Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 683 | 247 | 63 | 38 | 108 | 10 | 26 | 82 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002 | 0/0 | 683 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0003 | 0/0 | 683 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0004 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0005 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0006 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2052 | 229 | 52 | 34 | 107 | 10 | 24 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0002 | 0/0 | 2052 | 5 | 4 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0003 | 0/0 | 2052 | 4 | 3 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0004 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0005 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0006 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0007 | 0/0 | 2052 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0008 | 0/0 | 2052 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0009 | 0/0 | 2052 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0010 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0011 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0012 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0013 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| c0014 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2388 | 113 | 15 | 22 | 58 | 6 | 11 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0002 | 0/1 | 2388 | 78 | 7 | 13 | 45 | 4 | 8 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0003 | 0/0 | 2388 | 19 | 16 | 2 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0004 | 0/0 | 2388 | 16 | 13 | 1 | 0 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0005 | 0/0 | 2388 | 12 | 11 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0006 | 0/0 | 2388 | 6 | 0 | 0 | 4 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0007 | 0/0 | 2388 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0008 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0009 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0010 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0011 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0012 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0013 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0014 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0015 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0016 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0017 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| t0018 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2052 | 229 | 52 | 34 | 107 | 10 | 24 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0002 | 0/0 | 2052 | 5 | 4 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0003 | 0/0 | 2052 | 4 | 3 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0006 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0008 | 0/0 | 2052 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0009 | 0/0 | 2052 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0010 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0014 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002c0004 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002c0005 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0003c0007 | 0/0 | 2052 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0004c0011 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0005c0012 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0006c0013 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | 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 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0002 | 0/1 | 4439 | 78 | 7 | 13 | 45 | 4 | 8 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0003 | 0/0 | 4439 | 19 | 16 | 2 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0004 | 0/0 | 4439 | 9 | 7 | 0 | 0 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0005 | 0/0 | 4439 | 7 | 7 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0006 | 0/0 | 4439 | 6 | 0 | 0 | 4 | 0 | 2 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0009 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0010 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0012 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0015 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0016 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0001t0018 | 0/0 | 4439 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0002t0005 | 0/0 | 4439 | 5 | 4 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0003t0004 | 0/0 | 4439 | 4 | 3 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0006t0011 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0006t0014 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0006t0017 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0008t0001 | 0/0 | 4439 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0009t0007 | 0/0 | 4439 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0010t0001 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0001c0014t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002c0004t0004 | 0/0 | 4439 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002c0005t0008 | 0/0 | 4439 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0002c0005t0013 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0003c0007t0001 | 0/0 | 4439 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0004c0011t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0005c0012t0001 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| a0006c0013t0001 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | copy fasta | chr5 | 149136493 | 149265542 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0054 | 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 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0179 | 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 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0202 | 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 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0056 | 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 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0136 | 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 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0002g0233 | 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 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 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 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0088 | 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 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0089 | 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 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0001t0018g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0018 | 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 |
| a0001c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0003t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0006t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0008t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0009t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0009t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0010t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0001c0014t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0004t0004g0014 | 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 |
| a0002c0004t0004g0091 | 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 |
| a0002c0005t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0002c0005t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0003c0007t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0003c0007t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0004c0011t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0005c0012t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| a0006c0013t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0227 | EUR | GBR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0032 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01175 | hp2 | a0003 | c0007 | t0001 | g0147 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01192 | hp2 | a0003 | c0007 | t0001 | g0234 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0249 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0114 | AMR | PUR | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01261 | hp1 | a0001 | c0009 | t0007 | g0038 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0046 | 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 | g0166 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01884 | hp1 | a0001 | c0006 | t0017 | g0071 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02135 | hp1 | a0001 | c0014 | t0001 | g0095 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CDX | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0122 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0018 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02647 | hp1 | a0002 | c0005 | t0013 | g0020 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02683 | hp1 | a0001 | c0008 | t0001 | g0177 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02738 | hp1 | a0001 | c0001 | t0018 | g0238 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02738 | hp2 | a0001 | c0009 | t0007 | g0118 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02818 | hp1 | a0002 | c0004 | t0004 | g0014 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02897 | hp2 | a0006 | c0013 | t0001 | g0248 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0021 | 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 | g0085 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02976 | hp1 | a0001 | c0006 | t0011 | g0072 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03041 | hp2 | a0002 | c0004 | t0004 | g0090 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0111 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03486 | hp2 | a0001 | c0006 | t0014 | g0214 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03540 | hp2 | a0001 | c0010 | t0001 | g0218 | AFR | GWD | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0094 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0183 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18522 | hp2 | a0001 | c0002 | t0005 | g0217 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18942 | hp1 | a0001 | c0001 | t0016 | g0015 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18967 | hp2 | a0004 | c0011 | t0001 | g0135 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18978 | hp2 | a0001 | c0001 | t0010 | g0134 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19012 | hp1 | a0001 | c0001 | t0015 | g0206 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19054 | hp1 | a0005 | c0012 | t0001 | g0102 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA19240 | hp2 | a0002 | c0005 | t0008 | g0117 | AFR | YRI | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03471 | hp1 | a0002 | c0005 | t0008 | g0116 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| HG03471 | hp2 | a0002 | c0004 | t0004 | g0091 | AFR | MSL | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA21309 | hp1 | a0001 | c0003 | t0004 | g0123 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0100 | REF | REF | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0221 | REF | REF | ABLIM3_chr5_149136493_149265542 | ABLIM3 | chr5 | 149136493 | 149265542 |
| 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 | a0004 | 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 | a0006 | 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 | a0005 | 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 |
| 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 | a0001c0006a0001c0010 | 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 | a0001c0008a0001c0010 | 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 | a0001c0003a0002c0004 | 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 |
