Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22885 |
| ensemblid | ENSG00000173210.21 |
| hgncid | 29132 |
| symbol | ABLIM3 |
| name | actin binding LIM protein family member 3 |
| refseq_nuc | NM_014945.5 |
| refseq_prot | NP_055760.1 |
| ensembl_nuc | ENST00000309868.12 |
| ensembl_prot | ENSP00000310309.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 149141493 |
| end | 149260542 |
| strand | + |
| ver | v1.2 |
| region | chr5:149141493-149260542 |
| region5000 | chr5:149136493-149265542 |
| regionname0 | ABLIM3_chr5_149141493_149260542 |
| regionname5000 | ABLIM3_chr5_149136493_149265542 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 683 | 247 | 63 | 38 | 108 | 10 | 26 | 82 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| a0002 | 0/0 | 683 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| a0003 | 0/0 | 683 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| a0004 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| a0005 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| a0006 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | MNTSI others(678): Show |
chr5 | 149136493 | 149265542 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2049 | 229 | 52 | 34 | 107 | 10 | 24 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0002 | 0/0 | 2049 | 5 | 4 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0003 | 0/0 | 2049 | 4 | 3 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0006 | 0/0 | 2049 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0008 | 0/0 | 2049 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0009 | 0/0 | 2049 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0010 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0001c0014 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0002c0004 | 0/0 | 2049 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0002c0005 | 0/0 | 2049 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0003c0007 | 0/0 | 2049 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0004c0013 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0005c0011 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 | ||
| a0006c0012 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | ATGAA others(2044): Show |
chr5 | 149136493 | 149265542 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4439 | 104 | 13 | 19 | 55 | 6 | 10 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0002 | 0/1 | 4439 | 78 | 7 | 13 | 45 | 4 | 8 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0003 | 0/0 | 4439 | 19 | 16 | 2 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0004 | 0/0 | 4439 | 9 | 7 | 0 | 0 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0005 | 0/0 | 4439 | 7 | 7 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0006 | 0/0 | 4439 | 6 | 0 | 0 | 4 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0009 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0010 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0012 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0015 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0016 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0001t0018 | 0/0 | 4439 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0002t0005 | 0/0 | 4439 | 5 | 4 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0003t0004 | 0/0 | 4439 | 4 | 3 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0006t0011 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0006t0014 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0006t0017 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0008t0001 | 0/0 | 4439 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0009t0007 | 0/0 | 4439 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0010t0001 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0001c0014t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0002c0004t0004 | 0/0 | 4439 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0002c0005t0008 | 0/0 | 4439 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0002c0005t0013 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0003c0007t0001 | 0/0 | 4439 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0004c0013t0001 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0005c0011t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| a0006c0012t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | GCCCC others(4434): Show |
chr5 | 149136493 | 149265542 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0016g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0018g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0017g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0008t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0009t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0009t0007g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0010t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0014t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0004t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0004t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0004t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0005t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0005t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0005t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0003c0007t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0003c0007t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0004c0013t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0005c0011t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0006c0012t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | GBR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0031 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01175 | hp2 | a0003 | c0007 | t0001 | g0146 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01192 | hp2 | a0003 | c0007 | t0001 | g0233 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0248 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0113 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01261 | hp1 | a0001 | c0009 | t0007 | g0037 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01884 | hp1 | a0001 | c0006 | t0017 | g0070 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02135 | hp1 | a0001 | c0014 | t0001 | g0094 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0017 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02647 | hp1 | a0002 | c0005 | t0013 | g0019 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02683 | hp1 | a0001 | c0008 | t0001 | g0176 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02738 | hp1 | a0001 | c0001 | t0018 | g0237 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02738 | hp2 | a0001 | c0009 | t0007 | g0117 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02818 | hp1 | a0002 | c0004 | t0004 | g0013 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0215 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02897 | hp2 | a0004 | c0013 | t0001 | g0247 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02976 | hp1 | a0001 | c0006 | t0011 | g0071 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03041 | hp2 | a0002 | c0004 | t0004 | g0089 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0075 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0110 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03486 | hp2 | a0001 | c0006 | t0014 | g0213 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03540 | hp2 | a0001 | c0010 | t0001 | g0217 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0093 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0181 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0182 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0039 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18522 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18942 | hp1 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18967 | hp2 | a0005 | c0011 | t0001 | g0134 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18978 | hp2 | a0001 | c0001 | t0010 | g0133 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19012 | hp1 | a0001 | c0001 | t0015 | g0205 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19054 | hp1 | a0006 | c0012 | t0001 | g0101 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19240 | hp2 | a0002 | c0005 | t0008 | g0116 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0074 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03471 | hp1 | a0002 | c0005 | t0008 | g0115 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03471 | hp2 | a0002 | c0004 | t0004 | g0090 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA21309 | hp1 | a0001 | c0003 | t0004 | g0122 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0099 | REF | REF | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0220 | REF | REF | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149200354 | G | A | 1 | a0002 | 6 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
missense_variant | MODERATE | c.374G>A | p.Gly125Asp | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/24 | 623/4439 | 374/2052 | 125/683 | chr5 | 149200354 | |||
| chr5:149233236 | G | A | 1 | a0005 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.824G>A | p.Arg275Gln | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/24 | 1073/4439 | 824/2052 | 275/683 | chr5 | 149233236 | |||
| chr5:149239272 | T | A | 1 | a0003 | 2 | HG01175.hp2 HG01192.hp2 |
missense_variant | MODERATE | c.1069T>A | p.Ser357Thr | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/24 | 1318/4439 | 1069/2052 | 357/683 | chr5 | 149239272 | |||
| chr5:149239783 | C | T | 1 | a0004 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1099C>T | p.Arg367Trp | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/24 | 1348/4439 | 1099/2052 | 367/683 | chr5 | 149239783 | |||
| chr5:149242533 | G | C | 1 | a0006 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.1346G>C | p.Arg449Pro | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/24 | 1595/4439 | 1346/2052 | 449/683 | chr5 | 149242533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149200376 | G | A | 2 | a0001c0006 a0001c0010 |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.396G>A | p.Thr132Thr | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/24 | 645/4439 | 396/2052 | 132/683 | chr5 | 149200376 | |||
| chr5:149200412 | G | A | 1 | a0001c0002 | 5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.432G>A | p.Lys144Lys | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/24 | 681/4439 | 432/2052 | 144/683 | chr5 | 149200412 | |||
| chr5:149207114 | C | T | 1 | a0001c0010 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.555C>T | p.Leu185Leu | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/24 | 804/4439 | 555/2052 | 185/683 | chr5 | 149207114 | |||
| chr5:149233294 | C | T | 1 | a0001c0014 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.882C>T | p.Val294Val | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/24 | 1131/4439 | 882/2052 | 294/683 | chr5 | 149233294 | |||
| chr5:149242519 | C | A | 1 | a0001c0008 | 2 | HG01167.hp1 HG02683.hp1 |
synonymous_variant | LOW | c.1332C>A | p.Pro444Pro | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/24 | 1581/4439 | 1332/2052 | 444/683 | chr5 | 149242519 | |||
| chr5:149242522 | G | A | 2 | a0001c0008 a0001c0010 |
3 | HG01167.hp1 HG02683.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.1335G>A | p.Pro445Pro | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/24 | 1584/4439 | 1335/2052 | 445/683 | chr5 | 149242522 | |||
| chr5:149245008 | C | A | 2 | a0001c0003 a0002c0004 |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
synonymous_variant | LOW | c.1479C>A | p.Ser493Ser | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/24 | 1728/4439 | 1479/2052 | 493/683 | chr5 | 149245008 | |||
| chr5:149246504 | G | A | 1 | a0001c0009 | 2 | HG01261.hp1 HG02738.hp2 |
synonymous_variant | LOW | c.1509G>A | p.Ser503Ser | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/24 | 1758/4439 | 1509/2052 | 503/683 | chr5 | 149246504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149141537 | G | T | 1 | a0001c0001t0018 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 1/24 | 559 | chr5 | 149141537 | ||||||
| chr5:149258496 | G | C | 1 | a0001c0009t0007 | 2 | HG01261.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*92G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 92 | chr5 | 149258496 | ||||||
| chr5:149258528 | G | C | 1 | a0001c0001t0009 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 124 | chr5 | 149258528 | ||||||
| chr5:149258548 | G | A | 1 | a0001c0001t0010 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 144 | chr5 | 149258548 | ||||||
| chr5:149258932 | G | A | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(6): Show |
41 | HG00738.hp2 HG01071.hp1 HG01243.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 528 | chr5 | 149258932 | ||||||
| chr5:149259239 | C | T | 1 | a0001c0006t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 835 | chr5 | 149259239 | ||||||
| chr5:149259357 | C | T | 1 | a0001c0006t0014 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 953 | chr5 | 149259357 | ||||||
| chr5:149259499 | C | T | 2 | a0001c0001t0002 a0001c0001t0016 |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1095 | chr5 | 149259499 | ||||||
| chr5:149259630 | A | G | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(10): Show |
56 | HG00738.hp2 HG01071.hp1 HG01243.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1226A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1226 | chr5 | 149259630 | ||||||
| chr5:149259711 | A | G | 1 | a0002c0005t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1307 | chr5 | 149259711 | ||||||
| chr5:149259749 | A | T | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(7): Show |
43 | HG00738.hp2 HG01071.hp1 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1345A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1345 | chr5 | 149259749 | ||||||
| chr5:149259760 | G | T | 1 | a0001c0001t0012 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1356 | chr5 | 149259760 | ||||||
| chr5:149259774 | T | A | 4 | a0001c0001t0003 a0001c0006t0011 a0001c0009t0007 others(1): Show |
23 | HG00738.hp2 HG01071.hp1 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1370T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1370 | chr5 | 149259774 | ||||||
| chr5:149259895 | T | A | 1 | a0001c0006t0011 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1491 | chr5 | 149259895 | ||||||
| chr5:149259945 | C | T | 1 | a0001c0001t0015 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1541 | chr5 | 149259945 | ||||||
| chr5:149259995 | G | A | 1 | a0001c0001t0016 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1591G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1591 | chr5 | 149259995 | ||||||
| chr5:149260199 | G | A | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
140 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1795G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1795 | chr5 | 149260199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149141669 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-88+15G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 1/23 | chr5 | 149141669 | |||||||
| chr5:149141772 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0003g0001 others(2): Show |
6 | HG01496.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-88+118C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 1/23 | chr5 | 149141772 | |||||||
| chr5:149141862 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-87-147G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 1/23 | chr5 | 149141862 | |||||||
| chr5:149142236 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(211): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.13+128T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142236 | |||||||
| chr5:149142247 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG01884.hp2 HG04228.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.13+139T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142247 | |||||||
| chr5:149142281 | ACT | A | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | HG02896.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.13+176_13+177delCT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149142281 | ||||||
| chr5:149142312 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.13+204T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142312 | |||||||
| chr5:149142576 | A | C | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+468A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142576 | |||||||
| chr5:149142666 | G | A | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.13+558G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142666 | |||||||
| chr5:149142680 | G | T | 1 | a0001c0001t0003g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.13+572G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142680 | |||||||
| chr5:149142698 | C | G | 12 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(9): Show |
12 | HG00438.hp1 HG00673.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+590C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142698 | |||||||
| chr5:149142816 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0016g0014 |
2 | NA18942.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.13+708G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142816 | |||||||
| chr5:149142935 | A | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.13+827A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142935 | |||||||
| chr5:149142947 | C | T | 1 | a0001c0001t0006g0093 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.13+839C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149142947 | |||||||
| chr5:149143016 | C | G | 6 | a0001c0001t0003g0087 a0001c0001t0004g0088 a0001c0001t0004g0091 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+908C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143016 | |||||||
| chr5:149143138 | G | A | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+1030G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143138 | |||||||
| chr5:149143277 | T | G | 1 | a0001c0014t0001g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.13+1169T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143277 | |||||||
| chr5:149143314 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.13+1206G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143314 | |||||||
| chr5:149143316 | T | C | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.13+1208T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143316 | |||||||
| chr5:149143346 | G | C | 2 | a0001c0001t0001g0018 a0001c0003t0004g0017 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.13+1238G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143346 | |||||||
| chr5:149143460 | A | G | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.13+1352A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143460 | |||||||
| chr5:149143970 | C | A | 1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13+1862C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149143970 | |||||||
| chr5:149144143 | G | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(89): Show |
94 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+2035G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149144143 | |||||||
| chr5:149144355 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01071.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.13+2247A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149144355 | |||||||
| chr5:149145257 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.13+3149C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145257 | |||||||
| chr5:149145258 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.13+3150C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145258 | |||||||
| chr5:149145416 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.13+3308G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145416 | |||||||
| chr5:149145606 | T | C | 2 | a0001c0001t0001g0018 a0001c0003t0004g0017 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.13+3498T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145606 | |||||||
| chr5:149145778 | C | T | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+3670C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145778 | |||||||
| chr5:149145792 | C | CT | 35 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0111 others(32): Show |
35 | HG00738.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.13+3695dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149145792 | ||||||
| chr5:149145792 | C | CTT | 60 | a0001c0001t0001g0095 a0001c0001t0001g0128 a0001c0001t0001g0129 others(57): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.13+3694_13+3695dup others(2): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149145792 | ||||||
| chr5:149145889 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.13+3781G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145889 | |||||||
| chr5:149145925 | G | A | 90 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0111 others(87): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.13+3817G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149145925 | |||||||
| chr5:149146077 | C | A | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+3969C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146077 | |||||||
| chr5:149146080 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.13+3972C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146080 | |||||||
| chr5:149146503 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0002g0105 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.13+4395G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146503 | |||||||
| chr5:149146519 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.13+4411A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146519 | |||||||
| chr5:149146563 | G | A | 1 | a0001c0001t0006g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.13+4455G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146563 | |||||||
| chr5:149146606 | T | C | 90 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0111 others(87): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.13+4498T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146606 | |||||||
| chr5:149146723 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.13+4615T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146723 | |||||||
| chr5:149146801 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.13+4693C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146801 | |||||||
| chr5:149146954 | T | C | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+4846T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149146954 | |||||||
| chr5:149147004 | T | A | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+4896T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147004 | |||||||
| chr5:149147015 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+4907G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147015 | |||||||
| chr5:149147069 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0178 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.13+4961_13+4962ins others(19): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147069 | |||||||
| chr5:149147069 | T | TTC | 4 | a0001c0001t0002g0100 a0001c0002t0005g0214 a0001c0002t0005g0215 others(1): Show |
4 | HG01167.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+4980_13+4981dup others(2): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147069 | ||||||
| chr5:149147069 | T | TTCTC | 39 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(36): Show |
39 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.13+4978_13+4981dup others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147069 | ||||||
| chr5:149147069 | T | TTCTCTCT others(3): Show |
1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+4972_13+4981dup others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147069 | ||||||
| chr5:149147069 | T | TTCTCTCT others(7): Show |
14 | a0001c0001t0001g0081 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
14 | HG00597.hp1 HG00673.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.13+4968_13+4981dup others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147069 | ||||||
| chr5:149147069 | T | TTCTCTCT others(11): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03017.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.13+4964_13+4981dup others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147069 | ||||||
| chr5:149147101 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13+4993C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147101 | |||||||
| chr5:149147113 | ATGTG | A | 3 | a0001c0001t0001g0023 a0001c0001t0002g0025 a0001c0010t0001g0217 |
3 | HG03017.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+5026_13+5029del others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149147113 | ||||||
| chr5:149147340 | C | T | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+5232C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147340 | |||||||
| chr5:149147346 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0005g0069 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.13+5238G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147346 | |||||||
| chr5:149147437 | C | T | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+5329C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147437 | |||||||
| chr5:149147538 | G | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.13+5430G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147538 | |||||||
| chr5:149147723 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13+5615G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147723 | |||||||
| chr5:149147779 | T | G | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+5671T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149147779 | |||||||
| chr5:149148001 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.13+5893G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148001 | |||||||
| chr5:149148243 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+6135G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148243 | |||||||
| chr5:149148459 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.13+6351T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148459 | |||||||
| chr5:149148544 | C | T | 89 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0111 others(86): Show |
90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.13+6436C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148544 | |||||||
| chr5:149148606 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.13+6498G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148606 | |||||||
| chr5:149148630 | T | C | 7 | a0001c0001t0003g0087 a0001c0001t0004g0068 a0001c0001t0004g0088 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+6522T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148630 | |||||||
| chr5:149148656 | C | T | 19 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(16): Show |
19 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+6548C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148656 | |||||||
| chr5:149148678 | C | G | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+6570C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148678 | |||||||
| chr5:149148705 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.13+6597C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149148705 | |||||||
| chr5:149149125 | G | T | 23 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(20): Show |
23 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.13+7017G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149125 | |||||||
| chr5:149149201 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+7093C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149201 | |||||||
| chr5:149149419 | T | C | 23 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(20): Show |
23 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.13+7311T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149419 | |||||||
| chr5:149149469 | A | C | 19 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(16): Show |
19 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+7361A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149469 | |||||||
| chr5:149149502 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+7394G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149502 | |||||||
| chr5:149149540 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+7432A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149540 | |||||||
| chr5:149149679 | C | G | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+7571C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149149679 | |||||||
| chr5:149150148 | T | C | 16 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(13): Show |
16 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.13+8040T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149150148 | |||||||
| chr5:149150670 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.13+8562A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149150670 | |||||||
| chr5:149150862 | T | TCTCTGTG others(12): Show |
1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+8755_13+8773dup others(19): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149150862 | ||||||
| chr5:149150869 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0005g0069 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.13+8761G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149150869 | |||||||
| chr5:149150892 | A | G | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+8784A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149150892 | |||||||
| chr5:149151151 | C | T | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+9043C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149151151 | |||||||
| chr5:149151354 | G | A | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+9246G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149151354 | |||||||
| chr5:149151746 | A | G | 5 | a0001c0001t0003g0087 a0001c0001t0004g0088 a0001c0001t0005g0086 others(2): Show |
5 | HG02258.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.13+9638A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149151746 | |||||||
| chr5:149152005 | C | T | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+9897C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152005 | |||||||
| chr5:149152203 | G | T | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+10095G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152203 | |||||||
| chr5:149152308 | T | C | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+10200T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152308 | |||||||
| chr5:149152338 | G | A | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+10230G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152338 | |||||||
| chr5:149152420 | T | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(167): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.13+10312T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152420 | |||||||
| chr5:149152594 | G | C | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+10486G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152594 | |||||||
| chr5:149152834 | G | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.13+10726G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152834 | |||||||
| chr5:149152913 | C | T | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+10805C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152913 | |||||||
| chr5:149152936 | C | T | 1 | a0001c0008t0001g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.13+10828C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152936 | |||||||
| chr5:149152970 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.13+10862A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152970 | |||||||
| chr5:149152998 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13+10890G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149152998 | |||||||
| chr5:149153155 | C | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.13+11047C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153155 | |||||||
| chr5:149153332 | T | A | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+11224T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153332 | |||||||
| chr5:149153448 | A | T | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+11340A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153448 | |||||||
| chr5:149153465 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+11357G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153465 | |||||||
| chr5:149153527 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0002g0174 |
2 | NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.13+11419C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153527 | |||||||
| chr5:149153636 | T | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.13+11528T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153636 | |||||||
| chr5:149153705 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.13+11597C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153705 | |||||||
| chr5:149153843 | A | G | 19 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(16): Show |
19 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+11735A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153843 | |||||||
| chr5:149153852 | A | T | 1 | a0001c0001t0002g0066 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.13+11744A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153852 | |||||||
| chr5:149153863 | G | A | 2 | a0001c0001t0001g0018 a0001c0003t0004g0017 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.13+11755G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149153863 | |||||||
| chr5:149154060 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.13+11952C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154060 | |||||||
