Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2800 |
| ensemblid | ENSG00000136935.14 |
| hgncid | 4424 |
| symbol | GOLGA1 |
| name | golgin A1 |
| refseq_nuc | NM_002077.4 |
| refseq_prot | NP_002068.2 |
| ensembl_nuc | ENST00000373555.9 |
| ensembl_prot | ENSP00000362656.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 124878275 |
| end | 124941083 |
| strand | - |
| ver | v1.2 |
| region | chr9:124878275-124941083 |
| region5000 | chr9:124873275-124946083 |
| regionname0 | GOLGA1_chr9_124878275_124941083 |
| regionname5000 | GOLGA1_chr9_124873275_124946083 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 767 | 183 | 41 | 44 | 69 | 10 | 19 | 52 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0002 | 0/1 | 767 | 167 | 29 | 16 | 104 | 4 | 13 | 80 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0003 | 0/0 | 767 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0004 | 1/0 | 767 | 5 | 3 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0005 | 0/0 | 767 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0006 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0007 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0008 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0009 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0010 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| a0011 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | MFAKL others(762): Show |
chr9 | 124873275 | 124946083 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2301 | 173 | 33 | 44 | 67 | 10 | 19 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0001c0005 | 0/0 | 2301 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0001c0010 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0001c0014 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0002c0002 | 0/1 | 2301 | 103 | 18 | 14 | 60 | 4 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0002c0003 | 0/0 | 2301 | 59 | 7 | 1 | 44 | 0 | 7 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0002c0006 | 0/0 | 2301 | 5 | 4 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0003c0004 | 0/0 | 2301 | 11 | 9 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0003c0016 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0004c0007 | 1/0 | 2301 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0005c0008 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0006c0011 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0007c0009 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0008c0017 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0009c0013 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0010c0012 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 | ||
| a0011c0015 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | ATGTT others(2296): Show |
chr9 | 124873275 | 124946083 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 4875 | 101 | 25 | 29 | 31 | 4 | 12 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0003 | 0/0 | 4877 | 45 | 7 | 8 | 18 | 6 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0004 | 0/0 | 4877 | 18 | 0 | 6 | 11 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0008 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0010 | 0/0 | 4875 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0016 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0017 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0018 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0001c0001t0019 | 0/0 | 4875 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0001c0005t0005 | 0/0 | 4877 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0001c0010t0002 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0001c0014t0003 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0002t0001 | 0/1 | 4877 | 97 | 14 | 14 | 58 | 4 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0002t0008 | 0/0 | 4877 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0002t0011 | 0/0 | 4877 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0002t0020 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0003t0001 | 0/0 | 4877 | 55 | 4 | 1 | 43 | 0 | 7 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0003t0012 | 0/0 | 4877 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0003t0014 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0003t0015 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0002c0006t0003 | 0/0 | 4877 | 5 | 4 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0003c0004t0006 | 0/0 | 4878 | 6 | 5 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4873): Show |
chr9 | 124873275 | 124946083 |
| a0003c0004t0009 | 0/0 | 4878 | 4 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4873): Show |
chr9 | 124873275 | 124946083 |
| a0003c0004t0013 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0003c0016t0001 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0004c0007t0007 | 1/0 | 4877 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0005c0008t0002 | 0/0 | 4875 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0006c0011t0003 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0007c0009t0008 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0008c0017t0004 | 0/0 | 4877 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| a0009c0013t0002 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0010c0012t0002 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4870): Show |
chr9 | 124873275 | 124946083 |
| a0011c0015t0013 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | GGTTC others(4872): Show |
chr9 | 124873275 | 124946083 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0018g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0001t0019g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0005t0005g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0005t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0005t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0005t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0005t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0010t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0001c0014t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0011g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0002t0020g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0003t0015g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0006t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0006t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0006t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0006t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0002c0006t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0004t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0003c0016t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0004c0007t0007g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0004c0007t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0004c0007t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0004c0007t0007g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0005c0008t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0006c0011t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0007c0009t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0008c0017t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0009c0013t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0010c0012t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| a0011c0015t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0047 