Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84253 |
|---|---|
| ensemblid | ENSG00000136895.19 |
| hgncid | 25425 |
| symbol | GARNL3 |
| name | GTPase activating Rap/RanGAP domain like 3 |
| refseq_nuc | NM_032293.5 |
| refseq_prot | NP_115669.3 |
| ensembl_nuc | ENST00000373387.9 |
| ensembl_prot | ENSP00000362485.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 127264774 |
| end | 127393660 |
| strand | + |
| ver | v1.2 |
| region | chr9:127264774-127393660 |
| region5000 | chr9:127259774-127398660 |
| regionname0 | GARNL3_chr9_127264774_127393660 |
| regionname5000 | GARNL3_chr9_127259774_127398660 |
| 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 | 1013 | 294 | 74 | 47 | 130 | 16 | 25 | 97 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0002 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0003 | 0/0 | 1013 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0004 | 0/0 | 1013 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0005 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0006 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0007 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| 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 | 3042 | 273 | 56 | 45 | 129 | 16 | 25 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0002 | 0/0 | 3042 | 19 | 18 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0003 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0004 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0005 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0006 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0007 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0008 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0009 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| c0010 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| 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 | 1/1 | 511 | 298 | 75 | 48 | 132 | 15 | 26 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| t0002 | 0/0 | 511 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| t0003 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| 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 | 2 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| 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 | 3042 | 273 | 56 | 45 | 129 | 16 | 25 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0002 | 0/0 | 3042 | 19 | 18 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0006 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0009 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0002c0010 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0003c0003 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0004c0007 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0005c0008 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0006c0005 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0007c0004 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3552 | 271 | 55 | 45 | 129 | 15 | 25 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0001t0002 | 0/0 | 3552 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0001t0003 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0002t0001 | 0/0 | 3552 | 19 | 18 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0006t0001 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0001c0009t0001 | 0/0 | 3552 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0002c0010t0001 | 0/0 | 3552 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0003c0003t0001 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0004c0007t0001 | 0/0 | 3552 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0005c0008t0001 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0006c0005t0001 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| a0007c0004t0001 | 0/0 | 3552 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | copy fasta | chr9 | 127259774 | 127398660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0001c0009t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0002c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0004c0007t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0005c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0006c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| a0007c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | FIN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01074 | hp2 | a0007 | c0004 | t0001 | g0157 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01109 | hp1 | a0001 | c0009 | t0001 | g0040 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02027 | hp1 | a0001 | c0006 | t0001 | g0265 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02071 | hp2 | a0006 | c0005 | t0001 | g0229 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02145 | hp1 | a0004 | c0007 | t0001 | g0127 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03669 | hp2 | a0002 | c0010 | t0001 | g0065 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19004 | hp1 | a0005 | c0008 | t0001 | g0198 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | TSI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0204 | REF | REF | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0083 | REF | REF | GARNL3_chr9_127259774_127398660 | GARNL3 | chr9 | 127259774 | 127398660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127336221
|
C | T | 1 | a0002 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.967C>T | p.Arg323Cys | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/28 | 1071/3552 | 967/3042 | 323/1013 | chr9 | 127336221 | ||
| chr9:127339670
|
G | A | 1 | a0003 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1054G>A | p.Val352Ile | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/28 | 1158/3552 | 1054/3042 | 352/1013 | chr9 | 127339670 | ||
| chr9:127342326
|
T | A | 1 | a0007 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1243T>A | p.Leu415Met | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/28 | 1347/3552 | 1243/3042 | 415/1013 | chr9 | 127342326 | ||
| chr9:127344308
|
C | A | 1 | a0006 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.1325C>A | p.Ala442Asp | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/28 | 1429/3552 | 1325/3042 | 442/1013 | chr9 | 127344308 | ||
| chr9:127345461
|
G | A | 1 | a0004 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1415G>A | p.Gly472Glu | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/28 | 1519/3552 | 1415/3042 | 472/1013 | chr9 | 127345461 | ||
| chr9:127393195
|
G | C | 1 | a0005 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.2983G>C | p.Gly995Arg | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 28/28 | 3087/3552 | 2983/3042 | 995/1013 | chr9 | 127393195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127336130
|
G | A | 1 | a0001c0002 | 19 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
splice_region_variant&synonymous_variant | LOW | c.876G>A | p.Val292Val | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/28 | 980/3552 | 876/3042 | 292/1013 | chr9 | 127336130 | ||
| chr9:127344318
|
G | A | 1 | a0001c0006 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1335G>A | p.Ala445Ala | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/28 | 1439/3552 | 1335/3042 | 445/1013 | chr9 | 127344318 | ||
| chr9:127387322
|
C | T | 1 | a0001c0009 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.2518C>T | p.Leu840Leu | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/28 | 2622/3552 | 2518/3042 | 840/1013 | chr9 | 127387322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127264784
|
A | G | 1 | a0001c0001t0003 | 1 | HG02895.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/28 | 94 | chr9 | 127264784 | |||||
| chr9:127393366
|
A | G | 1 | a0001c0001t0002 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 28/28 | 112 | chr9 | 127393366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127265346
|
TA | T | 5 | a0001c0001t0001g0292a0001c0001t0001g0295a0001c0001t0001g0296others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+329delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127265346 | |||||
| chr9:127265817
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+796C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127265817 | ||||||
| chr9:127265873
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.144+852G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127265873 | ||||||
| chr9:127266128
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.144+1107C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266128 | ||||||
| chr9:127266167
|
G | A | 1 | a0007c0004t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.144+1146G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266167 | ||||||
| chr9:127266256
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144+1235G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266256 | ||||||
| chr9:127266502
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+1481G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266502 | ||||||
| chr9:127266578
|
A | C | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+1557A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266578 | ||||||
| chr9:127266834
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.144+1813T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127266834 | ||||||
| chr9:127267155
|
A | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+2134A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267155 | ||||||
| chr9:127267233
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+2212G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267233 | ||||||
| chr9:127267411
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.144+2390C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267411 | ||||||
| chr9:127267412
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144+2391G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267412 | ||||||
| chr9:127267623
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.144+2602G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267623 | ||||||
| chr9:127267721
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.144+2700T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267721 | ||||||
| chr9:127267939
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.144+2918G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267939 | ||||||
| chr9:127267948
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.144+2927T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127267948 | ||||||
| chr9:127268319
|
A | G | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+3298A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268319 | ||||||
| chr9:127268358
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.144+3337C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268358 | ||||||
| chr9:127268384
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.144+3363G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268384 | ||||||
| chr9:127268509
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144+3488T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268509 | ||||||
| chr9:127268657
|
C | T | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+3636C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268657 | ||||||
| chr9:127268710
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.144+3689T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127268710 | ||||||
| chr9:127269009
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.144+3988C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127269009 | ||||||
| chr9:127269570
|
A | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.144+4549A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127269570 | ||||||
| chr9:127269733
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.144+4712T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127269733 | ||||||
| chr9:127269772
|
GTTTTGTT | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00558.hp1 HG02027.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+4758_144+4764d others(9): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269772 | |||||
| chr9:127269786
|
G | GT | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.144+4780dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269786 | |||||
| chr9:127269786
|
G | GTT | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.144+4779_144+4780d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269786 | |||||
| chr9:127269786
|
G | GTTTTTTG others(4): Show |
1 | a0004c0007t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.144+4771_144+4772i others(13): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269786 | |||||
| chr9:127269786
|
G | GTTTTTTG others(3): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+4771_144+4772i others(12): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269786 | |||||
| chr9:127269786
|
G | GTTTTTTG others(4): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00735.hp2 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+4771_144+4772i others(13): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269786 | |||||
| chr9:127269787
|
T | TTTTTTGT others(1): Show |
22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+4771_144+4772i others(10): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127269787 | |||||
| chr9:127269815
|
A | C | 7 | a0001c0001t0001g0118a0001c0002t0001g0002a0001c0002t0001g0119others(4): Show | 8 | HG02809.hp2 HG03130.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+4794A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127269815 | ||||||
| chr9:127269876
|
C | G | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+4855C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127269876 | ||||||
| chr9:127270128
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.144+5107C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270128 | ||||||
| chr9:127270301
|
AATG | A | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+5284_144+5286d others(5): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127270301 | |||||
| chr9:127270321
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00735.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.144+5300T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270321 | ||||||
| chr9:127270402
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+5381C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270402 | ||||||
| chr9:127270425
|
C | T | 1 | a0001c0002t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.144+5404C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270425 | ||||||
| chr9:127270481
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.144+5460G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270481 | ||||||
| chr9:127270615
|
G | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+5594G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270615 | ||||||
| chr9:127270665
|
G | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 83 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.144+5644G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270665 | ||||||
| chr9:127270678
|
C | T | 20 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG01069.hp2 HG01496.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.144+5657C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270678 | ||||||
| chr9:127270694
|
C | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00438.hp1 HG02074.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+5673C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270694 | ||||||
| chr9:127270712
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.144+5691A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127270712 | ||||||
| chr9:127270879
|
TTGGCCAC others(1650): Show |
T | 18 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(15): Show | 19 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+5863_144+7519d others(2): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127270879 | |||||
| chr9:127271162
|
C | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0046others(19): Show | 22 | HG01069.hp2 HG01496.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.144+6141C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271162 | ||||||
| chr9:127271203
|
G | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 64 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.144+6182G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271203 | ||||||
| chr9:127271268
|
A | G | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0289others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+6247A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271268 | ||||||
| chr9:127271366
|
G | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+6345G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271366 | ||||||
| chr9:127271500
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.144+6479A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271500 | ||||||
| chr9:127271802
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.144+6781G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271802 | ||||||
| chr9:127271818
|
C | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00558.hp1 HG02027.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+6797C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271818 | ||||||
| chr9:127271936
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.144+6915A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271936 | ||||||
| chr9:127271996
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.144+6975A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127271996 | ||||||
| chr9:127272180
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.144+7159G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272180 | ||||||
| chr9:127272499
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0158others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.144+7478T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272499 | ||||||
| chr9:127272500
|
T | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0158others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.144+7479T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272500 | ||||||
| chr9:127272501
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0158others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.144+7480T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272501 | ||||||
| chr9:127272543
|
G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02155.hp1 NA18970.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+7522G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272543 | ||||||
| chr9:127272575
|
G | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.144+7554G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272575 | ||||||
| chr9:127272583
|
G | A | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+7562G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272583 | ||||||
| chr9:127272608
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.144+7587T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272608 | ||||||
| chr9:127272684
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0002t0001g0037others(2): Show | 5 | HG01099.hp2 HG01109.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+7663G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272684 | ||||||
| chr9:127272768
|
A | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.144+7747A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272768 | ||||||
| chr9:127272875
|
G | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+7854G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127272875 | ||||||
| chr9:127273131
|
C | T | 7 | a0001c0001t0001g0118a0001c0002t0001g0002a0001c0002t0001g0119others(4): Show | 8 | HG02809.hp2 HG03130.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+8110C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273131 | ||||||
| chr9:127273302
|
G | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | NA18942.hp1 NA18980.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+8281G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273302 | ||||||
| chr9:127273373
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.144+8352C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273373 | ||||||
| chr9:127273518
|
A | T | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+8497A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273518 | ||||||
| chr9:127273642
|
TG | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01516.hp2 HG02004.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+8623delG | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127273642 | |||||
| chr9:127273771
|
C | G | 1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.144+8750C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273771 | ||||||
| chr9:127273826
|
G | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 28 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.144+8805G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273826 | ||||||
| chr9:127273883
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0159a0001c0001t0001g0164others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.144+8862C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273883 | ||||||
| chr9:127273990
|
T | C | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+8969T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127273990 | ||||||
| chr9:127274043
|
G | T | 1 | a0001c0001t0001g0282 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.144+9022G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274043 | ||||||
| chr9:127274090
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+9069A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274090 | ||||||
| chr9:127274284
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.144+9263A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274284 | ||||||
| chr9:127274290
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.144+9269G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274290 | ||||||
| chr9:127274447
|
G | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 14 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.144+9426G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274447 | ||||||
| chr9:127274603
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+9582C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274603 | ||||||
| chr9:127274846
|
C | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+9825C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274846 | ||||||
| chr9:127274909
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.144+9888A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127274909 | ||||||
| chr9:127275126
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+10105A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275126 | ||||||
| chr9:127275169
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+10148T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275169 | ||||||
| chr9:127275195
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.144+10174C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275195 | ||||||
| chr9:127275297
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.144+10276T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275297 | ||||||
| chr9:127275457
|
T | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.144+10436T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275457 | ||||||
| chr9:127275542
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.144+10521G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275542 | ||||||
| chr9:127275662
|
C | CA | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+10648dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127275662 | |||||
| chr9:127275795
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+10774T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275795 | ||||||
| chr9:127275819
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.144+10798A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275819 | ||||||
| chr9:127275834
|
G | A | 18 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(15): Show | 19 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+10813G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275834 | ||||||
| chr9:127275915
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144+10894C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127275915 | ||||||
| chr9:127276130
|
C | CT | 50 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.144+11122dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127276130 | |||||
| chr9:127276130
|
CT | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.144+11122delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127276130 | |||||
| chr9:127276292
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02257.hp2 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144+11271A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127276292 | ||||||
| chr9:127276326
|
G | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+11305G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127276326 | ||||||
| chr9:127276379
|
C | CA | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.144+11359dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127276379 | |||||
| chr9:127276380
|
A | AT | 22 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 22 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.144+11372dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127276380 | |||||
| chr9:127276568
|
G | C | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+11547G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127276568 | ||||||
| chr9:127277049
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+12028A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277049 | ||||||
| chr9:127277127
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0173others(10): Show | 14 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.144+12106T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277127 | ||||||
| chr9:127277254
|
A | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.144+12233A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277254 | ||||||
| chr9:127277518
|
C | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.144+12497C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277518 | ||||||
| chr9:127277601
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+12580C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277601 | ||||||
| chr9:127277949
|
G | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.144+12928G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127277949 | ||||||
| chr9:127278227
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.145-12941A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127278227 | ||||||
| chr9:127278653
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.145-12515T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127278653 | ||||||
| chr9:127278772
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG01069.hp2 HG01496.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.145-12396C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127278772 | ||||||
