 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-6780C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497834 | |||||||
| chr12:71497835 | A | G | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.213-6779A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497835 | |||||||
| chr12:71497954 | C | T | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-6660C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71497954 | |||||||
| chr12:71498178 | G | A | 16 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(13): Show |
16 | HG00423.hp2 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.213-6436G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498178 | |||||||
| chr12:71498253 | C | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-6361C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498253 | |||||||
| chr12:71498261 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-6353T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498261 | |||||||
| chr12:71498320 | CA | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-6293delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498320 | |||||||
| chr12:71498556 | T | C | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-6058T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498556 | |||||||
| chr12:71498705 | A | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.213-5909A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498705 | |||||||
| chr12:71498719 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-5895A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71498719 | |||||||
| chr12:71499007 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-5607G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499007 | |||||||
| chr12:71499057 | T | A | 3 | a0001c0002t0001g0095 a0001c0002t0007g0186 a0001c0002t0007g0188 |
3 | HG01243.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.213-5557T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499057 | |||||||
| chr12:71499073 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-5541T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499073 | |||||||
| chr12:71499126 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.213-5488G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499126 | |||||||
| chr12:71499157 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.213-5457A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499157 | |||||||
| chr12:71499209 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0027 others(36): Show |
39 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.213-5405C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499209 | |||||||
| chr12:71499403 | A | C | 2 | a0001c0001t0001g0001 a0002c0003t0005g0175 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.213-5211A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499403 | |||||||
| chr12:71499513 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-5101T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499513 | |||||||
| chr12:71499874 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.213-4740C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499874 | |||||||
| chr12:71499895 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-4719A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499895 | |||||||
| chr12:71499974 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.213-4640G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71499974 | |||||||
| chr12:71500043 | T | G | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-4571T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500043 | |||||||
| chr12:71500143 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-4471T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500143 | |||||||
| chr12:71500194 | T | C | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-4420T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500194 | |||||||
| chr12:71500228 | C | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-4386C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500228 | |||||||
| chr12:71500301 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-4313T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500301 | |||||||
| chr12:71500304 | C | CT | 2 | a0001c0001t0006g0193 a0001c0002t0001g0057 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213-4309dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71500304 | ||||||
| chr12:71500793 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.213-3821G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500793 | |||||||
| chr12:71500853 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.213-3761C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500853 | |||||||
| chr12:71500925 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.213-3689C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71500925 | |||||||
| chr12:71501077 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-3537A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501077 | |||||||
| chr12:71501093 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.213-3521G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501093 | |||||||
| chr12:71501180 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-3434G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501180 | |||||||
| chr12:71501185 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-3429T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501185 | |||||||
| chr12:71501215 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.213-3399G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501215 | |||||||
| chr12:71501257 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.213-3357A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501257 | |||||||
| chr12:71501342 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.213-3272C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501342 | |||||||
| chr12:71501347 | C | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-3267C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501347 | |||||||
| chr12:71501437 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-3177T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501437 | |||||||
| chr12:71501491 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.213-3123A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501491 | |||||||
| chr12:71501596 | A | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-3018A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501596 | |||||||
| chr12:71501608 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-3006A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501608 | |||||||
| chr12:71501804 | A | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG00741.hp1 HG01071.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-2810A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501804 | |||||||
| chr12:71501822 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-2792G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501822 | |||||||
| chr12:71501951 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0002g0135 |
2 | HG01071.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.213-2663T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71501951 | |||||||
| chr12:71502007 | T | A | 1 | a0001c0001t0002g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.213-2607T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502007 | |||||||
| chr12:71502115 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-2499T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502115 | |||||||
| chr12:71502134 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.213-2480T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502134 | |||||||
| chr12:71502193 | C | CT | 9 | a0001c0001t0001g0172 a0001c0001t0002g0075 a0001c0001t0002g0129 others(6): Show |
9 | HG01106.hp2 HG01928.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.213-2400dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71502193 | ||||||
| chr12:71502341 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-2273G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502341 | |||||||
| chr12:71502410 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.213-2204C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502410 | |||||||
| chr12:71502432 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-2182G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502432 | |||||||
| chr12:71502517 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-2097A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502517 | |||||||
| chr12:71502704 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-1910T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502704 | |||||||
| chr12:71502774 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-1840G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502774 | |||||||
| chr12:71502880 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-1734A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502880 | |||||||
| chr12:71502920 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.213-1694G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71502920 | |||||||
| chr12:71503153 | TG | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-1460delG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503153 | |||||||
| chr12:71503218 | CA | C | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01433.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.213-1388delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 71503218 | ||||||
| chr12:71503451 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-1163A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503451 | |||||||
| chr12:71503484 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-1130T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503484 | |||||||
| chr12:71503652 | A | G | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213-962A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503652 | |||||||
| chr12:71503704 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG00438.hp2 HG02083.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.213-910A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503704 | |||||||
| chr12:71503883 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.213-731T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503883 | |||||||
| chr12:71503908 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.213-706T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71503908 | |||||||
| chr12:71504128 | T | A | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213-486T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504128 | |||||||
| chr12:71504141 | G | T | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213-473G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504141 | |||||||
| chr12:71504144 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.213-470G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504144 | |||||||
| chr12:71504147 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.213-467G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504147 | |||||||
| chr12:71504151 | T | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-463T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504151 | |||||||
| chr12:71504228 | A | G | 16 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(13): Show |
16 | HG00423.hp2 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.213-386A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504228 | |||||||
| chr12:71504413 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-201T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504413 | |||||||
| chr12:71504440 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-174T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504440 | |||||||
| chr12:71504507 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-107G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504507 | |||||||
| chr12:71504578 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.213-36T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 1/17 | chr12 | 71504578 | |||||||
| chr12:71504736 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+51T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71504736 | |||||||
| chr12:71504914 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.284+229G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71504914 | |||||||
| chr12:71505040 | C | T | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284+355C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505040 | |||||||
| chr12:71505275 | G | T | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284+590G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505275 | |||||||
| chr12:71505321 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+636T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505321 | |||||||
| chr12:71505412 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+727G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505412 | |||||||
| chr12:71505898 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+1213A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505898 | |||||||
| chr12:71505933 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+1248A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71505933 | |||||||
| chr12:71506155 | A | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.284+1470A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506155 | |||||||
| chr12:71506186 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+1501C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506186 | |||||||
| chr12:71506574 | T | C | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+1889T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506574 | |||||||
| chr12:71506597 | A | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+1912A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506597 | |||||||
| chr12:71506699 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+2014T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506699 | |||||||
| chr12:71506796 | G | A | 8 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+2111G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506796 | |||||||
| chr12:71506909 | T | A | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284+2224T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506909 | |||||||
| chr12:71506927 | C | T | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284+2242C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71506927 | |||||||
| chr12:71507028 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+2343C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507028 | |||||||
| chr12:71507217 | A | T | 1 | a0001c0001t0002g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284+2532A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507217 | |||||||
| chr12:71507413 | G | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+2728G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507413 | |||||||
| chr12:71507769 | G | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0027 others(38): Show |
41 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.284+3084G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507769 | |||||||
| chr12:71507908 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+3223T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507908 | |||||||
| chr12:71507916 | C | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284+3231C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507916 | |||||||
| chr12:71507959 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+3274A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71507959 | |||||||
| chr12:71508002 | C | T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+3317C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508002 | |||||||
| chr12:71508062 | CA | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(5): Show |
8 | HG00423.hp2 HG01257.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+3394delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71508062 | ||||||
| chr12:71508087 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.284+3402G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508087 | |||||||
| chr12:71508267 | A | G | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284+3582A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508267 | |||||||
| chr12:71508478 | G | A | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284+3793G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508478 | |||||||
| chr12:71508583 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+3898G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508583 | |||||||
| chr12:71508622 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284+3937C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508622 | |||||||
| chr12:71508625 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.284+3940G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508625 | |||||||
| chr12:71508697 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+4012C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508697 | |||||||
| chr12:71508734 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.284+4049T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508734 | |||||||
| chr12:71508752 | C | CA | 55 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0001g0169 others(52): Show |
55 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.284+4092dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71508752 | ||||||
| chr12:71508752 | C | CAA | 5 | a0001c0001t0002g0092 a0001c0001t0003g0068 a0001c0001t0003g0077 others(2): Show |
5 | HG01978.hp1 HG02132.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+4091_284+4092d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71508752 | ||||||
| chr12:71508752 | C | CAAA | 5 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+4090_284+4092d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71508752 | ||||||
| chr12:71508752 | CA | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0049 others(9): Show |
12 | HG00280.hp1 HG00423.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+4092delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71508752 | ||||||
| chr12:71508833 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+4148T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71508833 | |||||||
| chr12:71509003 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+4318A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509003 | |||||||
| chr12:71509082 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+4397G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509082 | |||||||
| chr12:71509230 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+4545T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509230 | |||||||
| chr12:71509424 | T | C | 3 | a0001c0001t0002g0058 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | NA18962.hp1 NA18971.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.284+4739T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509424 | |||||||
| chr12:71509464 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.284+4779T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509464 | |||||||
| chr12:71509500 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+4815G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509500 | |||||||
| chr12:71509544 | G | A | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+4859G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509544 | |||||||
| chr12:71509561 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+4876A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509561 | |||||||
| chr12:71509650 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG00609.hp1 NA18612.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.284+4965C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509650 | |||||||
| chr12:71509833 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5148G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509833 | |||||||
| chr12:71509919 | T | C | 2 | a0001c0001t0003g0149 a0001c0001t0004g0047 |
2 | NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.284+5234T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509919 | |||||||
| chr12:71509974 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5289A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71509974 | |||||||
| chr12:71510070 | A | G | 1 | a0003c0004t0001g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.284+5385A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510070 | |||||||
| chr12:71510222 | C | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5537C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510222 | |||||||
| chr12:71510399 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5714T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510399 | |||||||
| chr12:71510551 | C | A | 1 | a0001c0002t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.284+5866C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510551 | |||||||
| chr12:71510591 | T | TTTCA | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5907_284+5908i others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71510591 | ||||||
| chr12:71510593 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5908C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510593 | |||||||
| chr12:71510673 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+5988C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510673 | |||||||
| chr12:71510743 | TAAC | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6061_284+6063d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71510743 | ||||||