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0310 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0057 | EUR | FIN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | FIN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0205 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0215 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0192 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00639 | hp2 | a0003 | c0004 | t0009 | g0077 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01069 | hp2 | a0003 | c0004 | t0006 | g0104 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0309 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01074 | hp2 | a0005 | c0008 | t0002 | g0147 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01109 | hp1 | a0004 | c0007 | t0007 | g0013 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01167 | hp1 | a0002 | c0006 | t0003 | g0081 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0196 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0276 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01884 | hp1 | a0003 | c0004 | t0009 | g0103 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01884 | hp2 | a0003 | c0016 | t0001 | g0108 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0135 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02027 | hp1 | a0001 | c0001 | t0017 | g0236 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0184 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02055 | hp2 | a0006 | c0011 | t0003 | g0040 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02071 | hp2 | a0001 | c0001 | t0018 | g0140 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02145 | hp1 | a0001 | c0005 | t0005 | g0328 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CDX | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CDX | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02258 | hp1 | a0003 | c0004 | t0006 | g0107 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02258 | hp2 | a0002 | c0002 | t0011 | g0034 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02280 | hp1 | a0004 | c0007 | t0007 | g0076 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02451 | hp1 | a0001 | c0005 | t0005 | g0327 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02523 | hp1 | a0007 | c0009 | t0008 | g0043 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0206 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02572 | hp1 | a0004 | c0007 | t0007 | g0013 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02615 | hp2 | a0003 | c0004 | t0006 | g0106 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0045 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02683 | hp1 | a0008 | c0017 | t0004 | g0085 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0199 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02717 | hp2 | a0001 | c0005 | t0005 | g0006 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02723 | hp1 | a0003 | c0004 | t0006 | g0101 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0044 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0275 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02895 | hp1 | a0002 | c0006 | t0003 | g0082 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02897 | hp1 | a0002 | c0006 | t0003 | g0083 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02922 | hp1 | a0004 | c0007 | t0007 | g0075 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02965 | hp1 | a0002 | c0003 | t0014 | g0038 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02976 | hp2 | a0001 | c0005 | t0005 | g0006 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03130 | hp1 | a0001 | c0005 | t0005 | g0006 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03139 | hp1 | a0003 | c0004 | t0006 | g0244 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03139 | hp2 | a0001 | c0005 | t0005 | g0329 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03195 | hp1 | a0001 | c0005 | t0005 | g0037 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03195 | hp2 | a0002 | c0006 | t0003 | g0080 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0281 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03225 | hp2 | a0003 | c0004 | t0009 | g0102 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0323 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03486 | hp1 | a0002 | c0002 | t0020 | g0326 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03540 | hp1 | a0002 | c0006 | t0003 | g0084 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03540 | hp2 | a0002 | c0002 | t0011 | g0034 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03579 | hp1 | a0003 | c0004 | t0006 | g0105 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0253 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0186 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0282 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0209 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04115 | hp1 | a0010 | c0012 | t0002 | g0145 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0210 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0188 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18522 | hp2 | a0001 | c0005 | t0005 | g0037 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0203 | EAS | CHB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0207 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18977 | hp2 | a0001 | c0001 | t0010 | g0241 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18980 | hp2 | a0001 | c0010 | t0002 | g0091 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18981 | hp1 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18982 | hp2 | a0002 | c0002 | t0008 | g0268 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0214 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18985 | hp2 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18987 | hp1 | a0002 | c0003 | t0001 | g0213 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18987 | hp2 | a0002 | c0002 | t0008 | g0269 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0242 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0185 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0187 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0225 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19006 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0227 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19043 | hp1 | a0003 | c0004 | t0013 | g0079 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0224 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19077 | hp2 | a0001 | c0014 | t0003 | g0066 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20129 | hp1 | a0002 | c0002 | t0011 | g0312 | AFR | ASW | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ASW | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0272 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0239 | SAS | GIH | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | GIH | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02486 | hp2 | a0003 | c0004 | t0009 | g0100 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG02559 | hp2 | a0002 | c0003 | t0012 | g0112 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG03471 | hp2 | a0009 | c0013 | t0002 | g0163 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG06807 | hp1 | a0011 | c0015 | t0013 | g0078 | AFR | USA | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0222 | AFR | USA | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA18955 | hp2 | a0002 | c0003 | t0015 | g0200 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| NA21309 | hp2 | a0002 | c0003 | t0012 | g0111 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0291 | REF | REF | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| homoSapiens | grch38p0 | a0004 | c0007 | t0007 | g0267 | REF | REF | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124881887 | G | A | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2033C>T | p.Ala678Val | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/23 | 2351/4877 | 2033/2304 | 678/767 | chr9 | 124881887 | |||