| chr9:127278885
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.145-12283A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127278885 | ||||||
| chr9:127279150
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.145-12018A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127279150 | ||||||
| chr9:127279483
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-11685A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127279483 | ||||||
| chr9:127279510
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.145-11658C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127279510 | ||||||
| chr9:127279568
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00735.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.145-11600T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127279568 | ||||||
| chr9:127279995
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18955.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.145-11173T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127279995 | ||||||
| chr9:127280090
|
G | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0289others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-11078G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280090 | ||||||
| chr9:127280149
|
G | A | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-11019G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280149 | ||||||
| chr9:127280260
|
C | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.145-10908C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280260 | ||||||
| chr9:127280338
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.145-10830C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280338 | ||||||
| chr9:127280373
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.145-10795C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280373 | ||||||
| chr9:127280400
|
T | C | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-10768T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280400 | ||||||
| chr9:127280804
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145-10364C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127280804 | ||||||
| chr9:127281113
|
G | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.145-10055G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281113 | ||||||
| chr9:127281157
|
C | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-10011C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281157 | ||||||
| chr9:127281224
|
A | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.145-9944A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281224 | ||||||
| chr9:127281297
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.145-9871A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281297 | ||||||
| chr9:127281596
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02071.hp1 NA18982.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-9572G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281596 | ||||||
| chr9:127281722
|
T | G | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-9446T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281722 | ||||||
| chr9:127281960
|
A | G | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-9208A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127281960 | ||||||
| chr9:127282018
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.145-9150C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127282018 | ||||||
| chr9:127282141
|
A | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-9027A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127282141 | ||||||
| chr9:127282257
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-8911C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127282257 | ||||||
| chr9:127282733
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG03098.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.145-8435G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127282733 | ||||||
| chr9:127283272
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.145-7896G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283272 | ||||||
| chr9:127283530
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0004c0007t0001g0127 | 3 | HG02145.hp1 HG02717.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.145-7638C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283530 | ||||||
| chr9:127283544
|
C | G | 1 | a0001c0001t0001g0278 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.145-7624C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283544 | ||||||
| chr9:127283581
|
G | T | 11 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(8): Show | 11 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-7587G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283581 | ||||||
| chr9:127283772
|
T | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02486.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.145-7396T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283772 | ||||||
| chr9:127283773
|
C | T | 2 | a0001c0001t0001g0032a0001c0002t0001g0031 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.145-7395C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283773 | ||||||
| chr9:127283783
|
T | C | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-7385T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127283783 | ||||||
| chr9:127284029
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.145-7139A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284029 | ||||||
| chr9:127284100
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0159a0001c0001t0001g0164others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.145-7068C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284100 | ||||||
| chr9:127284173
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.145-6995G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284173 | ||||||
| chr9:127284361
|
T | A | 21 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.145-6807T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284361 | ||||||
| chr9:127284437
|
T | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.145-6731T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284437 | ||||||
| chr9:127284731
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.145-6437T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284731 | ||||||
| chr9:127284877
|
G | C | 2 | a0001c0001t0001g0128a0004c0007t0001g0127 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.145-6291G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127284877 | ||||||
| chr9:127285222
|
G | A | 6 | a0001c0001t0001g0165a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 6 | HG02074.hp1 NA18943.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-5946G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285222 | ||||||
| chr9:127285314
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.145-5854G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285314 | ||||||
| chr9:127285400
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.145-5768G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285400 | ||||||
| chr9:127285437
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-5731A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285437 | ||||||
| chr9:127285461
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.145-5707A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285461 | ||||||
| chr9:127285554
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.145-5614G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285554 | ||||||
| chr9:127285631
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.145-5537T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127285631 | ||||||
| chr9:127286017
|
CT | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-5148delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127286017 | |||||
| chr9:127286144
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.145-5024G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286144 | ||||||
| chr9:127286205
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.145-4963G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286205 | ||||||
| chr9:127286343
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.145-4825T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286343 | ||||||
| chr9:127286531
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.145-4637G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286531 | ||||||
| chr9:127286598
|
C | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.145-4570C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286598 | ||||||
| chr9:127286600
|
T | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.145-4568T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286600 | ||||||
| chr9:127286829
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-4339T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286829 | ||||||
| chr9:127286855
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-4313G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286855 | ||||||
| chr9:127286949
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.145-4219A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127286949 | ||||||
| chr9:127287467
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.145-3701T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127287467 | ||||||
| chr9:127287538
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.145-3630C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127287538 | ||||||
| chr9:127287846
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.145-3322G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127287846 | ||||||
| chr9:127287847
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0002g0224 | 2 | HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.145-3321A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127287847 | ||||||
| chr9:127288087
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.145-3081C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288087 | ||||||
| chr9:127288121
|
T | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-3047T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288121 | ||||||
| chr9:127288192
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.145-2976G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288192 | ||||||
| chr9:127288439
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00438.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.145-2729G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288439 | ||||||
| chr9:127288565
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.145-2603C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288565 | ||||||
| chr9:127288612
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-2556A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288612 | ||||||
| chr9:127288749
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.145-2419G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288749 | ||||||
| chr9:127288916
|
T | C | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-2252T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127288916 | ||||||
| chr9:127289027
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.145-2141C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127289027 | ||||||
| chr9:127289118
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.145-2050T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127289118 | ||||||
| chr9:127289161
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-2007G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127289161 | ||||||
| chr9:127289366
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.145-1802G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127289366 | ||||||
| chr9:127289729
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.145-1439A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127289729 | ||||||
| chr9:127290120
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.145-1048T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290120 | ||||||
| chr9:127290123
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.145-1045T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290123 | ||||||
| chr9:127290177
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.145-991G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290177 | ||||||
| chr9:127290283
|
AT | A | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-879delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127290283 | |||||
| chr9:127290300
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.145-868T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290300 | ||||||
| chr9:127290304
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.145-864A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290304 | ||||||
| chr9:127290310
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.145-858G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290310 | ||||||
| chr9:127290335
|
G | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.145-833G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290335 | ||||||
| chr9:127290414
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.145-754C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290414 | ||||||
| chr9:127290500
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0080 | 2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.145-668C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290500 | ||||||
| chr9:127290504
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0080 | 2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.145-664C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290504 | ||||||
| chr9:127290820
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-348T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290820 | ||||||
| chr9:127290826
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0039others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.145-342T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127290826 | ||||||
| chr9:127290944
|
GT | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.145-219delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 127290944 | |||||
| chr9:127291128
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0281 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.145-40A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 1/27 | chr9 | 127291128 | ||||||
| chr9:127291726
|
CT | C | 85 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.219+508delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127291726 | |||||
| chr9:127291726
|
CTT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.219+507_219+508del others(2): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127291726 | |||||
| chr9:127291772
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+530C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127291772 | ||||||
| chr9:127291873
|
G | A | 16 | a0001c0001t0001g0095a0001c0001t0001g0167a0001c0001t0001g0168others(13): Show | 16 | HG00558.hp2 HG02132.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.219+631G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127291873 | ||||||
| chr9:127292040
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.219+798C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292040 | ||||||
| chr9:127292073
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219+831A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292073 | ||||||
| chr9:127292093
|
A | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+851A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292093 | ||||||
| chr9:127292365
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0124a0001c0001t0001g0226others(3): Show | 6 | HG02056.hp1 HG02135.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+1123G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292365 | ||||||
| chr9:127292642
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219+1400G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292642 | ||||||
| chr9:127292667
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.219+1425C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292667 | ||||||
| chr9:127292688
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.219+1446A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292688 | ||||||
| chr9:127292904
|
G | T | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+1662G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292904 | ||||||
| chr9:127292968
|
T | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219+1726T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127292968 | ||||||
| chr9:127293048
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.219+1806C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293048 | ||||||
| chr9:127293286
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0043 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.219+2044C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293286 | ||||||
| chr9:127293506
|
G | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.219+2264G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293506 | ||||||
| chr9:127293522
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.219+2280G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293522 | ||||||
| chr9:127293565
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+2323A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293565 | ||||||
| chr9:127293963
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.219+2721C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127293963 | ||||||
| chr9:127294139
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+2897G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294139 | ||||||
| chr9:127294373
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219+3131C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294373 | ||||||
| chr9:127294390
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219+3148G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294390 | ||||||
| chr9:127294564
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.219+3322C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294564 | ||||||
| chr9:127294565
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.219+3323A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294565 | ||||||
| chr9:127294570
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219+3328G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294570 | ||||||
| chr9:127294691
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.219+3449A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294691 | ||||||
| chr9:127294839
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.219+3597C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294839 | ||||||
| chr9:127294856
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.219+3614G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294856 | ||||||
| chr9:127294995
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.219+3753T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127294995 | ||||||
| chr9:127295061
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.219+3819C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127295061 | ||||||
| chr9:127295587
|
A | G | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.219+4345A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127295587 | ||||||
| chr9:127295716
|
A | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+4474A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127295716 | ||||||
| chr9:127295726
|
C | CT | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+4496dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127295726 | |||||
| chr9:127295821
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.219+4579C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127295821 | ||||||
| chr9:127295847
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+4605A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127295847 | ||||||
| chr9:127296016
|
A | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219+4774A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127296016 | ||||||
| chr9:127296137
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.219+4895C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127296137 | ||||||
| chr9:127296300
|
G | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.219+5058G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127296300 | ||||||
| chr9:127296464
|
C | CT | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.219+5246dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127296464 | |||||
| chr9:127296464
|
C | CTT | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00423.hp2 HG02083.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.219+5245_219+5246d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127296464 | |||||
| chr9:127296464
|
CT | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 43 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+5246delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127296464 | |||||
| chr9:127296633
|
A | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.219+5391A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127296633 | ||||||
| chr9:127296777
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.219+5535G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127296777 | ||||||
| chr9:127297045
|
C | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+5803C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297045 | ||||||
| chr9:127297089
|
A | T | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+5847A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297089 | ||||||
| chr9:127297160
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.219+5918G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297160 | ||||||
| chr9:127297261
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+6019T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297261 | ||||||
| chr9:127297372
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+6130C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297372 | ||||||
| chr9:127297609
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+6367C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297609 | ||||||
| chr9:127297675
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+6433A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127297675 | ||||||
| chr9:127298047
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0173others(8): Show | 12 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+6805C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298047 | ||||||
| chr9:127298081
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.219+6839T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298081 | ||||||
| chr9:127298101
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+6859A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298101 | ||||||
| chr9:127298131
|
G | A | 1 | a0007c0004t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.219+6889G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298131 | ||||||
| chr9:127298186
|
G | GT | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219+6944_219+6945i others(3): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298186 | ||||||
| chr9:127298187
|
G | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+6945G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298187 | ||||||
| chr9:127298199
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01496.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.219+6957C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298199 | ||||||
| chr9:127298409
|
C | A | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.219+7167C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298409 | ||||||
| chr9:127298423
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+7181T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298423 | ||||||
| chr9:127298427
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.219+7185C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298427 | ||||||
| chr9:127298496
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.219+7254A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298496 | ||||||
| chr9:127298597
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0024others(28): Show | 33 | HG00558.hp1 HG02027.hp2 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.219+7355T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298597 | ||||||
| chr9:127298616
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.219+7374T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298616 | ||||||
| chr9:127298698
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.219+7456G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298698 | ||||||
| chr9:127298775
|
A | G | 17 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(14): Show | 17 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.219+7533A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298775 | ||||||
| chr9:127298931
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.219+7689A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298931 | ||||||
| chr9:127298982
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219+7740C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127298982 | ||||||
| chr9:127299014
|
AAGAG | A | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+7776_219+7779d others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127299014 | |||||
| chr9:127299023
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.219+7781A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299023 | ||||||
| chr9:127299054
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.219+7812C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299054 | ||||||
| chr9:127299088
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.219+7846G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299088 | ||||||
| chr9:127299102
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.219+7860G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299102 | ||||||
| chr9:127299320
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0001g0033a0001c0001t0001g0254a0001c0001t0001g0269others(1): Show | 4 | NA18522.hp1 NA19003.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+8082_219+8091d others(12): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127299320 | |||||
| chr9:127299321
|
AAAAAAAA others(2): Show |
A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.219+8083_219+8091d others(11): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127299321 | |||||
| chr9:127299322
|
AAAAAAAA others(1): Show |
A | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(8): Show | 11 | HG01981.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.219+8084_219+8091d others(10): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127299322 | |||||
| chr9:127299501
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.219+8259G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299501 | ||||||
| chr9:127299671
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219+8429T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299671 | ||||||