| 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 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(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 | a0001c0001t0002a0001c0001t0016 | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(76): 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 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(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 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(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 | a0001c0001t0003a0001c0006t0011a0001c0009t0007others(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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1795G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 24/24 | 1795 | chr5 | 149260199 |
| 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 | a0001c0001t0003g0003 | 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 | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0003g0004others(3): 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 | a0001c0001t0001g0256 | 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 | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(213): Show | 217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): 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 | a0001c0001t0001g0012a0001c0001t0002g0010a0001c0001t0002g0011 | 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 | a0001c0002t0005g0215a0001c0002t0005g0216a0001c0002t0005g0217 | 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 | a0001c0001t0001g0013 | 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 | a0001c0006t0014g0214 | 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 | a0002c0004t0004g0014 | 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 | a0001c0001t0003g0255 | 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 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(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 | a0001c0001t0002g0016a0001c0001t0016g0015 | 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 | 117 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(114): Show | 118 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(115): 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 | a0001c0001t0006g0094 | 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 | a0001c0001t0003g0088a0001c0001t0004g0089a0001c0001t0004g0092others(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 | a0001c0001t0003g0017 | 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 | a0001c0014t0001g0095 | 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 | a0001c0001t0001g0096 | 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 | a0002c0004t0004g0014 | 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 | a0001c0001t0001g0019a0001c0003t0004g0018 | 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 | a0001c0001t0005g0087 | 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 | a0002c0005t0013g0020 | 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 | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(91): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | 126 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(123): 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0010a0001c0001t0002g0011 | 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 | a0001c0001t0001g0019a0001c0003t0004g0018 | 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 | a0001c0006t0014g0214 | 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 | 36 | a0001c0001t0001g0082a0001c0001t0001g0107a0001c0001t0001g0112others(33): Show | 36 | HG00738.hp2 HG00741.hp2 HG01123.hp1 others(33): 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 | a0001c0001t0001g0096a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0005g0021a0001c0001t0005g0022 | 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 | 91 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(88): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0107a0001c0001t0002g0106 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0006g0128 | 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 | 91 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(88): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0005g0087 | 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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0002g0101a0001c0002t0005g0215a0001c0002t0005g0216others(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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0082a0001c0001t0001g0188a0001c0001t0001g0189others(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 | a0001c0001t0001g0190a0001c0001t0001g0191 | 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 | a0001c0001t0002g0178 | 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 | a0001c0001t0001g0024a0001c0001t0002g0026a0001c0010t0001g0218 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0004g0069a0001c0001t0005g0070 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): 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 | a0001c0001t0002g0178 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(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 | a0001c0001t0002g0026 | 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 | a0001c0001t0003g0088a0001c0001t0004g0069a0001c0001t0004g0089others(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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | 2 | a0001c0001t0002g0100a0001c0001t0002g0127 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0002g0025 | 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 | a0001c0001t0004g0069a0001c0001t0005g0070 | 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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0003g0088a0001c0001t0004g0089a0001c0001t0005g0087others(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 | a0001c0006t0014g0214 | 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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): 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 | a0001c0001t0002g0025 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0008t0001g0177 | 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 | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0003g0017 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0176a0001c0001t0002g0175 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0002g0067 | 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 | a0001c0001t0001g0019a0001c0003t0004g0018 | 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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0226 | 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 | a0001c0006t0014g0214 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): 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 | a0001c0006t0017g0071 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0001g0212a0001c0001t0003g0213 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0002t0005g0215a0001c0002t0005g0216a0001c0002t0005g0217 | 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 | a0001c0006t0014g0214 | 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 | a0001c0001t0004g0069a0001c0001t0005g0070a0002c0005t0013g0020 | 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 | a0001c0001t0004g0069a0001c0001t0005g0070a0002c0005t0013g0020 | 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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0002g0025a0001c0002t0005g0215a0001c0002t0005g0216others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 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 | a0001c0001t0003g0088a0001c0001t0004g0069a0001c0001t0004g0089others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0200a0001c0001t0002g0199 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | a0001c0001t0003g0088 | 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 | a0001c0006t0014g0214 | 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 | a0002c0005t0013g0020 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0004g0069a0001c0001t0005g0070 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0024others(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 | a0001c0001t0004g0069a0001c0001t0005g0070a0001c0006t0014g0214 | 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 | a0001c0001t0001g0252 | 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 | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): 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 | 149 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(146): 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0172a0005c0012t0001g0102 | 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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0212a0001c0001t0003g0213 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0202a0001c0001t0002g0104a0001c0001t0002g0227 | 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 | a0001c0001t0002g0171 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0001t0002g0201 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0002g0198 | 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 | a0001c0001t0001g0176a0001c0001t0002g0175 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0003g0017 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0001g0019a0001c0001t0001g0077a0001c0001t0001g0079others(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 | 133 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0029others(130): Show | 134 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(131): 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 | a0001c0001t0002g0106 | 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 | a0001c0001t0003g0108 | 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 | 193 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): 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 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | 134 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0024others(131): Show | 135 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(132): 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0003g0088a0001c0001t0004g0089a0002c0004t0004g0090others(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 | a0001c0001t0002g0052 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0002g0073a0001c0001t0004g0074a0001c0002t0005g0075others(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 | 89 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0096others(86): Show | 90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): 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 | a0001c0001t0004g0089 | 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 | a0001c0001t0004g0069a0001c0006t0014g0214 | 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 | a0001c0001t0001g0256a0001c0001t0003g0251 | 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 | a0001c0001t0003g0088a0001c0001t0004g0089a0002c0004t0004g0090others(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 | a0001c0001t0005g0229 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | 189 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.14-18206T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149165246 | ||||||
| chr5:149165293
|