| chr5:149154161 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.13+12053G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154161 | |||||||
| chr5:149154188 | C | T | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+12080C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154188 | |||||||
| chr5:149154189 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.13+12081A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154189 | |||||||
| chr5:149154313 | G | A | 1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+12205G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154313 | |||||||
| chr5:149154453 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13+12345C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154453 | |||||||
| chr5:149154507 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.13+12399C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154507 | |||||||
| chr5:149154548 | G | A | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+12440G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154548 | |||||||
| chr5:149154620 | T | C | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | HG02896.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.13+12512T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154620 | |||||||
| chr5:149154647 | T | G | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+12539T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154647 | |||||||
| chr5:149154658 | A | G | 3 | a0001c0001t0004g0068 a0001c0001t0005g0069 a0002c0005t0013g0019 |
3 | HG02055.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.13+12550A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154658 | |||||||
| chr5:149154999 | G | A | 3 | a0001c0001t0004g0068 a0001c0001t0005g0069 a0002c0005t0013g0019 |
3 | HG02055.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.13+12891G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149154999 | |||||||
| chr5:149155092 | G | T | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+12984G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155092 | |||||||
| chr5:149155299 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+13191C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155299 | |||||||
| chr5:149155321 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.13+13213C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155321 | |||||||
| chr5:149155332 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.13+13224A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155332 | |||||||
| chr5:149155391 | C | A | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+13283C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155391 | |||||||
| chr5:149155451 | G | A | 4 | a0001c0001t0002g0024 a0001c0002t0005g0214 a0001c0002t0005g0215 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+13343G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155451 | |||||||
| chr5:149155633 | T | G | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+13525T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155633 | |||||||
| chr5:149155776 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.13+13668G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155776 | |||||||
| chr5:149155796 | G | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18947.hp2 NA18963.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.13+13688G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155796 | |||||||
| chr5:149155888 | A | T | 7 | a0001c0001t0003g0087 a0001c0001t0004g0068 a0001c0001t0004g0088 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+13780A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149155888 | |||||||
| chr5:149156018 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+13910G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156018 | |||||||
| chr5:149156438 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.13+14330A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156438 | |||||||
| chr5:149156773 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+14665A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156773 | |||||||
| chr5:149156785 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+14677G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156785 | |||||||
| chr5:149156895 | G | T | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+14787G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156895 | |||||||
| chr5:149156900 | G | C | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+14792G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156900 | |||||||
| chr5:149156920 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.13+14812C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156920 | |||||||
| chr5:149156949 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.13+14841C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156949 | |||||||
| chr5:149156952 | C | T | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+14844C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149156952 | |||||||
| chr5:149157082 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0002g0198 |
2 | NA18995.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.13+14974G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157082 | |||||||
| chr5:149157104 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+14996G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157104 | |||||||
| chr5:149157246 | C | A | 1 | a0001c0001t0003g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13+15138C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157246 | |||||||
| chr5:149157353 | C | G | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13+15245C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157353 | |||||||
| chr5:149157524 | G | A | 1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13+15416G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157524 | |||||||
| chr5:149157799 | C | A | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+15691C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157799 | |||||||
| chr5:149157932 | A | T | 1 | a0001c0001t0002g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.13+15824A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149157932 | |||||||
| chr5:149158039 | C | T | 2 | a0001c0001t0004g0068 a0001c0001t0005g0069 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.13+15931C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149158039 | |||||||
| chr5:149158667 | G | A | 16 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(13): Show |
16 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.13+16559G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149158667 | |||||||
| chr5:149158821 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 others(3): Show |
6 | HG01071.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+16713T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149158821 | |||||||
| chr5:149158853 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.13+16745G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149158853 | |||||||
| chr5:149159077 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.13+16969A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149159077 | |||||||
| chr5:149159358 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.13+17250T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149159358 | |||||||
| chr5:149159454 | G | A | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+17346G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149159454 | |||||||
| chr5:149159537 | C | T | 136 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.13+17429C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149159537 | |||||||
| chr5:149160003 | CTTAT | C | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+17902_13+17905d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149160003 | ||||||
| chr5:149160025 | C | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0023 others(40): Show |
43 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.13+17917C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149160025 | |||||||
| chr5:149160224 | G | A | 3 | a0001c0001t0004g0068 a0001c0001t0005g0069 a0001c0006t0014g0213 |
3 | HG02055.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.13+18116G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149160224 | |||||||
| chr5:149160332 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.13+18224G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149160332 | |||||||
| chr5:149160424 | CTCTAG | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.13+18320_13+18324d others(7): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149160424 | ||||||
| chr5:149160461 | CA | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.13+18368delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149160461 | ||||||
| chr5:149160856 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.13+18748G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149160856 | |||||||
| chr5:149160985 | G | A | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+18877G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149160985 | |||||||
| chr5:149161170 | G | A | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.13+19062G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161170 | |||||||
| chr5:149161171 | C | T | 2 | a0001c0001t0001g0171 a0006c0012t0001g0101 |
2 | NA19011.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.13+19063C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161171 | |||||||
| chr5:149161313 | C | T | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+19205C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161313 | |||||||
| chr5:149161341 | G | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(24): Show |
27 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.13+19233G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161341 | |||||||
| chr5:149161413 | T | C | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.13+19305T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161413 | |||||||
| chr5:149161579 | G | T | 2 | a0001c0001t0001g0211 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.13+19471G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161579 | |||||||
| chr5:149161777 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.13+19669T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161777 | |||||||
| chr5:149161890 | CTG | C | 3 | a0001c0001t0001g0201 a0001c0001t0002g0103 a0001c0001t0002g0226 |
3 | HG00140.hp1 HG02083.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.13+19796_13+19797d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149161890 | ||||||
| chr5:149161927 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.13+19819C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149161927 | |||||||
| chr5:149162000 | A | G | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+19892A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162000 | |||||||
| chr5:149162064 | G | A | 18 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+19956G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162064 | |||||||
| chr5:149162103 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.13+19995C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162103 | |||||||
| chr5:149162211 | T | C | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+20103T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162211 | |||||||
| chr5:149162385 | T | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(25): Show |
28 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.13+20277T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162385 | |||||||
| chr5:149162389 | A | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.13+20281A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162389 | |||||||
| chr5:149162444 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.13+20336C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162444 | |||||||
| chr5:149162465 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.13+20357A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162465 | |||||||
| chr5:149162535 | G | T | 2 | a0001c0001t0001g0175 a0001c0001t0002g0174 |
2 | NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.13+20427G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162535 | |||||||
| chr5:149162537 | G | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.13+20429G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162537 | |||||||
| chr5:149162597 | C | T | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+20489C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162597 | |||||||
| chr5:149162606 | C | T | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+20498C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162606 | |||||||
| chr5:149162707 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.13+20599T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162707 | |||||||
| chr5:149162718 | G | A | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.13+20610G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162718 | |||||||
| chr5:149162843 | C | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.14-20609C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162843 | |||||||
| chr5:149162885 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-20567G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162885 | |||||||
| chr5:149162989 | G | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0078 others(16): Show |
19 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.14-20463G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149162989 | |||||||
| chr5:149163010 | G | A | 132 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0028 others(129): Show |
133 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.14-20442G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163010 | |||||||
| chr5:149163047 | A | T | 1 | a0001c0001t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.14-20405A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163047 | |||||||
| chr5:149163282 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-20170G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163282 | |||||||
| chr5:149163418 | G | GC | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.14-20033dupC | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149163418 | ||||||
| chr5:149163438 | C | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.14-20014C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163438 | |||||||
| chr5:149163552 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.14-19900G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163552 | |||||||
| chr5:149163565 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-19887C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163565 | |||||||
| chr5:149163682 | C | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14-19770C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163682 | |||||||
| chr5:149163757 | G | A | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.14-19695G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163757 | |||||||
| chr5:149163935 | G | A | 133 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0023 others(130): Show |
134 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.14-19517G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149163935 | |||||||
| chr5:149164047 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.14-19405C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164047 | |||||||
| chr5:149164063 | C | T | 5 | a0001c0001t0003g0087 a0001c0001t0004g0088 a0002c0004t0004g0089 others(2): Show |
5 | HG02647.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.14-19389C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164063 | |||||||
| chr5:149164082 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.14-19370G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164082 | |||||||
| chr5:149164128 | C | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.14-19324C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164128 | |||||||
| chr5:149164321 | G | T | 5 | a0001c0001t0002g0072 a0001c0001t0004g0073 a0001c0002t0005g0074 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-19131G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164321 | |||||||
| chr5:149164482 | A | G | 88 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0095 others(85): Show |
89 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.14-18970A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164482 | |||||||
| chr5:149164523 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-18929T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164523 | |||||||
| chr5:149164559 | C | T | 2 | a0001c0001t0004g0068 a0001c0006t0014g0213 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.14-18893C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164559 | |||||||
| chr5:149164575 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0003g0250 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.14-18877C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164575 | |||||||
| chr5:149164619 | A | C | 5 | a0001c0001t0003g0087 a0001c0001t0004g0088 a0002c0004t0004g0089 others(2): Show |
5 | HG02647.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.14-18833A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164619 | |||||||
| chr5:149164658 | G | A | 1 | a0001c0001t0005g0228 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14-18794G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164658 | |||||||
| chr5:149164668 | C | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.14-18784C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149164668 | |||||||
| chr5:149165246 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.14-18206T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165246 | |||||||
| chr5:149165293 | A | G | 82 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0111 others(79): Show |
83 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.14-18159A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165293 | |||||||
| chr5:149165494 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0009g0075 |
3 | HG01071.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.14-17958G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165494 | |||||||
| chr5:149165504 | T | G | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-17948T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165504 | |||||||
| chr5:149165799 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.14-17653T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165799 | |||||||
| chr5:149165812 | T | C | 82 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0111 others(79): Show |
83 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.14-17640T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165812 | |||||||
| chr5:149165968 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0255 a0001c0001t0002g0229 others(2): Show |
5 | HG02257.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-17484G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165968 | |||||||
| chr5:149166004 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
40 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.14-17448T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149166004 | |||||||
| chr5:149166179 | T | A | 131 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0023 others(128): Show |
132 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.14-17273T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149166179 | |||||||
| chr5:149166237 | T | C | 5 | a0001c0001t0002g0072 a0001c0001t0004g0073 a0001c0002t0005g0074 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-17215T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149166237 | |||||||
| chr5:149166674 | A | G | 1 | a0001c0001t0005g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.14-16778A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149166674 | |||||||
| chr5:149166784 | T | G | 133 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0023 others(130): Show |
134 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.14-16668T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149166784 | |||||||
| chr5:149167330 | T | C | 1 | a0001c0001t0003g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.14-16122T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167330 | |||||||
| chr5:149167446 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0002g0166 a0001c0001t0002g0173 |
3 | NA18747.hp1 NA18979.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.14-16006C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167446 | |||||||
| chr5:149167477 | T | C | 2 | a0001c0001t0001g0023 a0001c0010t0001g0217 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.14-15975T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167477 | |||||||
| chr5:149167562 | C | T | 1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.14-15890C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167562 | |||||||
| chr5:149167638 | G | C | 34 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0076 others(31): Show |
34 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.14-15814G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167638 | |||||||
| chr5:149167690 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.14-15762G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167690 | |||||||
| chr5:149167927 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
40 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.14-15525C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149167927 | |||||||
| chr5:149168012 | A | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG01978.hp1 HG03834.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-15440A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168012 | |||||||
| chr5:149168047 | T | C | 1 | a0001c0001t0005g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.14-15405T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168047 | |||||||
| chr5:149168061 | A | T | 1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.14-15391A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168061 | |||||||
| chr5:149168120 | G | C | 15 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0187 others(12): Show |
15 | HG00597.hp1 HG02056.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.14-15332G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168120 | |||||||
| chr5:149168197 | T | G | 1 | a0001c0008t0001g0031 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.14-15255T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168197 | |||||||
| chr5:149168266 | C | T | 3 | a0001c0001t0002g0179 a0001c0001t0004g0181 a0001c0001t0004g0182 |
3 | HG03491.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.14-15186C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168266 | |||||||
| chr5:149168409 | G | T | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | HG02896.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.14-15043G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168409 | |||||||
| chr5:149168431 | G | T | 3 | a0001c0001t0001g0023 a0001c0006t0014g0213 a0001c0010t0001g0217 |
3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.14-15021G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168431 | |||||||
| chr5:149168444 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
39 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.14-15008C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168444 | |||||||
| chr5:149168481 | A | T | 6 | a0001c0001t0003g0016 a0001c0001t0003g0087 a0001c0001t0004g0088 others(3): Show |
6 | HG02647.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-14971A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168481 | |||||||
| chr5:149168555 | A | G | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-14897A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168555 | |||||||
| chr5:149168670 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.14-14782G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168670 | |||||||
| chr5:149168856 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0022 others(199): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.14-14596G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168856 | |||||||
| chr5:149168960 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(187): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.14-14492A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168960 | |||||||
| chr5:149169024 | C | G | 64 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(61): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.14-14428C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169024 | |||||||
| chr5:149169064 | C | CACCACTG others(21): Show |
1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14-14363_14-14362i others(30): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169064 | C | CACCACTG others(49): Show |
1 | a0001c0001t0004g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.14-14363_14-14362i others(58): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169064 | C | CACCACTG others(105): Show |
2 | a0001c0001t0001g0249 a0001c0003t0004g0248 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.14-14363_14-14362i others(114): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169064 | C | CACCACTG others(133): Show |
2 | a0001c0001t0012g0110 a0001c0010t0001g0217 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.14-14363_14-14362i others(142): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169064 | C | CACCACTG others(161): Show |
1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-14363_14-14362i others(170): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169064 | C | CACCACTG others(357): Show |
1 | a0001c0001t0003g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.14-14363_14-14362i others(366): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169064 | ||||||
| chr5:149169085 | A | ACCCCTCA others(22): Show |
12 | a0001c0001t0001g0052 a0001c0001t0001g0081 a0001c0001t0001g0150 others(9): Show |
12 | HG00673.hp1 NA18747.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.14-14363_14-14362i others(31): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169085 | ||||||
| chr5:149169085 | A | ACCCCTCA others(50): Show |
7 | a0001c0001t0001g0132 a0001c0001t0001g0178 a0001c0001t0001g0189 others(4): Show |
7 | HG00673.hp2 HG02056.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-14363_14-14362i others(59): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169085 | ||||||
| chr5:149169085 | A | ACCCCTCA others(78): Show |
4 | a0001c0001t0001g0190 a0001c0001t0002g0152 a0001c0001t0006g0039 others(1): Show |
4 | HG02148.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-14363_14-14362i others(87): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169085 | ||||||
| chr5:149169085 | A | ACCCCTCA others(162): Show |
1 | a0001c0001t0002g0153 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.14-14363_14-14362i others(171): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169085 | ||||||
| chr5:149169086 | C | CCCCTCAA others(21): Show |
8 | a0001c0001t0003g0087 a0001c0001t0004g0088 a0001c0001t0005g0086 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-14363_14-14362i others(30): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149169086 | ||||||
| chr5:149169090 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0004g0068 a0001c0003t0004g0017 |
3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.14-14362C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169090 | |||||||
| chr5:149169246 | T | G | 1 | a0001c0001t0010g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.14-14206T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169246 | |||||||
| chr5:149169340 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.14-14112G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169340 | |||||||
| chr5:149169435 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-14017C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169435 | |||||||
| chr5:149169526 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.14-13926G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169526 | |||||||
| chr5:149169531 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.14-13921T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169531 | |||||||
| chr5:149169548 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(143): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.14-13904G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169548 | |||||||
| chr5:149169552 | A | T | 2 | a0001c0001t0009g0075 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.14-13900A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169552 | |||||||
| chr5:149169565 | C | T | 3 | a0001c0001t0001g0234 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.14-13887C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169565 | |||||||
| chr5:149169643 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.14-13809A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169643 | |||||||
| chr5:149169735 | C | T | 1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-13717C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169735 | |||||||
| chr5:149169758 | G | C | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01346.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-13694G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169758 | |||||||
| chr5:149169785 | C | T | 49 | a0001c0001t0001g0023 a0001c0001t0001g0081 a0001c0001t0001g0150 others(46): Show |
49 | HG00673.hp2 HG01346.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.14-13667C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169785 | |||||||
| chr5:149169974 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0234 a0001c0009t0007g0037 others(1): Show |
4 | HG01099.hp2 HG01261.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-13478C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149169974 | |||||||
| chr5:149170054 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0016g0014 |
2 | NA18942.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.14-13398G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170054 | |||||||
| chr5:149170173 | C | T | 1 | a0001c0001t0018g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.14-13279C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170173 | |||||||
| chr5:149170228 | T | TCTCTCTC others(8): Show |
1 | a0001c0001t0006g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.14-13224_14-13223i others(17): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170228 | |||||||
| chr5:149170228 | T | TCTCTCTC others(10): Show |
1 | a0001c0002t0005g0214 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.14-13224_14-13223i others(19): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170228 | |||||||
| chr5:149170228 | T | TTC | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0052 others(23): Show |
26 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.14-13189_14-13188d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTC | 13 | a0001c0001t0001g0035 a0001c0001t0001g0236 a0001c0001t0002g0024 others(10): Show |
13 | HG00438.hp1 HG00738.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.14-13191_14-13188d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTC | 78 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0032 others(75): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.14-13193_14-13188d others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(1): Show |
23 | a0001c0001t0001g0028 a0001c0001t0001g0097 a0001c0001t0001g0140 others(20): Show |
23 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.14-13195_14-13188d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(3): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0096 others(6): Show |
9 | HG00423.hp2 HG01978.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-13197_14-13188d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(5): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0163 a0001c0001t0006g0033 others(1): Show |
4 | HG02818.hp1 HG03669.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-13199_14-13188d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(7): Show |
3 | a0001c0001t0003g0114 a0002c0004t0004g0089 a0002c0005t0013g0019 |
3 | HG02647.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.14-13201_14-13188d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(9): Show |
2 | a0001c0001t0001g0210 a0001c0002t0005g0215 |
2 | HG02896.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.14-13203_14-13188d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(11): Show |
2 | a0001c0001t0006g0093 a0001c0002t0005g0216 |
2 | HG03688.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.14-13205_14-13188d others(20): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(13): Show |
4 | a0001c0001t0002g0198 a0001c0001t0004g0118 a0001c0001t0006g0034 others(1): Show |
4 | HG02896.hp1 HG03471.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-13207_14-13188d others(22): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTCTCTCT others(15): Show |
1 | a0001c0002t0005g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.14-13209_14-13188d others(24): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTTTCTCT others(3): Show |
1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-13223_14-13222i others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTTTCTCT others(7): Show |
1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.14-13223_14-13222i others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | T | TTTTTTCT others(5): Show |
1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14-13223_14-13222i others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170228 | TTC | T | 8 | a0001c0001t0001g0255 a0001c0001t0002g0152 a0001c0001t0002g0153 others(5): Show |
8 | HG01346.hp1 HG01952.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-13189_14-13188d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170228 | ||||||