| chr12:71510769 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6084C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510769 | |||||||
| chr12:71510813 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6128C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510813 | |||||||
| chr12:71510954 | G | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6269G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71510954 | |||||||
| chr12:71511010 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(114): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.284+6325A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511010 | |||||||
| chr12:71511180 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.284+6495C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511180 | |||||||
| chr12:71511236 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+6551C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511236 | |||||||
| chr12:71511307 | T | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.284+6622T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511307 | |||||||
| chr12:71511356 | C | CA | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6673dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71511356 | ||||||
| chr12:71511490 | T | A | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.284+6805T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511490 | |||||||
| chr12:71511630 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+6945A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71511630 | |||||||
| chr12:71512031 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.284+7346G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512031 | |||||||
| chr12:71512182 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284+7497G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512182 | |||||||
| chr12:71512214 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284+7529C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512214 | |||||||
| chr12:71512254 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+7569C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512254 | |||||||
| chr12:71512265 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+7580C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512265 | |||||||
| chr12:71512281 | C | T | 9 | a0001c0001t0002g0114 a0001c0001t0006g0187 a0001c0001t0006g0189 others(6): Show |
9 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+7596C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512281 | |||||||
| chr12:71512496 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.284+7811C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512496 | |||||||
| chr12:71512516 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+7831G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512516 | |||||||
| chr12:71512614 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+7929A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512614 | |||||||
| chr12:71512625 | G | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+7940G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512625 | |||||||
| chr12:71512673 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.284+7988A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512673 | |||||||
| chr12:71512706 | G | A | 1 | a0001c0009t0009g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+8021G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512706 | |||||||
| chr12:71512756 | TG | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+8072delG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512756 | |||||||
| chr12:71512806 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+8121A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512806 | |||||||
| chr12:71512918 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.284+8233T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512918 | |||||||
| chr12:71512947 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+8262C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71512947 | |||||||
| chr12:71513175 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+8490A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513175 | |||||||
| chr12:71513189 | C | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+8504C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513189 | |||||||
| chr12:71513295 | T | C | 10 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(7): Show |
10 | HG01243.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+8610T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513295 | |||||||
| chr12:71513448 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+8763T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513448 | |||||||
| chr12:71513641 | TA | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+8959delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71513641 | ||||||
| chr12:71513703 | A | G | 2 | a0001c0002t0001g0196 a0001c0002t0001g0198 |
2 | HG01069.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.284+9018A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513703 | |||||||
| chr12:71513743 | C | T | 41 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(38): Show |
41 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.284+9058C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513743 | |||||||
| chr12:71513913 | T | C | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284+9228T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513913 | |||||||
| chr12:71513965 | C | G | 1 | a0002c0003t0005g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.284+9280C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71513965 | |||||||
| chr12:71514104 | AAAAC | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+9435_284+9438d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71514104 | ||||||
| chr12:71514171 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.284+9486T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514171 | |||||||
| chr12:71514223 | T | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.284+9538T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514223 | |||||||
| chr12:71514288 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.284+9603G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514288 | |||||||
| chr12:71514321 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284+9636C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514321 | |||||||
| chr12:71514340 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.284+9655A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514340 | |||||||
| chr12:71514344 | G | A | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+9659G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514344 | |||||||
| chr12:71514387 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.284+9702T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514387 | |||||||
| chr12:71514485 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.284+9800T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514485 | |||||||
| chr12:71514495 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.284+9810A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514495 | |||||||
| chr12:71514507 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.284+9822G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514507 | |||||||
| chr12:71514517 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.284+9832C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514517 | |||||||
| chr12:71514542 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0082 others(49): Show |
52 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.284+9857T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514542 | |||||||
| chr12:71514567 | C | CA | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.285-9826dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71514567 | ||||||
| chr12:71514567 | C | CAA | 10 | a0001c0001t0001g0167 a0001c0001t0020g0097 a0001c0002t0010g0182 others(7): Show |
10 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-9827_285-9826d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71514567 | ||||||
| chr12:71514824 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.285-9582C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514824 | |||||||
| chr12:71514860 | G | A | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.285-9546G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71514860 | |||||||
| chr12:71515176 | G | A | 2 | a0001c0001t0003g0026 a0001c0001t0003g0133 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.285-9230G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71515176 | |||||||
| chr12:71515300 | A | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-9106A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71515300 | |||||||
| chr12:71515327 | T | G | 1 | a0001c0001t0002g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.285-9079T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71515327 | |||||||
| chr12:71515932 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.285-8474G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71515932 | |||||||
| chr12:71515938 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-8468A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71515938 | |||||||
| chr12:71516179 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(107): Show |
110 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.285-8227A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516179 | |||||||
| chr12:71516208 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.285-8198C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516208 | |||||||
| chr12:71516424 | G | A | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.285-7982G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516424 | |||||||
| chr12:71516445 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.285-7961C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516445 | |||||||
| chr12:71516450 | G | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.285-7956G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516450 | |||||||
| chr12:71516458 | C | G | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.285-7948C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516458 | |||||||
| chr12:71516597 | AC | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.285-7807delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71516597 | ||||||
| chr12:71516608 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.285-7798A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516608 | |||||||
| chr12:71516639 | C | A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.285-7767C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71516639 | |||||||
| chr12:71517002 | TA | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(110): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.285-7389delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71517002 | ||||||
| chr12:71517101 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-7305G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517101 | |||||||
| chr12:71517681 | A | C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.285-6725A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517681 | |||||||
| chr12:71517684 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0082 others(49): Show |
52 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.285-6722A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517684 | |||||||
| chr12:71517741 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(116): Show |
119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.285-6665C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517741 | |||||||
| chr12:71517777 | A | G | 5 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-6629A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517777 | |||||||
| chr12:71517926 | A | G | 1 | a0001c0001t0003g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.285-6480A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517926 | |||||||
| chr12:71517984 | C | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.285-6422C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71517984 | |||||||
| chr12:71518039 | C | T | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-6367C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518039 | |||||||
| chr12:71518295 | A | C | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-6111A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518295 | |||||||
| chr12:71518380 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.285-6026G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518380 | |||||||
| chr12:71518417 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-5989G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518417 | |||||||
| chr12:71518428 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.285-5978G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518428 | |||||||
| chr12:71518481 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0002g0166 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.285-5925C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518481 | |||||||
| chr12:71518568 | AT | A | 2 | a0001c0001t0004g0173 a0002c0003t0005g0175 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.285-5836delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 71518568 | ||||||
| chr12:71518718 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-5688T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518718 | |||||||
| chr12:71518724 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.285-5682C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518724 | |||||||
| chr12:71518949 | A | G | 49 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0167 others(46): Show |
49 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.285-5457A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71518949 | |||||||
| chr12:71519009 | C | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0027 others(38): Show |
41 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.285-5397C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519009 | |||||||
| chr12:71519161 | C | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0074 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.285-5245C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519161 | |||||||
| chr12:71519170 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0082 others(45): Show |
48 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.285-5236G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519170 | |||||||
| chr12:71519186 | A | G | 10 | a0001c0001t0002g0058 a0001c0001t0002g0147 a0001c0001t0002g0148 others(7): Show |
10 | HG01496.hp1 HG01993.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.285-5220A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519186 | |||||||
| chr12:71519233 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0002t0001g0016 others(1): Show |
4 | HG00280.hp2 HG02109.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-5173G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519233 | |||||||
| chr12:71519342 | C | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-5064C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519342 | |||||||
| chr12:71519404 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG00741.hp1 HG01071.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-5002G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519404 | |||||||
| chr12:71519502 | A | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-4904A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519502 | |||||||
| chr12:71519579 | G | A | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.285-4827G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519579 | |||||||
| chr12:71519658 | A | G | 2 | a0001c0001t0009g0005 a0002c0003t0005g0165 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.285-4748A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519658 | |||||||
| chr12:71519667 | A | C | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.285-4739A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519667 | |||||||
| chr12:71519668 | C | A | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285-4738C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519668 | |||||||
| chr12:71519855 | A | T | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.285-4551A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519855 | |||||||
| chr12:71519941 | G | C | 3 | a0001c0001t0001g0015 a0001c0002t0001g0016 a0001c0002t0021g0132 |
3 | HG00280.hp2 HG02300.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.285-4465G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71519941 | |||||||
| chr12:71520427 | G | C | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-3979G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71520427 | |||||||
| chr12:71520634 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-3772G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71520634 | |||||||
| chr12:71520706 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-3700G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71520706 | |||||||
| chr12:71520730 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-3676G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71520730 | |||||||
| chr12:71521120 | T | C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.285-3286T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521120 | |||||||
| chr12:71521165 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-3241T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521165 | |||||||
| chr12:71521172 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.285-3234C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521172 | |||||||
| chr12:71521224 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-3182A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521224 | |||||||
| chr12:71521570 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-2836C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521570 | |||||||
| chr12:71521612 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0004g0173 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.285-2794T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521612 | |||||||
| chr12:71521796 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.285-2610G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521796 | |||||||
| chr12:71521928 | T | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.285-2478T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521928 | |||||||
| chr12:71521994 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(123): Show |
126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.285-2412C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71521994 | |||||||
| chr12:71522073 | C | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-2333C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522073 | |||||||
| chr12:71522080 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.285-2326G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522080 | |||||||
| chr12:71522162 | T | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.285-2244T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522162 | |||||||
| chr12:71522227 | G | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-2179G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522227 | |||||||
| chr12:71522504 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.285-1902T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522504 | |||||||
| chr12:71522801 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-1605A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522801 | |||||||
| chr12:71522839 | C | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0091 |
3 | HG00735.hp1 HG02293.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.285-1567C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522839 | |||||||
| chr12:71522867 | G | A | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-1539G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71522867 | |||||||
| chr12:71523066 | C | T | 46 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0167 others(43): Show |
46 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.285-1340C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523066 | |||||||
| chr12:71523120 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0004g0173 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.285-1286T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523120 | |||||||
| chr12:71523280 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.285-1126C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523280 | |||||||
| chr12:71523285 | G | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG00741.hp1 HG01071.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-1121G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523285 | |||||||
| chr12:71523674 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-732A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523674 | |||||||
| chr12:71523909 | A | G | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.285-497A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71523909 | |||||||
| chr12:71524298 | T | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-108T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 2/17 | chr12 | 71524298 | |||||||
| chr12:71524613 | A | G | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+136A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524613 | |||||||