A | G | 83 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(80): Show | 84 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(81): 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0009g0076 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0129 | 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 | 83 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(80): Show | 84 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(81): 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 | a0001c0001t0001g0231a0001c0001t0001g0256a0001c0001t0002g0230others(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 | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): 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 | 132 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0024others(129): Show | 133 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(130): 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 | a0001c0001t0002g0073a0001c0001t0004g0074a0001c0002t0005g0075others(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 | a0001c0001t0005g0070 | 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 | 134 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0024others(131): Show | 135 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(132): 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 | a0001c0001t0003g0109 | 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 | a0001c0001t0001g0168a0001c0001t0002g0167a0001c0001t0002g0174 | 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 | a0001c0001t0001g0024a0001c0010t0001g0218 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0077others(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 | a0001c0001t0002g0025 | 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 | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): 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 | 15 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0049others(12): Show | 15 | HG01978.hp1 HG03834.hp2 NA18945.hp2 others(12): 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 | a0001c0001t0005g0070 | 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 | a0002c0005t0013g0020 | 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 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0188others(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 | a0001c0008t0001g0032 | 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 | a0001c0001t0002g0180a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0002t0005g0215a0001c0002t0005g0216a0001c0002t0005g0217 | 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 | a0001c0001t0001g0024a0001c0006t0014g0214a0001c0010t0001g0218 | 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 | 39 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(36): 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 | a0001c0001t0003g0017a0001c0001t0003g0088a0001c0001t0004g0089others(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 | a0001c0001t0003g0003 | 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 | a0001c0001t0002g0175 | 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0023others(201): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.14-14596G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168856 | ||||||
| chr5:149168960
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.14-14492A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149168960 | ||||||
| chr5:149169024
|
C | G | 65 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(62): 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0004g0078 | 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 | a0001c0001t0001g0250a0001c0003t0004g0249 | 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 | a0001c0001t0012g0111a0001c0010t0001g0218 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0003g0120 | 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 | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0001g0151others(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 | a0001c0001t0001g0133a0001c0001t0001g0179a0001c0001t0001g0190others(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 | a0001c0001t0001g0191a0001c0001t0002g0153a0001c0001t0006g0040others(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 | a0001c0001t0002g0154 | 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 | a0001c0001t0003g0088a0001c0001t0004g0089a0001c0001t0005g0087others(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 | a0001c0001t0001g0019a0001c0001t0004g0069a0001c0003t0004g0018 | 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 | a0001c0001t0010g0134 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0047 | 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 | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0009g0076a0001c0006t0011g0072 | 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 | a0001c0001t0001g0235a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | a0001c0001t0001g0037 | 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 | a0001c0006t0017g0071 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0001g0151others(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 | a0001c0001t0001g0142a0001c0001t0001g0235a0001c0009t0007g0038others(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 | a0001c0001t0002g0016a0001c0001t0016g0015 | 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 | a0001c0001t0018g0238 | 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 | a0001c0001t0006g0040 | 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 | a0001c0002t0005g0215 | 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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0053others(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 | a0001c0001t0001g0036a0001c0001t0001g0237a0001c0001t0002g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0033others(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 | a0001c0001t0001g0029a0001c0001t0001g0098a0001c0001t0001g0141others(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 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0097others(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 | a0001c0001t0001g0048a0001c0001t0001g0164a0001c0001t0006g0034others(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 | a0001c0001t0003g0115a0002c0004t0004g0090a0002c0005t0013g0020 | 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 | a0001c0001t0001g0211a0001c0002t0005g0216 | 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 | a0001c0001t0006g0094a0001c0002t0005g0217 | 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 | a0001c0001t0002g0199a0001c0001t0004g0119a0001c0001t0006g0035others(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 | a0001c0002t0005g0075 | 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 | a0001c0006t0017g0071 | 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 | a0001c0006t0014g0214 | 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 | a0001c0006t0011g0072 | 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 | a0001c0001t0001g0256a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0006t0017g0071others(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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(80): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): 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 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0058others(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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0143a0001c0001t0009g0076a0001c0009t0007g0038others(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 | a0001c0001t0003g0003 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(136): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0113others(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 | a0001c0001t0004g0182 | 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 | a0001c0001t0001g0036a0001c0001t0002g0011a0001c0001t0002g0158others(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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(97): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.14-11910A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171542 | ||||||
| chr5:149171602
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(136): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): 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 | a0001c0001t0001g0031a0001c0001t0001g0243 | 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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(136): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.14-11720T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171732 | ||||||
| chr5:149171908
|
GTTTCT | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): 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 | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.14-11537T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171915 | ||||||
| chr5:149171916
|
T | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.14-11536T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171916 | ||||||
| chr5:149171918
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.14-11534T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171918 | ||||||
| chr5:149171919
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.14-11533C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171919 | ||||||
| chr5:149171920
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): 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 | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): 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 | 136 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.14-11521T>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149171931 | ||||||
| chr5:149172532
|
C | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): 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 | a0001c0001t0001g0082a0001c0001t0001g0225a0001c0001t0002g0081 | 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0004g0119 | 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 | a0001c0006t0017g0071a0001c0010t0001g0218 | 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 | a0002c0004t0004g0091 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0140 | 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 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0027others(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 | a0001c0001t0001g0054a0001c0001t0001g0235a0001c0001t0002g0084others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0009g0076others(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 | a0001c0001t0002g0171a0001c0001t0002g0224a0001c0001t0003g0246others(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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0082a0001c0001t0001g0143a0001c0001t0001g0151others(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 | a0001c0001t0004g0078a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0082a0001c0001t0001g0143a0001c0001t0001g0151others(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 | 78 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(75): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0006g0034 | 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 | 78 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(75): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): 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 | a0001c0002t0005g0114 | 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 | a0001c0006t0011g0072a0001c0006t0014g0214a0001c0006t0017g0071others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0169a0001c0001t0002g0170 | 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 | a0001c0001t0001g0226 | 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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(136): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): 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 | a0001c0006t0011g0072a0001c0006t0014g0214a0001c0006t0017g0071others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0001g0144a0001c0001t0001g0236 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0002g0016a0001c0001t0016g0015 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0009t0007g0038others(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 | a0001c0010t0001g0218 | 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 | a0001c0001t0018g0238 | 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 | a0001c0001t0001g0212a0001c0001t0003g0213 | 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 | a0001c0001t0001g0219 | 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 | a0002c0004t0004g0091 | 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 | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0113others(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 | a0001c0001t0003g0088 | 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 | a0001c0001t0004g0119 | 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 | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | 134 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): 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 | a0001c0001t0003g0246 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0004g0069 | 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 | 10 | a0001c0001t0002g0153a0001c0001t0003g0004a0001c0001t0003g0005others(7): 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0002g0227 | 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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0009t0007g0038others(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 | a0001c0008t0001g0032 | 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 | a0001c0001t0001g0143a0001c0001t0002g0052a0001c0001t0002g0145others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0002g0199a0001c0001t0003g0003others(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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0003g0108a0001c0001t0003g0113a0001c0001t0003g0121others(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 | a0001c0001t0005g0087 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0009g0076 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0009g0076 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0004g0069 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0006t0017g0071a0001c0010t0001g0218 | 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 | a0001c0001t0004g0069 | 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 | a0001c0006t0017g0071 | 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 | a0001c0003t0004g0249 | 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 | a0001c0006t0017g0071a0001c0010t0001g0218 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0003g0108 | 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 | a0001c0001t0002g0125a0001c0001t0002g0185a0001c0001t0002g0186others(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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0001g0247a0001c0001t0002g0073 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | 99 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(96): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.14-125G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 2/23 | chr5 | 149183327 | ||||||