| chr9:124882568 | G | C | 1 | a0010 | 1 | HG04115.hp1 | missense_variant&splice_region_variant | MODERATE | c.1907C>G | p.Thr636Ser | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/23 | 2225/4877 | 1907/2304 | 636/767 | chr9 | 124882568 | |||
| chr9:124889187 | G | A | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1717C>T | p.Arg573Trp | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/23 | 2035/4877 | 1717/2304 | 573/767 | chr9 | 124889187 | |||
| chr9:124889479 | C | T | 1 | a0007 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1555G>A | p.Glu519Lys | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 17/23 | 1873/4877 | 1555/2304 | 519/767 | chr9 | 124889479 | |||
| chr9:124899366 | G | A | 1 | a0002 | 166 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(163): Show |
missense_variant | MODERATE | c.1274C>T | p.Thr425Met | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/23 | 1592/4877 | 1274/2304 | 425/767 | chr9 | 124899366 | |||
| chr9:124899472 | C | T | 1 | a0005 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1168G>A | p.Ala390Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/23 | 1486/4877 | 1168/2304 | 390/767 | chr9 | 124899472 | |||
| chr9:124908433 | G | C | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1009C>G | p.Gln337Glu | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/23 | 1327/4877 | 1009/2304 | 337/767 | chr9 | 124908433 | |||
| chr9:124911921 | A | C | 10 | a0001 a0002 a0003 others(7): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.949T>G | p.Leu317Val | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/23 | 1267/4877 | 949/2304 | 317/767 | chr9 | 124911921 | |||
| chr9:124921795 | T | C | 2 | a0003 a0011 |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
missense_variant | MODERATE | c.659A>G | p.Asn220Ser | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/23 | 977/4877 | 659/2304 | 220/767 | chr9 | 124921795 | |||
| chr9:124921796 | T | G | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.658A>C | p.Asn220His | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/23 | 976/4877 | 658/2304 | 220/767 | chr9 | 124921796 | |||
| chr9:124926719 | T | C | 1 | a0008 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.422A>G | p.Gln141Arg | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/23 | 740/4877 | 422/2304 | 141/767 | chr9 | 124926719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124881177 | T | C | 2 | a0001c0010 a0002c0002 |
103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
synonymous_variant | LOW | c.2217A>G | p.Glu739Glu | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/23 | 2535/4877 | 2217/2304 | 739/767 | chr9 | 124881177 | |||
| chr9:124882525 | A | T | 1 | a0002c0006 | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.1950T>A | p.Thr650Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/23 | 2268/4877 | 1950/2304 | 650/767 | chr9 | 124882525 | |||
| chr9:124888352 | A | C | 1 | a0001c0005 | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.1806T>G | p.Thr602Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/23 | 2124/4877 | 1806/2304 | 602/767 | chr9 | 124888352 | |||
| chr9:124889170 | G | A | 2 | a0003c0004 a0011c0015 |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.1734C>T | p.Ala578Ala | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/23 | 2052/4877 | 1734/2304 | 578/767 | chr9 | 124889170 | |||
| chr9:124921240 | T | C | 1 | a0001c0014 | 1 | NA19077.hp2 | splice_region_variant&synonymous_variant | LOW | c.732A>G | p.Arg244Arg | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/23 | 1050/4877 | 732/2304 | 244/767 | chr9 | 124921240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124878475 | T | G | 1 | a0003c0004t0006 | 6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2055A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2055 | chr9 | 124878475 | ||||||
| chr9:124878487 | G | A | 3 | a0001c0005t0005 a0003c0004t0013 a0011c0015t0013 |
10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2043C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2043 | chr9 | 124878487 | ||||||
| chr9:124878491 | G | A | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2039C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2039 | chr9 | 124878491 | ||||||
| chr9:124878503 | A | G | 1 | a0002c0003t0012 | 2 | HG02559.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2027T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2027 | chr9 | 124878503 | ||||||
| chr9:124878699 | T | TG | 2 | a0003c0004t0006 a0003c0004t0009 |
10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1830dupC | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1830 | chr9 | 124878699 | ||||||
| chr9:124878713 | C | T | 1 | a0002c0003t0012 | 2 | HG02559.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1817G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1817 | chr9 | 124878713 | ||||||
| chr9:124878759 | T | C | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*1771A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1771 | chr9 | 124878759 | ||||||
| chr9:124879319 | T | A | 1 | a0001c0001t0017 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1211A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1211 | chr9 | 124879319 | ||||||
| chr9:124879356 | C | T | 1 | a0002c0003t0015 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1174 | chr9 | 124879356 | ||||||
| chr9:124879386 | T | C | 3 | a0001c0001t0008 a0002c0002t0008 a0007c0009t0008 |
4 | HG02523.hp1 NA18982.hp2 NA18987.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1144A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1144 | chr9 | 124879386 | ||||||
| chr9:124879446 | G | A | 1 | a0001c0001t0018 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1084C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1084 | chr9 | 124879446 | ||||||
| chr9:124879448 | A | G | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1082 | chr9 | 124879448 | ||||||
| chr9:124879485 | G | A | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1045C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1045 | chr9 | 124879485 | ||||||
