Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64395 |
| ensemblid | ENSG00000087338.5 |
| hgncid | 23843 |
| symbol | GMCL1 |
| name | germ cell-less 1, spermatogenesis associated |
| refseq_nuc | NM_178439.5 |
| refseq_prot | NP_848526.1 |
| ensembl_nuc | ENST00000282570.4 |
| ensembl_prot | ENSP00000282570.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 69829660 |
| end | 69881384 |
| strand | + |
| ver | v1.2 |
| region | chr2:69829660-69881384 |
| region5000 | chr2:69824660-69886384 |
| regionname0 | GMCL1_chr2_69829660_69881384 |
| regionname5000 | GMCL1_chr2_69824660_69886384 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 515 | 385 | 90 | 66 | 179 | 14 | 34 | 141 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| a0002 | 0/0 | 515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| a0003 | 0/0 | 515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| a0004 | 0/0 | 515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| a0005 | 0/0 | 515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| a0006 | 0/0 | 515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | MGSLS others(510): Show |
chr2 | 69824660 | 69886384 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1545 | 327 | 75 | 42 | 160 | 14 | 34 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0002 | 0/0 | 1545 | 50 | 10 | 22 | 18 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0003 | 0/0 | 1545 | 3 | 3 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0004 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0005 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0007 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0001c0010 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0002c0012 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0003c0006 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0004c0009 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0005c0008 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 | ||
| a0006c0011 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | ATGGG others(1540): Show |
chr2 | 69824660 | 69886384 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4159 | 93 | 10 | 6 | 61 | 3 | 12 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0002 | 1/0 | 4161 | 82 | 11 | 16 | 37 | 6 | 11 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0003 | 0/0 | 4159 | 80 | 24 | 12 | 38 | 2 | 4 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0005 | 0/0 | 4161 | 16 | 14 | 2 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0007 | 0/0 | 4159 | 10 | 1 | 0 | 2 | 1 | 6 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0008 | 0/0 | 4158 | 5 | 0 | 0 | 4 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4153): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0009 | 0/0 | 4160 | 4 | 0 | 1 | 2 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0010 | 0/0 | 4160 | 3 | 3 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0011 | 0/0 | 4161 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0012 | 0/0 | 4160 | 3 | 0 | 2 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0013 | 0/0 | 4161 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0015 | 0/0 | 4159 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0016 | 0/0 | 4160 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0017 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0018 | 0/0 | 4160 | 2 | 1 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0020 | 0/0 | 4159 | 2 | 0 | 0 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0021 | 0/0 | 4159 | 2 | 0 | 0 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0022 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0023 | 0/0 | 4160 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0024 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0025 | 0/0 | 4158 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4153): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0026 | 0/0 | 4159 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0028 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0029 | 0/0 | 4158 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4153): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0030 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0031 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0032 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0033 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0001t0034 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0002t0004 | 0/0 | 4159 | 29 | 6 | 12 | 11 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0002t0006 | 0/0 | 4160 | 16 | 0 | 9 | 7 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0002t0007 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0002t0019 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0002t0027 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0003t0004 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0001c0003t0006 | 0/0 | 4160 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0004t0014 | 0/0 | 4160 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0005t0002 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0001c0007t0014 | 0/0 | 4160 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4155): Show |
chr2 | 69824660 | 69886384 |
| a0001c0010t0001 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0002c0012t0001 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0003c0006t0004 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| a0004c0009t0002 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0005c0008t0005 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4156): Show |
chr2 | 69824660 | 69886384 |
| a0006c0011t0001 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | GCTTT others(4154): Show |
chr2 | 69824660 | 69886384 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0001 | 0/0 | 6 | 1 | 0 | 1 | 3 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0030 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0003 | 0/0 | 5 | 1 | 2 | 1 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0011g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0012g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0013g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0013g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0016g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0016g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0018g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0018g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0020g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0020g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0021g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0022g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0023g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0024g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0026g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0028g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0029g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0030g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0031g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0032g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0033g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0001t0034g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0019g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0002t0027g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0003t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0003t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0003t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0004t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0004t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0005t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0007t0014g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0001c0010t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0002c0012t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0003c0006t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0004c0009t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0005c0008t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| a0006c0011t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0208 | EUR | GBR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0062 | EUR | FIN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00323 | hp1 | a0001 | c0001 | t0032 | g0258 | EUR | FIN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0304 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00423 | hp2 | a0001 | c0001 | t0015 | g0154 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00438 | hp2 | a0001 | c0001 | t0021 | g0175 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00597 | hp1 | a0002 | c0012 | t0001 | g0168 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00642 | hp1 | a0001 | c0002 | t0006 | g0002 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00673 | hp1 | a0001 | c0001 | t0021 | g0163 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0002 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0317 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG00741 | hp2 | a0001 | c0007 | t0014 | g0181 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01099 | hp2 | a0001 | c0002 | t0006 | g0002 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01106 | hp1 | a0001 | c0002 | t0006 | g0033 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01167 | hp2 | a0001 | c0001 | t0018 | g0036 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01169 | hp1 | a0001 | c0001 | t0026 | g0035 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01175 | hp1 | a0001 | c0002 | t0027 | g0308 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01192 | hp1 | a0001 | c0001 | t0012 | g0064 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0033 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01255 | hp1 | a0001 | c0005 | t0002 | g0218 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0318 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01257 | hp2 | a0001 | c0001 | t0012 | g0065 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01261 | hp2 | a0001 | c0002 | t0006 | g0002 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01346 | hp1 | a0001 | c0002 | t0006 | g0002 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0305 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01361 | hp1 | a0001 | c0002 | t0004 | g0314 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0173 | EUR | IBS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0329 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01928 | hp1 | a0001 | c0002 | t0004 | g0315 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01952 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01975 | hp1 | a0001 | c0001 | t0033 | g0136 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01975 | hp2 | a0001 | c0002 | t0006 | g0002 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01981 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02004 | hp1 | a0001 | c0002 | t0006 | g0322 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02074 | hp1 | a0001 | c0002 | t0004 | g0313 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02083 | hp2 | a0001 | c0010 | t0001 | g0137 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CDX | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0302 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0288 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0306 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0293 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02523 | hp1 | a0004 | c0009 | t0002 | g0271 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | KHV | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02622 | hp1 | a0001 | c0001 | t0023 | g0289 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02622 | hp2 | a0001 | c0002 | t0019 | g0115 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0034 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0323 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0110 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02818 | hp1 | a0001 | c0001 | t0025 | g0042 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02886 | hp1 | a0001 | c0001 | t0031 | g0108 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02895 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0287 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02922 | hp1 | a0001 | c0004 | t0014 | g0111 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02965 | hp1 | a0001 | c0001 | t0024 | g0292 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0325 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0324 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0214 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03041 | hp2 | a0005 | c0008 | t0005 | g0031 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03453 | hp1 | a0001 | c0004 | t0014 | g0112 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03486 | hp1 | a0001 | c0002 | t0019 | g0114 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0270 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0213 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0303 | AFR | ESN | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0321 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0215 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0252 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0025 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0294 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18940 | hp1 | a0006 | c0011 | t0001 | g0124 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18941 | hp1 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18941 | hp2 | a0001 | c0001 | t0015 | g0158 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18950 | hp2 | a0001 | c0001 | t0028 | g0017 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18961 | hp2 | a0001 | c0001 | t0008 | g0198 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0312 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0320 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0242 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18971 | hp1 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18978 | hp1 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0307 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18981 | hp2 | a0001 | c0001 | t0013 | g0209 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18982 | hp1 | a0001 | c0001 | t0029 | g0060 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18990 | hp2 | a0001 | c0002 | t0006 | g0328 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0254 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19004 | hp1 | a0001 | c0001 | t0020 | g0222 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0241 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19010 | hp2 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19011 | hp1 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19030 | hp1 | a0001 | c0001 | t0034 | g0199 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0109 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19056 | hp1 | a0001 | c0001 | t0008 | g0139 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0319 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0330 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0156 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19065 | hp1 | a0001 | c0001 | t0020 | g0223 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0310 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19072 | hp1 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19072 | hp2 | a0001 | c0001 | t0011 | g0268 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19074 | hp2 | a0001 | c0002 | t0006 | g0301 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0309 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19086 | hp2 | a0001 | c0002 | t0004 | g0331 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0332 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0327 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA19240 | hp2 | a0001 | c0003 | t0006 | g0326 | AFR | YRI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0216 | AFR | ASW | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0277 | EUR | TSI | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | GIH | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02486 | hp1 | a0003 | c0006 | t0004 | g0300 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02559 | hp1 | a0001 | c0001 | t0030 | g0082 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0291 | AFR | ACB | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | USA | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | USA | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0295 | AFR | LWK | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0146 | REF | REF | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0030 | REF | REF | GMCL1_chr2_69824660_69886384 | GMCL1 | chr2 | 69824660 | 69886384 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69854906 | A | G | 1 | a0002 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1018A>G | p.Ile340Val | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/14 | 1251/4161 | 1018/1548 | 340/515 | chr2 | 69854906 | |||
| chr2:69864908 | A | C | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1151A>C | p.Glu384Ala | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1384/4161 | 1151/1548 | 384/515 | chr2 | 69864908 | |||
| chr2:69864909 | A | T | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1152A>T | p.Glu384Asp | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1385/4161 | 1152/1548 | 384/515 | chr2 | 69864909 | |||