| chr12:71524636 | C | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(5): Show |
8 | HG00423.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+159C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524636 | |||||||
| chr12:71524720 | C | G | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.356+243C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524720 | |||||||
| chr12:71524746 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.356+269G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524746 | |||||||
| chr12:71524798 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG00741.hp1 HG01346.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.356+321A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524798 | |||||||
| chr12:71524842 | G | A | 6 | a0001c0001t0001g0082 a0001c0001t0002g0088 a0001c0001t0002g0089 others(3): Show |
6 | HG00140.hp1 HG00735.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+365G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524842 | |||||||
| chr12:71524946 | G | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(138): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.356+469G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71524946 | |||||||
| chr12:71525085 | C | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+608C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525085 | |||||||
| chr12:71525203 | G | A | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.356+726G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525203 | |||||||
| chr12:71525305 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.356+828A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525305 | |||||||
| chr12:71525333 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.356+856G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525333 | |||||||
| chr12:71525338 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.356+861G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525338 | |||||||
| chr12:71525406 | C | CT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.356+940dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71525406 | ||||||
| chr12:71525537 | A | C | 2 | a0001c0001t0002g0060 a0001c0009t0009g0009 |
2 | HG02965.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.356+1060A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525537 | |||||||
| chr12:71525902 | T | C | 1 | a0002c0003t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.356+1425T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525902 | |||||||
| chr12:71525929 | A | G | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.356+1452A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71525929 | |||||||
| chr12:71526080 | G | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.356+1603G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526080 | |||||||
| chr12:71526163 | C | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+1686C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526163 | |||||||
| chr12:71526437 | GA | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.356+1971delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71526437 | ||||||
| chr12:71526473 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.356+1996C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526473 | |||||||
| chr12:71526700 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+2223T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526700 | |||||||
| chr12:71526798 | G | C | 1 | a0001c0009t0009g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.356+2321G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526798 | |||||||
| chr12:71526819 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG00438.hp2 HG02083.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.356+2342G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526819 | |||||||
| chr12:71526970 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0003g0105 a0001c0001t0020g0097 |
3 | NA18612.hp2 NA19000.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.356+2493C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71526970 | |||||||
| chr12:71527040 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.356+2563C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527040 | |||||||
| chr12:71527051 | A | T | 1 | a0001c0001t0003g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.356+2574A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527051 | |||||||
| chr12:71527126 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(20): Show |
23 | HG00741.hp1 HG01071.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.356+2649T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527126 | |||||||
| chr12:71527314 | C | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(5): Show |
8 | HG00423.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+2837C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527314 | |||||||
| chr12:71527682 | C | G | 4 | a0001c0001t0003g0066 a0001c0001t0003g0098 a0001c0001t0003g0103 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.356+3205C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527682 | |||||||
| chr12:71527760 | A | G | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.356+3283A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527760 | |||||||
| chr12:71527762 | A | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.356+3285A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527762 | |||||||
| chr12:71527810 | C | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+3333C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527810 | |||||||
| chr12:71527886 | T | C | 1 | a0002c0003t0005g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.356+3409T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71527886 | |||||||
| chr12:71528083 | ATAAT | A | 38 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(35): Show |
38 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.356+3610_356+3613d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71528083 | ||||||
| chr12:71528091 | A | G | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.356+3614A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71528091 | |||||||
| chr12:71528378 | C | G | 2 | a0001c0002t0001g0176 a0002c0003t0005g0175 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.356+3901C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71528378 | |||||||
| chr12:71528526 | C | A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(5): Show |
8 | HG00423.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+4049C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71528526 | |||||||
| chr12:71528865 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.356+4388T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71528865 | |||||||
| chr12:71528911 | G | T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG00438.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.356+4434G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71528911 | |||||||
| chr12:71529192 | A | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.356+4715A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71529192 | |||||||
| chr12:71529435 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0074 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.356+4958G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71529435 | |||||||
| chr12:71529761 | A | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.356+5284A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71529761 | |||||||
| chr12:71529812 | T | C | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-5303T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71529812 | |||||||
| chr12:71529947 | T | G | 1 | a0004c0005t0011g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.357-5168T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71529947 | |||||||
| chr12:71530131 | A | AT | 4 | a0001c0001t0002g0146 a0001c0001t0003g0105 a0001c0001t0003g0106 others(1): Show |
4 | HG00609.hp1 NA18612.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-4978dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71530131 | ||||||
| chr12:71530233 | G | A | 3 | a0001c0002t0001g0176 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-4882G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71530233 | |||||||
| chr12:71530252 | AG | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-4862delG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71530252 | |||||||
| chr12:71530368 | A | C | 35 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(32): Show |
35 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.357-4747A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71530368 | |||||||
| chr12:71530452 | A | C | 1 | a0001c0001t0002g0114 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.357-4663A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71530452 | |||||||
| chr12:71530582 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357-4533G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71530582 | |||||||
| chr12:71530996 | G | GAA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.357-4103_357-4102d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71530996 | ||||||
| chr12:71530996 | G | GAAA | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0003g0155 others(5): Show |
8 | HG00423.hp2 HG03130.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-4104_357-4102d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71530996 | ||||||
| chr12:71530996 | GA | G | 11 | a0001c0001t0001g0059 a0001c0001t0002g0023 a0001c0001t0003g0117 others(8): Show |
11 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.357-4102delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71530996 | ||||||
| chr12:71531161 | A | G | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.357-3954A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531161 | |||||||
| chr12:71531302 | G | A | 2 | a0001c0001t0001g0015 a0001c0002t0001g0016 |
2 | HG00280.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.357-3813G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531302 | |||||||
| chr12:71531311 | A | T | 4 | a0001c0001t0003g0084 a0001c0001t0003g0122 a0001c0001t0004g0047 others(1): Show |
4 | HG01993.hp2 NA18998.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-3804A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531311 | |||||||
| chr12:71531532 | T | C | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.357-3583T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531532 | |||||||
| chr12:71531585 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
119 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.357-3530C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531585 | |||||||
| chr12:71531738 | C | T | 1 | a0001c0002t0002g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.357-3377C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531738 | |||||||
| chr12:71531748 | A | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-3367A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531748 | |||||||
| chr12:71531800 | G | A | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.357-3315G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531800 | |||||||
| chr12:71531847 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-3268G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531847 | |||||||
| chr12:71531978 | CT | C | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.357-3136delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71531978 | |||||||
| chr12:71532274 | A | G | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.357-2841A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532274 | |||||||
| chr12:71532549 | A | T | 1 | a0001c0001t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.357-2566A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532549 | |||||||
| chr12:71532636 | ATATTT | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-2476_357-2472d others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71532636 | ||||||
| chr12:71532663 | A | G | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.357-2452A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532663 | |||||||
| chr12:71532758 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.357-2357G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532758 | |||||||
| chr12:71532785 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.357-2330T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532785 | |||||||
| chr12:71532848 | A | G | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-2267A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532848 | |||||||
| chr12:71532940 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.357-2175C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532940 | |||||||
| chr12:71532967 | G | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.357-2148G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71532967 | |||||||
| chr12:71533173 | C | G | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.357-1942C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533173 | |||||||
| chr12:71533177 | T | C | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357-1938T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533177 | |||||||
| chr12:71533208 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
119 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.357-1907G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533208 | |||||||
| chr12:71533301 | C | A | 2 | a0001c0001t0002g0130 a0001c0001t0003g0154 |
2 | HG01517.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.357-1814C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533301 | |||||||
| chr12:71533363 | T | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-1752T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533363 | |||||||
| chr12:71533467 | T | C | 36 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0035 others(33): Show |
36 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.357-1648T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533467 | |||||||
| chr12:71533588 | A | T | 1 | a0001c0009t0009g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.357-1527A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533588 | |||||||
| chr12:71533821 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.357-1294T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533821 | |||||||
| chr12:71533887 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.357-1228A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533887 | |||||||
| chr12:71533917 | C | T | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.357-1198C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533917 | |||||||
| chr12:71533966 | G | C | 3 | a0001c0001t0002g0078 a0001c0001t0003g0077 a0012c0010t0003g0121 |
3 | NA18947.hp1 NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.357-1149G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71533966 | |||||||
| chr12:71534170 | G | GA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.357-937dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71534170 | ||||||
| chr12:71534502 | TA | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(5): Show |
8 | HG00423.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-607delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 71534502 | ||||||
| chr12:71534616 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0092 |
2 | HG01106.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.357-499C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71534616 | |||||||
| chr12:71534650 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.357-465C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71534650 | |||||||
| chr12:71534671 | C | A | 1 | a0001c0001t0004g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.357-444C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71534671 | |||||||
| chr12:71534722 | T | G | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.357-393T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71534722 | |||||||
| chr12:71535021 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0004g0052 others(2): Show |
5 | HG00423.hp2 NA18959.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.357-94T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 3/17 | chr12 | 71535021 | |||||||
| chr12:71535483 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0004g0052 others(2): Show |
5 | HG00423.hp2 NA18959.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+297G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71535483 | |||||||
| chr12:71535511 | TA | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.428+337delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71535511 | ||||||
| chr12:71535620 | G | T | 3 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0014g0054 |
3 | HG00423.hp2 NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.428+434G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71535620 | |||||||
| chr12:71535765 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+579A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71535765 | |||||||
| chr12:71535808 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.428+622G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71535808 | |||||||
| chr12:71536051 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.428+865C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536051 | |||||||
| chr12:71536361 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.428+1175G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536361 | |||||||
| chr12:71536539 | T | C | 2 | a0002c0003t0005g0032 a0002c0003t0005g0194 |
2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.428+1353T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536539 | |||||||
| chr12:71536651 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.428+1465C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536651 | |||||||
| chr12:71536795 | G | T | 1 | a0001c0009t0009g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.428+1609G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536795 | |||||||
| chr12:71536999 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 others(3): Show |
6 | HG00423.hp2 HG04115.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+1813A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71536999 | |||||||
| chr12:71537183 | C | CA | 11 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(8): Show |
11 | HG00735.hp2 HG01346.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+2013dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71537183 | ||||||
| chr12:71537183 | C | CAA | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+2012_428+2013d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71537183 | ||||||
| chr12:71537183 | CA | C | 34 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(31): Show |
34 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.428+2013delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71537183 | ||||||
| chr12:71537191 | A | AC | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.428+2005_428+2006i others(3): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537191 | |||||||
| chr12:71537242 | G | T | 6 | a0001c0001t0001g0167 a0001c0002t0010g0182 a0001c0002t0010g0183 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+2056G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537242 | |||||||
| chr12:71537274 | G | T | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.428+2088G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537274 | |||||||
| chr12:71537377 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00423.hp2 NA18959.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+2191G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537377 | |||||||
| chr12:71537474 | T | TAAGAA | 37 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0169 others(34): Show |
37 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.428+2306_428+2310d others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71537474 | ||||||
| chr12:71537535 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.428+2349T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537535 | |||||||
| chr12:71537561 | A | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428+2375A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537561 | |||||||
| chr12:71537574 | A | G | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.428+2388A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537574 | |||||||
| chr12:71537688 | G | A | 1 | a0002c0003t0005g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.428+2502G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537688 | |||||||
| chr12:71537794 | G | A | 2 | a0001c0009t0009g0009 a0009c0017t0018g0004 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.428+2608G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71537794 | |||||||
| chr12:71538240 | T | A | 1 | a0001c0002t0009g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428+3054T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538240 | |||||||
| chr12:71538330 | T | C | 38 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0169 others(35): Show |
38 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.428+3144T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538330 | |||||||
| chr12:71538384 | C | T | 4 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0002c0003t0001g0020 others(1): Show |
4 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+3198C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538384 | |||||||