| chr9:124879753 | CAT | C | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0018 others(5): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*775_*776delAT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 775 | chr9 | 124879753 | ||||||
| chr9:124879857 | A | T | 4 | a0001c0001t0003 a0001c0014t0003 a0002c0006t0003 others(1): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*673T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 673 | chr9 | 124879857 | ||||||
| chr9:124879952 | A | G | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*578T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 578 | chr9 | 124879952 | ||||||
| chr9:124880073 | T | C | 1 | a0001c0001t0019 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 457 | chr9 | 124880073 | ||||||
| chr9:124938807 | C | T | 1 | a0002c0002t0011 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-96G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/23 | 96 | chr9 | 124938807 | ||||||
| chr9:124940134 | T | C | 1 | a0001c0001t0010 | 4 | NA18977.hp2 NA18981.hp1 NA18990.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-184A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/23 | 1423 | chr9 | 124940134 | ||||||
| chr9:124941034 | G | T | 1 | a0002c0003t0014 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-269C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2323 | chr9 | 124941034 | ||||||
| chr9:124941050 | G | A | 1 | a0002c0002t0020 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-285C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2339 | chr9 | 124941050 | ||||||
| chr9:124941072 | C | A | 1 | a0001c0005t0005 | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-307G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2361 | chr9 | 124941072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124880643 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2224-33G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880643 | |||||||
| chr9:124880649 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0245 |
3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2224-39T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880649 | |||||||
| chr9:124880802 | G | C | 120 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(117): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.2224-192C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880802 | |||||||
| chr9:124880889 | T | C | 196 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(193): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2224-279A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880889 | |||||||
| chr9:124880897 | C | T | 323 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(320): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.2223+274G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880897 | |||||||
| chr9:124881132 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2223+39C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124881132 | |||||||
| chr9:124881306 | G | A | 1 | a0003c0004t0013g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2137-49C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881306 | |||||||
| chr9:124881327 | C | T | 2 | a0002c0002t0001g0306 a0002c0002t0001g0307 |
2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2137-70G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881327 | |||||||
| chr9:124881438 | C | G | 1 | a0002c0003t0014g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2137-181G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881438 | |||||||
| chr9:124881440 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2137-183A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881440 | |||||||
| chr9:124881481 | T | A | 106 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(103): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2137-224A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881481 | |||||||
| chr9:124881526 | G | A | 1 | a0002c0003t0001g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2136+258C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881526 | |||||||
| chr9:124881667 | A | G | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.2136+117T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881667 | |||||||
| chr9:124881672 | G | A | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2136+112C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881672 | |||||||
| chr9:124881710 | T | TG | 26 | a0002c0002t0001g0028 a0002c0002t0001g0030 a0002c0002t0001g0031 others(23): Show |
31 | HG00140.hp2 HG00673.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2136+73dupC | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881710 | |||||||
| chr9:124882017 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1966-63C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882017 | |||||||
| chr9:124882031 | G | A | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1966-77C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882031 | |||||||
| chr9:124882095 | T | G | 7 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(4): Show |
10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1966-141A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882095 | |||||||
| chr9:124882098 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1966-144C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882098 | |||||||
| chr9:124882123 | G | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1966-169C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882123 | |||||||
| chr9:124882163 | T | C | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1966-209A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882163 | |||||||
| chr9:124882214 | C | CCA | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1966-262_1966-261d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882214 | |||||||
| chr9:124882318 | C | T | 3 | a0002c0002t0001g0274 a0002c0002t0001g0275 a0002c0002t0001g0279 |
3 | HG00642.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1965+192G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882318 | |||||||
| chr9:124882319 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1965+191C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882319 | |||||||
| chr9:124882334 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1965+176C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882334 | |||||||
| chr9:124882336 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1965+174C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882336 | |||||||
| chr9:124882405 | G | T | 7 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(4): Show |
10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1965+105C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882405 | |||||||
| chr9:124882428 | C | T | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1965+82G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882428 | |||||||
| chr9:124882603 | G | A | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1906-34C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882603 | |||||||
| chr9:124882858 | G | A | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1906-289C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882858 | |||||||
| chr9:124882863 | G | A | 15 | a0002c0003t0001g0001 a0002c0003t0001g0185 a0002c0003t0001g0192 others(12): Show |