| chr5:149183418
|
C | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(81): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0042others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): 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 | 7 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(4): 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0132 | 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0003g0108 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0001g0031a0001c0001t0001g0243 | 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 | a0001c0001t0001g0142 | 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 | 4 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(1): Show | 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 | a0001c0001t0001g0031a0001c0001t0001g0097a0001c0001t0001g0099others(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 | a0001c0001t0001g0130a0001c0001t0002g0016a0001c0001t0002g0047others(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 | 144 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(141): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0009g0076others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0012g0111 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(99): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): 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 | a0001c0001t0002g0026 | 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 | a0001c0001t0004g0119 | 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 | a0002c0004t0004g0091 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 142 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(139): Show | 143 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.151+2452A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149186041 | ||||||
| chr5:149186052
|
A | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0155 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0001g0151a0001c0001t0002g0152a0001c0001t0002g0153others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): 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 | a0001c0006t0011g0072a0001c0006t0014g0214a0001c0006t0017g0071others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0003g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.151+3828A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187417 | ||||||
| chr5:149187532
|
A | G | 1 | a0001c0001t0002g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.151+3943A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149187532 | ||||||
| chr5:149187545
|
G | A | 1 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0179a0001c0001t0001g0190a0001c0001t0001g0191 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0009g0076 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0001g0042 | 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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0009g0076others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0009g0076 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0246 | 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 | a0001c0001t0001g0082a0001c0001t0001g0225a0001c0001t0002g0081 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0235a0001c0001t0002g0166a0001c0001t0002g0181others(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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0051others(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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0001g0169 | 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 | a0001c0006t0011g0072a0001c0006t0014g0214a0001c0006t0017g0071others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0184 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0250 | 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 | 92 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(89): Show | 93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0012g0111 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0010t0001g0218 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0009t0007g0038others(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 | a0001c0001t0005g0021a0001c0001t0005g0022 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0151others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0009g0076others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0174 | 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 | a0001c0001t0010g0134 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 91 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(88): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0121others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 144 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(141): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0002g0138 | 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 | a0001c0001t0002g0150 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | 96 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(93): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | 82 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): 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 | a0001c0001t0001g0228a0001c0001t0001g0237a0001c0003t0004g0249 | 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 | 144 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(141): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): 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 | a0002c0004t0004g0014 | 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 | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.152-4836T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193383 | ||||||
| chr5:149193440
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0003t0004g0123 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0012g0111 | 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 | 144 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(141): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.152-4340G>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 3/23 | chr5 | 149193879 | ||||||
| chr5:149194086
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0168a0001c0001t0001g0202 | 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 | a0001c0001t0004g0078 | 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0004g0119 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0004g0119a0001c0001t0005g0087a0001c0001t0012g0111 | 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 | 117 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0012g0111 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | 82 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | 144 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(141): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0012g0111 | 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0006t0011g0072a0001c0006t0014g0214a0001c0006t0017g0071others(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 | a0001c0001t0004g0078a0001c0001t0004g0092a0001c0001t0004g0093 | 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 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0082others(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 | a0001c0001t0002g0199a0001c0001t0006g0034a0001c0001t0006g0035others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0010t0001g0218 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0005g0022 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0056 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0002g0199 | 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 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0051others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0002g0025a0001c0001t0005g0087 | 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 | a0001c0003t0004g0249 | 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0009g0076 | 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 | a0001c0001t0002g0146a0003c0007t0001g0147a0003c0007t0001g0234 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0006t0017g0071a0001c0010t0001g0218 | 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 | a0001c0008t0001g0177 | 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 | a0001c0001t0012g0111 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0002g0067 | 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 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0004g0074others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0012g0111a0001c0006t0011g0072a0001c0006t0014g0214others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0037others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0002g0044 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0001t0010g0134 | 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 | a0001c0001t0010g0134 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0009t0007g0038others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0131others(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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0001t0002g0207a0001c0001t0012g0111 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0006t0011g0072 | 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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0001t0001g0002a0001c0001t0002g0002 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0112others(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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | a0001c0001t0001g0077a0001c0001t0001g0204 | 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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0001t0004g0119 | 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 | a0001c0008t0001g0032 | 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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): 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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | a0001c0001t0002g0052a0001c0001t0003g0003a0001c0001t0003g0232others(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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0006g0034 | 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 | 143 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(140): Show | 144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): 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 | a0001c0001t0004g0119 | 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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(97): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): 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 | a0001c0001t0002g0106 | 