| chr9:127299816
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219+8574C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127299816 | ||||||
| chr9:127300007
|
T | C | 1 | a0001c0002t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219+8765T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300007 | ||||||
| chr9:127300100
|
A | G | 62 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0062others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.219+8858A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300100 | ||||||
| chr9:127300251
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.219+9009G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300251 | ||||||
| chr9:127300265
|
T | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+9023T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300265 | ||||||
| chr9:127300279
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.219+9037T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300279 | ||||||
| chr9:127300318
|
G | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.219+9076G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300318 | ||||||
| chr9:127300707
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.219+9465G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127300707 | ||||||
| chr9:127301003
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.219+9761C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127301003 | ||||||
| chr9:127301603
|
A | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-10033A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127301603 | ||||||
| chr9:127301875
|
G | T | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-9761G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127301875 | ||||||
| chr9:127301925
|
C | CT | 22 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0078others(19): Show | 22 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.220-9678dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301925
|
CT | C | 13 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG00323.hp2 HG01109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.220-9678delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301925
|
CTT | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0026others(55): Show | 60 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.220-9679_220-9678d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301925
|
CTTT | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.220-9680_220-9678d others(5): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301925
|
CTTTT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0129others(8): Show | 11 | HG01081.hp1 HG01975.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-9681_220-9678d others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301925
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.220-9696_220-9678d others(21): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127301925 | |||||
| chr9:127301971
|
C | T | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.220-9665C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127301971 | ||||||
| chr9:127302004
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0070others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-9632G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302004 | ||||||
| chr9:127302141
|
C | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-9495C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302141 | ||||||
| chr9:127302189
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-9447G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302189 | ||||||
| chr9:127302224
|
G | C | 1 | a0007c0004t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.220-9412G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302224 | ||||||
| chr9:127302357
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-9279C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302357 | ||||||
| chr9:127302644
|
A | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(121): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.220-8992A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302644 | ||||||
| chr9:127302693
|
G | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(121): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.220-8943G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302693 | ||||||
| chr9:127302792
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-8844A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302792 | ||||||
| chr9:127302926
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-8710T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127302926 | ||||||
| chr9:127303015
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-8621G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127303015 | ||||||
| chr9:127303058
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220-8578G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127303058 | ||||||
| chr9:127303296
|
TTGTATGT others(5): Show |
T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.220-8332_220-8321d others(14): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127303296 | |||||
| chr9:127303525
|
TTTTTTAA others(13): Show |
T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-8105_220-8086d others(22): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127303525 | |||||
| chr9:127303531
|
A | T | 1 | a0001c0001t0001g0282 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.220-8105A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127303531 | ||||||
| chr9:127303541
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.220-8095G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127303541 | ||||||
| chr9:127303750
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.220-7886G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127303750 | ||||||
| chr9:127304169
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.220-7467C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304169 | ||||||
| chr9:127304437
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.220-7199C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304437 | ||||||
| chr9:127304530
|
C | CT | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.220-7083dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127304530 | |||||
| chr9:127304530
|
C | CTT | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.220-7084_220-7083d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127304530 | |||||
| chr9:127304530
|
CT | C | 45 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0064others(42): Show | 45 | HG00099.hp1 HG00642.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.220-7083delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127304530 | |||||
| chr9:127304530
|
CTTTTTTT others(3): Show |
C | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.220-7092_220-7083d others(12): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127304530 | |||||
| chr9:127304557
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.220-7079A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304557 | ||||||
| chr9:127304660
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-6976C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304660 | ||||||
| chr9:127304730
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220-6906T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304730 | ||||||
| chr9:127304767
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.220-6869C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304767 | ||||||
| chr9:127304925
|
A | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.220-6711A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127304925 | ||||||
| chr9:127305016
|
G | A | 1 | a0001c0009t0001g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.220-6620G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127305016 | ||||||
| chr9:127305222
|
TA | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-6405delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127305222 | |||||
| chr9:127305356
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.220-6280T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127305356 | ||||||
| chr9:127305443
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-6193G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127305443 | ||||||
| chr9:127306010
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.220-5626C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306010 | ||||||
| chr9:127306196
|
C | CA | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.220-5440_220-5439i others(3): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306196 | ||||||
| chr9:127306206
|
G | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(121): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.220-5430G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306206 | ||||||
| chr9:127306227
|
A | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.220-5409A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306227 | ||||||
| chr9:127306320
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.220-5316C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306320 | ||||||
| chr9:127306366
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(4): Show | 7 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-5270C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306366 | ||||||
| chr9:127306456
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.220-5180G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306456 | ||||||
| chr9:127306555
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.220-5081G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306555 | ||||||
| chr9:127306726
|
C | CA | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.220-4895dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127306726 | |||||
| chr9:127306785
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA18970.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.220-4851G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306785 | ||||||
| chr9:127306866
|
C | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-4770C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306866 | ||||||
| chr9:127306880
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220-4756G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306880 | ||||||
| chr9:127306923
|
A | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0089others(1): Show | 4 | HG00738.hp2 HG01496.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4713A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306923 | ||||||
| chr9:127306979
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.220-4657G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127306979 | ||||||
| chr9:127307169
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-4467A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127307169 | ||||||
| chr9:127307407
|
G | A | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.220-4229G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127307407 | ||||||
| chr9:127307502
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.220-4134T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127307502 | ||||||
| chr9:127307746
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | NA18946.hp1 NA18974.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.220-3890T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127307746 | ||||||
| chr9:127308007
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.220-3629T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308007 | ||||||
| chr9:127308013
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.220-3623A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308013 | ||||||
| chr9:127308044
|
C | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-3592C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308044 | ||||||
| chr9:127308142
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-3494A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308142 | ||||||
| chr9:127308293
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.220-3343T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308293 | ||||||
| chr9:127308372
|
T | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020 | 3 | HG02109.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.220-3264T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308372 | ||||||
| chr9:127308891
|
G | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(4): Show | 7 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-2745G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308891 | ||||||
| chr9:127308978
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0150 | 2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.220-2658T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127308978 | ||||||
| chr9:127309120
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0150 | 2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.220-2516G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309120 | ||||||
| chr9:127309151
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-2485G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309151 | ||||||
| chr9:127309280
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0001g0284 | 3 | HG00741.hp1 HG01981.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.220-2356T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309280 | ||||||
| chr9:127309467
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-2169C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309467 | ||||||
| chr9:127309501
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.220-2135C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309501 | ||||||
| chr9:127309733
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220-1903G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309733 | ||||||
| chr9:127309742
|
C | CA | 49 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0132others(46): Show | 50 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.220-1887dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127309742 | |||||
| chr9:127309797
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.220-1839A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309797 | ||||||
| chr9:127309962
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.220-1674A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309962 | ||||||
| chr9:127309965
|
C | T | 54 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0095others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.220-1671C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127309965 | ||||||
| chr9:127310173
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-1463G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127310173 | ||||||
| chr9:127310530
|
C | G | 29 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.220-1106C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127310530 | ||||||
| chr9:127310601
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.220-1035G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127310601 | ||||||
| chr9:127310727
|
T | C | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-909T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127310727 | ||||||
| chr9:127310773
|
C | CA | 23 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(20): Show | 23 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.220-843dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127310773 | |||||
| chr9:127310773
|
C | CAA | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.220-844_220-843dup others(2): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127310773 | |||||
| chr9:127310773
|
CA | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG00558.hp2 HG02698.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-843delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127310773 | |||||
| chr9:127311124
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 129 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.220-512C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311124 | ||||||
| chr9:127311151
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-485T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311151 | ||||||
| chr9:127311235
|
G | GA | 53 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(50): Show | 53 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.220-390dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 127311235 | |||||
| chr9:127311247
|
C | G | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-389C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311247 | ||||||
| chr9:127311467
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.220-169C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311467 | ||||||
| chr9:127311543
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-93G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311543 | ||||||
| chr9:127311584
|
A | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-52A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 2/27 | chr9 | 127311584 | ||||||
| chr9:127311813
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02486.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.319+78T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127311813 | ||||||
| chr9:127311863
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+128C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127311863 | ||||||
| chr9:127311876
|
A | G | 1 | a0003c0003t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.319+141A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127311876 | ||||||
| chr9:127312308
|
C | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.319+573C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312308 | ||||||
| chr9:127312316
|
C | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(4): Show | 7 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+581C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312316 | ||||||
| chr9:127312380
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.319+645C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312380 | ||||||
| chr9:127312492
|
T | TTAAAGTG others(324): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0156 | 2 | HG02135.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.319+769_319+770ins others(331): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
7 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145others(4): Show | 7 | NA18956.hp2 NA18975.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(324): Show |
1 | a0001c0001t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+769_319+770ins others(331): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
1 | a0001c0001t0001g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
5 | a0001c0001t0001g0081a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0154 | 3 | HG02083.hp2 NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312492
|
T | TTAAAGTG others(323): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0242a0001c0001t0001g0274 | 3 | HG02155.hp2 NA18961.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.319+769_319+770ins others(330): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312492 | |||||
| chr9:127312531
|
GA | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+800delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 127312531 | |||||
| chr9:127312542
|
T | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.319+807T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312542 | ||||||
| chr9:127312815
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18955.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.320-626G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312815 | ||||||
| chr9:127312856
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.320-585A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312856 | ||||||
| chr9:127312981
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-460G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312981 | ||||||
| chr9:127312989
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.320-452G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127312989 | ||||||
| chr9:127313159
|
A | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.320-282A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127313159 | ||||||
| chr9:127313215
|
C | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00438.hp1 HG02074.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-226C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127313215 | ||||||
| chr9:127313347
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.320-94G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127313347 | ||||||
| chr9:127313393
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0039others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.320-48C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 3/27 | chr9 | 127313393 | ||||||
| chr9:127313600
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.438+41A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313600 | ||||||
| chr9:127313692
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.438+133T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313692 | ||||||
| chr9:127313755
|
G | GA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00735.hp2 HG02145.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.438+207dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127313755 | |||||
| chr9:127313755
|
G | T | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.438+196G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313755 | ||||||
| chr9:127313755
|
GA | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.438+207delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127313755 | |||||
| chr9:127313756
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.438+197A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313756 | ||||||
| chr9:127313794
|
C | A | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.438+235C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313794 | ||||||
| chr9:127313880
|
T | C | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.438+321T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313880 | ||||||
| chr9:127313891
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+332G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127313891 | ||||||
| chr9:127314217
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.438+658T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314217 | ||||||
| chr9:127314251
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+692A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314251 | ||||||
| chr9:127314522
|
C | G | 47 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0095others(44): Show | 47 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.438+963C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314522 | ||||||
| chr9:127314537
|
T | TCCCTCCC others(9): Show |
1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.438+991_438+1006du others(17): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127314537 | |||||
| chr9:127314620
|
G | A | 1 | a0003c0003t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.438+1061G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314620 | ||||||
| chr9:127314694
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG03098.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.438+1135T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314694 | ||||||
| chr9:127314733
|
C | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.438+1174C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314733 | ||||||
| chr9:127314870
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.438+1311G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314870 | ||||||
| chr9:127314874
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+1315C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314874 | ||||||
| chr9:127314921
|
C | T | 2 | a0001c0001t0001g0106a0001c0002t0001g0071 | 2 | HG02132.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.438+1362C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314921 | ||||||
| chr9:127314922
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1363G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314922 | ||||||
| chr9:127314934
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.438+1375A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127314934 | ||||||
| chr9:127315086
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438+1527G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315086 | ||||||
| chr9:127315159
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.438+1600T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315159 | ||||||
| chr9:127315205
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.438+1646T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315205 | ||||||
| chr9:127315247
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.438+1688C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315247 | ||||||
| chr9:127315296
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.438+1737C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315296 | ||||||
| chr9:127315931
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.439-2132G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127315931 | ||||||
| chr9:127316147
|
C | A | 1 | a0003c0003t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.439-1916C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316147 | ||||||
| chr9:127316308
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.439-1755A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316308 | ||||||
| chr9:127316323
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1740C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316323 | ||||||
| chr9:127316365
|
G | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-1698G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316365 | ||||||
| chr9:127316520
|
G | A | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.439-1543G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316520 | ||||||
| chr9:127316542
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.439-1521G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316542 | ||||||
| chr9:127316609
|
GA | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-1447delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127316609 | |||||
| chr9:127316671
|
C | G | 7 | a0001c0001t0001g0165a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG02074.hp1 NA18943.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-1392C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316671 | ||||||
| chr9:127316724
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.439-1339C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316724 | ||||||
| chr9:127316734
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.439-1329A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316734 | ||||||
| chr9:127316794
|
A | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0060 | 3 | HG02109.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.439-1269A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316794 | ||||||
| chr9:127316952
|
CCCT | C | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.439-1106_439-1104d others(5): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127316952 | |||||
| chr9:127316965
|
G | A | 49 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(46): Show | 49 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.439-1098G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127316965 | ||||||
| chr9:127317000
|
G | C | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.439-1063G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317000 | ||||||
| chr9:127317186
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439-877T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317186 | ||||||
| chr9:127317463
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.439-600G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317463 | ||||||
| chr9:127317733
|
AAAC | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.439-311_439-309del others(3): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127317733 | |||||
| chr9:127317733
|
AAACAAC | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 7 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-314_439-309del others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 127317733 | |||||
| chr9:127317738
|
AC | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-324delC | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317738 | ||||||
| chr9:127317827
|
C | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-236C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317827 | ||||||
| chr9:127317952
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.439-111G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 4/27 | chr9 | 127317952 | ||||||
| chr9:127318139
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.503+12T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318139 | ||||||
| chr9:127318178
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0070others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.503+51C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318178 | ||||||
| chr9:127318271
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0070others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.503+144G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318271 | ||||||
| chr9:127318282
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.503+155C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318282 | ||||||
| chr9:127318608
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.503+481G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318608 | ||||||
| chr9:127318653
|
C | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.503+526C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318653 | ||||||
| chr9:127318656
|
GC | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.503+534delC | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 127318656 | |||||
| chr9:127318681
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+554A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318681 | ||||||
| chr9:127318696
|
T | G | 1 | a0001c0002t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.503+569T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318696 | ||||||
| chr9:127318714
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.503+587T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318714 | ||||||
| chr9:127318881
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.503+754A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127318881 | ||||||
| chr9:127319161
|
C | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.503+1034C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319161 | ||||||
| chr9:127319175
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.503+1048C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319175 | ||||||
| chr9:127319214
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.503+1087A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319214 | ||||||
| chr9:127319223
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.503+1096G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319223 | ||||||
| chr9:127319280
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.503+1153C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319280 | ||||||
| chr9:127319614
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.504-1101G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127319614 | ||||||
| chr9:127320119
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.504-596G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127320119 | ||||||
| chr9:127320451
|
T | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.504-264T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127320451 | ||||||
| chr9:127320470
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.504-245C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127320470 | ||||||
| chr9:127320593
|
A | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.504-122A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 5/27 | chr9 | 127320593 | ||||||
| chr9:127320861
|
T | G | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.567+83T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127320861 | ||||||
| chr9:127321024
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.567+246G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321024 | ||||||
| chr9:127321039
|
A | G | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.567+261A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321039 | ||||||
| chr9:127321062
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.567+284A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321062 | ||||||
| chr9:127321089
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.567+311G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321089 | ||||||
| chr9:127321197
|
G | A | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.567+419G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321197 | ||||||
| chr9:127321308
|
G | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | NA19004.hp2 NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.567+530G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321308 | ||||||
| chr9:127321602
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.567+824C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321602 | ||||||
| chr9:127321910
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.567+1132G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321910 | ||||||
| chr9:127321931
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0217 | 3 | NA18943.hp1 NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.567+1153G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127321931 | ||||||
| chr9:127322067
|
C | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1289C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322067 | ||||||
| chr9:127322186
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.567+1408T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322186 | ||||||
| chr9:127322283
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1505C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322283 | ||||||
| chr9:127322309
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.567+1531G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322309 | ||||||
| chr9:127322406
|
GA | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.567+1640delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 127322406 | |||||
| chr9:127322578
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.567+1800T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322578 | ||||||
| chr9:127322668
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.567+1890G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322668 | ||||||
| chr9:127322676
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1898C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127322676 | ||||||
| chr9:127323267
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.568-1802A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323267 | ||||||
| chr9:127323441
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.568-1628G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323441 | ||||||
| chr9:127323456
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.568-1613G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323456 | ||||||
| chr9:127323598
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 68 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.568-1471T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323598 | ||||||
| chr9:127323635
|
A | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.568-1434A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323635 | ||||||
| chr9:127323725
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.568-1344C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323725 | ||||||
| chr9:127323740
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-1329A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323740 | ||||||
| chr9:127323751
|
AC | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.568-1311delC | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 127323751 | |||||
| chr9:127323912
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.568-1157C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127323912 | ||||||
| chr9:127324155
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568-914G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324155 | ||||||
| chr9:127324205
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.568-864C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324205 | ||||||
| chr9:127324407
|
T | C | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.568-662T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324407 | ||||||
| chr9:127324491
|
A | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.568-578A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324491 | ||||||
| chr9:127324663
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.568-406G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324663 | ||||||
| chr9:127324868
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.568-201A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324868 | ||||||
| chr9:127324923
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.568-146T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324923 | ||||||
| chr9:127324946
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.568-123C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127324946 | ||||||
| chr9:127325018
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-51G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 6/27 | chr9 | 127325018 | ||||||
| chr9:127325132
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.594+37C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325132 | ||||||
| chr9:127325229
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0150 | 2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.594+134C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325229 | ||||||
| chr9:127325229
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+134C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325229 | ||||||
| chr9:127325271
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.594+176A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325271 | ||||||
| chr9:127325371
|
T | C | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+276T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325371 | ||||||
| chr9:127325682
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.594+587C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325682 | ||||||
| chr9:127325781
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+686C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325781 | ||||||
| chr9:127325916
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+821A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127325916 | ||||||
| chr9:127326309
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.594+1214T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127326309 | ||||||
| chr9:127326327
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1232C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127326327 | ||||||
| chr9:127326747
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.594+1652T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127326747 | ||||||
| chr9:127326857
|
A | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.594+1762A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127326857 | ||||||
| chr9:127326933
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.594+1838T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127326933 | ||||||
| chr9:127327000
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(4): Show | 7 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+1905T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327000 | ||||||
| chr9:127327044
|
C | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.594+1949C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327044 | ||||||
| chr9:127327207
|
C | T | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.594+2112C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327207 | ||||||
| chr9:127327208
|
G | C | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.594+2113G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327208 | ||||||
| chr9:127327213
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.594+2118G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327213 | ||||||
| chr9:127327363
|
G | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 7 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+2268G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327363 | ||||||
| chr9:127327368
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+2273G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327368 | ||||||
| chr9:127327496
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.594+2401G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327496 | ||||||
| chr9:127327504
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+2409C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327504 | ||||||
| chr9:127327925
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2830G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327925 | ||||||
| chr9:127327942
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.594+2847G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327942 | ||||||
| chr9:127327997
|
A | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.594+2902A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127327997 | ||||||
| chr9:127328082
|
A | G | 21 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00609.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.594+2987A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328082 | ||||||
| chr9:127328303
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.594+3208C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328303 | ||||||
| chr9:127328502
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.594+3407A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328502 | ||||||
| chr9:127328647
|
A | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.594+3552A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328647 | ||||||
| chr9:127328649
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.594+3554G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328649 | ||||||
| chr9:127328666
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00735.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+3571A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328666 | ||||||
| chr9:127328770
|
A | G | 54 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.595-3504A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328770 | ||||||
| chr9:127328804
|
C | A | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595-3470C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328804 | ||||||
| chr9:127328807
|
T | C | 54 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.595-3467T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127328807 | ||||||
| chr9:127329042
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0220a0001c0001t0001g0251others(1): Show | 5 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-3232C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127329042 | ||||||
| chr9:127329459
|
A | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0032others(45): Show | 48 | HG01069.hp2 HG01099.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.595-2815A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127329459 | ||||||
| chr9:127329598
|
G | A | 14 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(11): Show | 14 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.595-2676G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127329598 | ||||||
| chr9:127329613
|
C | CT | 66 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.595-2657dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127329613 | |||||
| chr9:127329763
|
G | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(9): Show | 12 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-2511G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127329763 | ||||||
| chr9:127329860
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595-2414A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127329860 | ||||||
| chr9:127330706
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-1568G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127330706 | ||||||
| chr9:127330720
|
G | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 88 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.595-1554G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127330720 | ||||||
| chr9:127330730
|
GAAA | G | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 88 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.595-1543_595-1541d others(5): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127330730 | ||||||
| chr9:127330934
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0057 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.595-1340G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127330934 | ||||||
| chr9:127330945
|
A | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0199others(1): Show | 4 | HG01106.hp1 NA18989.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-1329A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127330945 | ||||||
| chr9:127331206
|
T | C | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.595-1068T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331206 | ||||||
| chr9:127331269
|
G | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 88 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.595-1005G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331269 | ||||||
| chr9:127331431
|
T | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0037a0001c0002t0001g0038others(14): Show | 18 | HG01099.hp2 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.595-843T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331431 | ||||||
| chr9:127331504
|
GA | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0035others(28): Show | 31 | HG01069.hp2 HG01109.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.595-759delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331504 | |||||
| chr9:127331516
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.595-758C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331516 | ||||||
| chr9:127331625
|
C | T | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.595-649C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331625 | ||||||
| chr9:127331627
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-647A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331627 | ||||||
| chr9:127331669
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.595-605G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331669 | ||||||
| chr9:127331720
|
C | CTT | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0098others(8): Show | 11 | HG00140.hp2 HG01081.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.595-540_595-539dup others(2): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTGCTTT others(21): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0022 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.595-552_595-551ins others(28): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTGCTTT others(22): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020 | 3 | HG02109.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.595-552_595-551ins others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTGCTTT others(26): Show |
1 | a0001c0001t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.595-552_595-551ins others(33): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTT | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.595-541_595-539dup others(3): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTT | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.595-544_595-539dup others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(13): Show | 16 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.595-547_595-539dup others(9): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0241 | 3 | NA18956.hp1 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.595-548_595-539dup others(10): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0276 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.595-550_595-539dup others(12): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02155.hp1 HG03239.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-551_595-539dup others(13): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(7): Show |
58 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(55): Show | 59 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.595-552_595-539dup others(14): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0209others(2): Show | 5 | HG00438.hp1 HG01433.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-553_595-539dup others(15): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0235 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.595-539_595-538ins others(23): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(17): Show |
8 | a0001c0001t0001g0105a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG02071.hp2 HG02074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(24): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(18): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0106others(3): Show | 6 | HG01074.hp2 HG01891.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(25): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(19): Show |
9 | a0001c0001t0001g0118a0001c0001t0001g0249a0001c0001t0001g0251others(6): Show | 9 | HG00741.hp2 HG01070.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(26): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(20): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0181others(8): Show | 12 | HG00280.hp1 HG00323.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(27): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(21): Show |
10 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0163others(7): Show | 10 | HG00558.hp1 HG00609.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(28): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(22): Show |
13 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0159others(10): Show | 13 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.595-539_595-538ins others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0261 | 3 | HG01109.hp2 HG02647.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.595-539_595-538ins others(30): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331720
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.595-539_595-538ins others(31): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr9 | 127331720 | |||||
| chr9:127331916
|
G | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 117 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.595-358G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127331916 | ||||||
| chr9:127332020
|
G | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0213 | 2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.595-254G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127332020 | ||||||
| chr9:127332247
|
T | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(53): Show | 57 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.595-27T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 7/27 | chr9 | 127332247 | ||||||
| chr9:127332399
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+50G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 8/27 | chr9 | 127332399 | ||||||
| chr9:127332527
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.670+178A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 8/27 | chr9 | 127332527 | ||||||
| chr9:127332711
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671-312G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 8/27 | chr9 | 127332711 | ||||||
| chr9:127333148
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.769+27T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333148 | ||||||
| chr9:127333175
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.769+54A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333175 | ||||||
| chr9:127333432
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.769+311G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333432 | ||||||
| chr9:127333498
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.769+377A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333498 | ||||||
| chr9:127333935
|
C | G | 1 | a0001c0001t0001g0266 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.769+814C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333935 | ||||||
| chr9:127333969
|
A | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.769+848A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333969 | ||||||
| chr9:127333974
|
C | T | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.769+853C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127333974 | ||||||
| chr9:127334065
|
T | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 114 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.769+944T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334065 | ||||||
| chr9:127334099
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 119 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.769+978G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334099 | ||||||
| chr9:127334375
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770-855G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334375 | ||||||
| chr9:127334380
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.770-850G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334380 | ||||||
| chr9:127334594
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.770-636G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334594 | ||||||