| chr5:149170271 | C | CCTCT | 4 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-13165_14-13162d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149170271 | ||||||
| chr5:149170288 | C | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(78): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.14-13164C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170288 | |||||||
| chr5:149170292 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
7 | HG00423.hp1 NA18947.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.14-13160G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170292 | |||||||
| chr5:149170330 | C | T | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.14-13122C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170330 | |||||||
| chr5:149170754 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.14-12698A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170754 | |||||||
| chr5:149170778 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0009g0075 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-12674G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170778 | |||||||
| chr5:149170784 | T | C | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-12668T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170784 | |||||||
| chr5:149170830 | A | T | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-12622A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170830 | |||||||
| chr5:149170938 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(134): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.14-12514T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149170938 | |||||||
| chr5:149171154 | G | T | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(19): Show |
22 | HG00673.hp2 HG01346.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-12298G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171154 | |||||||
| chr5:149171181 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.14-12271G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171181 | |||||||
| chr5:149171205 | T | C | 8 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0112 others(5): Show |
8 | HG00738.hp2 HG01243.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-12247T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171205 | |||||||
| chr5:149171259 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.14-12193A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171259 | |||||||
| chr5:149171443 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0002g0010 a0001c0001t0002g0157 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.14-12009A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171443 | |||||||
| chr5:149171542 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(95): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.14-11910A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171542 | |||||||
| chr5:149171602 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(134): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.14-11850A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171602 | |||||||
| chr5:149171689 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0242 |
2 | NA18988.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.14-11763T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171689 | |||||||
| chr5:149171732 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(134): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.14-11720T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171732 | |||||||
| chr5:149171908 | GTTTCT | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11543_14-11539d others(7): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171908 | |||||||
| chr5:149171915 | T | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11537T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171915 | |||||||
| chr5:149171916 | T | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11536T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171916 | |||||||
| chr5:149171918 | T | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11534T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171918 | |||||||
| chr5:149171919 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11533C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171919 | |||||||
| chr5:149171920 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11532C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171920 | |||||||
| chr5:149171922 | CTATTCTA others(1): Show |
C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11528_14-11521d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149171922 | ||||||
| chr5:149171931 | T | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.14-11521T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171931 | |||||||
| chr5:149172532 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.14-10920C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149172532 | |||||||
| chr5:149172539 | G | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0224 a0001c0001t0002g0080 |
3 | NA18971.hp1 NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.14-10913G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149172539 | |||||||
| chr5:149172561 | G | C | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14-10891G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149172561 | |||||||
| chr5:149172775 | T | C | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-10677T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149172775 | |||||||
| chr5:149172923 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.14-10529T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149172923 | |||||||
| chr5:149173009 | T | C | 1 | a0001c0001t0002g0240 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.14-10443T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173009 | |||||||
| chr5:149173011 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.14-10441C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173011 | |||||||
| chr5:149173186 | G | C | 2 | a0001c0006t0017g0070 a0001c0010t0001g0217 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.14-10266G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173186 | |||||||
| chr5:149173623 | G | A | 1 | a0002c0004t0004g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14-9829G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173623 | |||||||
| chr5:149173734 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.14-9718A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173734 | |||||||
| chr5:149173848 | C | T | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.14-9604C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173848 | |||||||
| chr5:149173890 | C | T | 3 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0139 |
3 | NA18945.hp1 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.14-9562C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149173890 | |||||||
| chr5:149174021 | C | CA | 35 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0026 others(32): Show |
35 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.14-9407dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149174021 | ||||||
| chr5:149174021 | CA | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0234 a0001c0001t0002g0083 others(10): Show |
13 | HG00323.hp1 HG01884.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-9407delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149174021 | ||||||
| chr5:149174024 | A | C | 4 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0001t0009g0075 others(1): Show |
4 | HG01261.hp1 HG03098.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-9428A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149174024 | |||||||
| chr5:149174272 | TA | T | 7 | a0001c0001t0002g0170 a0001c0001t0002g0223 a0001c0001t0003g0245 others(4): Show |
7 | HG01168.hp1 HG02572.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-9166delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149174272 | ||||||
| chr5:149174583 | A | G | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-8869A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149174583 | |||||||
| chr5:149174722 | T | A | 37 | a0001c0001t0001g0081 a0001c0001t0001g0142 a0001c0001t0001g0150 others(34): Show |
37 | HG00673.hp2 HG01123.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.14-8730T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149174722 | |||||||
| chr5:149174813 | A | G | 3 | a0001c0001t0004g0077 a0001c0001t0004g0091 a0001c0001t0004g0092 |
3 | HG02572.hp1 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.14-8639A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149174813 | |||||||
| chr5:149174858 | A | G | 29 | a0001c0001t0001g0081 a0001c0001t0001g0142 a0001c0001t0001g0150 others(26): Show |
29 | HG00673.hp2 HG01123.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.14-8594A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149174858 | |||||||
| chr5:149175167 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(73): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.14-8285C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175167 | |||||||
| chr5:149175493 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.14-7959G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175493 | |||||||
| chr5:149175503 | T | A | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-7949T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175503 | |||||||
| chr5:149175636 | G | C | 1 | a0001c0001t0006g0033 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.14-7816G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175636 | |||||||
| chr5:149175727 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(73): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.14-7725C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175727 | |||||||
| chr5:149175902 | G | A | 1 | a0001c0002t0005g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14-7550G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149175902 | |||||||
| chr5:149176105 | G | A | 4 | a0001c0006t0011g0071 a0001c0006t0014g0213 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-7347G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176105 | |||||||
| chr5:149176149 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.14-7303T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176149 | |||||||
| chr5:149176181 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0002g0169 |
2 | NA18977.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.14-7271G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176181 | |||||||
| chr5:149176237 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.14-7215C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176237 | |||||||
| chr5:149176362 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(134): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.14-7090A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176362 | |||||||
| chr5:149176479 | G | A | 4 | a0001c0006t0011g0071 a0001c0006t0014g0213 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-6973G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176479 | |||||||
| chr5:149176493 | G | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.14-6959G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176493 | |||||||
| chr5:149176536 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.14-6916G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176536 | |||||||
| chr5:149176559 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0235 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.14-6893A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176559 | |||||||
| chr5:149176591 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.14-6861C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176591 | |||||||
| chr5:149176821 | A | T | 2 | a0001c0001t0002g0015 a0001c0001t0016g0014 |
2 | NA18942.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.14-6631A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149176821 | |||||||
| chr5:149177080 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.14-6372C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149177080 | |||||||
| chr5:149177464 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.14-5988A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149177464 | |||||||
| chr5:149177798 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-5654A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149177798 | |||||||
| chr5:149177856 | A | G | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-5596A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149177856 | |||||||
| chr5:149178033 | C | T | 1 | a0001c0001t0018g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.14-5419C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178033 | |||||||
| chr5:149178191 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.14-5261C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178191 | |||||||
| chr5:149178328 | A | C | 1 | a0001c0001t0001g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.14-5124A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178328 | |||||||
| chr5:149178359 | G | A | 1 | a0002c0004t0004g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14-5093G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178359 | |||||||
| chr5:149178498 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.14-4954C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178498 | |||||||
| chr5:149178698 | A | G | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-4754A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178698 | |||||||
| chr5:149178770 | T | C | 8 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0112 others(5): Show |
8 | HG00738.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-4682T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178770 | |||||||
| chr5:149178915 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.14-4537G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178915 | |||||||
| chr5:149178944 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.14-4508C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178944 | |||||||
| chr5:149178945 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.14-4507A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178945 | |||||||
| chr5:149178981 | C | T | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-4471C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178981 | |||||||
| chr5:149178982 | G | A | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-4470G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149178982 | |||||||
| chr5:149179280 | CAGG | C | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-4171_14-4169del others(3): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179280 | |||||||
| chr5:149179296 | CTGTT | C | 5 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(2): Show |
5 | HG01192.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-4130_14-4127del others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149179296 | ||||||
| chr5:149179296 | CTGTTTGT others(1): Show |
C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(129): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.14-4134_14-4127del others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149179296 | ||||||
| chr5:149179296 | CTGTTTGT others(5): Show |
C | 1 | a0001c0001t0003g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.14-4138_14-4127del others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149179296 | ||||||
| chr5:149179318 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.14-4134G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179318 | |||||||
| chr5:149179345 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.14-4107G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179345 | |||||||
| chr5:149179495 | G | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14-3957G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179495 | |||||||
| chr5:149179608 | A | AT | 9 | a0001c0001t0002g0152 a0001c0001t0003g0001 a0001c0001t0003g0005 others(6): Show |
10 | HG01243.hp2 HG02148.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-3833dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149179608 | ||||||
| chr5:149179608 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.14-3844A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179608 | |||||||
| chr5:149179891 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.14-3561C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179891 | |||||||
| chr5:149179980 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-3472A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149179980 | |||||||
| chr5:149180033 | A | T | 1 | a0001c0008t0001g0031 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.14-3419A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180033 | |||||||
| chr5:149180151 | A | G | 15 | a0001c0001t0001g0142 a0001c0001t0002g0051 a0001c0001t0002g0144 others(12): Show |
15 | HG01261.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.14-3301A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180151 | |||||||
| chr5:149180174 | C | T | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-3278C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180174 | |||||||
| chr5:149180175 | G | A | 19 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(16): Show |
19 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.14-3277G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180175 | |||||||
| chr5:149180324 | T | C | 38 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(35): Show |
38 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.14-3128T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180324 | |||||||
| chr5:149180346 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.14-3106T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180346 | |||||||
| chr5:149180614 | AACTC | A | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-2835_14-2832del others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 149180614 | ||||||
| chr5:149180761 | T | C | 16 | a0001c0001t0002g0051 a0001c0001t0002g0198 a0001c0001t0003g0004 others(13): Show |
16 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-2691T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180761 | |||||||
| chr5:149180776 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.14-2676G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180776 | |||||||
| chr5:149180801 | A | G | 5 | a0001c0001t0003g0107 a0001c0001t0003g0112 a0001c0001t0003g0120 others(2): Show |
5 | HG00738.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-2651A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180801 | |||||||
| chr5:149180984 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-2468C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149180984 | |||||||
| chr5:149181146 | A | G | 9 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(6): Show |
9 | HG01243.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.14-2306A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181146 | |||||||
| chr5:149181255 | A | C | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.14-2197A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181255 | |||||||
| chr5:149181327 | G | A | 9 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(6): Show |
9 | HG01243.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.14-2125G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181327 | |||||||
| chr5:149181334 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.14-2118G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181334 | |||||||
| chr5:149181449 | T | C | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-2003T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181449 | |||||||
| chr5:149181606 | C | G | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14-1846C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181606 | |||||||
| chr5:149181717 | T | C | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.14-1735T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181717 | |||||||
| chr5:149181750 | G | T | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-1702G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181750 | |||||||
| chr5:149181796 | C | T | 2 | a0001c0006t0017g0070 a0001c0010t0001g0217 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.14-1656C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181796 | |||||||
| chr5:149181797 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14-1655G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149181797 | |||||||
| chr5:149182058 | C | T | 1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-1394C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182058 | |||||||
| chr5:149182170 | T | C | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14-1282T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182170 | |||||||
| chr5:149182192 | G | T | 2 | a0001c0006t0017g0070 a0001c0010t0001g0217 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.14-1260G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182192 | |||||||
| chr5:149182497 | C | A | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-955C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182497 | |||||||
| chr5:149182527 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-925G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182527 | |||||||
| chr5:149182657 | A | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0184 a0001c0001t0002g0185 others(1): Show |
4 | HG00597.hp1 HG02165.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-795A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182657 | |||||||
| chr5:149182717 | C | T | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.14-735C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182717 | |||||||
| chr5:149182790 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0002g0072 |
2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.14-662A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182790 | |||||||
| chr5:149182835 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.14-617A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182835 | |||||||
| chr5:149182959 | A | C | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-493A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182959 | |||||||
| chr5:149182971 | T | C | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-481T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149182971 | |||||||
| chr5:149183266 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.14-186G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149183266 | |||||||
| chr5:149183273 | C | T | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-179C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149183273 | |||||||
| chr5:149183327 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(94): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.14-125G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149183327 | |||||||
| chr5:149183418 | C | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(79): Show |
84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.14-34C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149183418 | |||||||
| chr5:149183621 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.151+32A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149183621 | |||||||
| chr5:149183773 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+184G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149183773 | |||||||
| chr5:149183799 | C | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0041 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.151+210C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149183799 | |||||||
| chr5:149183828 | A | G | 6 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(3): Show |
6 | HG01243.hp2 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+239A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149183828 | |||||||
| chr5:149183964 | T | G | 33 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(30): Show |
33 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.151+375T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149183964 | |||||||
| chr5:149183971 | G | GT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(82): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.151+395dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149183971 | ||||||
| chr5:149183971 | G | GTT | 6 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(3): Show |
7 | HG02135.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+394_151+395dup others(2): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149183971 | ||||||
| chr5:149183971 | GT | G | 10 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+395delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149183971 | ||||||
| chr5:149183971 | GTTT | G | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+393_151+395del others(3): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149183971 | ||||||
| chr5:149184143 | C | A | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+554C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184143 | |||||||
| chr5:149184155 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.151+566A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184155 | |||||||
| chr5:149184301 | G | C | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+712G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184301 | |||||||
| chr5:149184638 | A | T | 1 | a0001c0001t0003g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.151+1049A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184638 | |||||||
| chr5:149184783 | A | C | 1 | a0001c0001t0002g0240 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.151+1194A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184783 | |||||||
| chr5:149184784 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0242 |
2 | NA18988.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.151+1195C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184784 | |||||||
| chr5:149184901 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.151+1312T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149184901 | |||||||
| chr5:149185032 | C | T | 3 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 |
4 | HG02615.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+1443C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185032 | |||||||
| chr5:149185033 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0098 others(1): Show |
4 | NA18963.hp2 NA18988.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+1444G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185033 | |||||||
| chr5:149185159 | G | C | 4 | a0001c0001t0001g0129 a0001c0001t0002g0015 a0001c0001t0002g0046 others(1): Show |
4 | NA18942.hp1 NA18949.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+1570G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185159 | |||||||
| chr5:149185194 | A | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.151+1605A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185194 | |||||||
| chr5:149185197 | T | C | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+1608T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185197 | |||||||
| chr5:149185202 | C | G | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+1613C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185202 | |||||||
| chr5:149185380 | G | A | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+1791G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185380 | |||||||
| chr5:149185547 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0001t0009g0075 others(2): Show |
5 | HG01261.hp1 HG02738.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+1958C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185547 | |||||||
| chr5:149185548 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+1959G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185548 | |||||||
| chr5:149185662 | T | C | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+2073T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185662 | |||||||
| chr5:149185780 | C | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(97): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.151+2191C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185780 | |||||||
| chr5:149185797 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.151+2208A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185797 | |||||||
| chr5:149185853 | A | G | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.151+2264A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185853 | |||||||
| chr5:149185914 | G | A | 1 | a0002c0004t0004g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.151+2325G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185914 | |||||||
| chr5:149185945 | A | C | 10 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+2356A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149185945 | |||||||
| chr5:149186041 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(137): Show |
142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.151+2452A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186041 | |||||||
| chr5:149186052 | A | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.151+2463A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186052 | |||||||
| chr5:149186112 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.151+2523C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186112 | |||||||
| chr5:149186186 | T | C | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+2597T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186186 | |||||||
| chr5:149186197 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.151+2608C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186197 | |||||||
| chr5:149186240 | C | T | 13 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+2651C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186240 | |||||||
| chr5:149186243 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.151+2654A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186243 | |||||||
| chr5:149186259 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+2670C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186259 | |||||||
| chr5:149186370 | C | T | 13 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+2781C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186370 | |||||||
| chr5:149186416 | GA | G | 6 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+2837delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149186416 | ||||||
| chr5:149186577 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.151+2988C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186577 | |||||||
| chr5:149186798 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+3209A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186798 | |||||||
| chr5:149186847 | C | CA | 8 | a0001c0001t0001g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 others(5): Show |
8 | HG01123.hp1 HG01346.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+3268dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149186847 | ||||||
| chr5:149186847 | CA | C | 12 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(9): Show |
12 | HG01243.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+3268delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149186847 | ||||||
| chr5:149186855 | A | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.151+3266A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186855 | |||||||
| chr5:149186919 | A | G | 4 | a0001c0006t0011g0071 a0001c0006t0014g0213 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3330A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186919 | |||||||
| chr5:149187359 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.151+3770G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187359 | |||||||
| chr5:149187406 | C | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+3817C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187406 | |||||||
| chr5:149187412 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+3823A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187412 | |||||||
| chr5:149187417 | A | G | 1 | a0001c0001t0003g0209 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.151+3828A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187417 | |||||||
| chr5:149187545 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+3956G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187545 | |||||||
| chr5:149187593 | TAC | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02056.hp1 HG03017.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.151+4005_151+4006d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187593 | |||||||
| chr5:149187689 | G | A | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+4100G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187689 | |||||||
| chr5:149187805 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+4216G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187805 | |||||||
| chr5:149187933 | T | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4344T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187933 | |||||||
| chr5:149187991 | G | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4402G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187991 | |||||||
| chr5:149188002 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4413A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188002 | |||||||
| chr5:149188042 | T | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4453T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188042 | |||||||
| chr5:149188291 | G | C | 10 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+4702G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188291 | |||||||
| chr5:149188309 | A | G | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151+4720A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188309 | |||||||