18 | HG00609.hp1 HG00673.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1906-294C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882863 | |||||||
| chr9:124882925 | A | G | 316 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(313): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1906-356T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882925 | |||||||
| chr9:124882962 | C | T | 14 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(11): Show |
17 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1906-393G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882962 | |||||||
| chr9:124882963 | G | A | 1 | a0001c0001t0004g0026 | 2 | HG00621.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1906-394C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882963 | |||||||
| chr9:124883006 | G | T | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1906-437C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883006 | |||||||
| chr9:124883104 | AT | A | 91 | a0001c0001t0002g0019 a0001c0001t0002g0117 a0001c0001t0002g0161 others(88): Show |
108 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1906-536delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883104 | |||||||
| chr9:124883185 | C | T | 4 | a0002c0002t0001g0278 a0002c0002t0001g0287 a0002c0002t0001g0289 others(1): Show |
4 | NA18964.hp2 NA18995.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-616G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883185 | |||||||
| chr9:124883258 | G | C | 109 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(106): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1906-689C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883258 | |||||||
| chr9:124883292 | CT | C | 17 | a0001c0001t0002g0128 a0001c0001t0004g0003 a0001c0001t0004g0026 others(14): Show |
21 | HG00621.hp1 HG01123.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1906-724delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883292 | |||||||
| chr9:124883609 | G | A | 2 | a0002c0002t0011g0034 a0002c0002t0011g0312 |
3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1906-1040C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883609 | |||||||
| chr9:124883848 | G | A | 2 | a0002c0002t0001g0318 a0002c0002t0001g0322 |
2 | HG02080.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1906-1279C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883848 | |||||||
| chr9:124883871 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1906-1302G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883871 | |||||||
| chr9:124883901 | GTTT | G | 3 | a0002c0002t0001g0002 a0002c0002t0001g0258 a0002c0002t0001g0261 |
6 | NA18989.hp1 NA18998.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-1335_1906-133 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883901 | |||||||
| chr9:124883937 | A | G | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1906-1368T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883937 | |||||||
| chr9:124883979 | T | G | 1 | a0002c0002t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1906-1410A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883979 | |||||||
| chr9:124884016 | A | T | 6 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0052 others(3): Show |
8 | NA18955.hp1 NA18960.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1906-1447T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884016 | |||||||
| chr9:124884016 | AT | A | 6 | a0001c0001t0003g0056 a0001c0001t0004g0233 a0002c0002t0001g0259 others(3): Show |
6 | HG00558.hp1 HG02486.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906-1448delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884016 | |||||||
| chr9:124884018 | T | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1906-1449A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884018 | |||||||
| chr9:124884034 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1906-1465G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884034 | |||||||
| chr9:124884074 | C | T | 58 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(55): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1906-1505G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884074 | |||||||
| chr9:124884246 | A | AGGTGAT | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1906-1683_1906-167 others(10): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884246 | |||||||
| chr9:124884400 | A | C | 2 | a0002c0002t0001g0306 a0002c0002t0001g0307 |
2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1906-1831T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884400 | |||||||
| chr9:124884405 | G | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1906-1836C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884405 | |||||||
| chr9:124884499 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1906-1930G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884499 | |||||||
| chr9:124884500 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1906-1931C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884500 | |||||||
| chr9:124884764 | C | G | 1 | a0001c0001t0003g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1906-2195G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884764 | |||||||
| chr9:124884777 | C | T | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1906-2208G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884777 | |||||||
| chr9:124884883 | G | C | 3 | a0002c0002t0001g0274 a0002c0002t0001g0275 a0002c0002t0001g0279 |
3 | HG00642.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1906-2314C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884883 | |||||||
| chr9:124885121 | G | A | 2 | a0003c0004t0013g0079 a0011c0015t0013g0078 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1906-2552C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885121 | |||||||
| chr9:124885133 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1906-2564G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885133 | |||||||
| chr9:124885188 | G | A | 1 | a0001c0001t0004g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1906-2619C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885188 | |||||||
| chr9:124885306 | G | A | 12 | a0002c0003t0012g0111 a0002c0003t0012g0112 a0003c0004t0006g0101 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1906-2737C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885306 | |||||||
| chr9:124885322 | C | CA | 9 | a0001c0001t0002g0183 a0001c0001t0016g0045 a0001c0005t0005g0006 others(6): Show |
12 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1906-2754dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | |||||||
| chr9:124885322 | C | CAA | 136 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(133): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1906-2755_1906-275 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | |||||||
| chr9:124885322 | C | CAAA | 6 | a0001c0001t0002g0114 a0001c0001t0002g0158 a0001c0001t0002g0165 others(3): Show |
6 | HG02622.hp2 NA18906.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-2756_1906-275 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | |||||||
| chr9:124885440 | A | G | 8 | a0001c0001t0016g0045 a0001c0005t0005g0006 a0001c0005t0005g0037 others(5): Show |