| chr9:127334908
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-322G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127334908 | ||||||
| chr9:127335027
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.770-203G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 9/27 | chr9 | 127335027 | ||||||
| chr9:127335379
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.873+46G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335379 | ||||||
| chr9:127335412
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+79C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335412 | ||||||
| chr9:127335416
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.873+83G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335416 | ||||||
| chr9:127335441
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+108T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335441 | ||||||
| chr9:127335528
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.873+195C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335528 | ||||||
| chr9:127335563
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.873+230A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335563 | ||||||
| chr9:127335641
|
C | CT | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.873+317dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 127335641 | |||||
| chr9:127335839
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.874-289A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335839 | ||||||
| chr9:127335864
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-264A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335864 | ||||||
| chr9:127335868
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-260A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 10/27 | chr9 | 127335868 | ||||||
| chr9:127336280
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+44T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127336280 | ||||||
| chr9:127336638
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.982+402T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127336638 | ||||||
| chr9:127336800
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+564G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127336800 | ||||||
| chr9:127337002
|
G | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 50 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.982+766G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337002 | ||||||
| chr9:127337013
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.982+777G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337013 | ||||||
| chr9:127337026
|
A | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.982+790A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337026 | ||||||
| chr9:127337177
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.983-939C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337177 | ||||||
| chr9:127337392
|
C | G | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.983-724C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337392 | ||||||
| chr9:127337888
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.983-228C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337888 | ||||||
| chr9:127337918
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.983-198T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127337918 | ||||||
| chr9:127338009
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.983-107G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127338009 | ||||||
| chr9:127338026
|
G | A | 63 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0061others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.983-90G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 11/27 | chr9 | 127338026 | ||||||
| chr9:127338173
|
CTT | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG03098.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1028+14_1028+15del others(2): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 127338173 | |||||
| chr9:127338625
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1028+464G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127338625 | ||||||
| chr9:127338793
|
T | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0151a0001c0001t0001g0153 | 3 | HG04115.hp1 HG04199.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1028+632T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127338793 | ||||||
| chr9:127338829
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0256 | 3 | HG00423.hp2 NA18983.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1028+668G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127338829 | ||||||
| chr9:127339113
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0005c0008t0001g0198 | 3 | HG01106.hp1 NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1029-532C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339113 | ||||||
| chr9:127339124
|
C | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1029-521C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339124 | ||||||
| chr9:127339144
|
A | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 134 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1029-501A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339144 | ||||||
| chr9:127339179
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1029-466C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339179 | ||||||
| chr9:127339229
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1029-416G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339229 | ||||||
| chr9:127339296
|
C | CA | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 122 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.1029-334dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 127339296 | |||||
| chr9:127339296
|
C | CAA | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG00423.hp2 NA18942.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-335_1029-334d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 127339296 | |||||
| chr9:127339489
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0177a0001c0001t0001g0231others(1): Show | 5 | HG00280.hp2 HG01258.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029-156G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339489 | ||||||
| chr9:127339496
|
A | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1029-149A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339496 | ||||||
| chr9:127339533
|
C | T | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1029-112C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339533 | ||||||
| chr9:127339538
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1029-107A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 12/27 | chr9 | 127339538 | ||||||
| chr9:127339886
|
G | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135+135G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127339886 | ||||||
| chr9:127340099
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1135+348G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340099 | ||||||
| chr9:127340183
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+432C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340183 | ||||||
| chr9:127340347
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135+596G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340347 | ||||||
| chr9:127340461
|
GC | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135+713delC | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr9 | 127340461 | |||||
| chr9:127340660
|
T | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1135+909T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340660 | ||||||
| chr9:127340672
|
T | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135+921T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340672 | ||||||
| chr9:127340725
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+974G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340725 | ||||||
| chr9:127340773
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1135+1022G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340773 | ||||||
| chr9:127340944
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0281 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1135+1193A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340944 | ||||||
| chr9:127340961
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1135+1210C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127340961 | ||||||
| chr9:127341119
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0150others(2): Show | 5 | HG00423.hp2 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136-1100C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341119 | ||||||
| chr9:127341247
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1136-972A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341247 | ||||||
| chr9:127341425
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1136-794A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341425 | ||||||
| chr9:127341524
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136-695A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341524 | ||||||
| chr9:127341609
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1136-610C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341609 | ||||||
| chr9:127341977
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1136-242G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127341977 | ||||||
| chr9:127342008
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1136-211G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127342008 | ||||||
| chr9:127342195
|
C | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136-24C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 13/27 | chr9 | 127342195 | ||||||
| chr9:127342405
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251+71C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342405 | ||||||
| chr9:127342549
|
A | T | 1 | a0001c0001t0001g0196 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1251+215A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342549 | ||||||
| chr9:127342604
|
A | C | 1 | a0001c0001t0002g0224 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1251+270A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342604 | ||||||
| chr9:127342843
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251+509G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342843 | ||||||
| chr9:127342892
|
CT | C | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1251+579delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr9 | 127342892 | |||||
| chr9:127342896
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1251+562T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342896 | ||||||
| chr9:127342897
|
T | C | 29 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG01109.hp2 HG01496.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1251+563T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127342897 | ||||||
| chr9:127343028
|
G | A | 1 | a0001c0006t0001g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1251+694G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343028 | ||||||
| chr9:127343218
|
G | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251+884G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343218 | ||||||
| chr9:127343296
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1252-939G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343296 | ||||||
| chr9:127343339
|
G | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(67): Show | 71 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1252-896G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343339 | ||||||
| chr9:127343553
|
G | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1252-682G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343553 | ||||||
| chr9:127343787
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(51): Show | 55 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1252-448A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 14/27 | chr9 | 127343787 | ||||||
| chr9:127344499
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 118 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1356+160C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/27 | chr9 | 127344499 | ||||||
| chr9:127345016
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1357-387T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/27 | chr9 | 127345016 | ||||||
| chr9:127345052
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357-351G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/27 | chr9 | 127345052 | ||||||
| chr9:127345130
|
A | AT | 50 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0061others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1357-267dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 127345130 | |||||
| chr9:127345299
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1357-104C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 15/27 | chr9 | 127345299 | ||||||
| chr9:127345685
|
A | G | 164 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1431+208A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127345685 | ||||||
| chr9:127345894
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(49): Show | 53 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1431+417A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127345894 | ||||||
| chr9:127345990
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1431+513A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127345990 | ||||||
| chr9:127346159
|
A | G | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1431+682A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127346159 | ||||||
| chr9:127346166
|
C | T | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1431+689C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127346166 | ||||||
| chr9:127346629
|
T | C | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1431+1152T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127346629 | ||||||
| chr9:127346812
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1431+1335G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127346812 | ||||||
| chr9:127347000
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0005c0008t0001g0198 | 3 | HG01106.hp1 NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1431+1523A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347000 | ||||||
| chr9:127347083
|
A | G | 60 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0061others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1431+1606A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347083 | ||||||
| chr9:127347255
|
C | CA | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-1661dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr9 | 127347255 | |||||
| chr9:127347396
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1432-1528T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347396 | ||||||
| chr9:127347467
|
T | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1432-1457T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347467 | ||||||
| chr9:127347640
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-1284T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347640 | ||||||
| chr9:127347731
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-1193A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347731 | ||||||
| chr9:127347777
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0280 | 2 | NA19007.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1432-1147G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127347777 | ||||||
| chr9:127348132
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0035others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1432-792C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127348132 | ||||||
| chr9:127348293
|
C | G | 60 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0061others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1432-631C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127348293 | ||||||
| chr9:127348436
|
G | A | 239 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1432-488G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127348436 | ||||||
| chr9:127348716
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1432-208A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127348716 | ||||||
| chr9:127348798
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1432-126G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 16/27 | chr9 | 127348798 | ||||||
| chr9:127349155
|
G | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543+120G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349155 | ||||||
| chr9:127349418
|
A | T | 103 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(100): Show | 104 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1543+383A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349418 | ||||||
| chr9:127349579
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1543+544C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349579 | ||||||
| chr9:127349609
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1543+574G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349609 | ||||||
| chr9:127349799
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+764T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349799 | ||||||
| chr9:127349952
|
T | C | 165 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1543+917T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349952 | ||||||
| chr9:127349955
|
G | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0111others(16): Show | 19 | HG02129.hp1 HG02135.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543+920G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127349955 | ||||||
| chr9:127350297
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1262G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350297 | ||||||
| chr9:127350640
|
G | A | 1 | a0001c0002t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1543+1605G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350640 | ||||||
| chr9:127350737
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1543+1702C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350737 | ||||||
| chr9:127350879
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0249a0001c0001t0001g0258others(1): Show | 4 | HG01361.hp2 HG03239.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1844G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350879 | ||||||
| chr9:127350921
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1886A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350921 | ||||||
| chr9:127350958
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1923G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127350958 | ||||||
| chr9:127351277
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134 | 3 | HG01081.hp2 HG01255.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1543+2242G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351277 | ||||||
| chr9:127351329
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1543+2294G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351329 | ||||||
| chr9:127351475
|
T | TA | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1544-2361dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 127351475 | |||||
| chr9:127351476
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1544-2370A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351476 | ||||||
| chr9:127351492
|
G | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1544-2354G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351492 | ||||||
| chr9:127351525
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1544-2321T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351525 | ||||||
| chr9:127351646
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1544-2200A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351646 | ||||||
| chr9:127351848
|
T | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0241a0001c0001t0001g0277 | 3 | NA18945.hp2 NA18956.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1544-1998T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351848 | ||||||
| chr9:127351916
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544-1930A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127351916 | ||||||
| chr9:127352085
|
C | T | 239 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1544-1761C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127352085 | ||||||
| chr9:127352549
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0195 | 2 | HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1544-1297C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127352549 | ||||||
| chr9:127352980
|
A | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1544-866A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127352980 | ||||||
| chr9:127353095
|
G | C | 15 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(12): Show | 15 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(12): Show |
intron_variant | MODIFIER | c.1544-751G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127353095 | ||||||
| chr9:127353314
|
C | T | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1544-532C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127353314 | ||||||
| chr9:127353481
|
C | CT | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00423.hp2 HG00609.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1544-349dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 127353481 | |||||
| chr9:127353481
|
CT | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0076others(11): Show | 14 | HG00738.hp2 HG01884.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1544-349delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 127353481 | |||||
| chr9:127353494
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0221 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1544-352T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127353494 | ||||||
| chr9:127353571
|
A | G | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1544-275A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127353571 | ||||||
| chr9:127353581
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1544-265C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 17/27 | chr9 | 127353581 | ||||||
| chr9:127353959
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1642+15C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127353959 | ||||||
| chr9:127354001
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1642+57G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127354001 | ||||||
| chr9:127354079
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1642+135A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127354079 | ||||||
| chr9:127354105
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1642+161G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127354105 | ||||||
| chr9:127354118
|
G | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0095others(37): Show | 40 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1642+174G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127354118 | ||||||
| chr9:127354132
|
G | T | 70 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1643-162G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 18/27 | chr9 | 127354132 | ||||||
| chr9:127354445
|
G | GT | 10 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0186others(7): Show | 10 | HG02027.hp2 HG02129.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.1759+46dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 127354445 | |||||
| chr9:127354547
|
G | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0046others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1759+137G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127354547 | ||||||
| chr9:127354724
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1759+314G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127354724 | ||||||
| chr9:127354837
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1759+427G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127354837 | ||||||
| chr9:127354845
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1759+435T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127354845 | ||||||
| chr9:127355106
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0296 | 2 | HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1760-191T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127355106 | ||||||
| chr9:127355244
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1760-53G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 19/27 | chr9 | 127355244 | ||||||
| chr9:127355582
|
C | A | 69 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1935+110C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127355582 | ||||||
| chr9:127355637
|
TA | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0248others(1): Show | 4 | HG02165.hp1 NA18961.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+168delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr9 | 127355637 | |||||
| chr9:127355692
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1935+220A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127355692 | ||||||
| chr9:127355784
|
A | G | 18 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0002t0001g0002others(15): Show | 19 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1935+312A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127355784 | ||||||
| chr9:127355825
|
A | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(13): Show | 16 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.1935+353A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127355825 | ||||||
| chr9:127355862
|
A | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1935+390A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127355862 | ||||||
| chr9:127356032
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1935+560A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356032 | ||||||
| chr9:127356050
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1935+578G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356050 | ||||||
| chr9:127356156
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1935+684G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356156 | ||||||
| chr9:127356303
|
C | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1935+831C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356303 | ||||||
| chr9:127356303
|
C | T | 15 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0105others(12): Show | 15 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.1935+831C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356303 | ||||||
| chr9:127356337
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(28): Show | 31 | HG00735.hp2 HG01109.hp1 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1935+865G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356337 | ||||||
| chr9:127356814
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1936-405A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356814 | ||||||
| chr9:127356867