| chr12:71538522 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0150 a0001c0001t0001g0171 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+3336T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538522 | |||||||
| chr12:71538666 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00423.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.428+3480C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538666 | |||||||
| chr12:71538735 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.428+3549G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538735 | |||||||
| chr12:71538800 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.428+3614G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538800 | |||||||
| chr12:71538827 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.428+3641C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538827 | |||||||
| chr12:71538851 | G | T | 1 | a0002c0003t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.428+3665G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71538851 | |||||||
| chr12:71539260 | G | C | 4 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0194 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+4074G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71539260 | |||||||
| chr12:71539532 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.428+4346C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71539532 | |||||||
| chr12:71539543 | T | G | 3 | a0001c0001t0001g0131 a0001c0009t0009g0009 a0009c0017t0018g0004 |
3 | HG02965.hp2 HG02970.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.428+4357T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71539543 | |||||||
| chr12:71539585 | T | C | 47 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0048 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.428+4399T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71539585 | |||||||
| chr12:71539606 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0002c0003t0001g0020 others(1): Show |
4 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+4420T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71539606 | |||||||
| chr12:71540169 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
136 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.428+4983G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540169 | |||||||
| chr12:71540315 | A | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+5129A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540315 | |||||||
| chr12:71540318 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.428+5132A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540318 | |||||||
| chr12:71540429 | A | G | 1 | a0001c0001t0003g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.428+5243A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540429 | |||||||
| chr12:71540484 | T | C | 55 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0048 others(52): Show |
55 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.428+5298T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540484 | |||||||
| chr12:71540596 | T | C | 2 | a0002c0003t0005g0032 a0002c0003t0005g0194 |
2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.428+5410T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540596 | |||||||
| chr12:71540746 | T | C | 12 | a0001c0001t0001g0059 a0001c0001t0002g0023 a0001c0001t0003g0117 others(9): Show |
12 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.428+5560T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540746 | |||||||
| chr12:71540895 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | NA18959.hp1 NA18960.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+5709T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71540895 | |||||||
| chr12:71541010 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
116 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.428+5824C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541010 | |||||||
| chr12:71541074 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+5888A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541074 | |||||||
| chr12:71541145 | G | A | 1 | a0002c0003t0005g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.428+5959G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541145 | |||||||
| chr12:71541162 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.428+5976G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541162 | |||||||
| chr12:71541217 | A | G | 2 | a0001c0002t0010g0183 a0001c0002t0010g0184 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.428+6031A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541217 | |||||||
| chr12:71541283 | A | G | 1 | a0001c0001t0004g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.428+6097A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541283 | |||||||
| chr12:71541295 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.428+6109T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541295 | |||||||
| chr12:71541607 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0004g0053 others(1): Show |
4 | NA18959.hp1 NA18965.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+6421A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71541607 | |||||||
| chr12:71542025 | A | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0007c0015t0001g0031 |
3 | HG01069.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428+6839A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542025 | |||||||
| chr12:71542073 | G | A | 13 | a0001c0001t0001g0059 a0001c0001t0001g0169 a0001c0001t0001g0170 others(10): Show |
13 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+6887G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542073 | |||||||
| chr12:71542103 | C | G | 39 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(36): Show |
39 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.428+6917C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542103 | |||||||
| chr12:71542126 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.428+6940C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542126 | |||||||
| chr12:71542182 | G | A | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.428+6996G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542182 | |||||||
| chr12:71542272 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.428+7086A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542272 | |||||||
| chr12:71542361 | A | T | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.428+7175A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542361 | |||||||
| chr12:71542389 | C | A | 5 | a0001c0001t0002g0067 a0001c0001t0002g0114 a0001c0001t0002g0151 others(2): Show |
5 | HG01099.hp1 HG01928.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+7203C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542389 | |||||||
| chr12:71542416 | T | C | 5 | a0001c0001t0001g0167 a0001c0002t0010g0183 a0001c0002t0010g0184 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+7230T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542416 | |||||||
| chr12:71542642 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.428+7456T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542642 | |||||||
| chr12:71542747 | G | A | 13 | a0001c0001t0001g0059 a0001c0001t0001g0169 a0001c0001t0001g0170 others(10): Show |
13 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+7561G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542747 | |||||||
| chr12:71542831 | G | C | 39 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(36): Show |
39 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.428+7645G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542831 | |||||||
| chr12:71542862 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.428+7676G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71542862 | |||||||
| chr12:71542870 | GA | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+7695delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71542870 | ||||||
| chr12:71543031 | A | AG | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.428+7846dupG | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71543031 | ||||||
| chr12:71543098 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.428+7912T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543098 | |||||||
| chr12:71543214 | C | G | 40 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(37): Show |
40 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.428+8028C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543214 | |||||||
| chr12:71543396 | A | T | 5 | a0001c0001t0001g0059 a0001c0002t0001g0196 a0001c0002t0001g0198 others(2): Show |
5 | HG01069.hp2 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+8210A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543396 | |||||||
| chr12:71543432 | G | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0092 |
2 | HG01106.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.428+8246G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543432 | |||||||
| chr12:71543457 | A | T | 13 | a0001c0001t0001g0059 a0001c0001t0001g0169 a0001c0001t0001g0170 others(10): Show |
13 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+8271A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543457 | |||||||
| chr12:71543653 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.428+8467C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543653 | |||||||
| chr12:71543866 | A | G | 39 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(36): Show |
39 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.428+8680A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543866 | |||||||
| chr12:71543870 | A | C | 1 | a0002c0003t0005g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.428+8684A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543870 | |||||||
| chr12:71543920 | C | T | 2 | a0001c0002t0001g0196 a0001c0002t0001g0198 |
2 | HG01069.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428+8734C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543920 | |||||||
| chr12:71543942 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0002g0096 others(1): Show |
4 | NA18747.hp1 NA18957.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+8756T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71543942 | |||||||
| chr12:71544087 | C | A | 1 | a0001c0002t0002g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.428+8901C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544087 | |||||||
| chr12:71544091 | A | T | 1 | a0001c0001t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.428+8905A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544091 | |||||||
| chr12:71544116 | C | T | 52 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0082 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.428+8930C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544116 | |||||||
| chr12:71544218 | C | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.429-8855C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544218 | |||||||
| chr12:71544233 | A | G | 13 | a0001c0001t0001g0059 a0001c0001t0001g0169 a0001c0001t0001g0170 others(10): Show |
13 | HG00323.hp1 HG01069.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-8840A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544233 | |||||||
| chr12:71544250 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG00423.hp1 HG02135.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.429-8823G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544250 | |||||||
| chr12:71544256 | ATTCT | A | 39 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(36): Show |
39 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.429-8814_429-8811d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71544256 | ||||||
| chr12:71544304 | TTTC | T | 43 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0177 others(40): Show |
43 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.429-8757_429-8755d others(5): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71544304 | ||||||
| chr12:71544314 | TTC | T | 10 | a0001c0001t0001g0128 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG01069.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-8757_429-8756d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71544314 | ||||||
| chr12:71544315 | TC | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.429-8757delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544315 | |||||||
| chr12:71544316 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.429-8757C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544316 | |||||||
| chr12:71544506 | G | A | 1 | a0001c0001t0017g0018 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429-8567G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544506 | |||||||
| chr12:71544536 | TA | T | 6 | a0001c0001t0002g0023 a0001c0001t0002g0070 a0001c0001t0003g0117 others(3): Show |
6 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.429-8524delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71544536 | ||||||
| chr12:71544624 | G | C | 5 | a0001c0001t0002g0023 a0001c0001t0003g0117 a0001c0001t0004g0069 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-8449G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544624 | |||||||
| chr12:71544650 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0004g0053 others(1): Show |
4 | NA18959.hp1 NA18965.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-8423C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544650 | |||||||
| chr12:71544752 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.429-8321G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71544752 | |||||||
| chr12:71544939 | T | TAAGAGGG others(67): Show |
1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.429-8117_429-8116i others(76): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71544939 | ||||||
| chr12:71545000 | C | T | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.429-8073C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545000 | |||||||
| chr12:71545117 | CAAAATA | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
176 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.429-7935_429-7930d others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71545117 | ||||||
| chr12:71545161 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429-7912T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545161 | |||||||
| chr12:71545205 | G | A | 1 | a0001c0001t0020g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.429-7868G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545205 | |||||||
| chr12:71545357 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.429-7716A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545357 | |||||||
| chr12:71545389 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0021g0132 |
2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.429-7684T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545389 | |||||||
| chr12:71545493 | G | A | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.429-7580G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545493 | |||||||
| chr12:71545556 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
173 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.429-7517T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545556 | |||||||
| chr12:71545779 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.429-7294T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545779 | |||||||
| chr12:71545955 | A | G | 9 | a0001c0001t0002g0058 a0001c0001t0002g0147 a0001c0001t0002g0148 others(6): Show |
9 | HG01496.hp1 HG01993.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-7118A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545955 | |||||||
| chr12:71545992 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.429-7081T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545992 | |||||||
| chr12:71545993 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
119 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.429-7080G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71545993 | |||||||
| chr12:71546080 | A | G | 53 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0167 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.429-6993A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546080 | |||||||
| chr12:71546115 | C | A | 1 | a0001c0002t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.429-6958C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546115 | |||||||
| chr12:71546116 | C | G | 1 | a0001c0002t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.429-6957C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546116 | |||||||
| chr12:71546292 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429-6781G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546292 | |||||||
| chr12:71546317 | A | AAT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(106): Show |
109 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.429-6739_429-6738d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71546317 | ||||||
| chr12:71546317 | A | AATAT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.429-6741_429-6738d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71546317 | ||||||
| chr12:71546317 | A | AATATAT | 3 | a0001c0001t0002g0070 a0001c0001t0002g0092 a0001c0001t0003g0106 |
3 | HG00609.hp1 HG02683.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.429-6743_429-6738d others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71546317 | ||||||
| chr12:71546349 | G | A | 1 | a0001c0002t0009g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.429-6724G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546349 | |||||||
| chr12:71546373 | T | G | 1 | a0001c0002t0009g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.429-6700T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546373 | |||||||
| chr12:71546431 | T | A | 1 | a0001c0002t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.429-6642T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546431 | |||||||
| chr12:71546505 | A | G | 32 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0059 others(29): Show |
32 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.429-6568A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546505 | |||||||
| chr12:71546518 | C | T | 1 | a0002c0003t0005g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.429-6555C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546518 | |||||||
| chr12:71546576 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(172): Show |
175 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.429-6497T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546576 | |||||||
| chr12:71546695 | A | G | 2 | a0001c0001t0001g0059 a0001c0002t0001g0198 |
2 | HG01069.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.429-6378A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546695 | |||||||
| chr12:71546766 | A | T | 1 | a0001c0001t0003g0025 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.429-6307A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546766 | |||||||
| chr12:71546792 | T | G | 42 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.429-6281T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546792 | |||||||
| chr12:71546898 | A | G | 1 | a0012c0010t0003g0121 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.429-6175A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546898 | |||||||
| chr12:71546925 | T | C | 1 | a0001c0002t0009g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.429-6148T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546925 | |||||||
| chr12:71546985 | T | C | 1 | a0001c0001t0002g0146 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.429-6088T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71546985 | |||||||
| chr12:71547022 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.429-6051G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547022 | |||||||
| chr12:71547088 | G | A | 14 | a0001c0001t0007g0191 a0001c0001t0009g0005 a0001c0001t0016g0071 others(11): Show |
14 | HG01069.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.429-5985G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547088 | |||||||
| chr12:71547132 | G | A | 2 | a0001c0001t0007g0191 a0013c0013t0004g0157 |
2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429-5941G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547132 | |||||||
| chr12:71547168 | G | A | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.429-5905G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547168 | |||||||
| chr12:71547246 | AC | A | 5 | a0001c0001t0001g0167 a0001c0002t0010g0183 a0001c0002t0010g0184 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-5826delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547246 | |||||||
| chr12:71547663 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.429-5410G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547663 | |||||||
| chr12:71547695 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.429-5378G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547695 | |||||||
| chr12:71547710 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0038 others(30): Show |
33 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.429-5363T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547710 | |||||||
| chr12:71547979 | AC | A | 63 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.429-5086delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71547979 | ||||||
| chr12:71547982 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0102 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.429-5091C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547982 | |||||||
| chr12:71547985 | C | T | 3 | a0001c0001t0007g0191 a0001c0002t0001g0057 a0013c0013t0004g0157 |