| chr2:69864913 | A | C | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1156A>C | p.Asn386His | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1389/4161 | 1156/1548 | 386/515 | chr2 | 69864913 | |||
| chr2:69864917 | A | G | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1160A>G | p.Lys387Arg | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1393/4161 | 1160/1548 | 387/515 | chr2 | 69864917 | |||
| chr2:69864918 | A | T | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1161A>T | p.Lys387Asn | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1394/4161 | 1161/1548 | 387/515 | chr2 | 69864918 | |||
| chr2:69864921 | A | T | 1 | a0006 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1164A>T | p.Glu388Asp | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1397/4161 | 1164/1548 | 388/515 | chr2 | 69864921 | |||
| chr2:69869846 | G | A | 1 | a0003 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1346G>A | p.Arg449Gln | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/14 | 1579/4161 | 1346/1548 | 449/515 | chr2 | 69869846 | |||
| chr2:69871750 | G | A | 1 | a0005 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1370G>A | p.Arg457His | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/14 | 1603/4161 | 1370/1548 | 457/515 | chr2 | 69871750 | |||
| chr2:69871756 | C | T | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1376C>T | p.Ala459Val | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/14 | 1609/4161 | 1376/1548 | 459/515 | chr2 | 69871756 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69837568 | T | C | 1 | a0001c0005 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.282T>C | p.Ser94Ser | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/14 | 515/4161 | 282/1548 | 94/515 | chr2 | 69837568 | |||
| chr2:69843151 | C | T | 1 | a0001c0004 | 2 | HG02922.hp1 HG03453.hp1 |
splice_region_variant&synonymous_variant | LOW | c.582C>T | p.Asp194Asp | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/14 | 815/4161 | 582/1548 | 194/515 | chr2 | 69843151 | |||
| chr2:69843259 | A | G | 1 | a0001c0003 | 3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
splice_region_variant&synonymous_variant | LOW | c.690A>G | p.Lys230Lys | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/14 | 923/4161 | 690/1548 | 230/515 | chr2 | 69843259 | |||
| chr2:69844173 | T | C | 3 | a0001c0002 a0001c0003 a0003c0006 |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
synonymous_variant | LOW | c.735T>C | p.Asn245Asn | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/14 | 968/4161 | 735/1548 | 245/515 | chr2 | 69844173 | |||
| chr2:69864912 | C | A | 1 | a0006c0011 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.1155C>A | p.Ile385Ile | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/14 | 1388/4161 | 1155/1548 | 385/515 | chr2 | 69864912 | |||
| chr2:69869730 | T | C | 1 | a0001c0007 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1230T>C | p.Arg410Arg | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/14 | 1463/4161 | 1230/1548 | 410/515 | chr2 | 69869730 | |||
| chr2:69869796 | A | G | 1 | a0001c0010 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1296A>G | p.Lys432Lys | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/14 | 1529/4161 | 1296/1548 | 432/515 | chr2 | 69869796 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69829734 | A | G | 11 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(8): Show |
110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-159A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/14 | 159 | chr2 | 69829734 | ||||||
| chr2:69829814 | G | A | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0016 others(4): Show |
25 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/14 | 79 | chr2 | 69829814 | ||||||
| chr2:69879063 | G | A | 1 | a0001c0001t0011 | 3 | NA18993.hp2 NA19007.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*59G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 59 | chr2 | 69879063 | ||||||
| chr2:69879113 | T | C | 1 | a0001c0001t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 109 | chr2 | 69879113 | ||||||
| chr2:69879700 | T | C | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*696T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 696 | chr2 | 69879700 | ||||||
| chr2:69879824 | A | C | 1 | a0001c0001t0031 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 820 | chr2 | 69879824 | ||||||
| chr2:69879936 | C | A | 1 | a0001c0001t0013 | 3 | NA18971.hp1 NA18978.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 932 | chr2 | 69879936 | ||||||
| chr2:69880196 | G | A | 2 | a0001c0001t0017 a0001c0001t0031 |
3 | HG02647.hp2 HG02886.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1192G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1192 | chr2 | 69880196 | ||||||
| chr2:69880263 | A | G | 1 | a0001c0001t0032 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1259A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1259 | chr2 | 69880263 | ||||||
| chr2:69880277 | A | G | 6 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0021 others(3): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1273A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1273 | chr2 | 69880277 | ||||||
| chr2:69880496 | A | C | 1 | a0001c0001t0034 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1492 | chr2 | 69880496 | ||||||
| chr2:69880608 | G | T | 1 | a0001c0001t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1604G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1604 | chr2 | 69880608 | ||||||
| chr2:69880721 | G | A | 2 | a0001c0001t0017 a0001c0001t0031 |
3 | HG02647.hp2 HG02886.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1717G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1717 | chr2 | 69880721 | ||||||
| chr2:69880735 | C | G | 1 | a0001c0001t0030 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1731C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1731 | chr2 | 69880735 | ||||||
| chr2:69880739 | T | A | 1 | a0001c0001t0030 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1735T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1735 | chr2 | 69880739 | ||||||
| chr2:69880740 | C | A | 1 | a0001c0001t0030 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1736C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1736 | chr2 | 69880740 | ||||||
| chr2:69880758 | G | A | 2 | a0001c0001t0022 a0001c0001t0023 |
2 | HG02280.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1754G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1754 | chr2 | 69880758 | ||||||
| chr2:69880791 | T | C | 1 | a0001c0001t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1787T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1787 | chr2 | 69880791 | ||||||
| chr2:69880803 | G | C | 1 | a0001c0001t0016 | 2 | HG02451.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1799G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1799 | chr2 | 69880803 | ||||||
| chr2:69880826 | C | T | 1 | a0001c0001t0015 | 3 | HG00423.hp2 NA18941.hp2 NA19072.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1822C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1822 | chr2 | 69880826 | ||||||
| chr2:69880842 | C | T | 1 | a0001c0002t0019 | 2 | HG02622.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1838C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1838 | chr2 | 69880842 | ||||||
| chr2:69880843 | G | A | 2 | a0001c0001t0018 a0001c0001t0026 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1839G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1839 | chr2 | 69880843 | ||||||
| chr2:69880847 | CA | C | 10 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(7): Show |
35 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1864delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1864 | INFO_REALIGN_3_PRIME | chr2 | 69880847 | |||||
| chr2:69880847 | CAA | C | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(18): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*1863_*1864delAA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1863 | INFO_REALIGN_3_PRIME | chr2 | 69880847 | |||||
| chr2:69880847 | CAAA | C | 3 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0029 |
7 | HG01515.hp2 HG02523.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1862_*1864delAAA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1862 | INFO_REALIGN_3_PRIME | chr2 | 69880847 | |||||
| chr2:69880939 | C | T | 6 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0027 others(3): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1935C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 1935 | chr2 | 69880939 | ||||||
| chr2:69881124 | T | A | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*2120T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 2120 | chr2 | 69881124 | ||||||
| chr2:69881315 | C | T | 1 | a0001c0001t0028 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2311C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 14/14 | 2311 | chr2 | 69881315 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69830232 | CG | C | 64 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0279 others(61): Show |
76 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.260+84delG | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69830232 | ||||||
| chr2:69830301 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.260+149C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830301 | |||||||
| chr2:69830316 | T | G | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.260+164T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830316 | |||||||
| chr2:69830368 | T | C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.260+216T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830368 | |||||||
| chr2:69830418 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.260+266G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830418 | |||||||
| chr2:69830468 | A | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01169.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.260+316A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830468 | |||||||
| chr2:69830643 | C | G | 2 | a0001c0001t0002g0274 a0001c0001t0002g0275 |
2 | HG02074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.260+491C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830643 | |||||||
| chr2:69830681 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+529G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830681 | |||||||
| chr2:69830720 | A | ATG | 40 | a0001c0001t0007g0327 a0001c0002t0004g0002 a0001c0002t0004g0011 others(37): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.260+570_260+571dup others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69830720 | ||||||
| chr2:69830763 | CT | C | 155 | a0001c0001t0001g0113 a0001c0001t0002g0013 a0001c0001t0002g0014 others(152): Show |
182 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.260+627delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69830763 | ||||||
| chr2:69830770 | T | C | 40 | a0001c0001t0007g0327 a0001c0002t0004g0002 a0001c0002t0004g0011 others(37): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.260+618T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830770 | |||||||
| chr2:69830893 | G | A | 24 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0279 others(21): Show |
25 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.260+741G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69830893 | |||||||
| chr2:69831328 | C | G | 40 | a0001c0001t0007g0327 a0001c0002t0004g0002 a0001c0002t0004g0011 others(37): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.260+1176C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831328 | |||||||
| chr2:69831365 | TA | T | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.260+1214delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831365 | |||||||
| chr2:69831416 | G | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260+1264G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831416 | |||||||
| chr2:69831477 | C | G | 2 | a0001c0001t0005g0298 a0001c0001t0005g0299 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.260+1325C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831477 | |||||||
| chr2:69831639 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.260+1487G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831639 | |||||||
| chr2:69831751 | C | G | 2 | a0001c0001t0005g0296 a0001c0001t0005g0297 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.260+1599C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831751 | |||||||
| chr2:69831863 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.260+1711C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831863 | |||||||
| chr2:69831948 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260+1796C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69831948 | |||||||
| chr2:69832155 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.260+2003G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832155 | |||||||
| chr2:69832219 | C | CA | 29 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0002g0207 others(26): Show |
30 | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.260+2083dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69832219 | ||||||
| chr2:69832219 | CA | C | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0002g0272 others(3): Show |
6 | HG02523.hp1 HG02897.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.260+2083delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69832219 | ||||||
| chr2:69832314 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.260+2162T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832314 | |||||||
| chr2:69832377 | A | C | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+2225A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832377 | |||||||
| chr2:69832399 | G | A | 1 | a0001c0001t0007g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.260+2247G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832399 | |||||||
| chr2:69832402 | C | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.260+2250C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832402 | |||||||
| chr2:69832421 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.260+2269T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832421 | |||||||
| chr2:69832457 | C | CACAT | 17 | a0001c0001t0003g0044 a0001c0001t0005g0031 a0001c0001t0005g0032 others(14): Show |
18 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.260+2319_260+2322d others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69832457 | ||||||
| chr2:69832475 | T | C | 86 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0038 others(83): Show |
101 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.260+2323T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832475 | |||||||
| chr2:69832666 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.260+2514G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832666 | |||||||
| chr2:69832692 | G | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.260+2540G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832692 | |||||||
| chr2:69832720 | T | C | 1 | a0001c0001t0013g0209 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.260+2568T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832720 | |||||||
| chr2:69832867 | A | G | 3 | a0001c0002t0004g0330 a0001c0002t0004g0331 a0001c0002t0004g0332 |
3 | NA19060.hp2 NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.260+2715A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69832867 | |||||||
| chr2:69833087 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.260+2935C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833087 | |||||||
| chr2:69833101 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.260+2949A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833101 | |||||||
| chr2:69833146 | T | G | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.260+2994T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833146 | |||||||
| chr2:69833167 | A | G | 1 | a0001c0001t0010g0295 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260+3015A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833167 | |||||||
| chr2:69833235 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.260+3083G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833235 | |||||||
| chr2:69833248 | C | CAGAATTT others(3963): Show |
1 | a0001c0001t0003g0045 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.260+3113_260+3114i others(3972): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 69833248 | ||||||
| chr2:69833274 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0037 others(31): Show |
37 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.260+3122G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833274 | |||||||
| chr2:69833433 | A | C | 24 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0279 others(21): Show |
25 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.260+3281A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833433 | |||||||
| chr2:69833459 | T | C | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.260+3307T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833459 | |||||||
| chr2:69833488 | C | T | 1 | a0001c0002t0004g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.260+3336C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833488 | |||||||
| chr2:69833686 | T | C | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.260+3534T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833686 | |||||||