11 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1905+2813T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885440 | |||||||
| chr9:124885442 | G | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1905+2811C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885442 | |||||||
| chr9:124885484 | CA | C | 178 | a0001c0001t0002g0142 a0001c0001t0003g0046 a0001c0001t0004g0003 others(175): Show |
207 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1905+2768delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885484 | |||||||
| chr9:124885521 | G | A | 90 | a0001c0001t0008g0042 a0002c0002t0001g0002 a0002c0002t0001g0004 others(87): Show |
106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1905+2732C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885521 | |||||||
| chr9:124885571 | GGGA | G | 177 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(174): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1905+2679_1905+268 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885571 | |||||||
| chr9:124885903 | C | T | 55 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(52): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1905+2350G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885903 | |||||||
| chr9:124885977 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1905+2276C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885977 | |||||||
| chr9:124885980 | G | A | 3 | a0003c0004t0009g0100 a0003c0004t0009g0102 a0003c0004t0009g0103 |
3 | HG01884.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1905+2273C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885980 | |||||||
| chr9:124886075 | A | G | 14 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0118 others(11): Show |
16 | HG00280.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1905+2178T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886075 | |||||||
| chr9:124886411 | G | GC | 48 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1841_1905+184 others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886411 | |||||||
| chr9:124886412 | G | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1841C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886412 | |||||||
| chr9:124886413 | C | G | 48 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1840G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886413 | |||||||
| chr9:124886568 | T | C | 1 | a0002c0003t0001g0215 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1905+1685A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886568 | |||||||
| chr9:124886634 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1905+1619T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886634 | |||||||
| chr9:124886649 | C | T | 40 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0021 others(37): Show |
43 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1905+1604G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886649 | |||||||
| chr9:124886655 | A | G | 1 | a0002c0002t0001g0029 | 2 | HG01099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1905+1598T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886655 | |||||||
| chr9:124886713 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1905+1540C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886713 | |||||||
| chr9:124886927 | G | A | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1905+1326C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886927 | |||||||
| chr9:124887087 | A | T | 1 | a0002c0002t0001g0308 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1905+1166T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887087 | |||||||
| chr9:124887142 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1905+1111G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887142 | |||||||
| chr9:124887266 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1905+987A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887266 | |||||||
| chr9:124887298 | A | T | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1905+955T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887298 | |||||||
| chr9:124887327 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0116 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1905+926C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887327 | |||||||
| chr9:124887339 | A | AGGGCTGG others(12): Show |
1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1905+895_1905+913d others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887339 | |||||||
| chr9:124887350 | G | A | 10 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+903C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887350 | |||||||
| chr9:124887401 | G | A | 1 | a0002c0002t0001g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1905+852C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887401 | |||||||
| chr9:124887428 | T | A | 8 | a0002c0003t0001g0023 a0002c0003t0001g0186 a0002c0003t0001g0189 others(5): Show |
9 | HG00558.hp1 HG00597.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1905+825A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887428 | |||||||
| chr9:124887519 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1905+734A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887519 | |||||||
| chr9:124887553 | G | A | 1 | a0002c0003t0014g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1905+700C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887553 | |||||||
| chr9:124887751 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1905+502C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887751 | |||||||
| chr9:124887868 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1905+385G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887868 | |||||||
| chr9:124888042 | G | C | 146 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(143): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1905+211C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888042 | |||||||
| chr9:124888048 | G | A | 6 | a0001c0001t0002g0167 a0001c0001t0002g0169 a0001c0001t0002g0179 others(3): Show |
6 | HG00408.hp1 HG02040.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1905+205C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888048 | |||||||
| chr9:124888072 | TGGA | T | 4 | a0001c0001t0003g0009 a0001c0001t0003g0053 a0001c0001t0003g0071 others(1): Show |
5 | NA18960.hp1 NA18961.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1905+178_1905+180d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888072 | |||||||
| chr9:124888545 | A | G | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-149T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888545 | |||||||
| chr9:124888576 | C | T | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1762-180G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888576 | |||||||
| chr9:124888630 | G | C | 167 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(164): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1762-234C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888630 | |||||||
| chr9:124888650 | T | C | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-254A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888650 | |||||||