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1936-352C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356867 | ||||||
| chr9:127356989
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-230G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127356989 | ||||||
| chr9:127357047
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1936-172C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127357047 | ||||||
| chr9:127357077
|
C | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1936-142C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127357077 | ||||||
| chr9:127357102
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1936-117C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127357102 | ||||||
| chr9:127357179
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1936-40G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 20/27 | chr9 | 127357179 | ||||||
| chr9:127357443
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2094+66C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127357443 | ||||||
| chr9:127357525
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2094+148G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127357525 | ||||||
| chr9:127357704
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2094+327G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127357704 | ||||||
| chr9:127357782
|
TA | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2094+418delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127357782 | |||||
| chr9:127357946
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 52 | HG00423.hp1 HG00735.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2094+569T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127357946 | ||||||
| chr9:127358010
|
G | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(28): Show | 31 | HG00423.hp1 HG00735.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2094+633G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358010 | ||||||
| chr9:127358011
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(28): Show | 31 | HG00423.hp1 HG00735.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2094+634G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358011 | ||||||
| chr9:127358228
|
G | A | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2094+851G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358228 | ||||||
| chr9:127358276
|
G | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+899G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358276 | ||||||
| chr9:127358436
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2094+1059G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358436 | ||||||
| chr9:127358522
|
GCT | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0032others(15): Show | 18 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2094+1148_2094+114 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127358522 | |||||
| chr9:127358718
|
T | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(13): Show | 16 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.2094+1341T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358718 | ||||||
| chr9:127358966
|
T | TG | 73 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2094+1596dupG | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127358966 | |||||
| chr9:127358997
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0172others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2094+1620T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127358997 | ||||||
| chr9:127359113
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2094+1736C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359113 | ||||||
| chr9:127359362
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2094+1985C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359362 | ||||||
| chr9:127359489
|
C | CA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00735.hp2 HG02145.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+2125dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127359489 | |||||
| chr9:127359489
|
CA | C | 91 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0035others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2094+2125delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127359489 | |||||
| chr9:127359510
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2094+2133C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359510 | ||||||
| chr9:127359594
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2094+2217T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359594 | ||||||
| chr9:127359735
|
C | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | NA18942.hp1 NA18980.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094+2358C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359735 | ||||||
| chr9:127359919
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+2542T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359919 | ||||||
| chr9:127359958
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0070others(2): Show | 6 | HG01099.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+2581C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127359958 | ||||||
| chr9:127360008
|
G | GA | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.2094+2640dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127360008 | |||||
| chr9:127360018
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00735.hp2 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+2641T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360018 | ||||||
| chr9:127360024
|
TTTG | T | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG02055.hp2 HG02109.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.2094+2660_2094+266 others(7): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127360024 | |||||
| chr9:127360120
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2094+2743A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360120 | ||||||
| chr9:127360168
|
CA | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2094+2792delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360168 | ||||||
| chr9:127360342
|
G | GA | 5 | a0001c0001t0001g0036a0001c0001t0001g0093a0001c0001t0001g0113others(2): Show | 5 | HG01346.hp1 HG02135.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+2974dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127360342 | |||||
| chr9:127360395
|
C | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+3018C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360395 | ||||||
| chr9:127360398
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2094+3021C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360398 | ||||||
| chr9:127360410
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+3033T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360410 | ||||||
| chr9:127360413
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2094+3036C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360413 | ||||||
| chr9:127360414
|
G | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02074.hp2 NA18953.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+3037G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360414 | ||||||
| chr9:127360419
|
C | T | 107 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0032others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2094+3042C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360419 | ||||||
| chr9:127360438
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2094+3061G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360438 | ||||||
| chr9:127360444
|
G | C | 73 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2094+3067G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360444 | ||||||
| chr9:127360476
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2094+3099C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360476 | ||||||
| chr9:127360509
|
T | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.2094+3132T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360509 | ||||||
| chr9:127360738
|
A | G | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.2094+3361A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360738 | ||||||
| chr9:127360901
|
G | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+3524G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360901 | ||||||
| chr9:127360970
|
A | G | 125 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.2094+3593A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127360970 | ||||||
| chr9:127361146
|
A | G | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2094+3769A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361146 | ||||||
| chr9:127361243
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2094+3866G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361243 | ||||||
| chr9:127361271
|
A | AAG | 71 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(68): Show | 72 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2094+3916_2094+391 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127361271 | |||||
| chr9:127361386
|
C | T | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0002t0001g0002others(14): Show | 18 | HG01109.hp2 HG01884.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.2095-3914C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361386 | ||||||
| chr9:127361465
|
A | C | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2095-3835A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361465 | ||||||
| chr9:127361524
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2095-3776G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361524 | ||||||
| chr9:127361885
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0042others(3): Show | 6 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2095-3415C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127361885 | ||||||
| chr9:127362068
|
C | CT | 33 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2095-3212dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127362068 | |||||
| chr9:127362072
|
T | TC | 15 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0046others(12): Show | 15 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.2095-3228_2095-322 others(5): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362072 | ||||||
| chr9:127362235
|
A | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(70): Show | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2095-3065A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362235 | ||||||
| chr9:127362235
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2095-3065A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362235 | ||||||
| chr9:127362235
|
AT | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2095-3050delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr9 | 127362235 | |||||
| chr9:127362266
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-3034A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362266 | ||||||
| chr9:127362287
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2095-3013C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362287 | ||||||
| chr9:127362348
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-2952A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362348 | ||||||
| chr9:127362357
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2095-2943C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362357 | ||||||
| chr9:127362672
|
T | C | 179 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.2095-2628T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362672 | ||||||
| chr9:127362905
|
G | A | 64 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2095-2395G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127362905 | ||||||
| chr9:127363049
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2095-2251T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363049 | ||||||
| chr9:127363050
|
G | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(13): Show | 16 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.2095-2250G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363050 | ||||||
| chr9:127363155
|
T | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0105a0001c0001t0001g0106others(10): Show | 13 | HG00423.hp1 HG02027.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2095-2145T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363155 | ||||||
| chr9:127363163
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2095-2137A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363163 | ||||||
| chr9:127363366
|
T | G | 38 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0059others(35): Show | 38 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2095-1934T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363366 | ||||||
| chr9:127363447
|
T | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2095-1853T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363447 | ||||||
| chr9:127363684
|
T | C | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2095-1616T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363684 | ||||||
| chr9:127363838
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2095-1462G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363838 | ||||||
| chr9:127363863
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2095-1437C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363863 | ||||||
| chr9:127363967
|
G | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2095-1333G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127363967 | ||||||
| chr9:127364209
|
G | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2095-1091G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127364209 | ||||||
| chr9:127365101
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2095-199C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127365101 | ||||||
| chr9:127365172
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095-128G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 21/27 | chr9 | 127365172 | ||||||
| chr9:127365412
|
C | CT | 51 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2161+57dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127365412 | |||||
| chr9:127365618
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2161+252T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127365618 | ||||||
| chr9:127365653
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2161+287G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127365653 | ||||||
| chr9:127365770
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2161+404G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127365770 | ||||||
| chr9:127365777
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0057others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2161+411T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127365777 | ||||||
| chr9:127365858
|
G | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0057others(49): Show | 53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.2161+492G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127365858 | ||||||
| chr9:127366023
|
T | C | 69 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.2161+657T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366023 | ||||||
| chr9:127366040
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2161+674A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366040 | ||||||
| chr9:127366199
|
A | G | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2161+833A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366199 | ||||||
| chr9:127366327
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2161+961G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366327 | ||||||
| chr9:127366506
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2161+1140G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366506 | ||||||
| chr9:127366628
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2161+1262G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366628 | ||||||
| chr9:127366674
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2161+1308A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366674 | ||||||
| chr9:127366928
|
A | G | 11 | a0001c0001t0001g0155a0001c0001t0001g0170a0001c0001t0001g0171others(8): Show | 11 | HG02165.hp1 NA18956.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.2161+1562A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127366928 | ||||||
| chr9:127366945
|
C | CT | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0057others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2161+1580dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127366945 | |||||
| chr9:127366972
|
AGTATCTT others(9): Show |
A | 1 | a0001c0001t0001g0291 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2161+1620_2161+163 others(20): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127366972 | |||||
| chr9:127367042
|
T | G | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+1676T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367042 | ||||||
| chr9:127367164
|
C | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2161+1798C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367164 | ||||||
| chr9:127367204
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2161+1838C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367204 | ||||||
| chr9:127367322
|
T | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2161+1956T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367322 | ||||||
| chr9:127367398
|
C | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2161+2032C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367398 | ||||||
| chr9:127367477
|
T | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0095others(33): Show | 36 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2161+2111T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367477 | ||||||
| chr9:127367528
|
A | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(73): Show | 77 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2161+2162A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367528 | ||||||
| chr9:127367608
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2161+2242A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367608 | ||||||
| chr9:127367725
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2161+2359A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367725 | ||||||
| chr9:127367728
|
C | T | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2161+2362C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367728 | ||||||
| chr9:127367860
|
TA | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2161+2496delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127367860 | |||||
| chr9:127367931
|
T | A | 1 | a0001c0002t0001g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2161+2565T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367931 | ||||||
| chr9:127367961
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2161+2595A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127367961 | ||||||
| chr9:127367967
|
GTATT | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0057others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2161+2606_2161+260 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127367967 | |||||
| chr9:127368008
|
C | CT | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(15): Show | 18 | HG00438.hp1 HG00735.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.2161+2666dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368008 | |||||
| chr9:127368008
|
CT | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(67): Show | 71 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2161+2666delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368008 | |||||
| chr9:127368008
|
CTT | C | 69 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0062others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2161+2665_2161+266 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368008 | |||||
| chr9:127368078
|
T | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(13): Show | 16 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.2161+2712T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368078 | ||||||
| chr9:127368323
|
T | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(14): Show | 17 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2161+2957T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368323 | ||||||
| chr9:127368330
|
C | CT | 14 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0105others(11): Show | 14 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.2161+2981dupT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368330 | |||||
| chr9:127368330
|
CT | C | 73 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2161+2981delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368330 | |||||
| chr9:127368363
|
C | T | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+2997C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368363 | ||||||
| chr9:127368543
|
C | G | 1 | a0001c0001t0001g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2161+3177C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368543 | ||||||
| chr9:127368610
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2161+3244C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368610 | ||||||
| chr9:127368774
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2161+3408A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368774 | ||||||
| chr9:127368910
|
G | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.2161+3544G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368910 | ||||||
| chr9:127368929
|
T | TCAAAA | 58 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0063others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2161+3584_2161+358 others(9): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127368929 | |||||
| chr9:127368941
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2161+3575A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368941 | ||||||
| chr9:127368962
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2161+3596A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368962 | ||||||
| chr9:127368965
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2161+3599T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127368965 | ||||||
| chr9:127369118
|
TA | T | 42 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 42 | HG00423.hp1 HG01070.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.2161+3770delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127369118 | |||||
| chr9:127369118
|
TAA | T | 65 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2161+3769_2161+377 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127369118 | |||||
| chr9:127369187
|
G | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.2161+3821G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369187 | ||||||
| chr9:127369188
|
A | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.2161+3822A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369188 | ||||||
| chr9:127369243
|
T | C | 19 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2161+3877T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369243 | ||||||
| chr9:127369247
|
G | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0105others(14): Show | 17 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2161+3881G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369247 | ||||||
| chr9:127369258
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2161+3892G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369258 | ||||||
| chr9:127369338
|
G | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0057others(49): Show | 53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.2161+3972G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369338 | ||||||
| chr9:127369394
|
G | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG01069.hp2 HG01496.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2161+4028G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369394 | ||||||
| chr9:127369480
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2161+4114C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369480 | ||||||
| chr9:127369509
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2161+4143G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369509 | ||||||
| chr9:127369579
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2161+4213G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369579 | ||||||
| chr9:127369678
|
G | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+4312G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369678 | ||||||
| chr9:127369717
|
A | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0095others(33): Show | 36 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2161+4351A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369717 | ||||||
| chr9:127369887
|
G | A | 19 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2161+4521G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369887 | ||||||
| chr9:127369945
|
A | G | 19 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2161+4579A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127369945 | ||||||
| chr9:127370057
|
CTG | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2161+4694_2161+469 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127370057 | |||||
| chr9:127370068
|
T | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+4702T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370068 | ||||||
| chr9:127370113
|
A | G | 80 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2161+4747A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370113 | ||||||
| chr9:127370216
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2161+4850T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370216 | ||||||
| chr9:127370267
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2161+4901A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370267 | ||||||
| chr9:127370385
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0151a0001c0001t0001g0153 | 3 | HG04115.hp1 HG04199.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2161+5019G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370385 | ||||||
| chr9:127370433
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2161+5067T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370433 | ||||||
| chr9:127370433
|
T | TGAAAA | 19 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2161+5071_2161+507 others(9): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127370433 | |||||
| chr9:127370591
|
C | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG02165.hp1 HG02735.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.2161+5225C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370591 | ||||||
| chr9:127370683
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG02055.hp2 HG02109.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.2161+5317C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370683 | ||||||
| chr9:127370823
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00735.hp2 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2161+5457G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127370823 | ||||||