| chr2:69833774 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.260+3622A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833774 | |||||||
| chr2:69833890 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0047 |
3 | HG01884.hp2 HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.261-3657G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69833890 | |||||||
| chr2:69834368 | C | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0006c0011t0001g0124 |
3 | NA18940.hp1 NA18947.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.261-3179C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834368 | |||||||
| chr2:69834389 | T | C | 2 | a0001c0002t0006g0010 a0001c0002t0006g0301 |
4 | HG00408.hp2 NA18941.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-3158T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834389 | |||||||
| chr2:69834431 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.261-3116G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834431 | |||||||
| chr2:69834456 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.261-3091G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834456 | |||||||
| chr2:69834473 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.261-3074T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834473 | |||||||
| chr2:69834753 | C | T | 1 | a0001c0001t0005g0287 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.261-2794C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834753 | |||||||
| chr2:69834770 | T | C | 2 | a0001c0001t0022g0288 a0001c0001t0023g0289 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.261-2777T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834770 | |||||||
| chr2:69834800 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.261-2747T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834800 | |||||||
| chr2:69834876 | C | G | 3 | a0001c0001t0017g0109 a0001c0001t0017g0110 a0001c0001t0031g0108 |
3 | HG02647.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.261-2671C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834876 | |||||||
| chr2:69834962 | C | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-2585C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834962 | |||||||
| chr2:69834999 | A | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.261-2548A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69834999 | |||||||
| chr2:69835084 | C | T | 3 | a0001c0001t0017g0109 a0001c0001t0017g0110 a0001c0001t0031g0108 |
3 | HG02647.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.261-2463C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835084 | |||||||
| chr2:69835144 | C | T | 86 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0038 others(83): Show |
101 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.261-2403C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835144 | |||||||
| chr2:69835228 | T | C | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.261-2319T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835228 | |||||||
| chr2:69835287 | C | T | 1 | a0001c0001t0034g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.261-2260C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835287 | |||||||
| chr2:69835316 | A | G | 6 | a0001c0001t0005g0032 a0001c0001t0005g0283 a0001c0001t0005g0284 others(3): Show |
7 | HG01167.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-2231A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835316 | |||||||
| chr2:69835322 | G | T | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
290 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.261-2225G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835322 | |||||||
| chr2:69835365 | G | A | 2 | a0001c0002t0004g0302 a0001c0002t0004g0303 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.261-2182G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835365 | |||||||
| chr2:69835424 | G | C | 1 | a0001c0001t0005g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261-2123G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835424 | |||||||
| chr2:69835498 | T | G | 40 | a0001c0001t0007g0327 a0001c0002t0004g0002 a0001c0002t0004g0011 others(37): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.261-2049T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835498 | |||||||
| chr2:69835657 | A | C | 1 | a0001c0001t0002g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.261-1890A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835657 | |||||||
| chr2:69835807 | T | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
194 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.261-1740T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835807 | |||||||
| chr2:69835895 | A | C | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.261-1652A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69835895 | |||||||
| chr2:69836146 | C | T | 1 | a0001c0001t0008g0198 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.261-1401C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836146 | |||||||
| chr2:69836183 | C | T | 79 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(76): Show |
91 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.261-1364C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836183 | |||||||
| chr2:69836251 | T | C | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-1296T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836251 | |||||||
| chr2:69836340 | T | C | 1 | a0001c0001t0003g0049 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.261-1207T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836340 | |||||||
| chr2:69836395 | C | T | 95 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0038 others(92): Show |
110 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.261-1152C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836395 | |||||||
| chr2:69836431 | G | C | 262 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
300 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.261-1116G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836431 | |||||||
| chr2:69836440 | C | T | 1 | a0001c0002t0006g0328 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.261-1107C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836440 | |||||||
| chr2:69836443 | G | A | 47 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(44): Show |
59 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.261-1104G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836443 | |||||||
| chr2:69836454 | A | G | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.261-1093A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836454 | |||||||
| chr2:69836528 | A | G | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
291 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.261-1019A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836528 | |||||||
| chr2:69836586 | C | T | 30 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(27): Show |
33 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.261-961C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836586 | |||||||
| chr2:69836641 | G | A | 75 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(72): Show |
90 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.261-906G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836641 | |||||||
| chr2:69836828 | T | C | 20 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(17): Show |
23 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.261-719T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836828 | |||||||
| chr2:69836857 | A | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261-690A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69836857 | |||||||
| chr2:69837023 | C | G | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
289 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.261-524C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837023 | |||||||
| chr2:69837065 | A | G | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.261-482A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837065 | |||||||
| chr2:69837148 | A | G | 30 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(27): Show |
33 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.261-399A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837148 | |||||||
| chr2:69837253 | C | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261-294C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837253 | |||||||
| chr2:69837269 | A | G | 5 | a0001c0001t0002g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-278A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837269 | |||||||
| chr2:69837287 | G | A | 6 | a0001c0001t0010g0290 a0001c0001t0010g0291 a0001c0001t0010g0295 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-260G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837287 | |||||||
| chr2:69837300 | C | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-247C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837300 | |||||||
| chr2:69837303 | C | T | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.261-244C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 1/13 | chr2 | 69837303 | |||||||
| chr2:69837708 | T | G | 1 | a0001c0005t0002g0218 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.384+38T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69837708 | |||||||
| chr2:69837795 | C | A | 123 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(120): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.384+125C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69837795 | |||||||
| chr2:69838003 | C | T | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.384+333C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838003 | |||||||
| chr2:69838009 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0006c0011t0001g0124 |
3 | NA18940.hp1 NA18947.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.384+339G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838009 | |||||||
| chr2:69838138 | G | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.384+468G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838138 | |||||||
| chr2:69838336 | C | CA | 51 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0037 others(48): Show |
62 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.384+694dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAA | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(75): Show |
87 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.384+693_384+694dup others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAA | 29 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0121 others(26): Show |
32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.384+692_384+694dup others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA | 14 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0159 others(11): Show |
15 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+688_384+694dup others(7): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0022 a0001c0001t0001g0151 a0001c0001t0001g0152 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+687_384+694dup others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(2): Show |
19 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0045 others(16): Show |
20 | HG00621.hp2 HG01069.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.384+686_384+694dup others(9): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(10): Show |
19 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.384+685_384+694dup others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
4 | HG01070.hp2 HG02015.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+684_384+694dup others(11): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0003g0053 a0001c0004t0014g0112 |
2 | HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.384+683_384+694dup others(12): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.384+680_384+694dup others(15): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.384+679_384+694dup others(16): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(10): Show |
1 | a0001c0004t0014g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+678_384+694dup others(17): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0003g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.384+676_384+694dup others(19): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0003g0049 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.384+673_384+694dup others(22): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | CA | C | 12 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(9): Show |
12 | HG00609.hp2 HG00621.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.384+694delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | CAA | C | 9 | a0001c0001t0003g0004 a0001c0001t0003g0044 a0001c0001t0003g0099 others(6): Show |
13 | HG03688.hp1 HG04115.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.384+693_384+694del others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0212 a0001c0001t0025g0042 |
2 | HG00735.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384+685_384+694del others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838336 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0004g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.384+684_384+694del others(11): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69838336 | ||||||
| chr2:69838399 | A | G | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.384+729A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838399 | |||||||
| chr2:69838549 | G | A | 1 | a0001c0001t0005g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+879G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838549 | |||||||
| chr2:69838686 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.385-771T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838686 | |||||||
| chr2:69838779 | C | A | 1 | a0001c0002t0004g0306 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.385-678C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838779 | |||||||
| chr2:69838808 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0145 |
3 | NA18747.hp1 NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.385-649G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838808 | |||||||
| chr2:69838865 | G | A | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.385-592G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838865 | |||||||
| chr2:69838900 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385-557C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838900 | |||||||
| chr2:69838970 | A | G | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.385-487A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69838970 | |||||||
| chr2:69839095 | G | A | 1 | a0001c0001t0007g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.385-362G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69839095 | |||||||
| chr2:69839122 | G | GC | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.385-333dupC | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69839122 | ||||||
| chr2:69839127 | TCAGGTGT others(1): Show |
T | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-326_385-319del others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69839127 | ||||||
| chr2:69839380 | T | C | 1 | a0001c0001t0005g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.385-77T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69839380 | |||||||
| chr2:69839434 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.385-23G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | chr2 | 69839434 | |||||||
| chr2:69839439 | C | CTT | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
splice_region_variant&intron_variant | LOW | c.385-9_385-8dupTT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 69839439 | ||||||
| chr2:69839588 | C | T | 1 | a0002c0012t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.481+35C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69839588 | |||||||
| chr2:69839732 | A | G | 1 | a0001c0003t0006g0326 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481+179A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69839732 | |||||||
| chr2:69839759 | A | C | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.481+206A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69839759 | |||||||
| chr2:69839790 | A | G | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.481+237A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69839790 | |||||||
| chr2:69839836 | AT | A | 120 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(117): Show |
144 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.481+294delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 69839836 | ||||||
| chr2:69840175 | A | G | 76 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(73): Show |
91 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.481+622A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840175 | |||||||
| chr2:69840226 | G | C | 7 | a0001c0001t0003g0054 a0001c0001t0003g0058 a0001c0001t0003g0059 others(4): Show |
7 | NA18944.hp2 NA18964.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+673G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840226 | |||||||
| chr2:69840327 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | NA18943.hp1 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.482-615G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840327 | |||||||
| chr2:69840424 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.482-518G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840424 | |||||||