| chr9:124888688 | CTTTA | C | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-296_1762-293d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888688 | |||||||
| chr9:124888706 | T | C | 167 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(164): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1762-310A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888706 | |||||||
| chr9:124888781 | G | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1761+362C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888781 | |||||||
| chr9:124888835 | G | A | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1761+308C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888835 | |||||||
| chr9:124888971 | T | A | 84 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(81): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1761+172A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888971 | |||||||
| chr9:124889059 | C | A | 1 | a0002c0002t0020g0326 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1761+84G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889059 | |||||||
| chr9:124889062 | C | T | 106 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(103): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1761+81G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889062 | |||||||
| chr9:124889105 | C | T | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0019g0135 |
3 | HG01952.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1761+38G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889105 | |||||||
| chr9:124889800 | C | G | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1498-264G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124889800 | |||||||
| chr9:124890000 | G | C | 22 | a0001c0001t0002g0020 a0001c0001t0002g0160 a0001c0001t0002g0167 others(19): Show |
23 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1497+389C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890000 | |||||||
| chr9:124890018 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1497+371T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890018 | |||||||
| chr9:124890092 | T | C | 1 | a0002c0002t0001g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1497+297A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890092 | |||||||
| chr9:124890181 | C | A | 47 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(44): Show |
53 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1497+208G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890181 | |||||||
| chr9:124890342 | G | A | 88 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(85): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1497+47C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890342 | |||||||
| chr9:124890381 | G | C | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1497+8C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890381 | |||||||
| chr9:124890532 | G | A | 11 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(8): Show |
11 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408-54C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890532 | |||||||
| chr9:124890562 | G | A | 1 | a0002c0002t0001g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1408-84C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890562 | |||||||
| chr9:124890720 | C | T | 3 | a0002c0003t0001g0225 a0002c0003t0001g0226 a0002c0003t0001g0227 |
3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1408-242G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890720 | |||||||
| chr9:124890726 | C | T | 102 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(99): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1408-248G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890726 | |||||||
| chr9:124890788 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1408-310C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890788 | |||||||
| chr9:124890820 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-342C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890820 | |||||||
| chr9:124890856 | AAAG | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-381_1408-379d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890856 | |||||||
| chr9:124890964 | G | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1408-486C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890964 | |||||||
| chr9:124891200 | C | G | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1408-722G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891200 | |||||||
| chr9:124891207 | C | A | 1 | a0001c0001t0002g0139 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1408-729G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891207 | |||||||
| chr9:124891222 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-744C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891222 | |||||||
| chr9:124891222 | G | C | 141 | a0001c0001t0008g0042 a0002c0002t0001g0002 a0002c0002t0001g0004 others(138): Show |
163 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1408-744C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891222 | |||||||
| chr9:124891306 | G | A | 2 | a0002c0003t0001g0187 a0002c0003t0001g0202 |
2 | NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1408-828C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891306 | |||||||
| chr9:124891378 | C | A | 1 | a0002c0002t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1408-900G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891378 | |||||||
| chr9:124891551 | T | A | 1 | a0002c0002t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1408-1073A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891551 | |||||||
| chr9:124891678 | CTT | C | 6 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(3): Show |
6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1202_1408-120 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891678 | |||||||
| chr9:124891681 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-1203C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891681 | |||||||
| chr9:124891764 | C | G | 4 | a0002c0002t0001g0029 a0002c0002t0001g0036 a0002c0002t0001g0256 others(1): Show |
6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1286G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891764 | |||||||
| chr9:124891770 | G | A | 1 | a0002c0002t0001g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1408-1292C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891770 | |||||||
| chr9:124891774 | A | G | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-1296T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891774 | |||||||
| chr9:124891978 | C | CAG | 318 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(315): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1408-1502_1408-150 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891978 | |||||||
| chr9:124892081 | G | T | 1 | a0002c0003t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1603C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892081 | |||||||
| chr9:124892249 | C | T | 1 | a0002c0003t0001g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1408-1771G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892249 | |||||||
| chr9:124892250 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408-1772C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892250 | |||||||