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 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0129others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0001g0133a0001c0001t0002g0016a0001c0001t0016g0015 | 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 | a0001c0001t0004g0069 | 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 | 81 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(78): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): 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 | 107 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(104): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0143others(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 | a0001c0001t0012g0111 | 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 | a0001c0001t0002g0170 | 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 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0143others(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 | 129 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(127): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(97): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0002g0160 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0098others(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 | a0001c0001t0004g0119 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0002g0186 | 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0005g0022 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0004g0119 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0209 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0107others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0002c0004t0004g0014a0002c0004t0004g0090a0002c0004t0004g0091others(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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0004g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.449-133A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | chr5 | 149206875 | ||||||
| chr5:149206888
|
A | AG | 256 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.449-118dupG | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr5 | 149206888 | |||||
| chr5:149207240
|
G | A | 2 | a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0209 | 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 | a0002c0004t0004g0014 | 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0001g0041a0001c0001t0002g0101a0001c0001t0002g0103others(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 | a0001c0008t0001g0032 | 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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0174 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | 104 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(101): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): 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 | a0001c0001t0001g0036a0001c0001t0002g0227 | 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 | 146 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(143): 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 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0209others(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 | a0001c0001t0002g0127a0001c0001t0002g0156a0001c0001t0002g0178 | 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 | 6 | a0001c0001t0002g0100a0001c0002t0005g0075a0001c0002t0005g0114others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(3): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0140others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0002g0052a0001c0001t0003g0246a0001c0001t0009g0076 | 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 | a0001c0001t0003g0232a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0001t0001g0143a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | 103 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(100): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0002g0145a0001c0001t0005g0021 | 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 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0143others(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 | 38 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0143others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(35): 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 | a0001c0001t0005g0070a0001c0001t0005g0254 | 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 | a0001c0001t0002g0240 | 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 | a0001c0001t0001g0024a0001c0001t0001g0143a0001c0001t0002g0145others(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 | a0001c0001t0001g0082a0001c0001t0001g0176a0001c0001t0001g0225others(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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0002g0138a0001c0001t0002g0170 | 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 | 133 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): 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 | a0001c0003t0004g0122a0001c0003t0004g0123 | 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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0001g0082a0001c0001t0001g0151a0001c0001t0001g0176others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0006t0014g0214 | 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 | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): 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 | a0001c0001t0003g0113 | 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0005g0110 | 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 | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.576-320A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 6/23 | chr5 | 149210406 | ||||||
| chr5:149210860
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.669+41T>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149210860 | ||||||
| chr5:149211057
|
T | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(110): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0045 | 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 | 37 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(34): 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 | 82 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0005g0087a0001c0001t0009g0076 | 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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0013a0001c0001t0010g0134 | 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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0024a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0143a0001c0001t0002g0025a0001c0001t0002g0145others(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 | a0001c0003t0004g0122a0001c0003t0004g0123a0002c0004t0004g0014others(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 | a0001c0001t0002g0010a0001c0001t0002g0166a0001c0001t0005g0110others(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 | a0001c0006t0011g0072 | 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 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0098 | 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 | a0001c0001t0001g0024a0001c0001t0004g0069a0001c0001t0004g0074others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0002g0010a0001c0001t0002g0166a0001c0001t0005g0110others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133a0001c0001t0001g0239 | 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 | a0001c0001t0001g0024a0001c0001t0004g0069a0001c0001t0004g0074others(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 | a0001c0001t0005g0021a0001c0001t0005g0022 | 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 | 112 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0045others(109): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): 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 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0151others(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 | 11 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(8): 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 | 89 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0054others(86): Show | 90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): 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 | 77 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0054others(74): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.670-3050G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149213909 | ||||||
| chr5:149213982
|
C | CCA | 152 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0036others(149): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): 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 | a0001c0006t0014g0214 | 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 | 37 | a0001c0001t0001g0019a0001c0001t0002g0025a0001c0001t0002g0166others(34): 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 | a0001c0001t0002g0030 | 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 | a0001c0001t0002g0166a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | 143 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(140): Show | 144 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(141): 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 | a0001c0001t0002g0233 | 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 | a0001c0001t0001g0188 | 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 | a0001c0003t0004g0249 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | 125 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(122): Show | 126 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.670-2045A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149214914 | ||||||
| chr5:149214985
|
T | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(1): Show | 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0004g0119others(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 | a0001c0001t0003g0210a0001c0001t0003g0255 | 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 | a0001c0001t0004g0078 | 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 | a0001c0003t0004g0122a0001c0003t0004g0123a0002c0004t0004g0014others(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 | a0001c0001t0002g0080a0001c0001t0002g0201 | 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 | 125 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(122): Show | 126 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(123): 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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | 239 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(236): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): 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 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0001t0006g0034others(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 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0001t0006g0034others(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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | 125 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(122): Show | 126 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(123): 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0001g0222 | 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 | a0001c0003t0004g0249 | 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 | 124 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(121): Show | 125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-481C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216478 | ||||||
| chr5:149216522
|
C | CT | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0003t0004g0122others(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 | 133 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(130): Show | 134 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(131): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | 124 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(121): Show | 125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-147G>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 7/23 | chr5 | 149216812 | ||||||
| chr5:149217130
|