| chr2:69840679 | C | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-263C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840679 | |||||||
| chr2:69840709 | T | TGTAACAT others(9): Show |
1 | a0001c0001t0002g0206 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.482-232_482-231ins others(16): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 69840709 | ||||||
| chr2:69840711 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.482-231C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840711 | |||||||
| chr2:69840732 | A | C | 31 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(28): Show |
34 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.482-210A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840732 | |||||||
| chr2:69840752 | TATTAA | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.482-184_482-180del others(5): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 69840752 | ||||||
| chr2:69840925 | G | A | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.482-17G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 3/13 | chr2 | 69840925 | |||||||
| chr2:69841126 | CT | C | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
289 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.579+93delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69841126 | ||||||
| chr2:69841150 | A | G | 1 | a0001c0001t0005g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.579+111A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841150 | |||||||
| chr2:69841206 | C | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.579+167C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841206 | |||||||
| chr2:69841235 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.579+196G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841235 | |||||||
| chr2:69841336 | ATGACT | A | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.579+303_579+307del others(5): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69841336 | ||||||
| chr2:69841371 | CAATT | C | 18 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(15): Show |
21 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+337_579+340del others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69841371 | ||||||
| chr2:69841495 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.579+456T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841495 | |||||||
| chr2:69841503 | G | T | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
298 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.579+464G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841503 | |||||||
| chr2:69841510 | A | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
109 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.579+471A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841510 | |||||||
| chr2:69841594 | A | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.579+555A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841594 | |||||||
| chr2:69841623 | G | A | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.579+584G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841623 | |||||||
| chr2:69841940 | G | T | 1 | a0001c0002t0004g0306 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.579+901G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841940 | |||||||
| chr2:69841976 | A | G | 6 | a0001c0002t0004g0302 a0001c0002t0004g0303 a0001c0002t0004g0321 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+937A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69841976 | |||||||
| chr2:69842013 | T | C | 33 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(30): Show |
36 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.579+974T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842013 | |||||||
| chr2:69842061 | A | G | 1 | a0001c0001t0003g0093 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.579+1022A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842061 | |||||||
| chr2:69842073 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.579+1034A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842073 | |||||||
| chr2:69842077 | A | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.579+1038A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842077 | |||||||
| chr2:69842144 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.580-1005A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842144 | |||||||
| chr2:69842198 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.580-951A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842198 | |||||||
| chr2:69842502 | G | A | 1 | a0001c0001t0005g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.580-647G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842502 | |||||||
| chr2:69842532 | C | T | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.580-617C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842532 | |||||||
| chr2:69842619 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(1): Show |
6 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-530C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842619 | |||||||
| chr2:69842827 | C | T | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.580-322C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842827 | |||||||
| chr2:69842908 | T | TC | 35 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(32): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.580-234dupC | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69842908 | ||||||
| chr2:69842913 | C | G | 1 | a0001c0001t0003g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.580-236C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842913 | |||||||
| chr2:69842915 | C | A | 2 | a0001c0003t0004g0324 a0001c0003t0004g0325 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.580-234C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842915 | |||||||
| chr2:69842974 | T | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.580-175T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69842974 | |||||||
| chr2:69842990 | T | TA | 14 | a0001c0001t0001g0022 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-142dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69842990 | ||||||
| chr2:69842990 | TA | T | 40 | a0001c0001t0001g0144 a0001c0001t0002g0230 a0001c0001t0003g0045 others(37): Show |
48 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.580-142delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69842990 | ||||||
| chr2:69842990 | TAA | T | 10 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(7): Show |
14 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-143_580-142del others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69842990 | ||||||
| chr2:69843008 | C | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0066 a0001c0001t0003g0086 |
3 | HG02257.hp2 HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.580-141C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | chr2 | 69843008 | |||||||
| chr2:69843052 | CT | C | 79 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(76): Show |
94 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.580-86delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 69843052 | ||||||
| chr2:69843287 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.692+26C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843287 | |||||||
| chr2:69843327 | A | G | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.692+66A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843327 | |||||||
| chr2:69843464 | A | G | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.692+203A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843464 | |||||||
| chr2:69843617 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(30): Show |
37 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.692+356C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843617 | |||||||
| chr2:69843883 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0229 a0001c0001t0002g0264 others(4): Show |
9 | NA18944.hp1 NA18951.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.693-248C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843883 | |||||||
| chr2:69843911 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-220A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843911 | |||||||
| chr2:69843913 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-218A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843913 | |||||||
| chr2:69843916 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-215G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843916 | |||||||
| chr2:69843919 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-212G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843919 | |||||||
| chr2:69843922 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-209T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843922 | |||||||
| chr2:69843926 | AACTGGAA others(16): Show |
A | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-203_693-181del others(23): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 69843926 | ||||||
| chr2:69843950 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.693-181A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69843950 | |||||||
| chr2:69843965 | TTAA | T | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.693-160_693-158del others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 69843965 | ||||||
| chr2:69844012 | G | A | 1 | a0001c0001t0003g0069 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.693-119G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69844012 | |||||||
| chr2:69844018 | AGT | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.693-112_693-111del others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69844018 | |||||||
| chr2:69844078 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.693-53A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 5/13 | chr2 | 69844078 | |||||||
| chr2:69844206 | T | C | 2 | a0001c0001t0002g0232 a0001c0001t0002g0267 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.758+10T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844206 | |||||||
| chr2:69844211 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.758+15A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844211 | |||||||
| chr2:69844299 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.758+103A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844299 | |||||||
| chr2:69844397 | A | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(38): Show |
48 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.758+201A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844397 | |||||||
| chr2:69844422 | G | A | 1 | a0001c0001t0005g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.758+226G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844422 | |||||||
| chr2:69844525 | T | G | 1 | a0001c0001t0003g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.758+329T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69844525 | |||||||
| chr2:69844531 | A | AAACTGT | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.758+336_758+341dup others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69844531 | ||||||
| chr2:69844544 | CT | C | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.758+367delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69844544 | ||||||
| chr2:69844544 | CTTT | C | 8 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(5): Show |
9 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.758+365_758+367del others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69844544 | ||||||
| chr2:69844544 | CTTTT | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.758+364_758+367del others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69844544 | ||||||
| chr2:69845065 | G | A | 2 | a0001c0001t0003g0095 a0001c0001t0003g0099 |
2 | NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.758+869G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845065 | |||||||
| chr2:69845207 | G | A | 2 | a0001c0001t0005g0298 a0001c0001t0005g0299 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.758+1011G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845207 | |||||||
| chr2:69845222 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0001c0001t0001g0278 |
3 | HG00609.hp1 HG02155.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.758+1026C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845222 | |||||||
| chr2:69845223 | G | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+1027G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845223 | |||||||
| chr2:69845240 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.758+1044A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845240 | |||||||
| chr2:69845332 | A | G | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.758+1136A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845332 | |||||||
| chr2:69845392 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.758+1196G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845392 | |||||||
| chr2:69845394 | G | A | 30 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(27): Show |
41 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.758+1198G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845394 | |||||||
| chr2:69845648 | A | T | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.758+1452A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845648 | |||||||
| chr2:69845881 | A | G | 20 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(17): Show |
23 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.759-1662A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69845881 | |||||||
| chr2:69845955 | A | AT | 9 | a0001c0001t0002g0207 a0001c0001t0002g0261 a0001c0001t0002g0269 others(6): Show |
10 | HG01167.hp2 HG01175.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.759-1572dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69845955 | ||||||
| chr2:69845955 | AT | A | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.759-1572delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69845955 | ||||||
| chr2:69846113 | G | T | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.759-1430G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846113 | |||||||
| chr2:69846119 | T | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.759-1424T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846119 | |||||||
| chr2:69846141 | C | T | 1 | a0001c0002t0006g0319 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.759-1402C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846141 | |||||||
| chr2:69846305 | G | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.759-1238G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846305 | |||||||
| chr2:69846473 | A | G | 1 | a0001c0001t0005g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.759-1070A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846473 | |||||||
| chr2:69846570 | A | T | 2 | a0001c0001t0003g0052 a0001c0001t0012g0065 |
2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.759-973A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846570 | |||||||
| chr2:69846571 | C | T | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
290 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.759-972C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846571 | |||||||
| chr2:69846614 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.759-929G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846614 | |||||||
| chr2:69846731 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.759-812T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846731 | |||||||
| chr2:69846786 | A | G | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.759-757A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846786 | |||||||
| chr2:69846827 | C | T | 1 | a0001c0001t0015g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.759-716C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69846827 | |||||||
| chr2:69846999 | A | AT | 52 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0002g0207 others(49): Show |
63 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.759-525dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 69846999 | ||||||
| chr2:69847156 | G | T | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.759-387G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69847156 | |||||||
| chr2:69847281 | A | G | 2 | a0001c0001t0022g0288 a0001c0001t0023g0289 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.759-262A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 6/13 | chr2 | 69847281 | |||||||
| chr2:69847652 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.843+25T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69847652 | |||||||
| chr2:69847754 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.843+127C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69847754 | |||||||
| chr2:69847879 | T | A | 1 | a0001c0002t0004g0307 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.843+252T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69847879 | |||||||
| chr2:69847939 | G | A | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+312G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69847939 | |||||||
| chr2:69847960 | TTAA | T | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+335_843+337del others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 69847960 | ||||||
| chr2:69848041 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.843+414A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69848041 | |||||||
| chr2:69848320 | CTCTT | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.843+695_843+698del others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 69848320 | ||||||