3 | HG02723.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.429-5088C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547985 | |||||||
| chr12:71547987 | C | A | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.429-5086C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547987 | |||||||
| chr12:71547992 | G | A | 2 | a0001c0001t0007g0191 a0013c0013t0004g0157 |
2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429-5081G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71547992 | |||||||
| chr12:71548025 | G | A | 1 | a0001c0001t0003g0112 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.429-5048G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71548025 | |||||||
| chr12:71548124 | T | C | 1 | a0001c0001t0003g0025 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.429-4949T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71548124 | |||||||
| chr12:71548301 | C | CTG | 11 | a0001c0001t0002g0116 a0001c0001t0016g0071 a0001c0002t0007g0188 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-4749_429-4748d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(3): Show |
10 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0038 others(7): Show |
10 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-4757_429-4748d others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(5): Show |
54 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.429-4759_429-4748d others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0128 a0001c0001t0003g0026 a0007c0015t0001g0031 |
3 | HG01361.hp2 HG02559.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.429-4761_429-4748d others(16): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0082 |
3 | HG02083.hp1 HG03492.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.429-4763_429-4748d others(18): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(13): Show |
1 | a0002c0003t0001g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.429-4767_429-4748d others(22): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(15): Show |
2 | a0001c0001t0001g0127 a0001c0002t0001g0016 |
2 | HG00280.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.429-4769_429-4748d others(24): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(17): Show |
3 | a0001c0001t0001g0180 a0001c0001t0002g0029 a0001c0002t0012g0006 |
3 | HG01192.hp1 HG02486.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.429-4771_429-4748d others(26): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548301 | C | CTGTGTGT others(19): Show |
1 | a0001c0002t0021g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.429-4748_429-4747i others(28): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548301 | ||||||
| chr12:71548321 | G | GTA | 2 | a0001c0001t0001g0101 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.429-4751_429-4750i others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548321 | ||||||
| chr12:71548321 | G | GTGTGTGT others(3): Show |
8 | a0001c0001t0001g0126 a0001c0001t0001g0171 a0001c0001t0001g0172 others(5): Show |
8 | HG00323.hp2 HG00741.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-4748_429-4747i others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548321 | ||||||
| chr12:71548321 | G | GTGTGTGT others(5): Show |
4 | a0001c0001t0001g0124 a0001c0001t0002g0158 a0001c0001t0002g0166 others(1): Show |
4 | HG00140.hp2 HG00423.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-4748_429-4747i others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548321 | ||||||
| chr12:71548321 | G | GTGTGTGT others(7): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(47): Show |
50 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.429-4748_429-4747i others(16): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548321 | ||||||
| chr12:71548321 | G | GTGTGTGT others(9): Show |
9 | a0001c0001t0001g0042 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG00323.hp1 HG00735.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-4748_429-4747i others(18): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548321 | ||||||
| chr12:71548359 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429-4714G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71548359 | |||||||
| chr12:71548815 | TAC | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(44): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.429-4225_429-4224d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548815 | ||||||
| chr12:71548815 | TACAC | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0124 others(11): Show |
14 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.429-4227_429-4224d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548815 | ||||||
| chr12:71548815 | TACACAC | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.429-4229_429-4224d others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548815 | ||||||
| chr12:71548815 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0127 a0001c0001t0001g0180 a0001c0001t0002g0029 others(6): Show |
9 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-4233_429-4224d others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71548815 | ||||||
| chr12:71548944 | A | C | 1 | a0001c0001t0002g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.429-4129A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71548944 | |||||||
| chr12:71549277 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.429-3796C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549277 | |||||||
| chr12:71549394 | G | C | 2 | a0001c0001t0001g0059 a0001c0009t0009g0009 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.429-3679G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549394 | |||||||
| chr12:71549468 | T | A | 53 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0169 others(50): Show |
53 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.429-3605T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549468 | |||||||
| chr12:71549599 | G | C | 50 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0002g0070 others(47): Show |
50 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.429-3474G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549599 | |||||||
| chr12:71549670 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
44 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.429-3403T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549670 | |||||||
| chr12:71549732 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.429-3341C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549732 | |||||||
| chr12:71549757 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
44 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.429-3316T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549757 | |||||||
| chr12:71549879 | CA | C | 7 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.429-3193delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71549879 | |||||||
| chr12:71550338 | A | G | 1 | a0001c0002t0021g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.429-2735A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71550338 | |||||||
| chr12:71550426 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0109 a0001c0001t0002g0094 |
3 | HG01261.hp2 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.429-2647C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71550426 | |||||||
| chr12:71550461 | CT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.429-2595delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71550461 | ||||||
| chr12:71550789 | C | T | 1 | a0002c0003t0013g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429-2284C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71550789 | |||||||
| chr12:71550997 | G | C | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.429-2076G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71550997 | |||||||
| chr12:71551108 | T | G | 5 | a0001c0001t0001g0127 a0001c0002t0001g0016 a0001c0002t0021g0132 others(2): Show |
5 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-1965T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71551108 | |||||||
| chr12:71551316 | C | G | 11 | a0001c0001t0016g0071 a0002c0003t0005g0032 a0002c0003t0005g0033 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-1757C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71551316 | |||||||
| chr12:71551399 | G | A | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.429-1674G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71551399 | |||||||
| chr12:71551792 | A | G | 53 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0169 others(50): Show |
53 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.429-1281A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71551792 | |||||||
| chr12:71552020 | G | A | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.429-1053G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552020 | |||||||
| chr12:71552410 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.429-663T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552410 | |||||||
| chr12:71552442 | G | A | 1 | a0002c0003t0005g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-631G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552442 | |||||||
| chr12:71552490 | G | A | 9 | a0001c0002t0001g0095 a0001c0002t0001g0197 a0001c0002t0001g0198 others(6): Show |
9 | HG01069.hp2 HG01243.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-583G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552490 | |||||||
| chr12:71552498 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.429-575G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552498 | |||||||
| chr12:71552567 | C | CA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(108): Show |
111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.429-490dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71552567 | ||||||
| chr12:71552567 | C | CAA | 6 | a0001c0001t0001g0041 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG02109.hp1 HG02135.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.429-491_429-490dup others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 71552567 | ||||||
| chr12:71552694 | A | G | 4 | a0001c0001t0001g0127 a0001c0002t0001g0016 a0002c0003t0001g0020 others(1): Show |
4 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-379A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552694 | |||||||
| chr12:71552792 | G | A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.429-281G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552792 | |||||||
| chr12:71552927 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.429-146G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71552927 | |||||||
| chr12:71553016 | T | C | 1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.429-57T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 4/17 | chr12 | 71553016 | |||||||
| chr12:71553393 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.644+105G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553393 | |||||||
| chr12:71553546 | C | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.644+258C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553546 | |||||||
| chr12:71553626 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
54 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.644+338A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553626 | |||||||
| chr12:71553866 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.644+578G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553866 | |||||||
| chr12:71553926 | A | T | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.644+638A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553926 | |||||||
| chr12:71553998 | G | A | 2 | a0001c0001t0004g0053 a0001c0001t0014g0054 |
2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.644+710G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71553998 | |||||||
| chr12:71554065 | G | C | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.644+777G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71554065 | |||||||
| chr12:71554228 | G | T | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.644+940G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71554228 | |||||||
| chr12:71554377 | GA | G | 53 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0169 others(50): Show |
53 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.644+1094delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 71554377 | ||||||
| chr12:71554774 | A | G | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+1486A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71554774 | |||||||
| chr12:71554974 | C | G | 7 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-1645C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71554974 | |||||||
| chr12:71555038 | C | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.645-1581C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555038 | |||||||
| chr12:71555444 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.645-1175A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555444 | |||||||
| chr12:71555590 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.645-1029A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555590 | |||||||
| chr12:71555659 | G | A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.645-960G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555659 | |||||||
| chr12:71555756 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.645-863T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555756 | |||||||
| chr12:71555787 | A | C | 2 | a0001c0001t0008g0011 a0001c0001t0008g0012 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.645-832A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555787 | |||||||
| chr12:71555859 | A | G | 3 | a0001c0001t0003g0084 a0001c0001t0004g0047 a0001c0001t0004g0055 |
3 | NA18998.hp2 NA19010.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.645-760A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555859 | |||||||
| chr12:71555962 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
44 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.645-657G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71555962 | |||||||
| chr12:71556335 | AC | A | 7 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-283delC | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71556335 | |||||||
| chr12:71556536 | G | A | 6 | a0001c0001t0001g0127 a0001c0002t0001g0016 a0001c0002t0012g0006 others(3): Show |
6 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-83G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 5/17 | chr12 | 71556536 | |||||||
| chr12:71556809 | G | A | 1 | a0001c0001t0006g0189 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.716+119G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71556809 | |||||||
| chr12:71556969 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
44 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.716+279G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71556969 | |||||||
| chr12:71557035 | G | T | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.716+345G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557035 | |||||||
| chr12:71557059 | G | A | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.716+369G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557059 | |||||||
| chr12:71557083 | A | G | 6 | a0001c0001t0001g0127 a0001c0002t0001g0016 a0001c0002t0012g0006 others(3): Show |
6 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.716+393A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557083 | |||||||
| chr12:71557102 | A | C | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.716+412A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557102 | |||||||
| chr12:71557218 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.716+528G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557218 | |||||||
| chr12:71557263 | TGA | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0029 |
2 | HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.716+574_716+575del others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557263 | |||||||
| chr12:71557437 | T | C | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.716+747T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557437 | |||||||
| chr12:71557539 | C | G | 6 | a0001c0001t0001g0127 a0001c0002t0001g0016 a0001c0002t0012g0006 others(3): Show |
6 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.716+849C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71557539 | |||||||
| chr12:71557997 | AT | A | 49 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0002g0070 others(46): Show |
49 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.716+1310delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 71557997 | ||||||
| chr12:71558089 | C | T | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.716+1399C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558089 | |||||||
| chr12:71558195 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(104): Show |
107 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.717-1391A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558195 | |||||||
| chr12:71558310 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.717-1276C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558310 | |||||||
| chr12:71558317 | A | G | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.717-1269A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558317 | |||||||
| chr12:71558328 | A | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0002g0070 others(46): Show |
49 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.717-1258A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558328 | |||||||
| chr12:71558739 | T | A | 2 | a0004c0005t0011g0199 a0004c0005t0019g0181 |
2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.717-847T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558739 | |||||||
| chr12:71558744 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.717-842G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558744 | |||||||
| chr12:71558761 | C | A | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.717-825C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558761 | |||||||
| chr12:71558807 | A | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.717-779A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71558807 | |||||||
| chr12:71559233 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.717-353G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71559233 | |||||||
| chr12:71559282 | AAG | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(99): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.717-300_717-299del others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 71559282 | ||||||
| chr12:71559302 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(100): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.717-284A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71559302 | |||||||
| chr12:71559342 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.717-244G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71559342 | |||||||
| chr12:71559535 | A | G | 1 | a0001c0006t0003g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.717-51A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71559535 | |||||||
| chr12:71559540 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.717-46T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 6/17 | chr12 | 71559540 | |||||||
| chr12:71559760 | G | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(40): Show |
43 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.785+106G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71559760 | |||||||
| chr12:71559762 | T | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(40): Show |
43 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.785+108T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71559762 | |||||||
| chr12:71559910 | T | C | 48 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0002g0070 others(45): Show |
48 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.785+256T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71559910 | |||||||
| chr12:71560101 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.785+447A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71560101 | |||||||
| chr12:71560415 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.785+761A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71560415 | |||||||
| chr12:71560478 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.785+824A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71560478 | |||||||
| chr12:71560724 | C | T | 7 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(4): Show |
7 | HG00280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-1057C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71560724 | |||||||
| chr12:71560759 | C | G | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-1022C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71560759 | |||||||
| chr12:71561001 | A | C | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.786-780A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561001 | |||||||
| chr12:71561010 | T | C | 1 | a0002c0003t0005g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-771T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561010 | |||||||
| chr12:71561133 | G | A | 3 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0001c0002t0021g0132 |
3 | HG00280.hp2 HG02486.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.786-648G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561133 | |||||||
| chr12:71561614 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.786-167T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561614 | |||||||