TG | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0004g0069 | 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 | 124 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(121): Show | 125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): 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 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0079others(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 | a0001c0001t0012g0111a0001c0006t0011g0072 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0003g0210 | 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 | a0001c0001t0001g0144a0001c0001t0001g0236 | 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 | 124 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(121): Show | 125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0201 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(139): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0025a0001c0001t0002g0166a0001c0001t0003g0017others(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 | a0001c0001t0001g0228 | 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 | 107 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(104): Show | 108 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(105): 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 | a0001c0001t0002g0140 | 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 | a0004c0011t0001g0135 | 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 | a0001c0001t0006g0128 | 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0012g0111a0001c0006t0011g0072 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0010t0001g0218 | 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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(139): 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0009g0076others(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 | a0001c0001t0003g0232 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(139): 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0006t0014g0214 | 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 | a0001c0001t0001g0008 | 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 | a0001c0008t0001g0032a0001c0008t0001g0177 | 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 | a0001c0001t0003g0210a0001c0001t0003g0255 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0002g0016a0001c0001t0016g0015 | 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 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0096 | 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 | 107 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(104): Show | 108 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(105): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0001g0173a0001c0001t0001g0212a0001c0001t0018g0238 | 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 | a0001c0001t0002g0166a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0002g0199 | 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 | a0001c0006t0011g0072 | 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 | 77 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(74): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): 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 | a0001c0001t0002g0056 | 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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(139): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0002g0084 | 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 | 140 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(137): Show | 141 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.757+5139T>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149222185 | ||||||
| chr5:149222211
|
C | T | 16 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(13): 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0004g0119others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0004g0119others(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 | a0001c0001t0001g0028a0001c0001t0001g0143a0001c0001t0001g0161others(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 | a0001c0001t0001g0057a0001c0001t0001g0126a0001c0001t0001g0148others(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 | 92 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(89): Show | 93 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(90): 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0004g0119others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0001g0107 | 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 | a0001c0003t0004g0122a0001c0003t0004g0123a0002c0004t0004g0014others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213 | 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 | a0001c0001t0002g0044 | 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0004g0069others(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 | a0001c0001t0004g0074a0001c0001t0006g0034a0001c0001t0006g0035others(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 | a0001c0001t0002g0156 | 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 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0058others(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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0003t0004g0249 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0010t0001g0218 | 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 | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): 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 | a0001c0003t0004g0249 | 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 | 138 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(135): Show | 139 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(136): 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 | a0001c0003t0004g0122a0001c0003t0004g0123a0002c0004t0004g0014others(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 |
74 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(71): Show | 75 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(72): 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | 95 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(92): Show | 96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.758-5322G>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 8/23 | chr5 | 149225327 | ||||||
| chr5:149225341
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): 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 | a0001c0001t0002g0227 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0001c0001t0003g0088a0001c0001t0003g0108a0001c0001t0003g0113others(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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(109): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): 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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0005g0070a0001c0001t0005g0229a0001c0001t0005g0254others(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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0005g0021others(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 | a0001c0001t0004g0069a0001c0001t0004g0119a0001c0001t0005g0110others(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 | a0001c0001t0004g0069a0001c0001t0004g0119a0001c0001t0005g0110 | 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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0001c0001t0005g0110a0001c0003t0004g0018a0001c0006t0014g0214 | 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 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0053others(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 | a0001c0001t0004g0078a0001c0001t0004g0092a0001c0001t0006g0035 | 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 | a0001c0001t0006g0094 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0009g0076 | 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 | a0002c0005t0013g0020 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0001c0001t0006g0244 | 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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0006g0034 | 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 | a0001c0001t0001g0019 | 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 | 4 | a0001c0001t0002g0100a0001c0001t0002g0158a0001c0001t0002g0174others(1): Show | 4 | HG01515.hp2 HG03688.hp1 NA18747.hp1 others(1): Show |
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 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0030others(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 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(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 | a0001c0001t0002g0025a0001c0001t0002g0201a0001c0001t0003g0017others(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 | a0001c0001t0004g0069a0001c0001t0004g0119 | 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 | a0001c0001t0003g0003 | 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 | a0001c0001t0003g0113a0001c0001t0003g0120a0001c0006t0011g0072 | 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 | a0001c0001t0003g0004a0001c0001t0003g0109a0001c0001t0003g0213 | 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 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(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 | a0001c0001t0003g0088 | 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 | a0001c0001t0002g0044 | 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0006g0035 | 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 | a0001c0003t0004g0249 | 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 | a0001c0001t0004g0069a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0010t0001g0218 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0004g0078a0001c0001t0004g0092a0001c0001t0004g0093others(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 | a0001c0001t0001g0082a0001c0001t0001g0133a0001c0001t0001g0168others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0161others(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 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0142others(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 | a0001c0001t0001g0033a0001c0001t0001g0202a0001c0001t0001g0219others(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 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0036others(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 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0151others(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 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0042others(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 | a0001c0001t0001g0060a0001c0001t0001g0143a0001c0001t0002g0242 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0086a0001c0001t0001g0163 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0097others(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 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0002g0056others(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 | a0001c0001t0001g0013a0001c0001t0001g0252 | 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 | a0001c0001t0001g0247a0001c0001t0005g0110 | 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 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0112others(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 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0250 | 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 | a0001c0006t0017g0071 | 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 | a0001c0001t0002g0242a0001c0003t0004g0018a0001c0006t0014g0214 | 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 | a0001c0001t0004g0069a0001c0001t0004g0119a0001c0003t0004g0018others(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 | a0001c0001t0001g0126a0001c0001t0004g0069a0001c0001t0004g0119others(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 | a0001c0001t0004g0069a0001c0001t0004g0119a0001c0001t0005g0110others(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 | a0001c0001t0001g0086a0001c0001t0004g0069a0001c0001t0004g0119others(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 | a0001c0001t0005g0110 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0002g0166a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0004g0069a0001c0001t0004g0074a0001c0001t0004g0089others(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 | a0002c0004t0004g0014 | 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 | 95 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(92): Show | 96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): 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 | a0001c0001t0004g0074a0001c0001t0004g0089 | 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 | a0001c0001t0002g0030a0001c0001t0002g0065a0001c0001t0002g0067others(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 | a0001c0001t0002g0181 | 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 | a0001c0001t0003g0088a0001c0001t0003g0108a0001c0001t0003g0109others(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 | 16 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(13): 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 | a0001c0001t0001g0049a0001c0001t0001g0142a0001c0001t0001g0143others(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 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(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 | a0001c0001t0002g0080a0001c0001t0002g0166a0001c0001t0002g0170others(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 | 90 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(87): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): 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 | a0001c0001t0004g0069a0001c0001t0005g0021a0001c0001t0005g0022others(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 | 138 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(135): Show | 139 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(136): 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 | a0001c0001t0004g0069a0001c0001t0004g0182a0001c0001t0004g0183others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0002g0230 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0001t0006g0034others(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 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0027others(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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0069a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0002g0150 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0003t0004g0018a0001c0006t0014g0214 | 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0001g0061a0001c0001t0004g0069a0001c0001t0005g0021others(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 | 122 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(119): Show | 123 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(120): 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 | a0001c0001t0004g0069 | 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 | a0001c0003t0004g0122a0001c0003t0004g0123a0002c0004t0004g0014others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0012g0111a0001c0006t0011g0072 | 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 | a0001c0001t0004g0069a0001c0001t0004g0182a0001c0001t0004g0183others(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 | a0001c0001t0012g0111a0001c0006t0011g0072 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022 | 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 | a0002c0005t0008g0117 | 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 | a0001c0001t0004g0069a0001c0001t0005g0021a0001c0001t0005g0022others(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 | 138 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(135): Show | 139 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(136): 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 | a0001c0001t0004g0069a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0004g0069a0001c0001t0004g0182a0001c0001t0004g0183others(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 | a0001c0001t0001g0253 | 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 | a0001c0001t0004g0069a0001c0001t0005g0021a0001c0001t0005g0022others(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 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0001t0006g0034others(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 | 104 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): 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 | a0001c0001t0012g0111 | 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 | a0001c0001t0001g0046a0001c0001t0001g0236 | 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 | a0001c0001t0002g0175 | 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0001c0001t0001g0097a0001c0001t0001g0099 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0024a0001c0006t0017g0071 | 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 | 97 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(94): Show | 98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): 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 | a0001c0001t0001g0173a0001c0001t0001g0212a0001c0001t0018g0238 | 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 | a0001c0001t0001g0208 | 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 | 105 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(102): Show | 106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.817-1169C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 9/23 | chr5 | 149232060 | ||||||
| chr5:149232112
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(104): Show | 108 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(105): 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 | a0001c0001t0005g0087 | 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 | 104 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): 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 | a0001c0001t0012g0111 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0010t0001g0218 | 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 | 105 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(102): Show | 106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): 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 | a0001c0001t0012g0111a0001c0006t0011g0072 | 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 | a0001c0001t0001g0019a0001c0001t0002g0084a0001c0001t0002g0154others(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 | 99 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(96): Show | 100 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(97): 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 | a0001c0001t0001g0019a0001c0001t0002g0084a0001c0001t0002g0154others(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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0004g0069 | 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 | 105 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(102): Show | 106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0003g0246 | 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 | a0001c0001t0004g0119 | 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 | a0002c0005t0013g0020 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0002g0150 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0006g0035 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087 | 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 | 74 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(71): Show | 75 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.889-1742C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149235706 | ||||||
| chr5:149235883
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | 130 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(127): Show | 131 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(128): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | 74 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(71): Show | 75 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.889-1065C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 10/23 | chr5 | 149236383 | ||||||
| chr5:149236424
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(94): Show | 98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0127 | 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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(137): 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0010t0001g0218 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0001g0141a0001c0001t0002g0139a0001c0001t0002g0175 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0002g0166 | 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 | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0002g0055a0001c0001t0002g0167a0001c0001t0002g0187others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1045-387C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149238861 | ||||||
| chr5:149238903
|
CA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0003g0088a0001c0001t0003g0108a0001c0001t0003g0109others(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 | 106 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(103): Show | 107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1045-103A>G | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239145 | ||||||
| chr5:149239186
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1045-62C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 11/23 | chr5 | 149239186 | ||||||
| chr5:149239189
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0001t0001g0019a0001c0001t0004g0078a0001c0001t0004g0092others(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 | 98 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0001t0009g0076others(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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0004g0069 | 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 | a0001c0006t0011g0072 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087others(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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0002g0159 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0003g0003a0001c0001t0003g0213a0001c0001t0005g0087 | 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 | a0001c0001t0002g0136 | 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 | 96 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0054others(93): Show | 97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0003g0246 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0002g0125a0001c0001t0002g0185a0001c0001t0002g0186 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0019a0001c0001t0003g0003a0001c0001t0003g0213others(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 | a0001c0001t0004g0069 | 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 | 118 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0045others(115): Show | 119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): 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 | a0001c0001t0002g0175 | 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 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0082others(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 | a0001c0001t0001g0019a0001c0001t0004g0074a0001c0001t0004g0078others(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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0050others(110): Show | 114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): 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 | a0001c0001t0001g0219 | 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 | 19 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(16): 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 | 106 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(103): Show | 107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): 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 | a0001c0001t0005g0021 | 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 | 106 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(103): Show | 107 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(104): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0001g0046 | 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 | 128 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(125): Show | 129 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(126): 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 | a0001c0001t0002g0025a0001c0001t0003g0017 | 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 | a0001c0001t0002g0101 | 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 | 121 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(118): Show | 122 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(119): 