| chr9:127371006
|
C | T | 1 | a0001c0001t0001g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2161+5640C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371006 | ||||||
| chr9:127371008
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2161+5642C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371008 | ||||||
| chr9:127371018
|
C | T | 77 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2161+5652C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371018 | ||||||
| chr9:127371044
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 25 | HG01099.hp2 HG02165.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2161+5678G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371044 | ||||||
| chr9:127371193
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2161+5827C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371193 | ||||||
| chr9:127371340
|
T | C | 18 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0046others(15): Show | 18 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2161+5974T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371340 | ||||||
| chr9:127371477
|
T | C | 168 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2161+6111T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371477 | ||||||
| chr9:127371794
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0177a0001c0001t0001g0231others(1): Show | 5 | HG00280.hp2 HG01258.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2161+6428A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371794 | ||||||
| chr9:127371981
|
G | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+6615G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127371981 | ||||||
| chr9:127372103
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2161+6737A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127372103 | ||||||
| chr9:127372266
|
C | G | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+6900C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127372266 | ||||||
| chr9:127372772
|
C | A | 163 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(160): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2161+7406C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127372772 | ||||||
| chr9:127373078
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0080others(1): Show | 4 | NA18988.hp1 NA18989.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2161+7712A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373078 | ||||||
| chr9:127373482
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2161+8116C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373482 | ||||||
| chr9:127373492
|
C | T | 17 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0105others(14): Show | 17 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2161+8126C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373492 | ||||||
| chr9:127373612
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2161+8246C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373612 | ||||||
| chr9:127373752
|
G | A | 15 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(12): Show | 15 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(12): Show |
intron_variant | MODIFIER | c.2161+8386G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373752 | ||||||
| chr9:127373792
|
T | G | 39 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 39 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.2161+8426T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373792 | ||||||
| chr9:127373856
|
A | G | 80 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2161+8490A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373856 | ||||||
| chr9:127373963
|
G | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2161+8597G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127373963 | ||||||
| chr9:127374132
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01069.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2161+8766C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374132 | ||||||
| chr9:127374158
|
A | G | 39 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 39 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.2161+8792A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374158 | ||||||
| chr9:127374216
|
A | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG02165.hp1 HG02735.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.2161+8850A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374216 | ||||||
| chr9:127374233
|
G | A | 64 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2161+8867G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374233 | ||||||
| chr9:127374265
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2161+8899C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374265 | ||||||
| chr9:127374476
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(168): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2162-8962T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374476 | ||||||
| chr9:127374902
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG02055.hp2 HG02109.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.2162-8536A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374902 | ||||||
| chr9:127374909
|
C | CA | 29 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0039others(26): Show | 29 | HG01516.hp2 HG01884.hp2 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.2162-8513dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127374909 | |||||
| chr9:127374909
|
C | CAAAA | 15 | a0001c0001t0001g0026a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG00423.hp1 HG02027.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2162-8516_2162-851 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127374909 | |||||
| chr9:127374923
|
A | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2162-8515A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374923 | ||||||
| chr9:127374925
|
AC | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | NA18942.hp1 NA18980.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.2162-8512delC | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374925 | ||||||
| chr9:127374926
|
C | A | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG02055.hp2 HG02109.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.2162-8512C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374926 | ||||||
| chr9:127374952
|
C | T | 18 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0046others(15): Show | 18 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2162-8486C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374952 | ||||||
| chr9:127374954
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0009t0001g0040 | 3 | HG01109.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2162-8484A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127374954 | ||||||
| chr9:127375088
|
T | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0257a0001c0001t0001g0269 | 3 | NA18953.hp1 NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2162-8350T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127375088 | ||||||
| chr9:127375420
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.2162-8018C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127375420 | ||||||
| chr9:127375467
|
G | GA | 12 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(9): Show | 12 | HG00609.hp1 HG01109.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.2162-7955dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127375467 | |||||
| chr9:127375625
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2162-7813C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127375625 | ||||||
| chr9:127375736
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG00280.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2162-7702A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127375736 | ||||||
| chr9:127375767
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2162-7671G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127375767 | ||||||
| chr9:127376312
|
G | A | 18 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0046others(15): Show | 18 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2162-7126G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376312 | ||||||
| chr9:127376344
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2162-7094G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376344 | ||||||
| chr9:127376363
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2162-7075C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376363 | ||||||
| chr9:127376453
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2162-6985A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376453 | ||||||
| chr9:127376470
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2162-6968G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376470 | ||||||
| chr9:127376479
|
G | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2162-6959G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376479 | ||||||
| chr9:127376498
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2162-6940A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376498 | ||||||
| chr9:127376508
|
G | A | 70 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2162-6930G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376508 | ||||||
| chr9:127376577
|
G | GCTTT | 43 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(40): Show | 43 | HG00423.hp1 HG01069.hp2 HG01496.hp1 others(40): Show |
intron_variant | MODIFIER | c.2162-6836_2162-683 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127376577 | |||||
| chr9:127376577
|
GCTTT | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0231 | 3 | HG00280.hp2 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2162-6836_2162-683 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127376577 | |||||
| chr9:127376598
|
C | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2162-6840C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376598 | ||||||
| chr9:127376784
|
C | T | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2162-6654C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376784 | ||||||
| chr9:127376855
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2162-6583C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127376855 | ||||||
| chr9:127377107
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0153 | 2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2162-6331A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377107 | ||||||
| chr9:127377330
|
AT | A | 63 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.2162-6106delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127377330 | |||||
| chr9:127377344
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2162-6094T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377344 | ||||||
| chr9:127377346
|
G | A | 2 | a0001c0002t0001g0119a0001c0002t0001g0121 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2162-6092G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377346 | ||||||
| chr9:127377398
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2162-6040A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377398 | ||||||
| chr9:127377486
|
T | C | 39 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 39 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.2162-5952T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377486 | ||||||
| chr9:127377498
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2162-5940A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377498 | ||||||
| chr9:127377750
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00735.hp2 HG01109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2162-5688T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377750 | ||||||
| chr9:127377792
|
C | CA | 6 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0142others(3): Show | 6 | HG01993.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2162-5625dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127377792 | |||||
| chr9:127377792
|
C | CAA | 18 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0046others(15): Show | 18 | HG01891.hp1 HG02027.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2162-5626_2162-562 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127377792 | |||||
| chr9:127377792
|
CA | C | 65 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(62): Show | 66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2162-5625delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127377792 | |||||
| chr9:127377792
|
CAA | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0042others(9): Show | 12 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2162-5626_2162-562 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127377792 | |||||
| chr9:127377899
|
G | C | 18 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0046others(15): Show | 18 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2162-5539G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127377899 | ||||||
| chr9:127378113
|
T | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2162-5325T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378113 | ||||||
| chr9:127378243
|
C | CAA | 12 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0032others(9): Show | 12 | HG02135.hp1 NA18945.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.2162-5177_2162-517 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378243 | |||||
| chr9:127378243
|
C | CAAAA | 18 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0105others(15): Show | 18 | HG00423.hp1 HG02027.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2162-5179_2162-517 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378243 | |||||
| chr9:127378243
|
CA | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(66): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2162-5176delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378243 | |||||
| chr9:127378253
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2162-5185A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378253 | ||||||
| chr9:127378337
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0152others(1): Show | 4 | NA18990.hp1 NA19007.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2162-5101C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378337 | ||||||
| chr9:127378384
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0189others(1): Show | 4 | HG02071.hp1 NA19009.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.2162-5054C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378384 | ||||||
| chr9:127378524
|
T | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 70 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2162-4914T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378524 | ||||||
| chr9:127378543
|
T | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2162-4895T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378543 | ||||||
| chr9:127378587
|
CA | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(100): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.2162-4833delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378587 | |||||
| chr9:127378587
|
CAA | C | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2162-4834_2162-483 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378587 | |||||
| chr9:127378587
|
CAAA | C | 36 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 36 | HG00423.hp1 HG01891.hp1 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.2162-4835_2162-483 others(7): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127378587 | |||||
| chr9:127378752
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2162-4686T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378752 | ||||||
| chr9:127378762
|
A | T | 16 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.2162-4676A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378762 | ||||||
| chr9:127378765
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2162-4673T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378765 | ||||||
| chr9:127378769
|
G | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(8): Show | 11 | HG02135.hp1 NA18950.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.2162-4669G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378769 | ||||||
| chr9:127378901
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2162-4537G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378901 | ||||||
| chr9:127378967
|
G | A | 3 | a0001c0002t0001g0193a0001c0002t0001g0214a0001c0002t0001g0215 | 3 | HG02622.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2162-4471G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127378967 | ||||||
| chr9:127379024
|
C | T | 1 | a0001c0006t0001g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2162-4414C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379024 | ||||||
| chr9:127379074
|
G | A | 64 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2162-4364G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379074 | ||||||
| chr9:127379259
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2162-4179C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379259 | ||||||
| chr9:127379761
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2162-3677G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379761 | ||||||
| chr9:127379797
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0261 | 2 | HG00438.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2162-3641T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379797 | ||||||
| chr9:127379846
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2162-3592T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379846 | ||||||
| chr9:127379908
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2162-3530G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379908 | ||||||
| chr9:127379918
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2162-3520A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379918 | ||||||
| chr9:127379932
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00735.hp2 HG01109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2162-3506C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379932 | ||||||
| chr9:127379978
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2162-3460G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379978 | ||||||
| chr9:127379996
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2162-3442A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127379996 | ||||||
| chr9:127380052
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2162-3386C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380052 | ||||||
| chr9:127380053
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2162-3385G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380053 | ||||||
| chr9:127380071
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2162-3367C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380071 | ||||||
| chr9:127380200
|
A | ATG | 41 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(38): Show | 43 | HG00099.hp2 HG00280.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.2162-3200_2162-319 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | ATGTG | 42 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 42 | HG00323.hp2 HG00642.hp1 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.2162-3202_2162-319 others(8): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | ATGTGTG | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(102): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2162-3204_2162-319 others(10): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | ATGTGTGT others(1): Show |
24 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0076others(21): Show | 24 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2162-3206_2162-319 others(12): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | ATGTGTGT others(3): Show |
14 | a0001c0001t0001g0078a0001c0001t0001g0089a0001c0001t0001g0090others(11): Show | 14 | HG00741.hp1 HG01099.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.2162-3208_2162-319 others(14): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0251 | 2 | HG01070.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.2162-3210_2162-319 others(16): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2162-3238A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380200 | ||||||
| chr9:127380200
|
ATG | A | 18 | a0001c0001t0001g0026a0001c0001t0001g0137a0001c0001t0001g0138others(15): Show | 18 | HG01258.hp2 HG01884.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.2162-3200_2162-319 others(6): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2162-3212_2162-319 others(18): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380200
|
ATGTGTGT others(11): Show |
A | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2162-3216_2162-319 others(22): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127380200 | |||||
| chr9:127380397
|
A | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(10): Show | 13 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.2162-3041A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380397 | ||||||
| chr9:127380453
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2162-2985G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380453 | ||||||
| chr9:127380475
|
C | T | 1 | a0001c0001t0001g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2162-2963C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380475 | ||||||
| chr9:127380572
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2162-2866G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380572 | ||||||
| chr9:127380644
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2162-2794G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380644 | ||||||
| chr9:127380719
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2162-2719C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380719 | ||||||
| chr9:127380834
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2162-2604A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380834 | ||||||
| chr9:127380902
|
G | T | 1 | a0006c0005t0001g0229 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2162-2536G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380902 | ||||||
| chr9:127380971
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2162-2467C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127380971 | ||||||
| chr9:127381129
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2162-2309G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381129 | ||||||
| chr9:127381129
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2162-2309G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381129 | ||||||
| chr9:127381136
|
CA | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2162-2298delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127381136 | |||||
| chr9:127381374
|
CT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2162-2055delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127381374 | |||||
| chr9:127381400
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG02074.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.2162-2038G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381400 | ||||||
| chr9:127381587
|
GCTTTTCT others(3): Show |
G | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG02155.hp2 NA18946.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.2162-1835_2162-182 others(14): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127381587 | |||||
| chr9:127381658
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2162-1780G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381658 | ||||||
| chr9:127381685
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2162-1753C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381685 | ||||||
| chr9:127381704
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2162-1734C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381704 | ||||||
| chr9:127381763
|
AT | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2162-1660delT | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr9 | 127381763 | |||||
| chr9:127381795
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG00642.hp1 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.2162-1643C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381795 | ||||||
| chr9:127381798
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(17): Show | 20 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2162-1640A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381798 | ||||||
| chr9:127381903
|
C | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 63 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2162-1535C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381903 | ||||||
| chr9:127381963
|
T | C | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2162-1475T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381963 | ||||||
| chr9:127381973
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2162-1465T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127381973 | ||||||
| chr9:127382154
|
G | C | 8 | a0001c0002t0001g0045a0001c0002t0001g0071a0001c0002t0001g0193others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2162-1284G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382154 | ||||||
| chr9:127382239
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2162-1199G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382239 | ||||||
| chr9:127382294
|
C | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0143others(9): Show | 12 | HG00438.hp1 HG00558.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.2162-1144C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382294 | ||||||
| chr9:127382309
|
A | T | 8 | a0001c0002t0001g0045a0001c0002t0001g0071a0001c0002t0001g0193others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2162-1129A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382309 | ||||||
| chr9:127382558
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2162-880G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382558 | ||||||
| chr9:127382621
|
A | T | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2162-817A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127382621 | ||||||
| chr9:127383345
|
G | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 83 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2162-93G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 22/27 | chr9 | 127383345 | ||||||
| chr9:127383601
|
T | C | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2269+56T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127383601 | ||||||
| chr9:127383764
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2269+219T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127383764 | ||||||
| chr9:127383909
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2269+364C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127383909 | ||||||
| chr9:127383937
|
A | C | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2269+392A>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127383937 | ||||||