| chr12:71561634 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.786-147A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561634 | |||||||
| chr12:71561745 | A | C | 1 | a0001c0001t0002g0089 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.786-36A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 7/17 | chr12 | 71561745 | |||||||
| chr12:71562095 | A | G | 1 | a0002c0003t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.857+243A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562095 | |||||||
| chr12:71562233 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.857+381A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562233 | |||||||
| chr12:71562243 | C | T | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857+391C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562243 | |||||||
| chr12:71562464 | CT | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+615delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71562464 | ||||||
| chr12:71562511 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0076 |
3 | HG00323.hp2 HG01106.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.857+659G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562511 | |||||||
| chr12:71562537 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.857+685C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562537 | |||||||
| chr12:71562682 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.857+830C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562682 | |||||||
| chr12:71562836 | C | T | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+984C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562836 | |||||||
| chr12:71562991 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.857+1139G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71562991 | |||||||
| chr12:71563012 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1160C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563012 | |||||||
| chr12:71563119 | G | A | 1 | a0001c0001t0003g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.857+1267G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563119 | |||||||
| chr12:71563121 | C | T | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.857+1269C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563121 | |||||||
| chr12:71563131 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1279A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563131 | |||||||
| chr12:71563161 | T | A | 6 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0001c0002t0021g0132 others(3): Show |
6 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+1309T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563161 | |||||||
| chr12:71563188 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1336C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563188 | |||||||
| chr12:71563189 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.857+1337A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563189 | |||||||
| chr12:71563353 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1501A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563353 | |||||||
| chr12:71563362 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1510T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563362 | |||||||
| chr12:71563382 | C | T | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.857+1530C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563382 | |||||||
| chr12:71563456 | T | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.857+1604T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563456 | |||||||
| chr12:71563511 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1659T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563511 | |||||||
| chr12:71563526 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1674T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563526 | |||||||
| chr12:71563550 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1698C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563550 | |||||||
| chr12:71563582 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.857+1730T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563582 | |||||||
| chr12:71563664 | A | T | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.857+1812A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563664 | |||||||
| chr12:71563711 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.857+1859T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563711 | |||||||
| chr12:71563849 | A | AGT | 3 | a0001c0002t0001g0016 a0001c0002t0021g0132 a0008c0014t0011g0200 |
3 | HG00280.hp2 HG02698.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.857+2020_857+2021d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563849 | ||||||
| chr12:71563849 | A | AGTGTGTG others(1): Show |
2 | a0004c0005t0011g0199 a0004c0005t0019g0181 |
2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857+2014_857+2021d others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563849 | ||||||
| chr12:71563849 | AGT | A | 3 | a0001c0001t0001g0019 a0001c0001t0007g0191 a0001c0001t0009g0005 |
3 | HG02055.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.857+2020_857+2021d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563849 | ||||||
| chr12:71563872 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.857+2020G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563872 | |||||||
| chr12:71563872 | G | GTA | 7 | a0001c0001t0001g0051 a0001c0001t0003g0090 a0001c0001t0003g0140 others(4): Show |
7 | HG00140.hp1 HG01109.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.857+2025_857+2026d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563872 | ||||||
| chr12:71563896 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(44): Show |
47 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.857+2044G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563896 | |||||||
| chr12:71563926 | ATGTACAC others(71): Show |
A | 3 | a0001c0002t0002g0107 a0001c0002t0002g0134 a0001c0002t0021g0132 |
3 | HG02698.hp1 HG03831.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.857+2084_857+2161d others(80): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563926 | ||||||
| chr12:71563926 | ATGTACAC others(149): Show |
A | 3 | a0001c0001t0001g0170 a0001c0001t0007g0191 a0001c0001t0016g0071 |
3 | HG02109.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.857+2084_857+2239d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563926 | ||||||
| chr12:71563926 | ATGTACAC others(188): Show |
A | 2 | a0001c0002t0001g0196 a0008c0014t0011g0200 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.857+2084_858-2274d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563926 | ||||||
| chr12:71563926 | ATGTACAC others(266): Show |
A | 2 | a0004c0005t0011g0199 a0004c0005t0019g0181 |
2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857+2084_858-2196d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563926 | ||||||
| chr12:71563931 | CACACACA others(110): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.857+2084_857+2200d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563931 | ||||||
| chr12:71563936 | A | G | 3 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0007c0015t0001g0031 |
3 | HG00280.hp2 HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.857+2084A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563936 | |||||||
| chr12:71563936 | ACACCGTG others(110): Show |
A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0002g0064 others(11): Show |
14 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.857+2127_857+2243d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(149): Show |
A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.857+2127_858-2270d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(188): Show |
A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0004g0173 others(1): Show |
4 | HG00741.hp1 HG02300.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+2127_858-2231d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(266): Show |
A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(43): Show |
46 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.857+2127_858-2153d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(305): Show |
A | 44 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0061 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.857+2127_858-2114d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(344): Show |
A | 1 | a0013c0013t0004g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+2127_858-2075d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563936 | ACACCGTG others(461): Show |
A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.857+2127_858-1958d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563936 | ||||||
| chr12:71563941 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0150 others(6): Show |
9 | HG00280.hp1 HG01257.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+2089G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563941 | |||||||
| chr12:71563970 | CACACGCA others(71): Show |
C | 2 | a0002c0003t0005g0195 a0006c0011t0003g0104 |
2 | HG01943.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.857+2127_857+2204d others(80): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563970 | ||||||
| chr12:71563979 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0150 others(8): Show |
11 | HG00280.hp1 HG00280.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.857+2127T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71563979 | |||||||
| chr12:71563979 | TGTGTATA others(71): Show |
T | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.857+2196_857+2273d others(80): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71563979 | ||||||
| chr12:71564009 | CACACGCA others(32): Show |
C | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.857+2196_857+2234d others(41): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564009 | ||||||
| chr12:71564048 | T | C | 13 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0150 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.857+2196T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564048 | |||||||
| chr12:71564058 | G | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0002g0064 others(11): Show |
14 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.857+2206G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564058 | |||||||
| chr12:71564097 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.857+2245G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564097 | |||||||
| chr12:71564130 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.858-2274C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564130 | |||||||
| chr12:71564136 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0004g0173 others(1): Show |
4 | HG00741.hp1 HG02300.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-2268G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564136 | |||||||
| chr12:71564175 | G | A | 3 | a0002c0003t0005g0032 a0002c0003t0005g0100 a0002c0003t0013g0010 |
3 | HG02257.hp2 HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.858-2229G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564175 | |||||||
| chr12:71564214 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(45): Show |
48 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.858-2190G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564214 | |||||||
| chr12:71564253 | G | A | 44 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0061 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.858-2151G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564253 | |||||||
| chr12:71564292 | G | A | 2 | a0001c0001t0001g0167 a0013c0013t0004g0157 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.858-2112G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564292 | |||||||
| chr12:71564312 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0002g0096 a0001c0001t0002g0147 |
3 | NA18957.hp1 NA18984.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.858-2092G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564312 | |||||||
| chr12:71564331 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.858-2073G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564331 | |||||||
| chr12:71564365 | G | A | 1 | a0004c0005t0011g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.858-2039G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564365 | |||||||
| chr12:71564432 | TCTGTACA others(32): Show |
T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(74): Show |
77 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.858-1933_858-1895d others(41): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564432 | ||||||
| chr12:71564443 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858-1961G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564443 | |||||||
| chr12:71564447 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858-1957C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564447 | |||||||
| chr12:71564451 | TATATATG others(223): Show |
T | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858-1946_858-1717d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564451 | ||||||
| chr12:71564466 | ACGTAACT others(111): Show |
A | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.858-1937_858-1820d others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564466 | |||||||
| chr12:71564471 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.858-1933A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564471 | |||||||
| chr12:71564487 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0133 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.858-1917G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564487 | |||||||
| chr12:71564526 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.858-1878G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564526 | |||||||
| chr12:71564584 | C | CGTATCTG others(70): Show |
1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.858-1763_858-1762i others(79): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564584 | ||||||
| chr12:71564603 | C | T | 2 | a0002c0003t0005g0195 a0006c0011t0003g0104 |
2 | HG01943.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.858-1801C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564603 | |||||||
| chr12:71564603 | CGTGTATA others(32): Show |
C | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.858-1790_858-1752d others(41): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564603 | ||||||
| chr12:71564607 | TATATATG others(67): Show |
T | 2 | a0002c0003t0005g0195 a0006c0011t0003g0104 |
2 | HG01943.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.858-1790_858-1717d others(76): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564607 | ||||||
| chr12:71564634 | A | C | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.858-1770A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564634 | |||||||
| chr12:71564642 | T | C | 7 | a0001c0001t0003g0084 a0001c0001t0004g0047 a0001c0001t0004g0055 others(4): Show |
7 | HG01496.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-1762T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564642 | |||||||
| chr12:71564646 | TATATATA others(28): Show |
T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.858-1688_858-1654d others(37): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564646 | ||||||
| chr12:71564653 | A | G | 3 | a0001c0001t0003g0084 a0001c0001t0004g0047 a0001c0001t0004g0055 |
3 | NA18998.hp2 NA19010.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.858-1751A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564653 | |||||||
| chr12:71564659 | A | ATACGTAT others(1): Show |
3 | a0001c0001t0003g0084 a0001c0001t0004g0047 a0001c0001t0004g0055 |
3 | NA18998.hp2 NA19010.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.858-1744_858-1743i others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564659 | ||||||
| chr12:71564669 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0004g0055 |
2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.858-1735A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564669 | |||||||
| chr12:71564670 | C | CACCG | 2 | a0001c0001t0003g0084 a0001c0001t0004g0055 |
2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.858-1734_858-1733i others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564670 | |||||||
| chr12:71564670 | CTGTATAT others(30): Show |
C | 1 | a0001c0001t0002g0120 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.858-1732_858-1696d others(39): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564670 | ||||||
| chr12:71564673 | TATATATA others(1): Show |
T | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-1716_858-1709d others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564673 | ||||||
| chr12:71564674 | A | G | 1 | a0001c0001t0004g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.858-1730A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564674 | |||||||
| chr12:71564680 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0004g0055 |
2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.858-1724A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564680 | |||||||
| chr12:71564681 | C | CATATATA others(102): Show |
1 | a0001c0001t0003g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.858-1715_858-1714i others(111): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564681 | ||||||
| chr12:71564681 | C | CATATATA others(102): Show |
1 | a0001c0001t0004g0055 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.858-1715_858-1714i others(111): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564681 | ||||||
| chr12:71564685 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0006g0189 a0001c0001t0006g0192 others(1): Show |
4 | HG02145.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-1719T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564685 | |||||||
| chr12:71564703 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0006g0189 a0001c0001t0006g0192 others(1): Show |
4 | HG02145.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-1701C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564703 | |||||||
| chr12:71564707 | G | GTA | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1690_858-1689d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564707 | ||||||
| chr12:71564709 | ATATATAC others(26): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.858-1688_858-1656d others(35): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564709 | ||||||
| chr12:71564720 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.858-1684T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564720 | |||||||
| chr12:71564738 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.858-1666C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564738 | |||||||
| chr12:71564738 | CACTG | C | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1665_858-1662d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564738 | |||||||
| chr12:71564744 | A | G | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1660A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564744 | |||||||
| chr12:71564775 | CTG | C | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1628_858-1627d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564775 | |||||||
| chr12:71564778 | C | A | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1626C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564778 | |||||||
| chr12:71564778 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.858-1626C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564778 | |||||||
| chr12:71564779 | A | C | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1625A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564779 | |||||||
| chr12:71564781 | A | G | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1623A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564781 | |||||||
| chr12:71564786 | C | T | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1618C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564786 | |||||||
| chr12:71564788 | T | G | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1616T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564788 | |||||||
| chr12:71564792 | T | C | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1612T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564792 | |||||||
| chr12:71564802 | T | TAC | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1595_858-1594d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564802 | ||||||
| chr12:71564814 | A | G | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1590A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564814 | |||||||
| chr12:71564819 | G | T | 3 | a0001c0001t0006g0189 a0001c0001t0006g0192 a0001c0001t0008g0013 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.858-1585G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564819 | |||||||
| chr12:71564833 | TAC | T | 8 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0133 others(5): Show |
8 | HG01243.hp1 HG01361.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.858-1562_858-1561d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564833 | ||||||
| chr12:71564867 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-1537G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564867 | |||||||
| chr12:71564908 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-1496A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564908 | |||||||