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 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 | a0001c0001t0003g0251 | 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 | a0001c0001t0002g0016 | 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 | 21 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(18): 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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(97): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0004g0069 | 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 | a0001c0010t0001g0218 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0172a0001c0001t0001g0245 | 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 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0051others(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 | a0001c0001t0002g0240 | 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 | a0001c0001t0001g0045 | 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 | 21 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(18): 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 | a0001c0006t0011g0072 | 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 | 21 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(18): 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 | 21 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(18): 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 | a0001c0001t0009g0076 | 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 | a0002c0004t0004g0014 | 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 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0033others(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 | 121 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(118): Show | 122 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(119): 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0002g0132 | 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 | 21 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(18): 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 | 19 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(16): 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 | a0001c0001t0002g0181 | 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 | a0001c0001t0001g0235 | 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 | 34 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0003g0003others(31): 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0006t0014g0214 | 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 | a0001c0002t0005g0217 | 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 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0004g0069others(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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(97): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): 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 | a0004c0011t0001g0135 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0005g0022 | 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 | 141 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0054others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(139): 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 | a0001c0001t0004g0182 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1699+11C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149247940 | ||||||
| chr5:149248034
|
C | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(91): Show | 95 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1699+105C>A | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 18/23 | chr5 | 149248034 | ||||||
| chr5:149248160
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(79): Show | 83 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(80): 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 | a0002c0005t0008g0117 | 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 | a0001c0001t0002g0025a0001c0001t0003g0017a0001c0009t0007g0038others(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 | a0001c0001t0004g0069 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0004g0074others(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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0228others(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 | 96 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(93): Show | 97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): 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 | a0001c0001t0003g0017a0001c0001t0004g0069a0001c0001t0005g0022others(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 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0058others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0033others(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 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0107others(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 | a0001c0001t0002g0025a0001c0001t0003g0017a0001c0001t0003g0109others(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 | a0001c0001t0001g0061a0001c0001t0001g0144a0001c0001t0003g0213others(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 | a0001c0001t0001g0029a0001c0001t0001g0235a0001c0001t0003g0003others(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 |
6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0007others(3): 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 | a0001c0001t0003g0120 | 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 | a0002c0005t0013g0020 | 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 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0049others(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 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0004g0074others(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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0002g0001others(73): Show | 77 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(74): 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 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0004g0074others(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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0019a0001c0001t0002g0073a0001c0001t0004g0074others(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 | a0001c0010t0001g0218 | 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 | 120 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0054others(117): Show | 121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): 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 | a0001c0001t0009g0076 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0037a0001c0001t0001g0222 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0003g0109a0001c0001t0003g0115a0001c0001t0003g0120 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022 | 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 | a0001c0001t0002g0055a0001c0001t0002g0167a0001c0001t0002g0187others(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 | a0001c0001t0003g0017a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | a0001c0001t0010g0134 | 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 | a0001c0001t0009g0076a0001c0006t0011g0072 | 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 | a0001c0001t0004g0119 | 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 | 119 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0054others(116): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): 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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | a0002c0005t0008g0117 | 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 | a0001c0001t0003g0232a0001c0001t0003g0246a0002c0005t0013g0020 | 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 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0070others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0098others(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 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0023others(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 | a0001c0006t0011g0072 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0003g0088a0001c0001t0003g0113 | 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 | 121 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0054others(118): Show | 122 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(119): 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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0009a0001c0001t0001g0231a0006c0013t0001g0248 | 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 | a0001c0001t0005g0087 | 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 | a0001c0001t0004g0074a0001c0001t0004g0089a0001c0006t0014g0214 | 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 | a0001c0001t0001g0008a0001c0001t0001g0256 | 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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | a0001c0001t0001g0208 | 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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0009t0007g0038a0001c0009t0007g0118 | 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 | a0001c0001t0002g0105 | 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 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0039others(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 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0058others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | 115 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0002others(112): Show | 116 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(113): 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 | a0001c0001t0003g0246 | 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 | 248 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1938+1344A>C | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149254181 | ||||||
| chr5:149254215
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0002others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): 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 | a0001c0002t0005g0075a0001c0002t0005g0114a0001c0002t0005g0215others(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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0006g0034a0001c0001t0006g0035a0001c0001t0006g0040others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0002g0136 | 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 | 104 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0002others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): 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 | a0001c0001t0004g0183 | 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 | a0001c0001t0002g0146 | 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 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0004g0089others(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 | a0001c0001t0006g0035 | 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 | a0002c0005t0008g0116a0002c0005t0008g0117 | 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 | a0001c0001t0001g0219 | 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 | 56 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(53): 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 | 77 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0002g0001others(74): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): 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 | a0001c0001t0002g0073a0001c0001t0002g0106 | 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 | a0001c0001t0005g0022 | 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 | a0001c0003t0004g0018a0001c0003t0004g0122a0001c0003t0004g0123others(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 | a0001c0006t0011g0072 | 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 | a0001c0006t0017g0071 | 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 | 79 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0002others(76): Show | 80 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(77): 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 | a0001c0001t0004g0182a0001c0001t0004g0183 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1939-21C>T | ABLIM3 | ENSG00000173210.21 | transcript | ENST00000309868.12 | protein_coding | 23/23 | chr5 | 149258270 |