| chr5:149188355 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151+4766T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188355 | |||||||
| chr5:149188424 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151+4835T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188424 | |||||||
| chr5:149188511 | G | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.151+4922G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188511 | |||||||
| chr5:149188593 | T | A | 13 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+5004T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188593 | |||||||
| chr5:149188692 | C | A | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+5103C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188692 | |||||||
| chr5:149188699 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+5110T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188699 | |||||||
| chr5:149188741 | C | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+5152C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188741 | |||||||
| chr5:149188849 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+5260A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188849 | |||||||
| chr5:149188857 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0001t0009g0075 others(2): Show |
5 | HG01261.hp1 HG02738.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+5268T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188857 | |||||||
| chr5:149188864 | A | G | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+5275A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188864 | |||||||
| chr5:149188889 | A | G | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+5300A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188889 | |||||||
| chr5:149188923 | A | C | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151+5334A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188923 | |||||||
| chr5:149188925 | A | G | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+5336A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149188925 | |||||||
| chr5:149189002 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0245 |
3 | HG02922.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.151+5413A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189002 | |||||||
| chr5:149189164 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0224 a0001c0001t0002g0080 |
3 | NA18971.hp1 NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.151+5575A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189164 | |||||||
| chr5:149189173 | C | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+5584C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189173 | |||||||
| chr5:149189249 | A | G | 4 | a0001c0001t0001g0234 a0001c0001t0002g0165 a0001c0001t0002g0180 others(1): Show |
4 | HG00673.hp1 HG01516.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+5660A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189249 | |||||||
| chr5:149189349 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.151+5760A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189349 | |||||||
| chr5:149189532 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0050 others(13): Show |
16 | HG00423.hp2 HG00609.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+5943C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189532 | |||||||
| chr5:149189587 | C | A | 1 | a0001c0001t0002g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.151+5998C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189587 | |||||||
| chr5:149189610 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.151+6021C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189610 | |||||||
| chr5:149189611 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+6022G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189611 | |||||||
| chr5:149189737 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+6148C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189737 | |||||||
| chr5:149189745 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.151+6156T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189745 | |||||||
| chr5:149189746 | T | C | 4 | a0001c0006t0011g0071 a0001c0006t0014g0213 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+6157T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189746 | |||||||
| chr5:149189829 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.151+6240G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189829 | |||||||
| chr5:149189880 | T | C | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151+6291T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189880 | |||||||
| chr5:149189886 | T | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+6297T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189886 | |||||||
| chr5:149189954 | A | G | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+6365A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149189954 | |||||||
| chr5:149190144 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.151+6555C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190144 | |||||||
| chr5:149190436 | T | C | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+6847T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190436 | |||||||
| chr5:149190490 | G | C | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+6901G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190490 | |||||||
| chr5:149190537 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+6948G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190537 | |||||||
| chr5:149190617 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.151+7028T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190617 | |||||||
| chr5:149190618 | T | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(87): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.151+7029T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190618 | |||||||
| chr5:149190637 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+7048G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190637 | |||||||
| chr5:149190655 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+7066G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190655 | |||||||
| chr5:149190773 | C | G | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.151+7184C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190773 | |||||||
| chr5:149190789 | A | G | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+7200A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190789 | |||||||
| chr5:149190820 | T | TC | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+7234dupC | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149190820 | ||||||
| chr5:149190869 | A | C | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151+7280A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190869 | |||||||
| chr5:149190886 | T | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+7297T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149190886 | |||||||
| chr5:149191118 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-7101G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191118 | |||||||
| chr5:149191136 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-7083G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191136 | |||||||
| chr5:149191143 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.152-7076T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191143 | |||||||
| chr5:149191227 | A | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6992A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191227 | |||||||
| chr5:149191251 | G | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152-6968G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191251 | |||||||
| chr5:149191279 | T | TA | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6935dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149191279 | ||||||
| chr5:149191297 | A | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6922A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191297 | |||||||
| chr5:149191380 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-6839T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191380 | |||||||
| chr5:149191451 | C | T | 25 | a0001c0001t0001g0032 a0001c0001t0001g0081 a0001c0001t0001g0150 others(22): Show |
25 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-6768C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191451 | |||||||
| chr5:149191469 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.152-6750G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191469 | |||||||
| chr5:149191542 | G | GA | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6673dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149191542 | ||||||
| chr5:149191571 | G | A | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-6648G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191571 | |||||||
| chr5:149191592 | GAAAAATA others(81): Show |
G | 18 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0001t0009g0075 others(15): Show |
18 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-6622_152-6535d others(90): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149191592 | ||||||
| chr5:149191697 | G | A | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-6522G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191697 | |||||||
| chr5:149191767 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6452A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191767 | |||||||
| chr5:149191821 | G | A | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-6398G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191821 | |||||||
| chr5:149191866 | T | C | 10 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-6353T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191866 | |||||||
| chr5:149191920 | C | T | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-6299C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191920 | |||||||
| chr5:149191945 | C | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6274C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191945 | |||||||
| chr5:149191983 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6236A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149191983 | |||||||
| chr5:149192040 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.152-6179G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192040 | |||||||
| chr5:149192057 | T | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-6162T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192057 | |||||||
| chr5:149192109 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0002g0003 a0001c0001t0002g0173 |
3 | NA18747.hp1 NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.152-6110G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192109 | |||||||
| chr5:149192222 | A | T | 1 | a0001c0001t0010g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-5997A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192222 | |||||||
| chr5:149192327 | G | GA | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-5888dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149192327 | ||||||
| chr5:149192493 | CG | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-5722delG | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149192493 | ||||||
| chr5:149192504 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.152-5715T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192504 | |||||||
| chr5:149192617 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.152-5602T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192617 | |||||||
| chr5:149192620 | G | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-5599G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192620 | |||||||
| chr5:149192624 | CAAAAAAA others(8): Show |
C | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-5578_152-5564d others(17): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149192624 | ||||||
| chr5:149192637 | GA | G | 14 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0120 others(11): Show |
14 | HG00738.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-5568delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149192637 | ||||||
| chr5:149192665 | T | C | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-5554T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192665 | |||||||
| chr5:149192721 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.152-5498C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192721 | |||||||
| chr5:149192753 | G | C | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-5466G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192753 | |||||||
| chr5:149192781 | CAAATCAT others(95): Show |
C | 13 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-5435_152-5334d others(2): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149192781 | ||||||
| chr5:149192812 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.152-5407T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192812 | |||||||
| chr5:149192924 | G | C | 1 | a0001c0001t0002g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.152-5295G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192924 | |||||||
| chr5:149192949 | C | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-5270C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149192949 | |||||||
| chr5:149193062 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(91): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.152-5157T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193062 | |||||||
| chr5:149193087 | G | A | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-5132G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193087 | |||||||
| chr5:149193197 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(77): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-5022T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193197 | |||||||
| chr5:149193351 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0236 a0001c0003t0004g0248 |
3 | HG01243.hp1 NA19007.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.152-4868C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193351 | |||||||
| chr5:149193352 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.152-4867G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193352 | |||||||
| chr5:149193353 | C | G | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.152-4866C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193353 | |||||||
| chr5:149193383 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(104): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.152-4836T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193383 | |||||||
| chr5:149193440 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(104): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.152-4779A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193440 | |||||||
| chr5:149193449 | C | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-4770C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193449 | |||||||
| chr5:149193477 | AT | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-4736delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149193477 | ||||||
| chr5:149193557 | G | T | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-4662G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193557 | |||||||
| chr5:149193668 | A | G | 1 | a0001c0003t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152-4551A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193668 | |||||||
| chr5:149193694 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.152-4525G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193694 | |||||||
| chr5:149193729 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-4490A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193729 | |||||||
| chr5:149193759 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-4460G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193759 | |||||||
| chr5:149193879 | G | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.152-4340G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193879 | |||||||
| chr5:149194086 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(104): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.152-4133C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194086 | |||||||
| chr5:149194128 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.152-4091G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194128 | |||||||
| chr5:149194133 | C | CA | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-4082dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149194133 | ||||||
| chr5:149194138 | G | C | 24 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(21): Show |
24 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-4081G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194138 | |||||||
| chr5:149194265 | A | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0201 |
2 | HG02083.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.152-3954A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194265 | |||||||
| chr5:149194356 | A | G | 1 | a0001c0001t0004g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.152-3863A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194356 | |||||||
| chr5:149194398 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152-3821A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194398 | |||||||
| chr5:149194416 | A | T | 35 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(32): Show |
35 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-3803A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194416 | |||||||
| chr5:149194607 | T | C | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-3612T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194607 | |||||||
| chr5:149194676 | G | A | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-3543G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194676 | |||||||
| chr5:149194680 | C | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.152-3539C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194680 | |||||||
| chr5:149194717 | A | G | 9 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(6): Show |
9 | HG01243.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-3502A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194717 | |||||||
| chr5:149194726 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3493A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194726 | |||||||
| chr5:149194811 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152-3408C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194811 | |||||||
| chr5:149194915 | T | C | 3 | a0001c0001t0004g0118 a0001c0001t0005g0086 a0001c0001t0012g0110 |
3 | HG02258.hp2 HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.152-3304T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194915 | |||||||
| chr5:149194939 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(112): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.152-3280C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194939 | |||||||
| chr5:149194993 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3226A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149194993 | |||||||
| chr5:149195116 | T | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-3103T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195116 | |||||||
| chr5:149195281 | T | C | 25 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0178 others(22): Show |
25 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-2938T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195281 | |||||||
| chr5:149195297 | T | C | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-2922T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195297 | |||||||
| chr5:149195386 | C | T | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.152-2833C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195386 | |||||||
| chr5:149195497 | G | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(77): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-2722G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195497 | |||||||
| chr5:149195601 | T | C | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.152-2618T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195601 | |||||||
| chr5:149195644 | C | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.152-2575C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195644 | |||||||
| chr5:149195822 | C | T | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-2397C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195822 | |||||||
| chr5:149195869 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-2350G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195869 | |||||||
| chr5:149195928 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-2291G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195928 | |||||||
| chr5:149195933 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-2286G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195933 | |||||||
| chr5:149195966 | C | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.152-2253C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195966 | |||||||
| chr5:149195987 | A | C | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-2232A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149195987 | |||||||
| chr5:149196058 | T | G | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-2161T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196058 | |||||||
| chr5:149196130 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.152-2089C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196130 | |||||||
| chr5:149196190 | C | T | 4 | a0001c0006t0011g0071 a0001c0006t0014g0213 a0001c0006t0017g0070 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-2029C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196190 | |||||||
| chr5:149196491 | A | G | 3 | a0001c0001t0004g0077 a0001c0001t0004g0091 a0001c0001t0004g0092 |
3 | HG02572.hp1 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.152-1728A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196491 | |||||||
| chr5:149196502 | T | C | 59 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0081 others(56): Show |
59 | HG00673.hp2 HG01123.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.152-1717T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196502 | |||||||
| chr5:149196604 | T | G | 5 | a0001c0001t0002g0198 a0001c0001t0006g0033 a0001c0001t0006g0034 others(2): Show |
5 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-1615T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196604 | |||||||
| chr5:149196637 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1582T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196637 | |||||||
| chr5:149196645 | G | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.152-1574G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196645 | |||||||
| chr5:149196690 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(135): Show |
138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.152-1529T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196690 | |||||||
| chr5:149196767 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.152-1452T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196767 | |||||||
| chr5:149196864 | G | T | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.152-1355G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196864 | |||||||
| chr5:149196976 | G | T | 168 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(165): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.152-1243G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196976 | |||||||
| chr5:149196991 | A | G | 6 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-1228A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149196991 | |||||||
| chr5:149197022 | G | A | 168 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(165): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.152-1197G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197022 | |||||||
| chr5:149197134 | G | A | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.152-1085G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197134 | |||||||
| chr5:149197414 | C | T | 168 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(165): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.152-805C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197414 | |||||||
| chr5:149197454 | C | T | 1 | a0001c0001t0005g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152-765C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197454 | |||||||
| chr5:149197479 | A | G | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152-740A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197479 | |||||||
| chr5:149197557 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-662C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197557 | |||||||
| chr5:149197625 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-594G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197625 | |||||||
| chr5:149197806 | T | C | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.152-413T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197806 | |||||||
| chr5:149197932 | G | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.152-287G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197932 | |||||||
| chr5:149197957 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.152-262C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197957 | |||||||
| chr5:149197958 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0050 others(15): Show |
18 | HG00423.hp2 HG00609.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-261G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149197958 | |||||||
| chr5:149197990 | ATTCTTTA others(56): Show |
A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.152-164_152-102del others(63): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr5 | 149197990 | ||||||
| chr5:149198070 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.152-149G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149198070 | |||||||
| chr5:149198151 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0005g0086 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152-68C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149198151 | |||||||
| chr5:149198449 | G | A | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.335+47G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149198449 | |||||||
| chr5:149198463 | C | T | 21 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(18): Show |
21 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.335+61C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149198463 | |||||||
| chr5:149198641 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.335+239G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149198641 | |||||||
| chr5:149198740 | A | G | 3 | a0001c0001t0002g0145 a0003c0007t0001g0146 a0003c0007t0001g0233 |
3 | HG01175.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.335+338A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149198740 | |||||||
| chr5:149198977 | T | C | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.335+575T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149198977 | |||||||
| chr5:149199003 | C | T | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.335+601C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199003 | |||||||
| chr5:149199073 | T | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(124): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.335+671T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199073 | |||||||
| chr5:149199093 | G | A | 2 | a0001c0006t0017g0070 a0001c0010t0001g0217 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.335+691G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199093 | |||||||
| chr5:149199127 | G | A | 1 | a0001c0008t0001g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.335+725G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199127 | |||||||
| chr5:149199308 | C | T | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.335+906C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199308 | |||||||
| chr5:149199379 | G | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-937G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199379 | |||||||
| chr5:149199406 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.336-910G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199406 | |||||||
| chr5:149199515 | T | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0004g0073 others(4): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.336-801T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199515 | |||||||
| chr5:149199544 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.336-772G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199544 | |||||||
| chr5:149199564 | G | T | 5 | a0001c0001t0012g0110 a0001c0006t0011g0071 a0001c0006t0014g0213 others(2): Show |
5 | HG01884.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-752G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199564 | |||||||
| chr5:149199574 | G | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.336-742G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199574 | |||||||
| chr5:149199741 | A | G | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.336-575A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199741 | |||||||
| chr5:149199745 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0036 others(26): Show |
29 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.336-571G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149199745 | |||||||
| chr5:149200004 | G | C | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.336-312G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149200004 | |||||||
| chr5:149200009 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.336-307T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149200009 | |||||||
| chr5:149200070 | G | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.336-246G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149200070 | |||||||
| chr5:149200245 | G | A | 1 | a0001c0001t0010g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.336-71G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149200245 | |||||||
| chr5:149200246 | C | A | 1 | a0001c0001t0010g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.336-70C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 4/23 | chr5 | 149200246 | |||||||
| chr5:149200462 | G | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.448+34G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200462 | |||||||
| chr5:149200712 | G | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.448+284G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200712 | |||||||
| chr5:149200722 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.448+294C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200722 | |||||||
| chr5:149200723 | G | A | 17 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(14): Show |
17 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.448+295G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200723 | |||||||
| chr5:149200727 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0002g0144 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+299C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200727 | |||||||
| chr5:149200741 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0130 others(6): Show |
9 | HG00621.hp1 HG01099.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.448+313A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200741 | |||||||
| chr5:149200828 | G | A | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.448+400G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200828 | |||||||
| chr5:149200839 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.448+411G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149200839 | |||||||
| chr5:149201038 | T | C | 17 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(14): Show |
17 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.448+610T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201038 | |||||||
| chr5:149201121 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0012g0110 |
2 | HG00438.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.448+693G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201121 | |||||||
| chr5:149201127 | C | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+699C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201127 | |||||||
| chr5:149201164 | C | T | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.448+736C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201164 | |||||||
| chr5:149201200 | GT | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.448+774delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr5 | 149201200 | ||||||
| chr5:149201249 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0003 |
2 | NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.448+821T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201249 | |||||||
| chr5:149201297 | C | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0111 others(4): Show |
7 | HG01071.hp2 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+869C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201297 | |||||||
| chr5:149201328 | C | T | 6 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+900C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201328 | |||||||
| chr5:149201406 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0203 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.448+978C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201406 | |||||||
| chr5:149201500 | G | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.448+1072G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201500 | |||||||
| chr5:149201547 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.448+1119G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201547 | |||||||
| chr5:149201605 | G | A | 1 | a0001c0008t0001g0031 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.448+1177G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201605 | |||||||