| chr12:71564944 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | NA18947.hp1 NA18947.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-1460C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564944 | |||||||
| chr12:71564945 | G | A | 6 | a0001c0001t0004g0069 a0001c0001t0004g0173 a0001c0001t0008g0011 others(3): Show |
6 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.858-1459G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564945 | |||||||
| chr12:71564961 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.858-1443G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564961 | |||||||
| chr12:71564978 | C | T | 2 | a0001c0001t0003g0143 a0001c0001t0007g0191 |
2 | HG02723.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.858-1426C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71564978 | |||||||
| chr12:71564983 | G | GTA | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-1410_858-1409d others(4): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71564983 | ||||||
| chr12:71565027 | A | AC | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.858-1377_858-1376i others(3): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565027 | |||||||
| chr12:71565032 | A | G | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.858-1372A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565032 | |||||||
| chr12:71565236 | C | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-1168C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565236 | |||||||
| chr12:71565421 | GCTATATA others(3): Show |
G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.858-982_858-973del others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565421 | |||||||
| chr12:71565421 | GCTATATA others(5): Show |
G | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.858-982_858-971del others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565421 | |||||||
| chr12:71565422 | C | CTATATAT others(5): Show |
2 | a0001c0002t0001g0016 a0001c0002t0021g0132 |
2 | HG00280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.858-971_858-960dup others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | C | CTATATAT others(9): Show |
1 | a0001c0002t0012g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.858-975_858-960dup others(16): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | C | CTATATAT others(11): Show |
4 | a0001c0002t0001g0196 a0001c0002t0002g0134 a0001c0016t0015g0056 others(1): Show |
4 | HG01496.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-977_858-960dup others(18): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | C | CTATATAT others(13): Show |
1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.858-979_858-960dup others(20): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | C | CTATATAT others(15): Show |
3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0009c0017t0018g0004 |
3 | HG02486.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.858-981_858-960dup others(22): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | C | CTATATAT others(17): Show |
1 | a0001c0002t0002g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.858-960_858-959ins others(24): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565422 | CTATATAT others(3): Show |
C | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858-969_858-960del others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565422 | ||||||
| chr12:71565439 | T | C | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0133 others(1): Show |
4 | HG01361.hp2 HG03239.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-965T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565439 | |||||||
| chr12:71565445 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.858-959G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565445 | |||||||
| chr12:71565472 | C | CAT | 3 | a0001c0002t0001g0057 a0001c0002t0001g0176 a0009c0017t0018g0004 |
3 | HG02965.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.858-916_858-915dup others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565472 | ||||||
| chr12:71565472 | CAT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.858-916_858-915del others(2): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 71565472 | ||||||
| chr12:71565594 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.858-810A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565594 | |||||||
| chr12:71565783 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.858-621G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565783 | |||||||
| chr12:71565815 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-589C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71565815 | |||||||
| chr12:71566001 | T | C | 10 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0068 others(7): Show |
10 | HG01099.hp2 HG01257.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.858-403T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71566001 | |||||||
| chr12:71566146 | C | T | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.858-258C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71566146 | |||||||
| chr12:71566221 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-183A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71566221 | |||||||
| chr12:71566232 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.858-172C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71566232 | |||||||
| chr12:71566322 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.858-82C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 8/17 | chr12 | 71566322 | |||||||
| chr12:71566497 | G | A | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.929+22G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 9/17 | chr12 | 71566497 | |||||||
| chr12:71566549 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.929+74G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 9/17 | chr12 | 71566549 | |||||||
| chr12:71566621 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.930-11C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 9/17 | chr12 | 71566621 | |||||||
| chr12:71566753 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.998+53G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 10/17 | chr12 | 71566753 | |||||||
| chr12:71566804 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.999-37T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 10/17 | chr12 | 71566804 | |||||||
| chr12:71567145 | T | G | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070+233T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567145 | |||||||
| chr12:71567210 | C | G | 3 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 |
3 | HG03098.hp1 HG03831.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1070+298C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567210 | |||||||
| chr12:71567316 | G | C | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070+404G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567316 | |||||||
| chr12:71567433 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1070+521C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567433 | |||||||
| chr12:71567537 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+625C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567537 | |||||||
| chr12:71567561 | T | C | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070+649T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567561 | |||||||
| chr12:71567607 | G | A | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070+695G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567607 | |||||||
| chr12:71567634 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1070+722A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567634 | |||||||
| chr12:71567710 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0001c0002t0021g0132 |
3 | HG00280.hp2 HG02486.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1070+798C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567710 | |||||||
| chr12:71567755 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1070+843C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567755 | |||||||
| chr12:71567820 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+908A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567820 | |||||||
| chr12:71567847 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+935T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567847 | |||||||
| chr12:71567859 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1070+947T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567859 | |||||||
| chr12:71567865 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1070+953C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567865 | |||||||
| chr12:71567917 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1005T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567917 | |||||||
| chr12:71567921 | A | G | 1 | a0001c0001t0004g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1070+1009A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567921 | |||||||
| chr12:71567969 | G | T | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1070+1057G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71567969 | |||||||
| chr12:71568019 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1070+1107G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568019 | |||||||
| chr12:71568282 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1370A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568282 | |||||||
| chr12:71568359 | A | G | 5 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070+1447A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568359 | |||||||
| chr12:71568686 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1774A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568686 | |||||||
| chr12:71568688 | G | A | 1 | a0002c0003t0005g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1070+1776G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568688 | |||||||
| chr12:71568695 | T | C | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1070+1783T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568695 | |||||||
| chr12:71568720 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1808A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568720 | |||||||
| chr12:71568728 | A | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1816A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568728 | |||||||
| chr12:71568889 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+1977T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568889 | |||||||
| chr12:71568901 | T | A | 1 | a0001c0001t0002g0142 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1070+1989T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568901 | |||||||
| chr12:71568909 | T | G | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070+1997T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568909 | |||||||
| chr12:71568981 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1070+2069A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71568981 | |||||||
| chr12:71569161 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1070+2249C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569161 | |||||||
| chr12:71569195 | A | G | 36 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(33): Show |
36 | HG00438.hp2 HG01109.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.1070+2283A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569195 | |||||||
| chr12:71569227 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1071-2287G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569227 | |||||||
| chr12:71569248 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1071-2266G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569248 | |||||||
| chr12:71569364 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1071-2150G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569364 | |||||||
| chr12:71569404 | T | C | 2 | a0001c0002t0001g0016 a0001c0002t0021g0132 |
2 | HG00280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1071-2110T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569404 | |||||||
| chr12:71569469 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1071-2045A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569469 | |||||||
| chr12:71569493 | A | G | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1071-2021A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569493 | |||||||
| chr12:71569515 | CA | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1071-1990delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 71569515 | ||||||
| chr12:71569548 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1071-1966G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569548 | |||||||
| chr12:71569619 | C | A | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1071-1895C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569619 | |||||||
| chr12:71569715 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-1799A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569715 | |||||||
| chr12:71569855 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
79 | HG00280.hp2 HG00438.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1071-1659C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569855 | |||||||
| chr12:71569896 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-1618A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71569896 | |||||||
| chr12:71570103 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-1411G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570103 | |||||||
| chr12:71570161 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1071-1353G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570161 | |||||||
| chr12:71570206 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-1308G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570206 | |||||||
| chr12:71570265 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1071-1249A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570265 | |||||||
| chr12:71570358 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-1156C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570358 | |||||||
| chr12:71570460 | T | C | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1071-1054T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570460 | |||||||
| chr12:71570521 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-993G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570521 | |||||||
| chr12:71570551 | T | C | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071-963T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570551 | |||||||
| chr12:71570604 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-910G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570604 | |||||||
| chr12:71570688 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-826T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570688 | |||||||
| chr12:71570829 | A | C | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1071-685A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570829 | |||||||
| chr12:71570861 | A | T | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1071-653A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570861 | |||||||
| chr12:71570875 | A | T | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1071-639A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570875 | |||||||
| chr12:71570886 | T | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-628T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570886 | |||||||
| chr12:71570933 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-581C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570933 | |||||||
| chr12:71570990 | T | A | 10 | a0001c0002t0001g0016 a0001c0002t0001g0196 a0001c0002t0002g0107 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1071-524T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71570990 | |||||||
| chr12:71571150 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1071-364G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71571150 | |||||||
| chr12:71571310 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(34): Show |
37 | HG00438.hp2 HG01109.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.1071-204A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71571310 | |||||||
| chr12:71571391 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1071-123A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 11/17 | chr12 | 71571391 | |||||||
| chr12:71571636 | T | G | 3 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0001c0002t0021g0132 |
3 | HG00280.hp2 HG02486.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1136+57T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71571636 | |||||||
| chr12:71571676 | G | A | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1136+97G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71571676 | |||||||
| chr12:71572036 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1136+457T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572036 | |||||||
| chr12:71572083 | C | CT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(55): Show |
58 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1136+519dupT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 71572083 | ||||||
| chr12:71572110 | G | C | 1 | a0001c0001t0002g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1136+531G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572110 | |||||||
| chr12:71572115 | G | A | 1 | a0003c0004t0001g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1136+536G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572115 | |||||||
| chr12:71572132 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1136+553G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572132 | |||||||
| chr12:71572144 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1136+565G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572144 | |||||||
| chr12:71572152 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1136+573G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572152 | |||||||
| chr12:71572163 | A | T | 1 | a0001c0016t0015g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1136+584A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572163 | |||||||
| chr12:71572218 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1137-632G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572218 | |||||||
| chr12:71572237 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1137-613C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572237 | |||||||
| chr12:71572372 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137-478G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572372 | |||||||
| chr12:71572377 | C | T | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1137-473C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572377 | |||||||
| chr12:71572430 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137-420C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572430 | |||||||
| chr12:71572484 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137-366G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572484 | |||||||
| chr12:71572499 | A | C | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1137-351A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572499 | |||||||
| chr12:71572558 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1137-292G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572558 | |||||||
| chr12:71572571 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137-279C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572571 | |||||||
| chr12:71572826 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-24A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 12/17 | chr12 | 71572826 | |||||||
| chr12:71573056 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(44): Show |
47 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1208+135G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573056 | |||||||
| chr12:71573201 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1208+280C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573201 | |||||||
| chr12:71573214 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1208+293A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573214 | |||||||
| chr12:71573295 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1208+374C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573295 | |||||||
| chr12:71573464 | A | G | 1 | a0005c0007t0006g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1208+543A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573464 | |||||||
| chr12:71573529 | AT | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(43): Show |
46 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1208+615delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71573529 | ||||||
| chr12:71573535 | T | A | 1 | a0001c0001t0014g0054 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1208+614T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573535 | |||||||
| chr12:71573536 | T | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1208+615T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573536 | |||||||
| chr12:71573536 | TA | T | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+621delA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71573536 | ||||||
| chr12:71573631 | T | C | 2 | a0001c0001t0003g0138 a0001c0001t0003g0140 |
2 | NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1208+710T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573631 | |||||||
| chr12:71573685 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1208+764A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573685 | |||||||