| chr2:69848451 | A | C | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.843+824A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69848451 | |||||||
| chr2:69848852 | A | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-800A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69848852 | |||||||
| chr2:69849038 | C | T | 1 | a0001c0002t0004g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.844-614C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69849038 | |||||||
| chr2:69849041 | A | G | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.844-611A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69849041 | |||||||
| chr2:69849453 | C | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0197 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.844-199C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69849453 | |||||||
| chr2:69849518 | T | C | 78 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
90 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.844-134T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 7/13 | chr2 | 69849518 | |||||||
| chr2:69849822 | A | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
299 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.934+80A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69849822 | |||||||
| chr2:69849897 | A | G | 4 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0259 others(1): Show |
4 | HG00323.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+155A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69849897 | |||||||
| chr2:69849953 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.934+211T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69849953 | |||||||
| chr2:69850032 | C | T | 1 | a0001c0002t0004g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.934+290C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850032 | |||||||
| chr2:69850104 | C | T | 2 | a0001c0001t0016g0293 a0001c0001t0016g0294 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.934+362C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850104 | |||||||
| chr2:69850106 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.934+364C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850106 | |||||||
| chr2:69850107 | G | A | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.934+365G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850107 | |||||||
| chr2:69850290 | A | G | 79 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(76): Show |
91 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.934+548A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850290 | |||||||
| chr2:69850301 | T | C | 79 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(76): Show |
91 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.934+559T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850301 | |||||||
| chr2:69850356 | AATGT | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.934+623_934+626del others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69850356 | ||||||
| chr2:69850524 | A | T | 1 | a0001c0001t0002g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.934+782A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850524 | |||||||
| chr2:69850603 | A | G | 1 | a0001c0001t0003g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.934+861A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850603 | |||||||
| chr2:69850699 | A | C | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.934+957A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850699 | |||||||
| chr2:69850764 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.934+1022C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850764 | |||||||
| chr2:69850842 | A | C | 1 | a0001c0001t0003g0076 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.934+1100A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850842 | |||||||
| chr2:69850853 | G | C | 1 | a0001c0001t0002g0219 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.934+1111G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850853 | |||||||
| chr2:69850944 | T | G | 1 | a0001c0001t0002g0266 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.934+1202T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69850944 | |||||||
| chr2:69851126 | T | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.934+1384T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851126 | |||||||
| chr2:69851178 | T | C | 13 | a0001c0001t0003g0004 a0001c0001t0003g0050 a0001c0001t0003g0093 others(10): Show |
17 | HG00621.hp1 NA18939.hp2 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.934+1436T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851178 | |||||||
| chr2:69851201 | T | A | 3 | a0001c0001t0005g0284 a0001c0001t0005g0285 a0001c0001t0005g0286 |
3 | HG01884.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.934+1459T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851201 | |||||||
| chr2:69851350 | G | A | 2 | a0001c0001t0003g0061 a0001c0001t0003g0073 |
2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.934+1608G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851350 | |||||||
| chr2:69851375 | G | T | 1 | a0001c0001t0005g0280 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.934+1633G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851375 | |||||||
| chr2:69851417 | G | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0279 a0001c0001t0005g0281 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+1675G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851417 | |||||||
| chr2:69851467 | G | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0089 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.934+1725G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851467 | |||||||
| chr2:69851542 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+1800G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851542 | |||||||
| chr2:69851564 | T | C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.934+1822T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851564 | |||||||
| chr2:69851592 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.934+1850G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851592 | |||||||
| chr2:69851776 | A | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.934+2034A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851776 | |||||||
| chr2:69851835 | A | G | 1 | a0001c0007t0014g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.934+2093A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69851835 | |||||||
| chr2:69852025 | G | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.934+2283G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852025 | |||||||
| chr2:69852063 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(1): Show |
6 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+2321A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852063 | |||||||
| chr2:69852114 | G | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0089 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.934+2372G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852114 | |||||||
| chr2:69852268 | C | G | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.934+2526C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852268 | |||||||
| chr2:69852287 | TCCACTTC others(3): Show |
T | 1 | a0001c0002t0004g0331 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.935-2535_935-2526d others(12): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852287 | |||||||
| chr2:69852400 | C | A | 1 | a0001c0002t0004g0302 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.935-2423C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852400 | |||||||
| chr2:69852461 | A | G | 2 | a0001c0001t0022g0288 a0001c0001t0023g0289 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.935-2362A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852461 | |||||||
| chr2:69852477 | T | TATTTATA others(2): Show |
39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-2345_935-2344i others(11): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69852477 | ||||||
| chr2:69852481 | A | ATAT | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-2342_935-2341i others(5): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852481 | |||||||
| chr2:69852501 | C | T | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.935-2322C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852501 | |||||||
| chr2:69852516 | C | T | 3 | a0001c0001t0010g0290 a0001c0001t0010g0291 a0001c0001t0024g0292 |
3 | HG02559.hp2 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.935-2307C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852516 | |||||||
| chr2:69852544 | C | CT | 8 | a0001c0001t0016g0293 a0001c0001t0016g0294 a0001c0001t0018g0034 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.935-2268dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69852544 | ||||||
| chr2:69852544 | C | CTGTT | 40 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(37): Show |
47 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.935-2278_935-2277i others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69852544 | ||||||
| chr2:69852544 | C | CTT | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.935-2269_935-2268d others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69852544 | ||||||
| chr2:69852544 | C | CTTTT | 37 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0019 others(34): Show |
42 | HG00621.hp1 HG01243.hp2 HG01433.hp2 others(39): Show |
intron_variant | MODIFIER | c.935-2271_935-2268d others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69852544 | ||||||
| chr2:69852568 | T | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-2255T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852568 | |||||||
| chr2:69852649 | C | T | 1 | a0003c0006t0004g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.935-2174C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852649 | |||||||
| chr2:69852670 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.935-2153C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852670 | |||||||
| chr2:69852773 | G | A | 2 | a0001c0001t0005g0298 a0001c0001t0005g0299 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.935-2050G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852773 | |||||||
| chr2:69852985 | A | G | 1 | a0001c0001t0005g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.935-1838A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852985 | |||||||
| chr2:69852994 | C | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0151 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.935-1829C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852994 | |||||||
| chr2:69852997 | A | G | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.935-1826A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69852997 | |||||||
| chr2:69853082 | G | A | 1 | a0001c0001t0007g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.935-1741G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69853082 | |||||||
| chr2:69853265 | C | A | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.935-1558C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69853265 | |||||||
| chr2:69853374 | CAGGTGCC others(1306): Show |
C | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.935-1447_935-135de others(1): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69853374 | ||||||
| chr2:69853765 | GA | G | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.935-1050delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69853765 | ||||||
| chr2:69853771 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.935-1052A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69853771 | |||||||
| chr2:69853928 | G | A | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.935-895G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69853928 | |||||||
| chr2:69854036 | C | T | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-787C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854036 | |||||||
| chr2:69854120 | G | GTAT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0151 others(23): Show |
27 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.935-675_935-673dup others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69854120 | ||||||
| chr2:69854120 | G | GTATTAT | 38 | a0001c0001t0001g0129 a0001c0001t0015g0158 a0001c0001t0016g0293 others(35): Show |
50 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-678_935-673dup others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69854120 | ||||||
| chr2:69854120 | GTAT | G | 82 | a0001c0001t0001g0005 a0001c0001t0002g0038 a0001c0001t0002g0250 others(79): Show |
94 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.935-675_935-673del others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69854120 | ||||||
| chr2:69854120 | GTATTATT others(8): Show |
G | 6 | a0001c0001t0002g0210 a0001c0001t0002g0237 a0001c0001t0002g0238 others(3): Show |
6 | HG00544.hp1 HG02027.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.935-687_935-673del others(15): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 69854120 | ||||||
| chr2:69854148 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.935-675T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854148 | |||||||
| chr2:69854190 | C | G | 3 | a0001c0001t0017g0109 a0001c0001t0017g0110 a0001c0001t0031g0108 |
3 | HG02647.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.935-633C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854190 | |||||||
| chr2:69854266 | CAGCCTCC others(3): Show |
C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.935-556_935-547del others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854266 | |||||||
| chr2:69854348 | A | G | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.935-475A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854348 | |||||||
| chr2:69854369 | G | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.935-454G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854369 | |||||||
| chr2:69854744 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.935-79C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 8/13 | chr2 | 69854744 | |||||||
| chr2:69855152 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1072+192A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855152 | |||||||
| chr2:69855159 | A | G | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1072+199A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855159 | |||||||
| chr2:69855216 | C | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072+256C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855216 | |||||||
| chr2:69855284 | G | T | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1072+324G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855284 | |||||||
| chr2:69855288 | A | T | 1 | a0001c0001t0002g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1072+328A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855288 | |||||||
| chr2:69855307 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0180 |
3 | HG02080.hp2 NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1072+347G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855307 | |||||||
| chr2:69855332 | A | G | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1072+372A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855332 | |||||||
| chr2:69855626 | A | G | 1 | a0001c0001t0005g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1072+666A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855626 | |||||||
| chr2:69855764 | G | A | 28 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1072+804G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855764 | |||||||
| chr2:69855852 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1072+892G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69855852 | |||||||
| chr2:69856479 | G | C | 2 | a0001c0001t0005g0298 a0001c0001t0005g0299 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1072+1519G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856479 | |||||||
| chr2:69856625 | T | TC | 41 | a0001c0001t0002g0221 a0001c0001t0003g0003 a0001c0001t0003g0015 others(38): Show |
48 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1072+1667dupC | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856625 | ||||||
| chr2:69856640 | C | CT | 11 | a0001c0001t0002g0220 a0001c0001t0002g0226 a0001c0001t0002g0227 others(8): Show |
11 | HG01109.hp1 HG01952.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.1072+1708dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856640 | ||||||
| chr2:69856640 | CT | C | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(85): Show |
100 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1072+1708delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856640 | ||||||
| chr2:69856640 | CTT | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(124): Show |
149 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1072+1707_1072+170 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856640 | ||||||
| chr2:69856640 | CTTT | C | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0003g0039 others(8): Show |
12 | HG00280.hp2 HG01975.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072+1706_1072+170 others(7): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856640 | ||||||
| chr2:69856640 | CTTTT | C | 9 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1072+1705_1072+170 others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69856640 | ||||||