| chr5:149201895 | C | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.448+1467C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201895 | |||||||
| chr5:149201928 | G | A | 8 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.448+1500G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201928 | |||||||
| chr5:149201950 | C | T | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.448+1522C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149201950 | |||||||
| chr5:149202093 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1665T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202093 | |||||||
| chr5:149202097 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1669A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202097 | |||||||
| chr5:149202123 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1695T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202123 | |||||||
| chr5:149202169 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1741C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202169 | |||||||
| chr5:149202171 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1743A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202171 | |||||||
| chr5:149202175 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1747C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202175 | |||||||
| chr5:149202177 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1749T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202177 | |||||||
| chr5:149202178 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1750A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202178 | |||||||
| chr5:149202179 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1751C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202179 | |||||||
| chr5:149202180 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1752T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202180 | |||||||
| chr5:149202182 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1754T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202182 | |||||||
| chr5:149202188 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1760T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202188 | |||||||
| chr5:149202189 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1761G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202189 | |||||||
| chr5:149202192 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.448+1764A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202192 | |||||||
| chr5:149202212 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.448+1784G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202212 | |||||||
| chr5:149202265 | C | T | 4 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+1837C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202265 | |||||||
| chr5:149202286 | G | A | 19 | a0001c0001t0002g0051 a0001c0001t0003g0004 a0001c0001t0003g0231 others(16): Show |
19 | HG01884.hp1 HG02258.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.448+1858G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202286 | |||||||
| chr5:149202294 | A | G | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.448+1866A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202294 | |||||||
| chr5:149202407 | G | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.448+1979G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202407 | |||||||
| chr5:149202442 | T | C | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448+2014T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202442 | |||||||
| chr5:149202449 | G | A | 1 | a0001c0001t0006g0033 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.448+2021G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149202449 | |||||||
| chr5:149203070 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(138): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.448+2642A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203070 | |||||||
| chr5:149203208 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.448+2780C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203208 | |||||||
| chr5:149203319 | TAC | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(95): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.448+2892_448+2893d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203319 | |||||||
| chr5:149203389 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.448+2961T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203389 | |||||||
| chr5:149203395 | GCAATCAG others(14): Show |
G | 17 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0128 others(14): Show |
17 | HG00280.hp1 HG00738.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.448+2968_448+2988d others(23): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203395 | |||||||
| chr5:149203447 | C | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.448+3019C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203447 | |||||||
| chr5:149203572 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.448+3144T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203572 | |||||||
| chr5:149203638 | A | T | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+3210A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203638 | |||||||
| chr5:149203669 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0002g0015 a0001c0001t0016g0014 |
3 | NA18942.hp1 NA18949.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.448+3241C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203669 | |||||||
| chr5:149203690 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.448+3262C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203690 | |||||||
| chr5:149203702 | CATT | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(76): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.448+3282_448+3284d others(5): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr5 | 149203702 | ||||||
| chr5:149203767 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(102): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.449-3241T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203767 | |||||||
| chr5:149203767 | T | G | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.449-3241T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203767 | |||||||
| chr5:149203911 | G | T | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-3097G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203911 | |||||||
| chr5:149203957 | G | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0142 others(8): Show |
11 | HG01261.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.449-3051G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149203957 | |||||||
| chr5:149204176 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.449-2832G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204176 | |||||||
| chr5:149204226 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.449-2782G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204226 | |||||||
| chr5:149204422 | A | T | 12 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0142 others(9): Show |
12 | HG01261.hp1 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-2586A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204422 | |||||||
| chr5:149204431 | C | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(124): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.449-2577C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204431 | |||||||
| chr5:149204534 | A | C | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.449-2474A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204534 | |||||||
| chr5:149204570 | G | A | 6 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-2438G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204570 | |||||||
| chr5:149204923 | G | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0044 others(95): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.449-2085G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149204923 | |||||||
| chr5:149205062 | G | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1946G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205062 | |||||||
| chr5:149205068 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.449-1940T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205068 | |||||||
| chr5:149205146 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.449-1862G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205146 | |||||||
| chr5:149205315 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.449-1693G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205315 | |||||||
| chr5:149205346 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.449-1662G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205346 | |||||||
| chr5:149205390 | A | G | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1618A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205390 | |||||||
| chr5:149205416 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0097 others(3): Show |
6 | HG02083.hp1 NA18945.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-1592A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205416 | |||||||
| chr5:149205559 | T | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.449-1449T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205559 | |||||||
| chr5:149205660 | T | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1348T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205660 | |||||||
| chr5:149205684 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.449-1324G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205684 | |||||||
| chr5:149205792 | G | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.449-1216G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205792 | |||||||
| chr5:149205794 | A | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.449-1214A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205794 | |||||||
| chr5:149205907 | A | G | 1 | a0001c0001t0005g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.449-1101A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149205907 | |||||||
| chr5:149206151 | C | A | 1 | a0001c0001t0001g0012 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.449-857C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206151 | |||||||
| chr5:149206268 | T | G | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.449-740T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206268 | |||||||
| chr5:149206331 | G | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-677G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206331 | |||||||
| chr5:149206362 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.449-646T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206362 | |||||||
| chr5:149206438 | A | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-570A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206438 | |||||||
| chr5:149206480 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0106 others(3): Show |
6 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-528T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206480 | |||||||
| chr5:149206514 | T | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-494T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206514 | |||||||
| chr5:149206540 | C | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-468C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206540 | |||||||
| chr5:149206630 | T | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-378T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206630 | |||||||
| chr5:149206738 | T | C | 4 | a0002c0004t0004g0013 a0002c0004t0004g0089 a0002c0004t0004g0090 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-270T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206738 | |||||||
| chr5:149206789 | T | C | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.449-219T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206789 | |||||||
| chr5:149206829 | C | G | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.449-179C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206829 | |||||||
| chr5:149206873 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.449-135G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206873 | |||||||
| chr5:149206875 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.449-133A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206875 | |||||||
| chr5:149207240 | G | A | 2 | a0001c0001t0004g0073 a0001c0001t0004g0088 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.575+106G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207240 | |||||||
| chr5:149207250 | G | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+116G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207250 | |||||||
| chr5:149207309 | G | C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+175G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207309 | |||||||
| chr5:149207314 | T | G | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+180T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207314 | |||||||
| chr5:149207316 | T | TCCCTCTG others(27): Show |
1 | a0001c0001t0001g0208 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.575+184_575+217dup others(34): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149207316 | ||||||
| chr5:149207338 | C | T | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.575+204C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207338 | |||||||
| chr5:149207352 | G | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+218G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207352 | |||||||
| chr5:149207426 | C | T | 8 | a0001c0001t0001g0040 a0001c0001t0002g0100 a0001c0001t0002g0102 others(5): Show |
8 | HG00280.hp1 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.575+292C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207426 | |||||||
| chr5:149207501 | G | A | 1 | a0001c0008t0001g0031 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.575+367G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207501 | |||||||
| chr5:149207618 | A | G | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.575+484A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207618 | |||||||
| chr5:149207647 | T | G | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.575+513T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207647 | |||||||
| chr5:149207653 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0002g0003 a0001c0001t0002g0173 |
3 | NA18747.hp1 NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.575+519G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207653 | |||||||
| chr5:149207958 | C | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.575+824C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207958 | |||||||
| chr5:149207990 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(99): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.575+856T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149207990 | |||||||
| chr5:149208277 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0002g0226 |
2 | HG00140.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.575+1143C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208277 | |||||||
| chr5:149208350 | GTC | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.575+1251_575+1252d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208350 | ||||||
| chr5:149208350 | GTCTC | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0208 others(2): Show |
5 | HG01167.hp1 HG02572.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.575+1249_575+1252d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208350 | ||||||
| chr5:149208366 | CTCTCTCT others(23): Show |
C | 3 | a0001c0001t0002g0126 a0001c0001t0002g0155 a0001c0001t0002g0177 |
3 | HG00323.hp1 HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.575+1244_575+1273d others(32): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208366 | ||||||
| chr5:149208368 | CTCTCTCT others(21): Show |
C | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+1246_575+1273d others(30): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208368 | ||||||
| chr5:149208370 | CTCTCTCT others(19): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.575+1248_575+1273d others(28): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208370 | ||||||
| chr5:149208372 | CTCTCTCT others(17): Show |
C | 6 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0139 others(3): Show |
6 | HG00738.hp2 HG02896.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.575+1250_575+1273d others(26): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208372 | ||||||
| chr5:149208378 | CTCTCTCT others(11): Show |
C | 10 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(7): Show |
10 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.575+1253_575+1270d others(20): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208378 | ||||||
| chr5:149208380 | CTCTCTCA others(9): Show |
C | 3 | a0001c0001t0002g0051 a0001c0001t0003g0245 a0001c0001t0009g0075 |
3 | HG02922.hp1 HG03098.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.575+1253_575+1268d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208380 | ||||||
| chr5:149208382 | CTCTCAAT others(7): Show |
C | 4 | a0001c0001t0003g0231 a0001c0003t0004g0121 a0001c0003t0004g0122 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+1253_575+1266d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208382 | ||||||
| chr5:149208386 | CAATTTCT others(3): Show |
C | 3 | a0001c0001t0001g0142 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.575+1253_575+1262d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208386 | |||||||
| chr5:149208388 | ATTTCTCT others(13): Show |
A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(99): Show |
104 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.575+1256_575+1275d others(22): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149208388 | ||||||
| chr5:149208390 | T | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.575+1256T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208390 | |||||||
| chr5:149208396 | T | C | 2 | a0001c0001t0002g0144 a0001c0001t0005g0020 |
2 | HG02965.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.575+1262T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208396 | |||||||
| chr5:149208407 | T | A | 37 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0142 others(34): Show |
37 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.575+1273T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208407 | |||||||
| chr5:149208408 | G | A | 37 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0142 others(34): Show |
37 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.575+1274G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208408 | |||||||
| chr5:149208445 | T | A | 2 | a0001c0001t0005g0069 a0001c0001t0005g0253 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.575+1311T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208445 | |||||||
| chr5:149208511 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.575+1377A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208511 | |||||||
| chr5:149208749 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0142 a0001c0001t0002g0144 others(4): Show |
7 | HG01261.hp1 HG02630.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+1615C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208749 | |||||||
| chr5:149208770 | A | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0175 a0001c0001t0001g0224 others(1): Show |
4 | NA18971.hp1 NA19057.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.575+1636A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208770 | |||||||
| chr5:149208976 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.576-1750C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149208976 | |||||||
| chr5:149209002 | C | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.576-1724C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209002 | |||||||
| chr5:149209123 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.576-1603C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209123 | |||||||
| chr5:149209201 | A | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0169 |
2 | NA18975.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.576-1525A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209201 | |||||||
| chr5:149209283 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(128): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.576-1443G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209283 | |||||||
| chr5:149209425 | C | A | 17 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(14): Show |
17 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.576-1301C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209425 | |||||||
| chr5:149209460 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.576-1266T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209460 | |||||||
| chr5:149209521 | C | T | 2 | a0001c0003t0004g0121 a0001c0003t0004g0122 |
2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.576-1205C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209521 | |||||||
| chr5:149209679 | G | T | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.576-1047G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209679 | |||||||
| chr5:149209783 | G | T | 22 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0001g0175 others(19): Show |
22 | HG00673.hp2 HG01123.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.576-943G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209783 | |||||||
| chr5:149209917 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.576-809T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209917 | |||||||
| chr5:149209959 | C | G | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.576-767C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149209959 | |||||||
| chr5:149209985 | T | TTCTC | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.576-740_576-737dup others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr5 | 149209985 | ||||||
| chr5:149210060 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.576-666A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149210060 | |||||||
| chr5:149210146 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.576-580G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149210146 | |||||||
| chr5:149210386 | C | T | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.576-340C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149210386 | |||||||
| chr5:149210406 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.576-320A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149210406 | |||||||
| chr5:149210860 | T | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.669+41T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149210860 | |||||||
| chr5:149211057 | T | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(108): Show |
113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.669+238T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211057 | |||||||
| chr5:149211093 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.669+274G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211093 | |||||||
| chr5:149211097 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+278G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211097 | |||||||
| chr5:149211100 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.669+281A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211100 | |||||||
| chr5:149211142 | T | TTTTA | 36 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0052 others(33): Show |
37 | HG00673.hp2 HG00741.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.669+348_669+351dup others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149211142 | ||||||
| chr5:149211171 | A | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0035 others(77): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.669+352A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211171 | |||||||
| chr5:149211182 | T | A | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+363T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211182 | |||||||
| chr5:149211183 | G | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+364G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211183 | |||||||
| chr5:149211460 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.669+641T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211460 | |||||||
| chr5:149211509 | G | T | 2 | a0001c0001t0005g0086 a0001c0001t0009g0075 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.669+690G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211509 | |||||||
| chr5:149211530 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.669+711G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211530 | |||||||
| chr5:149211642 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.669+823A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149211642 | |||||||
| chr5:149212080 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0010g0133 |
2 | NA18978.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.669+1261C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212080 | |||||||
| chr5:149212289 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.669+1470C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212289 | |||||||
| chr5:149212361 | G | A | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+1542G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212361 | |||||||
| chr5:149212449 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0004g0073 a0001c0001t0004g0088 |
3 | HG02630.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.669+1630A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212449 | |||||||
| chr5:149212461 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.669+1642T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212461 | |||||||
| chr5:149212497 | G | A | 8 | a0001c0001t0001g0142 a0001c0001t0002g0024 a0001c0001t0002g0144 others(5): Show |
8 | HG01261.hp1 HG01884.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+1678G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212497 | |||||||
| chr5:149212676 | A | G | 6 | a0001c0003t0004g0121 a0001c0003t0004g0122 a0002c0004t0004g0013 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+1857A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212676 | |||||||
| chr5:149212835 | G | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0005g0109 others(6): Show |
9 | HG01243.hp2 HG01516.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+2016G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212835 | |||||||
| chr5:149212848 | G | A | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.669+2029G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212848 | |||||||
| chr5:149212998 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0097 |
3 | NA18945.hp2 NA18947.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.669+2179C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149212998 | |||||||
| chr5:149213103 | A | AT | 6 | a0001c0001t0001g0023 a0001c0001t0004g0068 a0001c0001t0004g0073 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+2285dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149213103 | ||||||
| chr5:149213111 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.669+2292C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213111 | |||||||
| chr5:149213140 | A | C | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669+2321A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213140 | |||||||
| chr5:149213271 | C | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0005g0109 others(6): Show |
9 | HG01243.hp2 HG01516.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+2452C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213271 | |||||||
| chr5:149213284 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.669+2465T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213284 | |||||||
| chr5:149213304 | T | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0238 |
2 | NA18986.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.669+2485T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213304 | |||||||
| chr5:149213450 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0004g0068 a0001c0001t0004g0073 others(2): Show |
5 | HG02630.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+2631G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213450 | |||||||
| chr5:149213455 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.669+2636G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213455 | |||||||
| chr5:149213639 | A | G | 110 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0044 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.669+2820A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213639 | |||||||
| chr5:149213740 | C | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0150 others(17): Show |
20 | HG01123.hp1 HG01346.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.669+2921C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213740 | |||||||
| chr5:149213761 | G | A | 10 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(7): Show |
11 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+2942G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213761 | |||||||
| chr5:149213813 | A | AT | 87 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0053 others(84): Show |
89 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.669+3006dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149213813 | ||||||
| chr5:149213909 | G | A | 76 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0053 others(73): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.670-3050G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213909 | |||||||
| chr5:149213982 | C | CCA | 150 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0035 others(147): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.670-2977_670-2976i others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213982 | |||||||
| chr5:149214021 | G | A | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.670-2938G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214021 | |||||||
| chr5:149214177 | C | T | 36 | a0001c0001t0001g0018 a0001c0001t0002g0024 a0001c0001t0002g0165 others(33): Show |
37 | HG01071.hp1 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.670-2782C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214177 | |||||||
| chr5:149214266 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.670-2693G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214266 | |||||||
| chr5:149214294 | G | A | 3 | a0001c0001t0002g0165 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.670-2665G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214294 | |||||||
| chr5:149214395 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(138): Show |
143 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.670-2564C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214395 | |||||||
| chr5:149214396 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.670-2563G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214396 | |||||||
| chr5:149214567 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.670-2392G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214567 | |||||||
| chr5:149214668 | A | T | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.670-2291A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214668 | |||||||
| chr5:149214907 | G | A | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-2052G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214907 | |||||||
| chr5:149214914 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(120): Show |
125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-2045A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214914 | |||||||
| chr5:149214985 | T | C | 3 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 |
4 | HG02615.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-1974T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214985 | |||||||
| chr5:149214992 | C | T | 8 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0004g0118 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-1967C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214992 | |||||||
| chr5:149215122 | A | G | 2 | a0001c0001t0003g0209 a0001c0001t0003g0254 |
2 | HG02698.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.670-1837A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215122 | |||||||
| chr5:149215384 | G | A | 1 | a0001c0001t0004g0077 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.670-1575G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215384 | |||||||
| chr5:149215395 | G | A | 6 | a0001c0003t0004g0121 a0001c0003t0004g0122 a0002c0004t0004g0013 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-1564G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215395 | |||||||
| chr5:149215432 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0200 |
2 | HG02135.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.670-1527C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215432 | |||||||
| chr5:149215483 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(120): Show |
125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-1476T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215483 | |||||||
| chr5:149215493 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.670-1466C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215493 | |||||||
| chr5:149215522 | TA | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.670-1426delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149215522 | ||||||
| chr5:149215532 | AAG | A | 8 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0006g0033 others(5): Show |
8 | HG03688.hp2 HG04115.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-1425_670-1424d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149215532 | ||||||
| chr5:149215535 | A | G | 8 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0006g0033 others(5): Show |