| chr9:127383999
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18955.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2269+454G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127383999 | ||||||
| chr9:127384002
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2269+457G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384002 | ||||||
| chr9:127384058
|
G | A | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2269+513G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384058 | ||||||
| chr9:127384365
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0200others(1): Show | 4 | HG02129.hp2 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2270-662G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384365 | ||||||
| chr9:127384374
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2270-653G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384374 | ||||||
| chr9:127384437
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2270-590A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384437 | ||||||
| chr9:127384517
|
C | G | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2270-510C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384517 | ||||||
| chr9:127384690
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00735.hp2 HG01109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2270-337G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 23/27 | chr9 | 127384690 | ||||||
| chr9:127385327
|
G | A | 66 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.2388+182G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385327 | ||||||
| chr9:127385419
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0162a0001c0001t0001g0172others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2388+274G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385419 | ||||||
| chr9:127385700
|
A | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(55): Show | 59 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.2388+555A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385700 | ||||||
| chr9:127385739
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(50): Show | 54 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.2388+594C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385739 | ||||||
| chr9:127385902
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2388+757C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385902 | ||||||
| chr9:127385927
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2388+782T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385927 | ||||||
| chr9:127385987
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2388+842C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127385987 | ||||||
| chr9:127386041
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2388+896A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386041 | ||||||
| chr9:127386085
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2388+940A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386085 | ||||||
| chr9:127386198
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(7): Show | 10 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-995T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386198 | ||||||
| chr9:127386305
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2389-888T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386305 | ||||||
| chr9:127386335
|
C | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0075others(46): Show | 50 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2389-858C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386335 | ||||||
| chr9:127386461
|
G | A | 71 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2389-732G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386461 | ||||||
| chr9:127386492
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2389-701G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386492 | ||||||
| chr9:127386502
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2389-691C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386502 | ||||||
| chr9:127386536
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2389-657A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386536 | ||||||
| chr9:127386546
|
T | G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2389-647T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386546 | ||||||
| chr9:127386668
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2389-525T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386668 | ||||||
| chr9:127386683
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2389-510G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386683 | ||||||
| chr9:127386790
|
A | G | 1 | a0004c0007t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2389-403A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386790 | ||||||
| chr9:127386843
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2389-350A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127386843 | ||||||
| chr9:127387041
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2389-152G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127387041 | ||||||
| chr9:127387124
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2389-69G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 24/27 | chr9 | 127387124 | ||||||
| chr9:127387371
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02055.hp1 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2527+40T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127387371 | ||||||
| chr9:127387392
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2527+61G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127387392 | ||||||
| chr9:127387481
|
C | G | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2527+150C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127387481 | ||||||
| chr9:127387743
|
C | CA | 13 | a0001c0001t0001g0209a0001c0001t0001g0249a0001c0001t0001g0280others(10): Show | 13 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2527+429dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 127387743 | |||||
| chr9:127387999
|
A | G | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2527+668A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127387999 | ||||||
| chr9:127388315
|
C | CA | 13 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0162others(10): Show | 14 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2528-571dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 127388315 | |||||
| chr9:127388315
|
CA | C | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2528-571delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 127388315 | |||||
| chr9:127388315
|
CAA | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(13): Show | 16 | HG02129.hp1 HG02135.hp1 HG03491.hp1 others(13): Show |
intron_variant | MODIFIER | c.2528-572_2528-571d others(4): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 127388315 | |||||
| chr9:127388342
|
G | T | 2 | a0001c0001t0001g0019a0001c0002t0001g0031 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2528-562G>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388342 | ||||||
| chr9:127388505
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2528-399G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388505 | ||||||
| chr9:127388597
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2528-307G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388597 | ||||||
| chr9:127388651
|
G | A | 8 | a0001c0002t0001g0045a0001c0002t0001g0071a0001c0002t0001g0193others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2528-253G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388651 | ||||||
| chr9:127388655
|
A | AGTCTTTT others(4): Show |
1 | a0001c0001t0001g0247 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2528-248_2528-238d others(13): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 127388655 | |||||
| chr9:127388753
|
C | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 68 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2528-151C>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388753 | ||||||
| chr9:127388847
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2528-57G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 25/27 | chr9 | 127388847 | ||||||
| chr9:127389305
|
T | C | 69 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0056others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.2743+186T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389305 | ||||||
| chr9:127389315
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2743+196A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389315 | ||||||
| chr9:127389603
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0200others(1): Show | 4 | HG02129.hp2 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2743+484G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389603 | ||||||
| chr9:127389647
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(10): Show | 13 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.2743+528C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389647 | ||||||
| chr9:127389659
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2743+540C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389659 | ||||||
| chr9:127389667
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2743+548T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389667 | ||||||
| chr9:127389675
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2743+556T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389675 | ||||||
| chr9:127389798
|
A | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(10): Show | 13 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.2743+679A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389798 | ||||||
| chr9:127389853
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2743+734C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127389853 | ||||||
| chr9:127389921
|
T | TA | 71 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 72 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2744-694dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr9 | 127389921 | |||||
| chr9:127389921
|
TA | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(34): Show | 37 | HG01069.hp1 HG01358.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.2744-694delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr9 | 127389921 | |||||
| chr9:127390147
|
A | T | 63 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0061others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.2744-494A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127390147 | ||||||
| chr9:127390243
|
T | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2744-398T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127390243 | ||||||
| chr9:127390537
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2744-104A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 26/27 | chr9 | 127390537 | ||||||
| chr9:127390777
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2870+10G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127390777 | ||||||
| chr9:127390832
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2870+65G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127390832 | ||||||
| chr9:127390923
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0081others(10): Show | 13 | HG02129.hp1 HG02135.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.2870+156C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127390923 | ||||||
| chr9:127390945
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2870+178C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127390945 | ||||||
| chr9:127390954
|
T | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG02074.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.2870+187T>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127390954 | ||||||
| chr9:127391058
|
G | A | 8 | a0001c0002t0001g0045a0001c0002t0001g0071a0001c0002t0001g0193others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2870+291G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391058 | ||||||
| chr9:127391121
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2870+354C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391121 | ||||||
| chr9:127391291
|
T | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2870+524T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391291 | ||||||
| chr9:127391406
|
T | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0228 | 2 | HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2870+639T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391406 | ||||||
| chr9:127391470
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2870+703C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391470 | ||||||
| chr9:127391495
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2870+728C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391495 | ||||||
| chr9:127391524
|
C | CA | 29 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00735.hp2 HG01109.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2870+767dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391524 | |||||
| chr9:127391524
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG02074.hp2 NA18953.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(15): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391524 | |||||
| chr9:127391524
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(16): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391524 | |||||
| chr9:127391533
|
A | AAAAAAAA others(64): Show |
1 | a0001c0001t0001g0078 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(73): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(39): Show |
1 | a0004c0007t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(48): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(40): Show |
1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(49): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(52): Show |
2 | a0001c0001t0001g0257a0002c0010t0001g0065 | 2 | HG03669.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(61): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(56): Show |
1 | a0001c0001t0001g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(65): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(62): Show |
1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(71): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(53): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0146 | 2 | HG01081.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(62): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(57): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG00140.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(66): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(63): Show |
1 | a0001c0001t0001g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(72): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(50): Show |
1 | a0001c0001t0001g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(59): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(54): Show |
1 | a0001c0001t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(63): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(56): Show |
1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(65): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(58): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0132others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(67): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(35): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0256 | 2 | HG01346.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(44): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(49): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0094 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(58): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(51): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0147 | 2 | NA18988.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(60): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(57): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0154 | 2 | NA19064.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(66): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(36): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0283 | 3 | HG01071.hp2 HG02165.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(45): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(47): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(40): Show |
2 | a0001c0001t0001g0201a0001c0001t0001g0227 | 2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(49): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0001g0102 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(53): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(54): Show |
1 | a0001c0001t0001g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(63): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(62): Show |
1 | a0001c0001t0001g0284 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(71): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(68): Show |
1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(77): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(33): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0195 | 3 | HG01433.hp1 HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(42): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0092 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(44): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(43): Show |
1 | a0001c0001t0001g0103 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(52): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(51): Show |
1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(60): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(53): Show |
1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(62): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(59): Show |
1 | a0001c0001t0001g0077 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(68): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(61): Show |
1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(70): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(20): Show |
5 | a0001c0001t0001g0249a0001c0001t0001g0252a0001c0001t0001g0258others(2): Show | 5 | HG01099.hp1 HG03239.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0285 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(31): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(47): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(42): Show |
1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(51): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(53): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(56): Show |
1 | a0001c0001t0001g0152 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(65): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0228 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(26): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0181 | 3 | HG00280.hp1 HG00323.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(28): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(21): Show |
12 | a0001c0001t0001g0136a0001c0001t0001g0166a0001c0001t0001g0220others(9): Show | 12 | HG01952.hp1 HG02004.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(30): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0230a0001c0001t0001g0264 | 2 | NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(32): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(43): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0104 | 2 | NA18980.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(52): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(45): Show |
2 | a0001c0001t0001g0226a0001c0001t0001g0269 | 2 | HG02056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(54): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(57): Show |
1 | a0001c0001t0001g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(66): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(20): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0159others(11): Show | 14 | HG00558.hp1 HG00673.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2870+767_2870+768i others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0271a0007c0004t0001g0157 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(31): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0001g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(43): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(40): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0056 | 2 | NA18964.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(49): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(42): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | NA18942.hp1 NA19077.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(51): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(53): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(48): Show |
1 | a0001c0001t0001g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(57): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0251a0001c0001t0001g0266 | 2 | HG01070.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(28): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(30): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0255 | 2 | HG00609.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(32): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(43): Show |
3 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0225 | 3 | HG01358.hp2 HG02723.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(52): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(53): Show |
1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(62): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0278 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(27): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(20): Show |
3 | a0001c0001t0001g0167a0001c0001t0001g0168a0003c0003t0001g0069 | 3 | HG02257.hp1 NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(31): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(48): Show |
1 | a0001c0001t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(57): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(28): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0001g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(42): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0002g0224 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(48): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(48): Show |
1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(57): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(29): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAGAA others(17): Show |
1 | a0001c0002t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2870+767_2870+768i others(26): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAGAA others(29): Show |
2 | a0001c0002t0001g0214a0001c0002t0001g0288 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(38): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAGAA others(31): Show |
2 | a0001c0002t0001g0193a0001c0002t0001g0215 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(40): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAGAA others(33): Show |
1 | a0001c0002t0001g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2870+767_2870+768i others(42): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | AAAAAGAA others(35): Show |
2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2870+767_2870+768i others(44): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391533 | |||||
| chr9:127391533
|
A | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0210a0001c0001t0001g0212 | 3 | HG00735.hp1 HG01515.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2870+766A>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391533 | ||||||
| chr9:127391535
|
T | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 48 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2870+768T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391535 | ||||||
| chr9:127391537
|
T | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG00735.hp2 HG02074.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2870+770T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391537 | ||||||
| chr9:127391539
|
T | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02074.hp2 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.2870+772T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391539 | ||||||
| chr9:127391552
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(7): Show | 10 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2870+785A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391552 | ||||||
| chr9:127391610
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2870+843A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127391610 | ||||||
| chr9:127391700
|
C | CA | 22 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG00735.hp2 HG01109.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2870+951dupA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391700 | |||||
| chr9:127391700
|
CA | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(74): Show | 78 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2870+951delA | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr9 | 127391700 | |||||
| chr9:127392209
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2871-874G>C | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392209 | ||||||
| chr9:127392329
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2871-754C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392329 | ||||||
| chr9:127392418
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2871-665G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392418 | ||||||
| chr9:127392420
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2871-663G>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392420 | ||||||
| chr9:127392703
|
T | A | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2871-380T>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392703 | ||||||
| chr9:127392825
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(9): Show | 12 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2871-258C>T | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392825 | ||||||
| chr9:127392868
|
A | AG | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG02074.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.2871-215_2871-214i others(3): Show |
GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392868 | ||||||
| chr9:127392869
|
C | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG02074.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.2871-214C>A | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392869 | ||||||
| chr9:127392978
|
T | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2871-105T>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127392978 | ||||||
| chr9:127393052
|
A | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2871-31A>G | GARNL3 | ENSG00000136895.19 | transcript | ENST00000373387.9 | protein_coding | 27/27 | chr9 | 127393052 |