| chr2:69856650 | T | G | 1 | a0001c0002t0006g0328 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1072+1690T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856650 | |||||||
| chr2:69856651 | T | G | 39 | a0001c0001t0025g0042 a0001c0002t0004g0002 a0001c0002t0004g0011 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1072+1691T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856651 | |||||||
| chr2:69856652 | T | G | 4 | a0001c0001t0018g0034 a0001c0002t0007g0020 a0001c0002t0019g0114 others(1): Show |
5 | HG02622.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+1692T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856652 | |||||||
| chr2:69856653 | T | G | 4 | a0001c0001t0018g0036 a0001c0001t0026g0035 a0001c0004t0014g0111 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072+1693T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856653 | |||||||
| chr2:69856656 | T | G | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1072+1696T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856656 | |||||||
| chr2:69856668 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | NA18943.hp1 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1072+1708T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856668 | |||||||
| chr2:69856749 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1072+1789C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856749 | |||||||
| chr2:69856936 | C | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1072+1976C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69856936 | |||||||
| chr2:69857075 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1072+2115A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857075 | |||||||
| chr2:69857087 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1072+2127A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857087 | |||||||
| chr2:69857174 | A | G | 30 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(27): Show |
41 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1072+2214A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857174 | |||||||
| chr2:69857250 | C | T | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072+2290C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857250 | |||||||
| chr2:69857347 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1072+2387A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857347 | |||||||
| chr2:69857467 | C | T | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1072+2507C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857467 | |||||||
| chr2:69857611 | C | T | 1 | a0001c0001t0012g0065 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1072+2651C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857611 | |||||||
| chr2:69857649 | A | G | 3 | a0001c0001t0015g0150 a0001c0001t0015g0154 a0001c0001t0015g0158 |
3 | HG00423.hp2 NA18941.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1072+2689A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857649 | |||||||
| chr2:69857657 | G | A | 1 | a0001c0001t0016g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1072+2697G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857657 | |||||||
| chr2:69857764 | A | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1072+2804A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857764 | |||||||
| chr2:69857778 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1072+2818A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857778 | |||||||
| chr2:69857845 | T | G | 134 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(131): Show |
159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1072+2885T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857845 | |||||||
| chr2:69857997 | T | A | 1 | a0001c0001t0005g0280 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1072+3037T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69857997 | |||||||
| chr2:69858073 | T | C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1072+3113T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858073 | |||||||
| chr2:69858085 | C | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0240 a0001c0001t0011g0029 others(3): Show |
6 | HG00597.hp2 HG02523.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1072+3125C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858085 | |||||||
| chr2:69858087 | A | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072+3127A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858087 | |||||||
| chr2:69858284 | G | T | 8 | a0001c0001t0002g0008 a0001c0001t0002g0219 a0001c0001t0002g0250 others(5): Show |
9 | HG02074.hp2 NA18943.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073-2994G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858284 | |||||||
| chr2:69858394 | A | G | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1073-2884A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858394 | |||||||
| chr2:69858473 | G | A | 1 | a0001c0002t0004g0304 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1073-2805G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858473 | |||||||
| chr2:69858571 | T | G | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1073-2707T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858571 | |||||||
| chr2:69858696 | T | G | 5 | a0001c0001t0002g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-2582T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858696 | |||||||
| chr2:69858829 | G | A | 131 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(128): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1073-2449G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858829 | |||||||
| chr2:69858870 | G | A | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1073-2408G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858870 | |||||||
| chr2:69858877 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0183 a0001c0001t0001g0185 |
3 | HG03017.hp1 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1073-2401G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858877 | |||||||
| chr2:69858914 | G | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1073-2364G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69858914 | |||||||
| chr2:69859060 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1073-2218C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859060 | |||||||
| chr2:69859101 | G | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1073-2177G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859101 | |||||||
| chr2:69859144 | C | CA | 64 | a0001c0001t0001g0118 a0001c0001t0001g0131 a0001c0001t0001g0151 others(61): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1073-2111dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859144 | ||||||
| chr2:69859144 | C | CAA | 7 | a0001c0001t0003g0090 a0001c0002t0004g0303 a0001c0002t0004g0315 others(4): Show |
7 | HG00738.hp2 HG01175.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-2112_1073-211 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859144 | ||||||
| chr2:69859144 | CA | C | 15 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0001t0001g0179 others(12): Show |
15 | HG01517.hp2 HG02027.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1073-2111delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859144 | ||||||
| chr2:69859144 | CAAAAAAA | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(13): Show |
19 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1073-2117_1073-211 others(11): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859144 | ||||||
| chr2:69859168 | T | A | 1 | a0001c0001t0002g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1073-2110T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859168 | |||||||
| chr2:69859231 | A | G | 74 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1073-2047A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859231 | |||||||
| chr2:69859236 | A | G | 5 | a0001c0001t0002g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-2042A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859236 | |||||||
| chr2:69859293 | G | C | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-1985G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859293 | |||||||
| chr2:69859322 | A | AAT | 10 | a0001c0001t0001g0127 a0001c0001t0003g0063 a0001c0001t0018g0034 others(7): Show |
11 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1073-1941_1073-194 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859322 | ||||||
| chr2:69859348 | T | A | 41 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(38): Show |
52 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1073-1930T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859348 | |||||||
| chr2:69859405 | A | G | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-1873A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859405 | |||||||
| chr2:69859596 | C | T | 74 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1073-1682C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859596 | |||||||
| chr2:69859742 | T | TAAA | 37 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(34): Show |
41 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1073-1522_1073-152 others(7): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAA | 21 | a0001c0001t0001g0142 a0001c0001t0003g0003 a0001c0001t0003g0016 others(18): Show |
27 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1073-1524_1073-152 others(9): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAA | 16 | a0001c0001t0003g0015 a0001c0001t0003g0017 a0001c0001t0003g0051 others(13): Show |
17 | HG00438.hp1 HG00621.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1073-1525_1073-152 others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(4): Show |
6 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-1530_1073-152 others(15): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(5): Show |
1 | a0001c0002t0019g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1073-1531_1073-152 others(16): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(6): Show |
23 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0306 others(20): Show |
32 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1073-1532_1073-152 others(17): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(7): Show |
14 | a0001c0002t0004g0012 a0001c0002t0004g0033 a0001c0002t0004g0302 others(11): Show |
16 | HG00423.hp1 HG01106.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1073-1533_1073-152 others(18): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(8): Show |
4 | a0001c0001t0003g0091 a0001c0001t0007g0025 a0001c0002t0004g0303 others(1): Show |
5 | HG01243.hp2 HG01358.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073-1534_1073-152 others(19): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(9): Show |
16 | a0001c0001t0002g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1073-1535_1073-152 others(20): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(10): Show |
13 | a0001c0001t0003g0004 a0001c0001t0003g0019 a0001c0001t0003g0039 others(10): Show |
18 | HG00621.hp1 HG02145.hp1 HG02895.hp1 others(15): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(21): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(11): Show |
8 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(5): Show |
8 | HG01433.hp2 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(22): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(12): Show |
1 | a0001c0001t0003g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1073-1520_1073-151 others(23): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(13): Show |
6 | a0001c0001t0001g0126 a0001c0001t0001g0185 a0001c0001t0003g0066 others(3): Show |
6 | HG02818.hp2 HG03017.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(24): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(14): Show |
25 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0037 others(22): Show |
28 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(25): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(15): Show |
21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0118 others(18): Show |
24 | HG00544.hp2 HG00673.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(26): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(16): Show |
10 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0133 others(7): Show |
10 | HG01515.hp2 HG01517.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(27): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(17): Show |
3 | a0001c0001t0001g0182 a0001c0001t0021g0175 a0001c0001t0034g0199 |
3 | HG00438.hp2 NA19030.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1073-1520_1073-151 others(28): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TAAAAAAA others(21): Show |
1 | a0001c0001t0001g0130 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1073-1520_1073-151 others(32): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69859742 | ||||||
| chr2:69859742 | T | TCAAAAAA others(14): Show |
1 | a0001c0001t0001g0131 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1073-1536_1073-153 others(25): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859742 | |||||||
| chr2:69859742 | T | TCTAAAAA others(14): Show |
2 | a0001c0001t0001g0132 a0001c0001t0007g0067 |
2 | NA18747.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1073-1536_1073-153 others(25): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859742 | |||||||
| chr2:69859742 | T | TCTAAAAA others(15): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0145 |
2 | NA18947.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1073-1536_1073-153 others(26): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859742 | |||||||
| chr2:69859742 | T | TCTAAAAA others(18): Show |
1 | a0001c0001t0001g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1073-1536_1073-153 others(29): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859742 | |||||||
| chr2:69859742 | T | TTAAAAAA others(14): Show |
1 | a0001c0007t0014g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1073-1536_1073-153 others(25): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859742 | |||||||
| chr2:69859810 | C | T | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1073-1468C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859810 | |||||||
| chr2:69859870 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1073-1408G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859870 | |||||||
| chr2:69859896 | A | C | 1 | a0003c0006t0004g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1073-1382A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69859896 | |||||||
| chr2:69860006 | A | AT | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-1269dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 69860006 | ||||||
| chr2:69860010 | A | T | 8 | a0001c0001t0002g0009 a0001c0001t0002g0229 a0001c0001t0002g0264 others(5): Show |
11 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1073-1268A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860010 | |||||||
| chr2:69860027 | T | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1073-1251T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860027 | |||||||
| chr2:69860105 | G | T | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1073-1173G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860105 | |||||||
| chr2:69860172 | G | A | 1 | a0001c0002t0004g0310 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1073-1106G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860172 | |||||||
| chr2:69860206 | G | T | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1073-1072G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860206 | |||||||
| chr2:69860327 | C | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-951C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860327 | |||||||
| chr2:69860492 | A | G | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1073-786A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860492 | |||||||
| chr2:69860498 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1073-780G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860498 | |||||||
| chr2:69860587 | A | T | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1073-691A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860587 | |||||||
| chr2:69860679 | G | T | 1 | a0001c0001t0023g0289 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1073-599G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860679 | |||||||
| chr2:69860685 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1073-593G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860685 | |||||||
| chr2:69860775 | C | A | 4 | a0001c0001t0009g0241 a0001c0001t0009g0242 a0001c0001t0020g0222 others(1): Show |
4 | NA18969.hp2 NA19004.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-503C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860775 | |||||||
| chr2:69860790 | G | C | 4 | a0001c0001t0009g0241 a0001c0001t0009g0242 a0001c0001t0020g0222 others(1): Show |
4 | NA18969.hp2 NA19004.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-488G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860790 | |||||||
| chr2:69860884 | A | C | 122 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(119): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1073-394A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860884 | |||||||
| chr2:69860896 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1073-382G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69860896 | |||||||
| chr2:69861081 | G | C | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-197G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69861081 | |||||||