8 | HG03688.hp2 HG04115.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-1424A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215535 | |||||||
| chr5:149215641 | C | T | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-1318C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215641 | |||||||
| chr5:149215722 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(120): Show |
125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-1237A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215722 | |||||||
| chr5:149215797 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.670-1162G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215797 | |||||||
| chr5:149215925 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.670-1034G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149215925 | |||||||
| chr5:149216079 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-880G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216079 | |||||||
| chr5:149216191 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.670-768C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216191 | |||||||
| chr5:149216226 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.670-733G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216226 | |||||||
| chr5:149216429 | G | T | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.670-530G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216429 | |||||||
| chr5:149216478 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(119): Show |
124 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.670-481C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216478 | |||||||
| chr5:149216522 | C | CT | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.670-425dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149216522 | ||||||
| chr5:149216522 | CT | C | 8 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0003t0004g0121 others(5): Show |
8 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-425delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr5 | 149216522 | ||||||
| chr5:149216568 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(128): Show |
133 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.670-391T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216568 | |||||||
| chr5:149216764 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.670-195A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216764 | |||||||
| chr5:149216792 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-167G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216792 | |||||||
| chr5:149216812 | G | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(119): Show |
124 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.670-147G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216812 | |||||||
| chr5:149217130 | TG | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.757+86delG | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149217130 | ||||||
| chr5:149217179 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.757+133C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217179 | |||||||
| chr5:149217278 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(119): Show |
124 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.757+232G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217278 | |||||||
| chr5:149217464 | A | C | 8 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0001c0001t0001g0078 others(5): Show |
8 | HG00280.hp2 HG00438.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.757+418A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217464 | |||||||
| chr5:149217539 | C | T | 2 | a0001c0001t0012g0110 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.757+493C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217539 | |||||||
| chr5:149217668 | G | A | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+622G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217668 | |||||||
| chr5:149217676 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.757+630C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217676 | |||||||
| chr5:149217677 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0235 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.757+631G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217677 | |||||||
| chr5:149217815 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(119): Show |
124 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.757+769A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217815 | |||||||
| chr5:149217896 | G | C | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.757+850G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149217896 | |||||||
| chr5:149218027 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757+981C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218027 | |||||||
| chr5:149218028 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.757+982G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218028 | |||||||
| chr5:149218053 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 |
3 | HG01071.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.757+1007T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218053 | |||||||
| chr5:149218061 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.757+1015G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218061 | |||||||
| chr5:149218075 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.757+1029T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218075 | |||||||
| chr5:149218121 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(136): Show |
141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.757+1075T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218121 | |||||||
| chr5:149218266 | T | C | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.757+1220T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218266 | |||||||
| chr5:149218321 | G | A | 5 | a0001c0001t0002g0024 a0001c0001t0002g0165 a0001c0001t0003g0016 others(2): Show |
5 | HG01261.hp1 HG01516.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+1275G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218321 | |||||||
| chr5:149218403 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.757+1357G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218403 | |||||||
| chr5:149218569 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.757+1523C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218569 | |||||||
| chr5:149218809 | C | G | 1 | a0001c0001t0002g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.757+1763C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218809 | |||||||
| chr5:149218817 | G | A | 1 | a0005c0011t0001g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.757+1771G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218817 | |||||||
| chr5:149218860 | C | G | 1 | a0001c0001t0006g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.757+1814C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218860 | |||||||
| chr5:149218874 | G | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.757+1828G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218874 | |||||||
| chr5:149218886 | T | G | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+1840T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218886 | |||||||
| chr5:149218968 | A | G | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+1922A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149218968 | |||||||
| chr5:149219000 | G | A | 2 | a0001c0001t0012g0110 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.757+1954G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219000 | |||||||
| chr5:149219029 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(4): Show |
7 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+1983G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219029 | |||||||
| chr5:149219077 | G | T | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.757+2031G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219077 | |||||||
| chr5:149219118 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(136): Show |
141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.757+2072T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219118 | |||||||
| chr5:149219203 | T | C | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+2157T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219203 | |||||||
| chr5:149219340 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.757+2294G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219340 | |||||||
| chr5:149219543 | G | A | 28 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(25): Show |
28 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.757+2497G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219543 | |||||||
| chr5:149219546 | A | G | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+2500A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219546 | |||||||
| chr5:149219701 | C | T | 17 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.757+2655C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219701 | |||||||
| chr5:149219767 | T | C | 7 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0009g0075 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+2721T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219767 | |||||||
| chr5:149219933 | G | T | 1 | a0001c0001t0003g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.757+2887G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219933 | |||||||
| chr5:149219959 | CAG | C | 17 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.757+2914_757+2915d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149219959 | |||||||
| chr5:149220118 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(136): Show |
141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.757+3072A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220118 | |||||||
| chr5:149220154 | G | GT | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.757+3109dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149220154 | ||||||
| chr5:149220243 | G | A | 1 | a0001c0006t0014g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.757+3197G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220243 | |||||||
| chr5:149220395 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.757+3349T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220395 | |||||||
| chr5:149220398 | G | A | 2 | a0001c0008t0001g0031 a0001c0008t0001g0176 |
2 | HG01167.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.757+3352G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220398 | |||||||
| chr5:149220421 | T | C | 2 | a0001c0001t0003g0209 a0001c0001t0003g0254 |
2 | HG02698.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.757+3375T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220421 | |||||||
| chr5:149220470 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.757+3424T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220470 | |||||||
| chr5:149220516 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.757+3470G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220516 | |||||||
| chr5:149220543 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.757+3497C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220543 | |||||||
| chr5:149220645 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.757+3599C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220645 | |||||||
| chr5:149220765 | A | C | 2 | a0001c0001t0002g0015 a0001c0001t0016g0014 |
2 | NA18942.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.757+3719A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220765 | |||||||
| chr5:149220782 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0095 |
3 | HG01261.hp2 HG01516.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.757+3736G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220782 | |||||||
| chr5:149220861 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.757+3815T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220861 | |||||||
| chr5:149220938 | C | G | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.757+3892C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149220938 | |||||||
| chr5:149221028 | A | G | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+3982A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221028 | |||||||
| chr5:149221035 | T | C | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+3989T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221035 | |||||||
| chr5:149221130 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0211 a0001c0001t0018g0237 |
3 | HG01168.hp2 HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.757+4084G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221130 | |||||||
| chr5:149221282 | C | T | 3 | a0001c0001t0002g0165 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.757+4236C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221282 | |||||||
| chr5:149221352 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.757+4306G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221352 | |||||||
| chr5:149221515 | G | T | 1 | a0001c0001t0002g0198 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.757+4469G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221515 | |||||||
| chr5:149221522 | G | A | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757+4476G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221522 | |||||||
| chr5:149221680 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(73): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.757+4634A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221680 | |||||||
| chr5:149221850 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.757+4804C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221850 | |||||||
| chr5:149221883 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(136): Show |
141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.757+4837A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221883 | |||||||
| chr5:149221907 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.757+4861C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149221907 | |||||||
| chr5:149222117 | TTAA | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.757+5081_757+5083d others(5): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149222117 | ||||||
| chr5:149222157 | A | T | 9 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.757+5111A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222157 | |||||||
| chr5:149222185 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.757+5139T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222185 | |||||||
| chr5:149222185 | T | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(135): Show |
140 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.757+5139T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222185 | |||||||
| chr5:149222211 | C | T | 15 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(12): Show |
16 | HG00738.hp2 HG02615.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.757+5165C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222211 | |||||||
| chr5:149222253 | C | T | 34 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+5207C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222253 | |||||||
| chr5:149222413 | A | G | 8 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0004g0118 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.757+5367A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222413 | |||||||
| chr5:149222570 | A | G | 28 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(25): Show |
28 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.757+5524A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222570 | |||||||
| chr5:149222578 | G | A | 8 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0004g0118 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.757+5532G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222578 | |||||||
| chr5:149222661 | C | CT | 26 | a0001c0001t0001g0027 a0001c0001t0001g0142 a0001c0001t0001g0160 others(23): Show |
26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.757+5639dupT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149222661 | ||||||
| chr5:149222661 | CT | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0125 a0001c0001t0001g0147 others(2): Show |
5 | HG02922.hp2 HG04184.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+5639delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149222661 | ||||||
| chr5:149222661 | CTTTTTTT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(87): Show |
92 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.757+5633_757+5639d others(9): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149222661 | ||||||
| chr5:149222661 | CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0004g0118 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.757+5627_757+5639d others(15): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149222661 | ||||||
| chr5:149222808 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.757+5762T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222808 | |||||||
| chr5:149222881 | T | C | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+5835T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222881 | |||||||
| chr5:149222886 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.757+5840T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222886 | |||||||
| chr5:149222899 | T | A | 6 | a0001c0003t0004g0121 a0001c0003t0004g0122 a0002c0004t0004g0013 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+5853T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222899 | |||||||
| chr5:149222906 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.757+5860G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222906 | |||||||
| chr5:149222926 | A | T | 2 | a0001c0001t0003g0004 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.757+5880A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222926 | |||||||
| chr5:149222939 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.757+5893C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222939 | |||||||
| chr5:149223114 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.757+6068G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223114 | |||||||
| chr5:149223122 | AT | A | 29 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0004g0068 others(26): Show |
29 | HG01071.hp1 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.757+6087delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149223122 | ||||||
| chr5:149223122 | ATT | A | 7 | a0001c0001t0004g0073 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
7 | HG02630.hp1 HG03688.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.757+6086_757+6087d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149223122 | ||||||
| chr5:149223170 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.757+6124T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223170 | |||||||
| chr5:149223262 | T | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
14 | HG00423.hp1 HG02056.hp1 HG03017.hp2 others(11): Show |
intron_variant | MODIFIER | c.757+6216T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223262 | |||||||
| chr5:149223390 | C | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.757+6344C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223390 | |||||||
| chr5:149223790 | G | A | 32 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(29): Show |
32 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.757+6744G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223790 | |||||||
| chr5:149223841 | A | T | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.757+6795A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149223841 | |||||||
| chr5:149224010 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.758-6639A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224010 | |||||||
| chr5:149224018 | G | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-6631G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224018 | |||||||
| chr5:149224021 | C | CATGGCCA others(14): Show |
2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-6628_758-6627i others(23): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224021 | |||||||
| chr5:149224157 | C | T | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.758-6492C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224157 | |||||||
| chr5:149224320 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(250): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.758-6329T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224320 | |||||||
| chr5:149224820 | A | T | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.758-5829A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224820 | |||||||
| chr5:149224893 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(133): Show |
138 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.758-5756A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224893 | |||||||
| chr5:149224910 | G | A | 6 | a0001c0003t0004g0121 a0001c0003t0004g0122 a0002c0004t0004g0013 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-5739G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149224910 | |||||||
| chr5:149225231 | A | ACCTCTAT others(8): Show |
73 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(70): Show |
74 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.758-5418_758-5417i others(17): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225231 | |||||||
| chr5:149225289 | C | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 |
3 | HG01071.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.758-5360C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225289 | |||||||
| chr5:149225313 | A | G | 26 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-5336A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225313 | |||||||
| chr5:149225327 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(90): Show |
95 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.758-5322G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225327 | |||||||
| chr5:149225341 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.758-5308C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225341 | |||||||
| chr5:149225394 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.758-5255G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225394 | |||||||
| chr5:149225431 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.758-5218T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225431 | |||||||
| chr5:149225562 | A | T | 26 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-5087A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225562 | |||||||
| chr5:149225660 | T | C | 26 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-4989T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225660 | |||||||
| chr5:149225687 | C | A | 7 | a0001c0001t0003g0087 a0001c0001t0003g0107 a0001c0001t0003g0112 others(4): Show |
7 | HG00738.hp2 HG02698.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.758-4962C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225687 | |||||||
| chr5:149225915 | TCATATAT others(1): Show |
T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(107): Show |
112 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.758-4725_758-4718d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225915 | ||||||
| chr5:149225924 | C | T | 26 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-4725C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225924 | |||||||
| chr5:149225937 | A | ATATATAT others(3): Show |
2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.758-4709_758-4708i others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225937 | ||||||
| chr5:149225937 | A | ATATATAT others(1): Show |
5 | a0001c0001t0005g0069 a0001c0001t0005g0228 a0001c0001t0005g0253 others(2): Show |
5 | HG02055.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4709_758-4708i others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225937 | ||||||
| chr5:149225937 | A | ATATATG | 13 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0005g0020 others(10): Show |
13 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.758-4709_758-4708i others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225937 | ||||||
| chr5:149225941 | G | A | 5 | a0001c0001t0004g0068 a0001c0001t0004g0118 a0001c0001t0005g0109 others(2): Show |
5 | HG02572.hp2 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4708G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225941 | |||||||
| chr5:149225945 | G | A | 3 | a0001c0001t0004g0068 a0001c0001t0004g0118 a0001c0001t0005g0109 |
3 | HG02896.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4704G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225945 | |||||||
| chr5:149225949 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4700G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225949 | |||||||
| chr5:149225951 | ATATAATA others(22): Show |
A | 3 | a0001c0001t0005g0109 a0001c0003t0004g0017 a0001c0006t0014g0213 |
3 | HG02572.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.758-4696_758-4668d others(31): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225951 | ||||||
| chr5:149225958 | A | ATG | 5 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0052 others(2): Show |
5 | HG01515.hp1 NA18949.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4667_758-4666d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225958 | ||||||
| chr5:149225958 | ATGTG | A | 3 | a0001c0001t0004g0077 a0001c0001t0004g0091 a0001c0001t0006g0034 |
3 | HG02572.hp1 NA18522.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.758-4669_758-4666d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225958 | ||||||
| chr5:149225958 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0006g0093 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.758-4675_758-4666d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225958 | ||||||
| chr5:149225960 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.758-4689G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225960 | |||||||
| chr5:149225962 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.758-4687G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225962 | |||||||
| chr5:149225964 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.758-4685G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225964 | |||||||
| chr5:149225966 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4683G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225966 | |||||||
| chr5:149225966 | GTGTGTGT others(29): Show |
G | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.758-4681_758-4646d others(38): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225966 | ||||||
| chr5:149225966 | GTGTGTGT others(31): Show |
G | 3 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0009g0075 |
3 | HG02630.hp1 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.758-4681_758-4644d others(40): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225966 | ||||||
| chr5:149225966 | GTGTGTGT others(33): Show |
G | 1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.758-4681_758-4642d others(42): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225966 | ||||||
| chr5:149225966 | GTGTGTGT others(35): Show |
G | 15 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(12): Show |
15 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.758-4681_758-4640d others(44): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225966 | ||||||
| chr5:149225968 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4681G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225968 | |||||||
| chr5:149225970 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4679G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225970 | |||||||
| chr5:149225970 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0006g0243 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.758-4677_758-4664d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225970 | ||||||
| chr5:149225972 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4677G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225972 | |||||||
| chr5:149225972 | GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-4675_758-4654d others(24): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225972 | ||||||
| chr5:149225972 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0006g0033 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.758-4675_758-4648d others(30): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225972 | ||||||
| chr5:149225974 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.758-4673_758-4662d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225974 | ||||||
| chr5:149225974 | GTGTGTGT others(13): Show |
G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0173 a0001c0001t0002g0184 |
3 | HG01515.hp2 HG03688.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.758-4673_758-4654d others(22): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225974 | ||||||
| chr5:149225974 | GTGTGTGT others(15): Show |
G | 15 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0029 others(12): Show |
16 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.758-4673_758-4652d others(24): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225974 | ||||||
| chr5:149225974 | GTGTGTGT others(17): Show |
G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(51): Show |
54 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.758-4673_758-4650d others(26): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225974 | ||||||
| chr5:149225974 | GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0200 a0001c0001t0003g0016 others(2): Show |
5 | HG01261.hp1 HG02135.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4673_758-4648d others(28): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225974 | ||||||
| chr5:149225976 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0118 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.758-4673G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225976 | |||||||
| chr5:149225976 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0003g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.758-4671_758-4662d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(9): Show |
G | 3 | a0001c0001t0003g0112 a0001c0001t0003g0119 a0001c0006t0011g0071 |
3 | HG02818.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.758-4671_758-4656d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0108 a0001c0001t0003g0212 |
3 | HG01071.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.758-4671_758-4654d others(20): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(13): Show |
G | 11 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(8): Show |
11 | HG00738.hp2 HG02698.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.758-4671_758-4652d others(22): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0003g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.758-4671_758-4650d others(24): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.758-4671_758-4648d others(26): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225976 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.758-4671_758-4644d others(30): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225976 | ||||||
| chr5:149225978 | G | A | 1 | a0001c0001t0006g0034 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.758-4671G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225978 | |||||||
| chr5:149225978 | GTGTGTAT others(9): Show |
G | 1 | a0001c0003t0004g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.758-4669_758-4654d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225978 | ||||||
| chr5:149225980 | G | A | 5 | a0001c0001t0004g0068 a0001c0001t0004g0077 a0001c0001t0004g0091 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4669G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225980 | |||||||
| chr5:149225980 | GTGTATAT others(3): Show |
G | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.758-4667_758-4658d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225980 | ||||||
| chr5:149225980 | GTGTATAT others(5): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.758-4667_758-4656d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225980 | ||||||
| chr5:149225982 | G | A | 6 | a0001c0001t0004g0077 a0001c0001t0004g0091 a0001c0001t0004g0092 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.758-4667G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225982 | |||||||
| chr5:149225982 | G | GTATA | 8 | a0001c0001t0001g0081 a0001c0001t0001g0132 a0001c0001t0001g0167 others(5): Show |
8 | HG01167.hp1 HG02148.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-4625_758-4622d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.758-4635_758-4622d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.758-4637_758-4622d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTA | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0160 others(9): Show |
12 | HG01123.hp2 HG01168.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.758-4623_758-4622d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATA | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0141 others(13): Show |
16 | HG01099.hp2 HG01175.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.758-4625_758-4622d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATA | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0201 a0001c0001t0001g0218 others(2): Show |
5 | HG02083.hp1 HG03486.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-4627_758-4622d others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(1): Show |
G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0035 others(6): Show |
9 | HG00140.hp2 HG01346.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.758-4629_758-4622d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0150 others(4): Show |
7 | HG00642.hp2 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.758-4631_758-4622d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(5): Show |