| chr12:71573913 | T | TAA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1208+1002_1208+100 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71573913 | ||||||
| chr12:71573913 | T | TAAA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(54): Show |
57 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1208+1001_1208+100 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71573913 | ||||||
| chr12:71573941 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1208+1020C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573941 | |||||||
| chr12:71573963 | G | A | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1208+1042G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573963 | |||||||
| chr12:71573986 | C | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1208+1065C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71573986 | |||||||
| chr12:71574030 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1208+1109C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574030 | |||||||
| chr12:71574085 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1208+1164C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574085 | |||||||
| chr12:71574091 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1208+1170C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574091 | |||||||
| chr12:71574099 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1208+1178C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574099 | |||||||
| chr12:71574159 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1208+1238C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574159 | |||||||
| chr12:71574238 | G | A | 13 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(10): Show |
13 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1208+1317G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574238 | |||||||
| chr12:71574295 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1208+1374C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574295 | |||||||
| chr12:71574301 | C | CA | 10 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 others(7): Show |
10 | HG00280.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1208+1402dupA | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71574301 | ||||||
| chr12:71574301 | C | CAA | 67 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0124 others(64): Show |
67 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1208+1401_1208+140 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71574301 | ||||||
| chr12:71574301 | C | CAAA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1208+1400_1208+140 others(7): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71574301 | ||||||
| chr12:71574301 | C | CAAAA | 13 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0185 others(10): Show |
13 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1208+1399_1208+140 others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71574301 | ||||||
| chr12:71574379 | C | T | 1 | a0008c0014t0011g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1208+1458C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574379 | |||||||
| chr12:71574405 | C | T | 13 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(10): Show |
13 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1208+1484C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574405 | |||||||
| chr12:71574474 | G | A | 15 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0002c0003t0001g0020 others(12): Show |
15 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208+1553G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574474 | |||||||
| chr12:71574481 | C | A | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1208+1560C>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574481 | |||||||
| chr12:71574500 | T | A | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+1579T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574500 | |||||||
| chr12:71574866 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1208+1945A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574866 | |||||||
| chr12:71574965 | C | T | 2 | a0001c0001t0003g0141 a0001c0001t0003g0160 |
2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1208+2044C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574965 | |||||||
| chr12:71574998 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1208+2077T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71574998 | |||||||
| chr12:71575145 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1208+2224G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575145 | |||||||
| chr12:71575183 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0185 a0001c0001t0002g0145 |
3 | HG02083.hp2 NA18959.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1208+2262G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575183 | |||||||
| chr12:71575188 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0002g0174 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1208+2267G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575188 | |||||||
| chr12:71575600 | A | G | 1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1209-2325A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575600 | |||||||
| chr12:71575715 | A | AAT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(36): Show |
39 | HG00323.hp2 HG00438.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1209-2203_1209-220 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575715 | ||||||
| chr12:71575715 | AAT | A | 5 | a0001c0002t0002g0134 a0004c0005t0011g0199 a0004c0005t0019g0181 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1209-2203_1209-220 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575715 | ||||||
| chr12:71575720 | ATATGTGT others(3): Show |
A | 1 | a0001c0001t0003g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1209-2203_1209-219 others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575720 | ||||||
| chr12:71575722 | A | ATATATGT others(3): Show |
1 | a0001c0001t0007g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1209-2202_1209-220 others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | ATATGTG | 3 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02109.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1209-2202_1209-220 others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | ATATGTGT others(1): Show |
7 | a0001c0001t0001g0019 a0001c0001t0002g0145 a0001c0001t0004g0069 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209-2202_1209-220 others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | ATATGTGT others(3): Show |
1 | a0001c0001t0016g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1209-2202_1209-220 others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | ATGTG | 3 | a0001c0001t0004g0164 a0001c0001t0004g0168 a0001c0001t0006g0193 |
3 | HG01884.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209-2169_1209-216 others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | ATGTGTG | 5 | a0001c0001t0006g0187 a0001c0001t0006g0189 a0001c0001t0006g0192 others(2): Show |
5 | HG01361.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-2171_1209-216 others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1209-2203A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575722 | |||||||
| chr12:71575722 | ATG | A | 8 | a0001c0001t0001g0002 a0001c0001t0002g0029 a0001c0001t0002g0060 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-2167_1209-216 others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | ATGTG | A | 6 | a0001c0002t0001g0095 a0002c0003t0001g0020 a0002c0003t0001g0125 others(3): Show |
6 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209-2169_1209-216 others(8): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | ATGTGTG | A | 12 | a0001c0002t0001g0198 a0001c0002t0007g0186 a0001c0002t0007g0188 others(9): Show |
12 | HG01069.hp2 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1209-2171_1209-216 others(10): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | ATGTGTGT others(1): Show |
A | 10 | a0001c0001t0003g0068 a0001c0001t0003g0077 a0001c0001t0003g0099 others(7): Show |
10 | HG01978.hp1 HG04115.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1209-2173_1209-216 others(12): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | ATGTGTGT others(3): Show |
A | 38 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0065 others(35): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1209-2175_1209-216 others(14): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575722 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0003g0141 a0001c0001t0003g0160 |
2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1209-2177_1209-216 others(16): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 71575722 | ||||||
| chr12:71575724 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0017 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1209-2201G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575724 | |||||||
| chr12:71575726 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0002g0029 a0001c0001t0002g0060 |
3 | HG03490.hp1 HG03490.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1209-2199G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575726 | |||||||
| chr12:71575735 | T | C | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1209-2190T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575735 | |||||||
| chr12:71575778 | T | C | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1209-2147T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575778 | |||||||
| chr12:71575872 | A | G | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1209-2053A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575872 | |||||||
| chr12:71575902 | G | A | 1 | a0010c0012t0001g0040 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1209-2023G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575902 | |||||||
| chr12:71575958 | A | G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0114 others(3): Show |
6 | HG00735.hp2 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209-1967A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71575958 | |||||||
| chr12:71576005 | G | A | 2 | a0001c0001t0003g0141 a0001c0001t0003g0160 |
2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1209-1920G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71576005 | |||||||
| chr12:71576034 | A | G | 3 | a0001c0002t0001g0016 a0001c0002t0012g0006 a0001c0002t0021g0132 |
3 | HG00280.hp2 HG02486.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1209-1891A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71576034 | |||||||
| chr12:71576105 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1209-1820A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71576105 | |||||||
| chr12:71576496 | C | G | 13 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(10): Show |
13 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209-1429C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71576496 | |||||||
| chr12:71576636 | T | A | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1209-1289T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71576636 | |||||||
| chr12:71577006 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1209-919G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577006 | |||||||
| chr12:71577154 | T | C | 1 | a0003c0004t0002g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1209-771T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577154 | |||||||
| chr12:71577159 | A | C | 1 | a0001c0002t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1209-766A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577159 | |||||||
| chr12:71577162 | T | A | 1 | a0001c0001t0002g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1209-763T>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577162 | |||||||
| chr12:71577358 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1209-567T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577358 | |||||||
| chr12:71577436 | G | C | 1 | a0003c0004t0002g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1209-489G>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577436 | |||||||
| chr12:71577464 | C | G | 11 | a0001c0001t0001g0041 a0001c0001t0002g0063 a0001c0001t0002g0163 others(8): Show |
11 | HG01928.hp1 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-461C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577464 | |||||||
| chr12:71577533 | A | G | 6 | a0001c0001t0001g0127 a0002c0003t0001g0020 a0002c0003t0001g0125 others(3): Show |
6 | HG00741.hp1 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-392A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577533 | |||||||
| chr12:71577582 | C | T | 8 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(5): Show |
8 | HG02486.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-343C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577582 | |||||||
| chr12:71577589 | G | T | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1209-336G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577589 | |||||||
| chr12:71577706 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1209-219C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 13/17 | chr12 | 71577706 | |||||||
| chr12:71578033 | A | T | 1 | a0001c0001t0003g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1280+37A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578033 | |||||||
| chr12:71578189 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1280+193A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578189 | |||||||
| chr12:71578202 | G | A | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1280+206G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578202 | |||||||
| chr12:71578559 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1281-245A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578559 | |||||||
| chr12:71578573 | A | C | 1 | a0001c0001t0003g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1281-231A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578573 | |||||||
| chr12:71578649 | C | G | 8 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(5): Show |
8 | HG02486.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-155C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578649 | |||||||
| chr12:71578721 | G | T | 1 | a0009c0017t0018g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1281-83G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578721 | |||||||
| chr12:71578733 | GT | G | 5 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-69delT | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 71578733 | ||||||
| chr12:71578740 | T | C | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-64T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 14/17 | chr12 | 71578740 | |||||||
| chr12:71578968 | T | G | 1 | a0001c0002t0021g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1406+39T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71578968 | |||||||
| chr12:71579124 | T | G | 2 | a0001c0001t0001g0185 a0001c0001t0002g0146 |
2 | NA18612.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1406+195T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579124 | |||||||
| chr12:71579286 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1406+357C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579286 | |||||||
| chr12:71579330 | C | T | 8 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(5): Show |
8 | HG02486.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1406+401C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579330 | |||||||
| chr12:71579569 | G | A | 4 | a0001c0002t0001g0196 a0001c0002t0002g0107 a0001c0002t0002g0134 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406+640G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579569 | |||||||
| chr12:71579601 | A | G | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1406+672A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579601 | |||||||
| chr12:71579730 | G | A | 12 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0133 others(9): Show |
12 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407-548G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579730 | |||||||
| chr12:71579752 | T | C | 8 | a0002c0003t0005g0032 a0002c0003t0005g0033 a0002c0003t0005g0100 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407-526T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579752 | |||||||
| chr12:71579995 | C | T | 5 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1407-283C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71579995 | |||||||
| chr12:71580007 | C | G | 18 | a0001c0002t0001g0016 a0001c0002t0001g0057 a0001c0002t0001g0176 others(15): Show |
18 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1407-271C>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 15/17 | chr12 | 71580007 | |||||||
| chr12:71580517 | C | T | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1552+94C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71580517 | |||||||
| chr12:71580518 | G | A | 9 | a0001c0001t0001g0178 a0001c0002t0001g0196 a0001c0002t0002g0107 others(6): Show |
9 | HG01346.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1552+95G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71580518 | |||||||
| chr12:71580569 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1552+146A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71580569 | |||||||
| chr12:71580596 | G | A | 1 | a0001c0002t0021g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1552+173G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71580596 | |||||||
| chr12:71580778 | G | T | 3 | a0004c0005t0011g0199 a0004c0005t0019g0181 a0008c0014t0011g0200 |
3 | HG02486.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1552+355G>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71580778 | |||||||
| chr12:71581035 | A | G | 22 | a0001c0001t0001g0178 a0001c0002t0001g0196 a0001c0002t0002g0107 others(19): Show |
22 | HG00741.hp1 HG01175.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1552+612A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581035 | |||||||
| chr12:71581053 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1552+630T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581053 | |||||||
| chr12:71581063 | G | A | 27 | a0001c0001t0001g0178 a0001c0002t0001g0016 a0001c0002t0001g0057 others(24): Show |
27 | HG00280.hp2 HG00741.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1552+640G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581063 | |||||||
| chr12:71581359 | A | C | 9 | a0001c0001t0001g0178 a0001c0002t0001g0196 a0001c0002t0002g0107 others(6): Show |
9 | HG01346.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1552+936A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581359 | |||||||
| chr12:71581596 | T | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0191 |
3 | HG02109.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1553-860T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581596 | |||||||
| chr12:71581733 | G | A | 1 | a0001c0001t0009g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1553-723G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581733 | |||||||
| chr12:71581801 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1553-655T>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581801 | |||||||
| chr12:71581899 | A | G | 1 | a0007c0015t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1553-557A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71581899 | |||||||
| chr12:71582132 | G | A | 5 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553-324G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 16/17 | chr12 | 71582132 | |||||||
| chr12:71582766 | C | T | 5 | a0001c0002t0001g0016 a0001c0002t0001g0057 a0001c0002t0001g0176 others(2): Show |
5 | HG00280.hp2 HG02486.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1636+227C>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71582766 | |||||||
| chr12:71582916 | A | C | 1 | a0012c0010t0003g0121 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1636+377A>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71582916 | |||||||
| chr12:71582942 | GAGGA | G | 16 | a0001c0001t0004g0052 a0001c0001t0004g0069 a0001c0016t0015g0056 others(13): Show |
16 | HG00423.hp2 HG00741.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1636+422_1636+425d others(6): Show |
LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 71582942 | ||||||
| chr12:71582956 | G | A | 10 | a0001c0001t0001g0178 a0001c0001t0004g0173 a0001c0002t0001g0196 others(7): Show |
10 | HG01346.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1636+417G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71582956 | |||||||
| chr12:71582996 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1636+457A>G | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71582996 | |||||||
| chr12:71583047 | T | C | 5 | a0002c0003t0001g0020 a0002c0003t0001g0125 a0002c0003t0002g0083 others(2): Show |
5 | HG00741.hp1 HG01175.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1636+508T>C | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71583047 | |||||||
| chr12:71583164 | G | A | 1 | a0010c0012t0001g0040 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1637-483G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71583164 | |||||||
| chr12:71583285 | G | A | 2 | a0001c0002t0001g0057 a0001c0002t0001g0176 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637-362G>A | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71583285 | |||||||
| chr12:71583566 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1637-81A>T | LGR5 | ENSG00000139292.13 | transcript | ENST00000266674.10 | protein_coding | 17/17 | chr12 | 71583566 |