| chr2:69861082 | AT | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-195delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69861082 | |||||||
| chr2:69861084 | C | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-194C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69861084 | |||||||
| chr2:69861085 | C | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-193C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69861085 | |||||||
| chr2:69861271 | A | G | 3 | a0001c0001t0003g0054 a0001c0001t0003g0059 a0001c0001t0029g0060 |
3 | NA18982.hp1 NA19070.hp1 NA19078.hp2 |
splice_region_variant&intron_variant | LOW | c.1073-7A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 9/13 | chr2 | 69861271 | |||||||
| chr2:69861398 | T | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0047 |
3 | HG01884.hp2 HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1142+51T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861398 | |||||||
| chr2:69861537 | A | C | 1 | a0001c0001t0002g0220 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1142+190A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861537 | |||||||
| chr2:69861587 | A | G | 6 | a0001c0001t0010g0290 a0001c0001t0010g0291 a0001c0001t0010g0295 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1142+240A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861587 | |||||||
| chr2:69861636 | C | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1142+289C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861636 | |||||||
| chr2:69861722 | T | C | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1142+375T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861722 | |||||||
| chr2:69861810 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1142+463C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861810 | |||||||
| chr2:69861811 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1142+464G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861811 | |||||||
| chr2:69861880 | C | T | 19 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(16): Show |
23 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1142+533C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861880 | |||||||
| chr2:69861998 | A | G | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1142+651A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69861998 | |||||||
| chr2:69862012 | AAAAC | A | 33 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0019 others(30): Show |
38 | HG00621.hp1 HG01243.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1142+681_1142+684d others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 69862012 | ||||||
| chr2:69862192 | T | C | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1142+845T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862192 | |||||||
| chr2:69862631 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0179 others(2): Show |
5 | HG02083.hp2 NA18942.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1142+1284T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862631 | |||||||
| chr2:69862694 | A | G | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1142+1347A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862694 | |||||||
| chr2:69862760 | A | C | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1142+1413A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862760 | |||||||
| chr2:69862776 | G | C | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1142+1429G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862776 | |||||||
| chr2:69862862 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1142+1515C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862862 | |||||||
| chr2:69862935 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1142+1588T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69862935 | |||||||
| chr2:69863111 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(63): Show |
72 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1142+1764G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863111 | |||||||
| chr2:69863144 | G | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1143-1756G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863144 | |||||||
| chr2:69863199 | A | C | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1143-1701A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863199 | |||||||
| chr2:69863407 | G | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143-1493G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863407 | |||||||
| chr2:69863447 | C | G | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1143-1453C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863447 | |||||||
| chr2:69863542 | G | A | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1143-1358G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863542 | |||||||
| chr2:69863703 | T | A | 1 | a0001c0001t0018g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1143-1197T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863703 | |||||||
| chr2:69863781 | C | T | 74 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1119C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863781 | |||||||
| chr2:69863825 | T | C | 5 | a0001c0001t0002g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143-1075T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69863825 | |||||||
| chr2:69864071 | C | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1143-829C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864071 | |||||||
| chr2:69864114 | T | C | 241 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1143-786T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864114 | |||||||
| chr2:69864167 | A | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1143-733A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864167 | |||||||
| chr2:69864235 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1143-665A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864235 | |||||||
| chr2:69864590 | C | CT | 23 | a0001c0001t0001g0037 a0001c0001t0001g0140 a0001c0001t0001g0159 others(20): Show |
24 | HG00597.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1143-288dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 69864590 | ||||||
| chr2:69864590 | C | CTT | 98 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
108 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1143-289_1143-288d others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 69864590 | ||||||
| chr2:69864590 | CT | C | 16 | a0001c0001t0002g0205 a0001c0001t0002g0228 a0001c0001t0002g0243 others(13): Show |
17 | HG00609.hp2 HG01123.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.1143-288delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 69864590 | ||||||
| chr2:69864590 | CTT | C | 109 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(106): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1143-289_1143-288d others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 69864590 | ||||||
| chr2:69864640 | T | C | 74 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-260T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864640 | |||||||
| chr2:69864860 | A | G | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1143-40A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 10/13 | chr2 | 69864860 | |||||||
| chr2:69865015 | T | A | 2 | a0001c0001t0001g0182 a0001c0010t0001g0137 |
2 | HG02083.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1218+40T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865015 | |||||||
| chr2:69865064 | C | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+89C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865064 | |||||||
| chr2:69865115 | G | A | 1 | a0006c0011t0001g0124 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1218+140G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865115 | |||||||
| chr2:69865241 | A | C | 14 | a0001c0001t0002g0029 a0001c0001t0002g0210 a0001c0001t0002g0237 others(11): Show |
14 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1218+266A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865241 | |||||||
| chr2:69865386 | G | A | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1218+411G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865386 | |||||||
| chr2:69865477 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0002c0012t0001g0168 |
3 | HG00597.hp1 HG02027.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1218+502A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865477 | |||||||
| chr2:69865546 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1218+571G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865546 | |||||||
| chr2:69865584 | G | A | 1 | a0001c0001t0012g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1218+609G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865584 | |||||||
| chr2:69865612 | C | T | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+637C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865612 | |||||||
| chr2:69865627 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1218+652G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865627 | |||||||
| chr2:69865665 | T | G | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1218+690T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865665 | |||||||
| chr2:69865979 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0142 a0001c0001t0001g0169 others(4): Show |
9 | NA18961.hp2 NA18965.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+1004G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69865979 | |||||||
| chr2:69866020 | G | A | 6 | a0001c0002t0004g0302 a0001c0002t0004g0303 a0001c0002t0004g0321 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+1045G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866020 | |||||||
| chr2:69866110 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+1135G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866110 | |||||||
| chr2:69866249 | GA | G | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1218+1289delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69866249 | ||||||
| chr2:69866507 | C | T | 4 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0259 others(1): Show |
4 | HG00323.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+1532C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866507 | |||||||
| chr2:69866515 | T | C | 239 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1218+1540T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866515 | |||||||
| chr2:69866524 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1218+1549A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866524 | |||||||
| chr2:69866708 | TC | T | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1218+1735delC | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69866708 | ||||||
| chr2:69866748 | A | G | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1218+1773A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866748 | |||||||
| chr2:69866766 | A | G | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1218+1791A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866766 | |||||||
| chr2:69866778 | G | A | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1218+1803G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866778 | |||||||
| chr2:69866907 | G | T | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+1932G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69866907 | |||||||
| chr2:69866952 | C | CT | 50 | a0001c0001t0001g0135 a0001c0001t0001g0204 a0001c0001t0018g0034 others(47): Show |
62 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1218+1987dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69866952 | ||||||
| chr2:69867005 | C | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1218+2030C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867005 | |||||||
| chr2:69867134 | C | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+2159C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867134 | |||||||
| chr2:69867284 | G | A | 1 | a0001c0002t0004g0331 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1218+2309G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867284 | |||||||
| chr2:69867358 | C | T | 36 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(33): Show |
47 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1219-2361C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867358 | |||||||
| chr2:69867379 | A | C | 1 | a0001c0001t0008g0139 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1219-2340A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867379 | |||||||
| chr2:69867591 | T | C | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-2128T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867591 | |||||||
| chr2:69867772 | T | C | 2 | a0001c0003t0004g0324 a0001c0003t0004g0325 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1219-1947T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69867772 | |||||||
| chr2:69868236 | T | TA | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
114 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1219-1471dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69868236 | ||||||
| chr2:69868381 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1219-1338A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868381 | |||||||
| chr2:69868510 | A | C | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1219-1209A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868510 | |||||||
| chr2:69868573 | T | A | 1 | a0001c0002t0004g0318 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1219-1146T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868573 | |||||||
| chr2:69868574 | T | A | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1219-1145T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868574 | |||||||
| chr2:69868659 | C | T | 42 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(39): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1219-1060C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868659 | |||||||
| chr2:69868664 | C | T | 1 | a0001c0001t0034g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1219-1055C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868664 | |||||||
| chr2:69868665 | G | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1219-1054G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868665 | |||||||
| chr2:69868974 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-745G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868974 | |||||||
| chr2:69868988 | A | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0142 a0001c0001t0001g0192 others(1): Show |
6 | NA18961.hp2 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1219-731A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69868988 | |||||||
| chr2:69869014 | A | C | 1 | a0001c0001t0003g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-705A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869014 | |||||||
| chr2:69869023 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-696C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869023 | |||||||
| chr2:69869046 | A | C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1219-673A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869046 | |||||||
| chr2:69869055 | C | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-664C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869055 | |||||||
| chr2:69869113 | T | TTGG | 48 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0025g0042 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1219-605_1219-603d others(5): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869113 | ||||||
| chr2:69869178 | G | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-541G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869178 | |||||||
| chr2:69869249 | C | CA | 13 | a0001c0001t0001g0161 a0001c0001t0002g0221 a0001c0001t0002g0259 others(10): Show |
13 | HG02145.hp2 HG02683.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1219-451dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869249 | ||||||
| chr2:69869249 | CA | C | 47 | a0001c0001t0001g0140 a0001c0001t0002g0206 a0001c0001t0002g0247 others(44): Show |
58 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1219-451delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869249 | ||||||
| chr2:69869332 | C | T | 13 | a0001c0001t0003g0004 a0001c0001t0003g0050 a0001c0001t0003g0093 others(10): Show |
17 | HG00621.hp1 NA18939.hp2 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219-387C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869332 | |||||||
| chr2:69869417 | C | CA | 16 | a0001c0001t0001g0141 a0001c0001t0002g0048 a0001c0001t0002g0207 others(13): Show |
16 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-279dupA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869417 | ||||||
| chr2:69869417 | CA | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1219-279delA | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869417 | ||||||
| chr2:69869417 | CAA | C | 11 | a0001c0001t0001g0140 a0001c0001t0003g0070 a0001c0001t0007g0270 others(8): Show |
11 | HG01358.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-280_1219-279d others(4): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869417 | ||||||
| chr2:69869417 | CAAA | C | 34 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(31): Show |
45 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1219-281_1219-279d others(5): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 69869417 | ||||||
| chr2:69869611 | G | A | 1 | a0001c0001t0003g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-108G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869611 | |||||||