G | 20 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0041 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.758-4633_758-4622d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(7): Show |
G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0142 a0001c0001t0002g0241 |
3 | HG04228.hp1 NA18986.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.758-4635_758-4622d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(11): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.758-4639_758-4622d others(20): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(15): Show |
G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0162 |
2 | HG00423.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.758-4643_758-4622d others(24): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225982 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.758-4645_758-4622d others(26): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149225982 | ||||||
| chr5:149225984 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0096 others(3): Show |
6 | HG01515.hp1 NA18963.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-4665A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225984 | |||||||
| chr5:149225986 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0002g0055 others(5): Show |
8 | HG02572.hp2 HG02896.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.758-4663A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225986 | |||||||
| chr5:149225988 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0251 |
2 | HG03669.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.758-4661A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225988 | |||||||
| chr5:149225990 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0005g0109 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.758-4659A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225990 | |||||||
| chr5:149225992 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0111 others(3): Show |
6 | HG00140.hp2 HG01346.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.758-4657A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225992 | |||||||
| chr5:149225994 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0111 a0001c0001t0001g0249 |
3 | HG02055.hp2 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.758-4655A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225994 | |||||||
| chr5:149225996 | A | G | 1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.758-4653A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225996 | |||||||
| chr5:149225998 | A | G | 3 | a0001c0001t0002g0241 a0001c0003t0004g0017 a0001c0006t0014g0213 |
3 | HG02572.hp2 HG03486.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.758-4651A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225998 | |||||||
| chr5:149226000 | A | G | 4 | a0001c0001t0004g0068 a0001c0001t0004g0118 a0001c0003t0004g0017 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.758-4649A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226000 | |||||||
| chr5:149226002 | A | G | 6 | a0001c0001t0001g0125 a0001c0001t0004g0068 a0001c0001t0004g0118 others(3): Show |
6 | HG02572.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.758-4647A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226002 | |||||||
| chr5:149226004 | A | G | 5 | a0001c0001t0004g0068 a0001c0001t0004g0118 a0001c0001t0005g0109 others(2): Show |
5 | HG02572.hp2 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-4645A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226004 | |||||||
| chr5:149226006 | A | G | 4 | a0001c0001t0001g0085 a0001c0001t0004g0068 a0001c0001t0004g0118 others(1): Show |
4 | HG01071.hp2 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.758-4643A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226006 | |||||||
| chr5:149226008 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.758-4641A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226008 | |||||||
| chr5:149226117 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.758-4532C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226117 | |||||||
| chr5:149226192 | A | C | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-4457A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226192 | |||||||
| chr5:149226224 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-4425C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226224 | |||||||
| chr5:149226236 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.758-4413C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226236 | |||||||
| chr5:149226249 | A | G | 3 | a0001c0001t0002g0165 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.758-4400A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226249 | |||||||
| chr5:149226287 | C | T | 2 | a0001c0001t0003g0004 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.758-4362C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226287 | |||||||
| chr5:149226319 | A | C | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-4330A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226319 | |||||||
| chr5:149226437 | T | C | 26 | a0001c0001t0004g0068 a0001c0001t0004g0073 a0001c0001t0004g0088 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-4212T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226437 | |||||||
| chr5:149226470 | G | A | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.758-4179G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226470 | |||||||
| chr5:149226489 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(90): Show |
95 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.758-4160A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226489 | |||||||
| chr5:149226537 | A | C | 2 | a0001c0001t0004g0073 a0001c0001t0004g0088 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.758-4112A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226537 | |||||||
| chr5:149226593 | C | T | 4 | a0001c0001t0002g0029 a0001c0001t0002g0064 a0001c0001t0002g0066 others(1): Show |
4 | NA18945.hp1 NA18955.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.758-4056C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226593 | |||||||
| chr5:149226682 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.758-3967G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226682 | |||||||
| chr5:149226837 | G | A | 10 | a0001c0001t0003g0087 a0001c0001t0003g0107 a0001c0001t0003g0108 others(7): Show |
10 | HG00738.hp2 HG02698.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.758-3812G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226837 | |||||||
| chr5:149226852 | C | G | 15 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(12): Show |
16 | HG00738.hp2 HG02615.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.758-3797C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149226852 | |||||||
| chr5:149227070 | C | CA | 17 | a0001c0001t0001g0048 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG01099.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.758-3557dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149227070 | ||||||
| chr5:149227070 | CA | C | 14 | a0001c0001t0001g0038 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
14 | HG01071.hp1 HG01071.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.758-3557delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149227070 | ||||||
| chr5:149227070 | CAAAAA | C | 7 | a0001c0001t0002g0079 a0001c0001t0002g0165 a0001c0001t0002g0169 others(4): Show |
7 | HG01261.hp1 HG01516.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.758-3561_758-3557d others(7): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149227070 | ||||||
| chr5:149227070 | CAAAAAA | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(85): Show |
90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.758-3562_758-3557d others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 149227070 | ||||||
| chr5:149227119 | T | C | 18 | a0001c0001t0004g0068 a0001c0001t0005g0020 a0001c0001t0005g0021 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-3530T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227119 | |||||||
| chr5:149227193 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(133): Show |
138 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.758-3456A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227193 | |||||||
| chr5:149227396 | G | A | 26 | a0001c0001t0004g0068 a0001c0001t0004g0181 a0001c0001t0004g0182 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-3253G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227396 | |||||||
| chr5:149227435 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.758-3214T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227435 | |||||||
| chr5:149227465 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.758-3184G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227465 | |||||||
| chr5:149227753 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.758-2896G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227753 | |||||||
| chr5:149227821 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.758-2828G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227821 | |||||||
| chr5:149227989 | C | T | 8 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0006g0033 others(5): Show |
8 | HG03688.hp2 HG04115.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-2660C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149227989 | |||||||
| chr5:149228171 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0026 others(27): Show |
30 | HG00323.hp2 HG00423.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.758-2478G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228171 | |||||||
| chr5:149228247 | A | G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.758-2402A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228247 | |||||||
| chr5:149228380 | T | C | 18 | a0001c0001t0004g0068 a0001c0001t0005g0020 a0001c0001t0005g0021 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-2269T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228380 | |||||||
| chr5:149228384 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.758-2265G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228384 | |||||||
| chr5:149228573 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.758-2076A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228573 | |||||||
| chr5:149228701 | T | C | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-1948T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228701 | |||||||
| chr5:149228812 | G | A | 2 | a0001c0003t0004g0017 a0001c0006t0014g0213 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.758-1837G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228812 | |||||||
| chr5:149228815 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.758-1834A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149228815 | |||||||
| chr5:149229128 | C | T | 19 | a0001c0001t0001g0060 a0001c0001t0004g0068 a0001c0001t0005g0020 others(16): Show |
19 | HG00609.hp1 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.758-1521C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229128 | |||||||
| chr5:149229289 | A | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(117): Show |
122 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.758-1360A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229289 | |||||||
| chr5:149229356 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.758-1293C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229356 | |||||||
| chr5:149229431 | G | A | 6 | a0001c0003t0004g0121 a0001c0003t0004g0122 a0002c0004t0004g0013 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-1218G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229431 | |||||||
| chr5:149229439 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.758-1210G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229439 | |||||||
| chr5:149229482 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.758-1167A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229482 | |||||||
| chr5:149229599 | A | G | 2 | a0001c0001t0012g0110 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.758-1050A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229599 | |||||||
| chr5:149229621 | G | A | 26 | a0001c0001t0004g0068 a0001c0001t0004g0181 a0001c0001t0004g0182 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-1028G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229621 | |||||||
| chr5:149229773 | G | A | 2 | a0001c0001t0012g0110 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.758-876G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229773 | |||||||
| chr5:149229785 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.758-864A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229785 | |||||||
| chr5:149229853 | G | A | 1 | a0002c0005t0008g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.758-796G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149229853 | |||||||
| chr5:149230145 | G | C | 18 | a0001c0001t0004g0068 a0001c0001t0005g0020 a0001c0001t0005g0021 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-504G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230145 | |||||||
| chr5:149230165 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(133): Show |
138 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.758-484C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230165 | |||||||
| chr5:149230183 | A | G | 18 | a0001c0001t0004g0068 a0001c0001t0005g0020 a0001c0001t0005g0021 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-466A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230183 | |||||||
| chr5:149230283 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.758-366A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230283 | |||||||
| chr5:149230436 | T | G | 26 | a0001c0001t0004g0068 a0001c0001t0004g0181 a0001c0001t0004g0182 others(23): Show |
26 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.758-213T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230436 | |||||||
| chr5:149230478 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.758-171C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230478 | |||||||
| chr5:149230526 | A | G | 18 | a0001c0001t0004g0068 a0001c0001t0005g0020 a0001c0001t0005g0021 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-123A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230526 | |||||||
| chr5:149230559 | G | T | 8 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0006g0033 others(5): Show |
8 | HG03688.hp2 HG04115.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-90G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149230559 | |||||||
| chr5:149230713 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
splice_region_variant&intron_variant | LOW | c.816+6C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149230713 | |||||||
| chr5:149231001 | G | A | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+294G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231001 | |||||||
| chr5:149231064 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0235 |
2 | HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.816+357A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231064 | |||||||
| chr5:149231125 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.816+418T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231125 | |||||||
| chr5:149231157 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.816+450T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231157 | |||||||
| chr5:149231244 | G | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.816+537G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231244 | |||||||
| chr5:149231457 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.816+750C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231457 | |||||||
| chr5:149231523 | C | G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.816+816C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231523 | |||||||
| chr5:149231644 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.816+937C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231644 | |||||||
| chr5:149231665 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | NA18963.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.816+958C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231665 | |||||||
| chr5:149231739 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.816+1032C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231739 | |||||||
| chr5:149231952 | C | T | 2 | a0001c0001t0001g0023 a0001c0006t0017g0070 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.816+1245C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231952 | |||||||
| chr5:149231965 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(92): Show |
97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.816+1258G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231965 | |||||||
| chr5:149231991 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0211 a0001c0001t0018g0237 |
3 | HG01168.hp2 HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.817-1238G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149231991 | |||||||
| chr5:149232031 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.817-1198A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232031 | |||||||
| chr5:149232060 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.817-1169C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232060 | |||||||
| chr5:149232112 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.817-1117G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232112 | |||||||
| chr5:149232177 | G | A | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.817-1052G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232177 | |||||||
| chr5:149232378 | G | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.817-851G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232378 | |||||||
| chr5:149232378 | G | T | 1 | a0001c0001t0012g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-851G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232378 | |||||||
| chr5:149232433 | T | C | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.817-796T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232433 | |||||||
| chr5:149232454 | T | C | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817-775T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232454 | |||||||
| chr5:149232498 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.817-731A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232498 | |||||||
| chr5:149232737 | T | C | 2 | a0001c0001t0012g0110 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.817-492T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232737 | |||||||
| chr5:149232758 | AG | A | 13 | a0001c0001t0001g0018 a0001c0001t0002g0083 a0001c0001t0002g0153 others(10): Show |
13 | HG00140.hp1 HG01071.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-470delG | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232758 | |||||||
| chr5:149232759 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(94): Show |
99 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.817-470G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232759 | |||||||
| chr5:149232760 | T | A | 13 | a0001c0001t0001g0018 a0001c0001t0002g0083 a0001c0001t0002g0153 others(10): Show |
13 | HG00140.hp1 HG01071.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-469T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232760 | |||||||
| chr5:149233025 | CT | C | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-203delT | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149233025 | |||||||
| chr5:149233056 | G | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.817-173G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149233056 | |||||||
| chr5:149233426 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+126G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233426 | |||||||
| chr5:149233484 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.888+184G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233484 | |||||||
| chr5:149233485 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.888+185C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233485 | |||||||
| chr5:149233600 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.888+300A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233600 | |||||||
| chr5:149233619 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.888+319C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233619 | |||||||
| chr5:149233626 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.888+326C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233626 | |||||||
| chr5:149233750 | C | G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.888+450C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233750 | |||||||
| chr5:149233840 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.888+540C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233840 | |||||||
| chr5:149233851 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.888+551G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149233851 | |||||||
| chr5:149234254 | G | A | 1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.888+954G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234254 | |||||||
| chr5:149234257 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.888+957G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234257 | |||||||
| chr5:149234612 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.888+1312G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234612 | |||||||
| chr5:149234843 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 |
3 | HG01071.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.888+1543G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234843 | |||||||
| chr5:149234857 | G | T | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.888+1557G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234857 | |||||||
| chr5:149234887 | G | A | 1 | a0001c0001t0006g0034 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.888+1587G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149234887 | |||||||
| chr5:149235061 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.888+1761G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235061 | |||||||
| chr5:149235134 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.888+1834C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235134 | |||||||
| chr5:149235361 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.888+2061C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235361 | |||||||
| chr5:149235607 | G | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 |
3 | HG01071.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.889-1841G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235607 | |||||||
| chr5:149235706 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(70): Show |
74 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.889-1742C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235706 | |||||||
| chr5:149235883 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.889-1565T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235883 | |||||||
| chr5:149235915 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.889-1533C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235915 | |||||||
| chr5:149235916 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(125): Show |
130 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.889-1532A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235916 | |||||||
| chr5:149236059 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.889-1389C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236059 | |||||||
| chr5:149236171 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.889-1277G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236171 | |||||||
| chr5:149236383 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(70): Show |
74 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.889-1065C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236383 | |||||||
| chr5:149236424 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(92): Show |
97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.889-1024G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236424 | |||||||
| chr5:149236435 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.889-1013C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236435 | |||||||
| chr5:149236488 | G | T | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.889-960G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236488 | |||||||
| chr5:149236541 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(134): Show |
139 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.889-907G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236541 | |||||||
| chr5:149236553 | C | T | 18 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.889-895C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236553 | |||||||
| chr5:149236594 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.889-854C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236594 | |||||||
| chr5:149236691 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(4): Show |
7 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-757G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236691 | |||||||
| chr5:149236723 | G | T | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.889-725G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236723 | |||||||
| chr5:149236932 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.889-516C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236932 | |||||||
| chr5:149237235 | T | C | 2 | a0001c0001t0003g0004 a0001c0001t0003g0212 |
2 | HG01071.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.889-213T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149237235 | |||||||
| chr5:149237696 | C | T | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+93C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149237696 | |||||||
| chr5:149237806 | C | A | 3 | a0001c0001t0001g0140 a0001c0001t0002g0138 a0001c0001t0002g0174 |
3 | NA18960.hp1 NA18979.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1044+203C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149237806 | |||||||
| chr5:149237880 | C | T | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+277C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149237880 | |||||||
| chr5:149238009 | C | T | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+406C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238009 | |||||||
| chr5:149238127 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+524G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238127 | |||||||
| chr5:149238169 | A | C | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1044+566A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238169 | |||||||
| chr5:149238375 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1044+772C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238375 | |||||||
| chr5:149238425 | A | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1044+822A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238425 | |||||||
| chr5:149238434 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1045-814G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238434 | |||||||
| chr5:149238455 | C | A | 4 | a0001c0001t0002g0054 a0001c0001t0002g0166 a0001c0001t0002g0186 others(1): Show |
4 | HG02071.hp2 HG02080.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-793C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238455 | |||||||
| chr5:149238759 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-489C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238759 | |||||||
| chr5:149238861 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1045-387C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238861 | |||||||
| chr5:149238903 | CA | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1045-343delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 149238903 | ||||||
| chr5:149238992 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1045-256G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238992 | |||||||
| chr5:149239010 | T | C | 10 | a0001c0001t0003g0087 a0001c0001t0003g0107 a0001c0001t0003g0108 others(7): Show |
10 | HG00738.hp2 HG02698.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045-238T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239010 | |||||||
| chr5:149239145 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1045-103A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239145 | |||||||
| chr5:149239186 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1045-62C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239186 | |||||||
| chr5:149239189 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1045-59G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239189 | |||||||
| chr5:149239309 | T | C | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1074+32T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | chr5 | 149239309 | |||||||
| chr5:149239401 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1074+124G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | chr5 | 149239401 | |||||||
| chr5:149239416 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1074+139G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | chr5 | 149239416 | |||||||
| chr5:149239426 | C | G | 6 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+149C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | chr5 | 149239426 | |||||||
| chr5:149239454 | A | T | 4 | a0001c0001t0001g0018 a0001c0001t0004g0077 a0001c0001t0004g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+177A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | chr5 | 149239454 | |||||||
| chr5:149239626 | AG | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(93): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1075-127delG | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr5 | 149239626 | ||||||
| chr5:149239919 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1204+31G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149239919 | |||||||
| chr5:149239987 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1204+99C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149239987 | |||||||
| chr5:149240009 | G | A | 4 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0009g0075 others(1): Show |
4 | HG02630.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+121G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240009 | |||||||
| chr5:149240054 | C | T | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204+166C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240054 | |||||||
| chr5:149240091 | T | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1204+203T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240091 | |||||||
| chr5:149240270 | C | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1204+382C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240270 | |||||||
| chr5:149240306 | G | A | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1205-370G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240306 | |||||||
| chr5:149240506 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1205-170G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240506 | |||||||
| chr5:149240550 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(4): Show |
7 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1205-126G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240550 | |||||||
| chr5:149240554 | C | T | 4 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 others(1): Show |
4 | HG01071.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-122C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240554 | |||||||
| chr5:149240661 | T | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1205-15T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 13/23 | chr5 | 149240661 | |||||||
| chr5:149240785 | C | T | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1303+11C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149240785 | |||||||
| chr5:149240888 | C | T | 36 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0040 others(33): Show |
36 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1303+114C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149240888 | |||||||
| chr5:149240972 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1303+198G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149240972 | |||||||
| chr5:149240996 | C | T | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1303+222C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149240996 | |||||||
| chr5:149241013 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(12): Show |
15 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1303+239G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241013 | |||||||
| chr5:149241039 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1303+265G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241039 | |||||||
| chr5:149241074 | G | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1303+300G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241074 | |||||||
| chr5:149241128 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1303+354C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241128 | |||||||
| chr5:149241163 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0212 a0001c0001t0005g0086 |
3 | HG01071.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1303+389A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241163 | |||||||
| chr5:149241267 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1303+493A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241267 | |||||||
| chr5:149241285 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0053 others(91): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1303+511G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241285 | |||||||
| chr5:149241294 | T | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1303+520T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241294 | |||||||
| chr5:149241307 | A | G | 11 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(8): Show |
11 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303+533A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241307 | |||||||
| chr5:149241412 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1303+638A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241412 | |||||||
| chr5:149241425 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(6): Show |
9 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303+651C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241425 | |||||||
| chr5:149241498 | C | A | 3 | a0001c0001t0002g0124 a0001c0001t0002g0184 a0001c0001t0002g0185 |
3 | HG00597.hp1 HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1303+724C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241498 | |||||||
| chr5:149241498 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1303+724C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241498 | |||||||
| chr5:149241619 | C | G | 17 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1303+845C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241619 | |||||||
| chr5:149241811 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1304-680C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241811 | |||||||
| chr5:149241821 | G | A | 17 | a0001c0001t0001g0018 a0001c0001t0003g0004 a0001c0001t0003g0212 others(14): Show |
17 | HG01071.hp1 HG02258.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1304-670G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241821 | |||||||
| chr5:149241834 | T | C | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1304-657T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241834 | |||||||
| chr5:149241889 | G | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0044 others(113): Show |
118 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1304-602G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241889 | |||||||
| chr5:149241984 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1304-507C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149241984 | |||||||
| chr5:149242059 | C | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0001c0001t0001g0081 others(3): Show |
6 | HG00438.hp2 NA18949.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-432C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149242059 | |||||||
| chr5:149242148 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0004g0073 a0001c0001t0004g0077 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304-343G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149242148 | |||||||
| chr5:149242242 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1304-249T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149242242 | |||||||
| chr5:149242249 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1304-242C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149242249 | |||||||
| chr5:149242282 | G | A | 18 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(15): Show |
19 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.1304-209G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 14/23 | chr5 | 149242282 | |||||||
| chr5:149242766 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(102): Show |
106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1351+228A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149242766 | |||||||
| chr5:149242772 | C | G | 1 | a0001c0001t0005g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1351+234C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149242772 | |||||||
| chr5:149242782 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(102): Show |
106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1351+244C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149242782 | |||||||
| chr5:149242912 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1351+374G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149242912 | |||||||
| chr5:149242947 | T | A | 18 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1351+409T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149242947 | |||||||
| chr5:149243015 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1351+477T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243015 | |||||||
| chr5:149243075 | G | T | 1 | a0001c0001t0005g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1351+537G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243075 | |||||||
| chr5:149243318 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1351+780C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243318 | |||||||
| chr5:149243466 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1351+928G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243466 | |||||||
| chr5:149243535 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(123): Show |
128 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1351+997A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243535 | |||||||
| chr5:149243560 | G | C | 2 | a0001c0001t0002g0024 a0001c0001t0003g0016 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1351+1022G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243560 | |||||||
| chr5:149243636 | G | C | 1 | a0001c0001t0002g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1351+1098G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243636 | |||||||
| chr5:149243654 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(116): Show |
121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1351+1116G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243654 | |||||||
| chr5:149243749 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1352-1132C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149243749 | |||||||
| chr5:149244132 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1352-749C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149244132 | |||||||
| chr5:149244258 | C | G | 1 | a0001c0001t0002g0015 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1352-623C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149244258 | |||||||
| chr5:149244428 | G | A | 20 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(17): Show |
21 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-453G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149244428 | |||||||
| chr5:149244647 | G | A | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-234G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 15/23 | chr5 | 149244647 | |||||||
| chr5:149245335 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(96): Show |
100 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1486+320G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245335 | |||||||
| chr5:149245387 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1486+372A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245387 | |||||||
| chr5:149245432 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1486+417G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245432 | |||||||
| chr5:149245447 | G | C | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1486+432G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245447 | |||||||
| chr5:149245460 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1486+445G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245460 | |||||||
| chr5:149245474 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0244 |
2 | NA18955.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1486+459C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245474 | |||||||
| chr5:149245595 | G | GTAGTGGC others(16): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0050 others(11): Show |
14 | HG01433.hp2 HG01496.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1486+598_1486+599i others(25): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr5 | 149245595 | ||||||
| chr5:149245639 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1486+624T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245639 | |||||||
| chr5:149245699 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1486+684C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245699 | |||||||
| chr5:149245856 | C | T | 20 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(17): Show |
21 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1487-626C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245856 | |||||||
| chr5:149245898 | C | T | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1487-584C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245898 | |||||||
| chr5:149245955 | G | A | 20 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(17): Show |
21 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1487-527G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149245955 | |||||||
| chr5:149246119 | C | T | 20 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(17): Show |
21 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1487-363C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149246119 | |||||||
| chr5:149246309 | G | T | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1487-173G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149246309 | |||||||
| chr5:149246408 | T | C | 1 | a0002c0004t0004g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1487-74T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149246408 | |||||||
| chr5:149246409 | T | A | 53 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0032 others(50): Show |
53 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1487-73T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149246409 | |||||||
| chr5:149246409 | TA | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(116): Show |
121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1487-63delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr5 | 149246409 | ||||||
| chr5:149246453 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1487-29C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 16/23 | chr5 | 149246453 | |||||||
| chr5:149246645 | T | C | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1551+99T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149246645 | |||||||
| chr5:149247025 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1551+479G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247025 | |||||||
| chr5:149247150 | T | C | 20 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(17): Show |
21 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1551+604T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247150 | |||||||
| chr5:149247155 | A | C | 18 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(15): Show |
19 | HG00738.hp2 HG01071.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.1551+609A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247155 | |||||||
| chr5:149247197 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1552-585C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247197 | |||||||
| chr5:149247221 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1552-561A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247221 | |||||||
| chr5:149247274 | C | G | 33 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0003g0001 others(30): Show |
34 | HG00738.hp2 HG01071.hp1 HG02572.hp1 others(31): Show |
intron_variant | MODIFIER | c.1552-508C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247274 | |||||||
| chr5:149247277 | G | T | 3 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0006t0014g0213 |
3 | HG02630.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1552-505G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247277 | |||||||
| chr5:149247336 | C | T | 1 | a0001c0002t0005g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1552-446C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247336 | |||||||
| chr5:149247376 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0004g0068 others(17): Show |
20 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.1552-406T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247376 | |||||||
| chr5:149247491 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(96): Show |
100 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1552-291G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247491 | |||||||
| chr5:149247497 | T | C | 1 | a0005c0011t0001g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-285T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247497 | |||||||
| chr5:149247599 | G | A | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1552-183G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247599 | |||||||
| chr5:149247652 | G | A | 1 | a0001c0001t0005g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1552-130G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247652 | |||||||
| chr5:149247689 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0053 others(136): Show |
141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1552-93G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247689 | |||||||
| chr5:149247712 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1552-70C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247712 | |||||||
| chr5:149247726 | A | G | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1552-56A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 17/23 | chr5 | 149247726 | |||||||
| chr5:149247940 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1699+11C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149247940 | |||||||
| chr5:149248034 | C | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(90): Show |
94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1699+105C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248034 | |||||||
| chr5:149248160 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1699+231T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248160 | |||||||
| chr5:149248179 | G | A | 1 | a0002c0005t0008g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1699+250G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248179 | |||||||
| chr5:149248242 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0003g0016 a0001c0009t0007g0037 others(1): Show |
4 | HG01261.hp1 HG02738.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1699+313C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248242 | |||||||
| chr5:149248269 | T | C | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1699+340T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248269 | |||||||
| chr5:149248327 | C | A | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1699+398C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248327 | |||||||
| chr5:149248462 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0004g0073 others(17): Show |
20 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1699+533C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248462 | |||||||
| chr5:149248625 | G | A | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1699+696G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248625 | |||||||
| chr5:149248689 | C | CA | 25 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0227 others(22): Show |
25 | HG01516.hp1 HG01975.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.1699+781dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248689 | ||||||
| chr5:149248689 | C | CAA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(91): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1699+780_1699+781d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248689 | ||||||
| chr5:149248689 | C | CAAA | 9 | a0001c0001t0003g0016 a0001c0001t0004g0068 a0001c0001t0005g0021 others(6): Show |
9 | HG02055.hp1 HG02258.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1699+779_1699+781d others(5): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248689 | ||||||
| chr5:149248689 | CA | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0057 others(2): Show |
5 | HG01515.hp1 HG02683.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1699+781delA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248689 | ||||||
| chr5:149248689 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1699+770_1699+781d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248689 | ||||||
| chr5:149248859 | G | GAC | 35 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0032 others(32): Show |
35 | HG00280.hp2 HG00621.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1700-917_1700-916d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACAC | 7 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0106 others(4): Show |
7 | HG00438.hp2 HG02165.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1700-919_1700-916d others(6): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACAC | 8 | a0001c0001t0002g0024 a0001c0001t0003g0016 a0001c0001t0003g0108 others(5): Show |
8 | HG02723.hp1 HG02886.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1700-921_1700-916d others(8): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACACA others(1): Show |
5 | a0001c0001t0001g0060 a0001c0001t0001g0143 a0001c0001t0003g0212 others(2): Show |
5 | HG00609.hp1 HG01071.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1700-923_1700-916d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACACA others(3): Show |
11 | a0001c0001t0001g0028 a0001c0001t0001g0234 a0001c0001t0003g0004 others(8): Show |
11 | HG02135.hp1 HG02698.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1700-925_1700-916d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACACA others(5): Show |
5 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0107 others(2): Show |
6 | HG00738.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1700-927_1700-916d others(14): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACACA others(7): Show |
1 | a0001c0001t0003g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1700-929_1700-916d others(16): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | G | GACACACA others(9): Show |
1 | a0002c0005t0013g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1700-931_1700-916d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | GAC | G | 27 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0048 others(24): Show |
27 | HG00423.hp2 HG00738.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1700-917_1700-916d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | GACACACA others(1): Show |
G | 14 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0004g0073 others(11): Show |
14 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1700-923_1700-916d others(10): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | GACACACA others(3): Show |
G | 13 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1700-925_1700-916d others(12): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | GACACACA others(9): Show |
G | 11 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(8): Show |
11 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1700-931_1700-916d others(18): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248859 | GACACACA others(13): Show |
G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0002g0002 others(72): Show |
76 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1700-935_1700-916d others(22): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 149248859 | ||||||
| chr5:149248877 | C | T | 13 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0004g0073 others(10): Show |
13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1700-938C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248877 | |||||||
| chr5:149248879 | C | T | 13 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1700-936C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248879 | |||||||
| chr5:149248898 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1700-917A>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248898 | |||||||
| chr5:149248919 | T | C | 26 | a0001c0001t0001g0018 a0001c0001t0002g0072 a0001c0001t0004g0073 others(23): Show |
26 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.1700-896T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248919 | |||||||
| chr5:149248962 | G | A | 1 | a0001c0010t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1700-853G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248962 | |||||||
| chr5:149248992 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0053 others(116): Show |
120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1700-823C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248992 | |||||||
| chr5:149249014 | C | G | 1 | a0001c0001t0009g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1700-801C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249014 | |||||||
| chr5:149249188 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1700-627T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249188 | |||||||
| chr5:149249225 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0221 |
2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1700-590G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249225 | |||||||
| chr5:149249347 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1700-468A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249347 | |||||||
| chr5:149249396 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1700-419G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249396 | |||||||
| chr5:149249434 | T | C | 3 | a0001c0001t0003g0108 a0001c0001t0003g0114 a0001c0001t0003g0119 |
3 | HG02723.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1700-381T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249434 | |||||||
| chr5:149249787 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1700-28A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149249787 | |||||||
| chr5:149250123 | T | C | 4 | a0001c0001t0002g0054 a0001c0001t0002g0166 a0001c0001t0002g0186 others(1): Show |
4 | HG02071.hp2 HG02080.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+279T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 19/23 | chr5 | 149250123 | |||||||
| chr5:149250164 | GAC | G | 3 | a0001c0001t0003g0016 a0001c0009t0007g0037 a0001c0009t0007g0117 |
3 | HG01261.hp1 HG02738.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1730-279_1730-278d others(4): Show |
ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr5 | 149250164 | ||||||
| chr5:149250183 | A | G | 1 | a0001c0001t0010g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1730-264A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 19/23 | chr5 | 149250183 | |||||||
| chr5:149250284 | C | T | 2 | a0001c0001t0009g0075 a0001c0006t0011g0071 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1730-163C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 19/23 | chr5 | 149250284 | |||||||
| chr5:149250606 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1788+101G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149250606 | |||||||
| chr5:149250628 | C | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0053 others(115): Show |
119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1788+123C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149250628 | |||||||
| chr5:149250737 | T | C | 12 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(9): Show |
12 | HG02572.hp1 HG02630.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1788+232T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149250737 | |||||||
| chr5:149250993 | G | A | 1 | a0002c0005t0008g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1789-366G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149250993 | |||||||
| chr5:149251002 | T | C | 3 | a0001c0001t0003g0231 a0001c0001t0003g0245 a0002c0005t0013g0019 |
3 | HG02647.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1789-357T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149251002 | |||||||
| chr5:149251211 | G | A | 11 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0069 others(8): Show |
11 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1789-148G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149251211 | |||||||
| chr5:149251270 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1789-89G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149251270 | |||||||
| chr5:149251292 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1789-67G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 20/23 | chr5 | 149251292 | |||||||
| chr5:149251525 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0097 others(3): Show |
6 | HG02083.hp1 NA18945.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849+106C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251525 | |||||||
| chr5:149251689 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0022 others(26): Show |
29 | HG00323.hp2 HG00423.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1849+270C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251689 | |||||||
| chr5:149251704 | G | A | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1849+285G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251704 | |||||||
| chr5:149251810 | C | G | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1849+391C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251810 | |||||||
| chr5:149251820 | G | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0112 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1850-381G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251820 | |||||||
| chr5:149251870 | T | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0053 others(117): Show |
121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1850-331T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251870 | |||||||
| chr5:149251909 | C | T | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1850-292C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251909 | |||||||
| chr5:149251910 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1850-291G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251910 | |||||||
| chr5:149251988 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1850-213A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149251988 | |||||||
| chr5:149252095 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0230 a0004c0013t0001g0247 |
3 | HG02897.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1850-106A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 21/23 | chr5 | 149252095 | |||||||
| chr5:149252494 | T | A | 1 | a0001c0001t0005g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1858-263T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 22/23 | chr5 | 149252494 | |||||||
| chr5:149252546 | T | C | 3 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0006t0014g0213 |
3 | HG02630.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1858-211T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 22/23 | chr5 | 149252546 | |||||||
| chr5:149252854 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0255 |
2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1938+17G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149252854 | |||||||
| chr5:149252940 | A | G | 23 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(20): Show |
23 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1938+103A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149252940 | |||||||
| chr5:149253037 | C | T | 23 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(20): Show |
23 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1938+200C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253037 | |||||||
| chr5:149253038 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1938+201C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253038 | |||||||
| chr5:149253286 | A | C | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+449A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253286 | |||||||
| chr5:149253344 | A | G | 2 | a0001c0009t0007g0037 a0001c0009t0007g0117 |
2 | HG01261.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1938+507A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253344 | |||||||
| chr5:149253412 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1938+575T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253412 | |||||||
| chr5:149253621 | G | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0038 others(3): Show |
6 | HG00323.hp2 HG00642.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+784G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253621 | |||||||
| chr5:149253644 | T | C | 26 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0057 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1938+807T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253644 | |||||||
| chr5:149253673 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1938+836A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253673 | |||||||
| chr5:149253796 | C | T | 17 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(14): Show |
17 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1938+959C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253796 | |||||||
| chr5:149253861 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0002g0002 a0001c0001t0002g0003 others(111): Show |
115 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1938+1024G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253861 | |||||||
| chr5:149253946 | T | G | 1 | a0001c0001t0003g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1938+1109T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149253946 | |||||||
| chr5:149254181 | A | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1938+1344A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254181 | |||||||
| chr5:149254215 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0002g0002 a0001c0001t0002g0003 others(94): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1938+1378T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254215 | |||||||
| chr5:149254232 | G | A | 5 | a0001c0002t0005g0074 a0001c0002t0005g0113 a0001c0002t0005g0214 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+1395G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254232 | |||||||
| chr5:149254674 | C | T | 10 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(7): Show |
10 | HG02572.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1938+1837C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254674 | |||||||
| chr5:149254947 | C | A | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1938+2110C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254947 | |||||||
| chr5:149255301 | A | C | 6 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0039 others(3): Show |
6 | HG03688.hp2 HG04204.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1938+2464A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149255301 | |||||||
| chr5:149255950 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1939-2341C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149255950 | |||||||
| chr5:149256163 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1939-2128C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256163 | |||||||
| chr5:149256533 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0002g0002 a0001c0001t0002g0003 others(100): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1939-1758A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256533 | |||||||
| chr5:149256775 | T | A | 1 | a0001c0001t0004g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1939-1516T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256775 | |||||||
| chr5:149256830 | G | T | 1 | a0001c0001t0002g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1939-1461G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256830 | |||||||
| chr5:149256899 | G | C | 11 | a0001c0001t0004g0073 a0001c0001t0004g0077 a0001c0001t0004g0088 others(8): Show |
11 | HG02572.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1939-1392G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256899 | |||||||
| chr5:149256968 | T | G | 1 | a0001c0001t0006g0034 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1939-1323T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149256968 | |||||||
| chr5:149257021 | A | G | 2 | a0002c0005t0008g0115 a0002c0005t0008g0116 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1939-1270A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257021 | |||||||
| chr5:149257034 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1939-1257G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257034 | |||||||
| chr5:149257287 | A | G | 55 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(52): Show |
56 | HG00738.hp2 HG01071.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1939-1004A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257287 | |||||||
| chr5:149257299 | C | CA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0002g0002 others(73): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1939-977dupA | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 149257299 | ||||||
| chr5:149257392 | A | G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0105 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1939-899A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257392 | |||||||
| chr5:149257710 | A | G | 1 | a0001c0001t0005g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1939-581A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257710 | |||||||
| chr5:149257859 | C | T | 7 | a0001c0003t0004g0017 a0001c0003t0004g0121 a0001c0003t0004g0122 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939-432C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257859 | |||||||
| chr5:149257922 | T | C | 1 | a0001c0006t0011g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1939-369T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257922 | |||||||
| chr5:149257933 | G | T | 1 | a0001c0006t0017g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1939-358G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149257933 | |||||||
| chr5:149258170 | C | G | 78 | a0001c0001t0001g0003 a0001c0001t0002g0002 a0001c0001t0002g0003 others(75): Show |
79 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1939-121C>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149258170 | |||||||
| chr5:149258270 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1939-21C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149258270 |