| chr2:69869685 | A | G | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1219-34A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 11/13 | chr2 | 69869685 | |||||||
| chr2:69869969 | A | G | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1364+105A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69869969 | |||||||
| chr2:69870111 | G | A | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1364+247G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69870111 | |||||||
| chr2:69870603 | G | C | 124 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(121): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1364+739G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69870603 | |||||||
| chr2:69870721 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1364+857C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69870721 | |||||||
| chr2:69870824 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0008g0173 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1365-921T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69870824 | |||||||
| chr2:69871038 | G | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365-707G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871038 | |||||||
| chr2:69871093 | T | TCACAATA others(1): Show |
3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365-650_1365-643d others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 69871093 | ||||||
| chr2:69871156 | G | GA | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1365-589_1365-588i others(3): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871156 | |||||||
| chr2:69871157 | T | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1365-588T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871157 | |||||||
| chr2:69871158 | G | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1365-587G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871158 | |||||||
| chr2:69871286 | G | T | 1 | a0001c0001t0002g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1365-459G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871286 | |||||||
| chr2:69871299 | C | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0179 others(2): Show |
5 | HG02083.hp2 NA18942.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365-446C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871299 | |||||||
| chr2:69871403 | G | A | 1 | a0001c0002t0004g0323 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1365-342G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871403 | |||||||
| chr2:69871411 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1365-334G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871411 | |||||||
| chr2:69871530 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0113 a0001c0001t0001g0172 others(1): Show |
5 | NA18939.hp1 NA18987.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365-215A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871530 | |||||||
| chr2:69871651 | CAG | C | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1365-91_1365-90del others(2): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 69871651 | ||||||
| chr2:69871676 | A | G | 261 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
299 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1365-69A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 12/13 | chr2 | 69871676 | |||||||
| chr2:69872085 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1452+253A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872085 | |||||||
| chr2:69872168 | A | G | 1 | a0001c0001t0034g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1452+336A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872168 | |||||||
| chr2:69872283 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(1): Show |
6 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452+451A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872283 | |||||||
| chr2:69872292 | A | G | 76 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(73): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1452+460A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872292 | |||||||
| chr2:69872524 | G | T | 1 | a0001c0002t0004g0313 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1452+692G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872524 | |||||||
| chr2:69872902 | T | A | 1 | a0001c0001t0003g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1452+1070T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872902 | |||||||
| chr2:69872966 | G | T | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1134G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69872966 | |||||||
| chr2:69873019 | T | C | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452+1187T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873019 | |||||||
| chr2:69873190 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1452+1358A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873190 | |||||||
| chr2:69873241 | T | C | 1 | a0001c0001t0005g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1452+1409T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873241 | |||||||
| chr2:69873407 | A | G | 1 | a0001c0001t0002g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1452+1575A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873407 | |||||||
| chr2:69873468 | A | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1636A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873468 | |||||||
| chr2:69873516 | A | T | 1 | a0001c0001t0002g0266 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1452+1684A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873516 | |||||||
| chr2:69873566 | A | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1452+1734A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873566 | |||||||
| chr2:69873655 | G | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02615.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1823G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873655 | |||||||
| chr2:69873727 | G | A | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1452+1895G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69873727 | |||||||
| chr2:69873946 | C | CT | 124 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(121): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1452+2129dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69873946 | ||||||
| chr2:69874123 | T | A | 3 | a0001c0001t0002g0210 a0001c0001t0002g0237 a0001c0001t0002g0261 |
3 | HG00544.hp1 HG02027.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1452+2291T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874123 | |||||||
| chr2:69874365 | T | TTTTG | 47 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(44): Show |
59 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1452+2545_1452+254 others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69874365 | ||||||
| chr2:69874391 | T | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1452+2559T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874391 | |||||||
| chr2:69874548 | C | T | 1 | a0001c0001t0018g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1452+2716C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874548 | |||||||
| chr2:69874700 | T | C | 1 | a0001c0001t0025g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1452+2868T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874700 | |||||||
| chr2:69874716 | T | C | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1452+2884T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874716 | |||||||
| chr2:69874757 | T | C | 116 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(113): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1452+2925T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874757 | |||||||
| chr2:69874870 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1452+3038T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874870 | |||||||
| chr2:69874892 | C | T | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1452+3060C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874892 | |||||||
| chr2:69874926 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1452+3094A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69874926 | |||||||
| chr2:69875076 | A | G | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1452+3244A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875076 | |||||||
| chr2:69875166 | C | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0179 |
3 | NA18942.hp1 NA18960.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1452+3334C>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875166 | |||||||
| chr2:69875603 | C | G | 116 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(113): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1453-3306C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875603 | |||||||
| chr2:69875700 | CT | C | 19 | a0001c0001t0002g0276 a0001c0001t0015g0150 a0001c0002t0004g0011 others(16): Show |
23 | HG00423.hp1 HG01169.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1453-3196delT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69875700 | ||||||
| chr2:69875746 | A | G | 5 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453-3163A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875746 | |||||||
| chr2:69875858 | C | CT | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(59): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1453-3045dupT | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69875858 | ||||||
| chr2:69875933 | G | A | 1 | a0001c0001t0003g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1453-2976G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875933 | |||||||
| chr2:69875937 | A | G | 18 | a0001c0001t0003g0004 a0001c0001t0003g0044 a0001c0001t0003g0050 others(15): Show |
22 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1453-2972A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69875937 | |||||||
| chr2:69876108 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0128 others(4): Show |
7 | HG00544.hp2 HG02080.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-2801C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876108 | |||||||
| chr2:69876169 | A | C | 1 | a0001c0001t0002g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1453-2740A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876169 | |||||||
| chr2:69876176 | G | T | 3 | a0001c0003t0004g0324 a0001c0003t0004g0325 a0001c0003t0006g0326 |
3 | HG02965.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1453-2733G>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876176 | |||||||
| chr2:69876372 | T | C | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1453-2537T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876372 | |||||||
| chr2:69876428 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1453-2481A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876428 | |||||||
| chr2:69876669 | A | G | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-2240A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876669 | |||||||
| chr2:69876670 | T | C | 77 | a0001c0001t0002g0038 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1453-2239T>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876670 | |||||||
| chr2:69876714 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1453-2195C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876714 | |||||||
| chr2:69876722 | C | T | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1453-2187C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876722 | |||||||
| chr2:69876776 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1453-2133A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876776 | |||||||
| chr2:69876822 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1453-2087A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876822 | |||||||
| chr2:69876845 | C | T | 6 | a0001c0001t0007g0025 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-2064C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876845 | |||||||
| chr2:69876850 | G | A | 2 | a0001c0001t0017g0109 a0001c0001t0017g0110 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1453-2059G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69876850 | |||||||
| chr2:69877141 | A | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1768A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877141 | |||||||
| chr2:69877153 | A | C | 10 | a0001c0001t0002g0008 a0001c0001t0002g0219 a0001c0001t0002g0224 others(7): Show |
11 | HG02074.hp2 NA18943.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.1453-1756A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877153 | |||||||
| chr2:69877181 | A | C | 18 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0047 others(15): Show |
21 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1453-1728A>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877181 | |||||||
| chr2:69877183 | G | C | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1453-1726G>C | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877183 | |||||||
| chr2:69877492 | A | G | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1453-1417A>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877492 | |||||||
| chr2:69877639 | C | G | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1270C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877639 | |||||||
| chr2:69877686 | CAG | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453-1213_1453-121 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877686 | ||||||
| chr2:69877706 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1453-1203T>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877706 | |||||||
| chr2:69877706 | T | TTG | 29 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0019 others(26): Show |
34 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1453-1176_1453-117 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | T | TTGTG | 5 | a0001c0001t0003g0076 a0001c0001t0003g0089 a0001c0001t0003g0091 others(2): Show |
5 | HG01243.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453-1178_1453-117 others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | T | TTGTGTG | 20 | a0001c0002t0004g0002 a0001c0002t0004g0033 a0001c0002t0004g0302 others(17): Show |
27 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1453-1180_1453-117 others(10): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | T | TTGTGTGT others(1): Show |
15 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0304 others(12): Show |
19 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1453-1182_1453-117 others(12): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | T | TTGTGTGT others(3): Show |
4 | a0001c0002t0004g0310 a0001c0002t0004g0312 a0001c0002t0004g0314 others(1): Show |
4 | HG01361.hp1 NA18964.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1184_1453-117 others(14): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | TTG | T | 101 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(98): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1453-1176_1453-117 others(6): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877706 | TTGTG | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1453-1178_1453-117 others(8): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877706 | ||||||
| chr2:69877733 | T | A | 1 | a0001c0001t0003g0045 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1453-1176T>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877733 | |||||||
| chr2:69877771 | ATCT | A | 3 | a0001c0002t0007g0020 a0001c0002t0019g0114 a0001c0002t0019g0115 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1133_1453-113 others(7): Show |
GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 69877771 | ||||||
| chr2:69877814 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1453-1095G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877814 | |||||||
| chr2:69877834 | C | G | 2 | a0001c0004t0014g0111 a0001c0004t0014g0112 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1453-1075C>G | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877834 | |||||||
| chr2:69877963 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1453-946G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69877963 | |||||||
| chr2:69878252 | G | A | 1 | a0001c0001t0010g0295 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1453-657G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878252 | |||||||
| chr2:69878521 | A | T | 1 | a0001c0001t0003g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1453-388A>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878521 | |||||||
| chr2:69878674 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1453-235C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878674 | |||||||
| chr2:69878680 | G | A | 39 | a0001c0002t0004g0002 a0001c0002t0004g0011 a0001c0002t0004g0012 others(36): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1453-229G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878680 | |||||||
| chr2:69878721 | C | T | 1 | a0001c0001t0007g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1453-188C>T | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878721 | |||||||
| chr2:69878832 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1453-77G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878832 | |||||||
| chr2:69878886 | G | A | 47 | a0001c0001t0018g0034 a0001c0001t0018g0036 a0001c0001t0026g0035 others(44): Show |
59 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1453-23G>A | GMCL1 | ENSG00000087338.5 | transcript | ENST00000282570.4 | protein_coding | 13/13 | chr2 | 69878886 |