| chr9:124892252 | G | C | 1 | a0002c0003t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1774C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892252 | |||||||
| chr9:124892253 | C | G | 1 | a0002c0003t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1775G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892253 | |||||||
| chr9:124892315 | G | A | 1 | a0002c0003t0001g0196 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1408-1837C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892315 | |||||||
| chr9:124892338 | T | C | 149 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(146): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1408-1860A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892338 | |||||||
| chr9:124892707 | C | T | 1 | a0002c0002t0001g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1408-2229G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892707 | |||||||
| chr9:124892793 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2315C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892793 | |||||||
| chr9:124892888 | C | T | 1 | a0002c0002t0001g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1408-2410G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892888 | |||||||
| chr9:124892893 | T | C | 1 | a0002c0002t0001g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1408-2415A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892893 | |||||||
| chr9:124892932 | C | CA | 138 | a0001c0001t0008g0042 a0001c0001t0010g0240 a0002c0002t0001g0002 others(135): Show |
160 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1408-2455dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892932 | |||||||
| chr9:124892954 | G | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0126 others(6): Show |
11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1408-2476C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892954 | |||||||
| chr9:124892977 | A | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2499T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892977 | |||||||
| chr9:124892999 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2521A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892999 | |||||||
| chr9:124893106 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1408-2628G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893106 | |||||||
| chr9:124893226 | T | A | 1 | a0011c0015t0013g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1408-2748A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893226 | |||||||
| chr9:124893311 | C | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0245 |
3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1408-2833G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893311 | |||||||
| chr9:124893486 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1408-3008G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893486 | |||||||
| chr9:124893546 | G | A | 1 | a0002c0003t0001g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1408-3068C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893546 | |||||||
| chr9:124893554 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-3076G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893554 | |||||||
| chr9:124893677 | C | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-3199G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893677 | |||||||
| chr9:124893817 | T | C | 11 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0118 others(8): Show |
13 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-3339A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893817 | |||||||
| chr9:124893888 | T | G | 1 | a0001c0001t0002g0292 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1408-3410A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893888 | |||||||
| chr9:124893924 | G | A | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1408-3446C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893924 | |||||||
| chr9:124893947 | C | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1408-3469G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893947 | |||||||
| chr9:124894276 | C | G | 2 | a0002c0003t0001g0253 a0002c0003t0001g0282 |
2 | HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1408-3798G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894276 | |||||||
| chr9:124894380 | T | TTG | 11 | a0001c0001t0003g0057 a0001c0001t0004g0229 a0001c0005t0005g0006 others(8): Show |
14 | HG00280.hp1 HG00738.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1408-3904_1408-390 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | |||||||
| chr9:124894380 | TTG | T | 186 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(183): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1408-3904_1408-390 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | |||||||
| chr9:124894380 | TTGTG | T | 10 | a0001c0001t0002g0020 a0001c0001t0002g0170 a0001c0001t0002g0172 others(7): Show |
11 | HG01167.hp1 HG01884.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408-3906_1408-390 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | |||||||
| chr9:124894482 | C | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1408-4004G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894482 | |||||||
| chr9:124894536 | A | G | 4 | a0002c0002t0001g0029 a0002c0002t0001g0036 a0002c0002t0001g0256 others(1): Show |
6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+4013T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894536 | |||||||
| chr9:124894585 | G | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1407+3964C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894585 | |||||||
| chr9:124894650 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1407+3899A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894650 | |||||||
| chr9:124894747 | A | G | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1407+3802T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894747 | |||||||
| chr9:124894900 | C | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0116 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1407+3649G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894900 | |||||||
| chr9:124894949 | C | CACATCCA others(27): Show |
1 | a0002c0002t0020g0326 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+3599_1407+360 others(38): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894949 | |||||||
| chr9:124894949 | C | CCCATCCA others(27): Show |
89 | a0001c0001t0008g0042 a0002c0002t0001g0002 a0002c0002t0001g0004 others(86): Show |
105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1407+3566_1407+359 others(38): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894949 | |||||||
| chr9:124894961 | A | G | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+3588T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894961 | |||||||
| chr9:124894965 | A | T | 5 | a0001c0001t0002g0021 a0001c0001t0002g0118 a0001c0001t0002g0136 others(2): Show |
6 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+3584T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894965 | |||||||
| chr9:124894969 | ATCCACAA others(10): Show |
A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407+3563_1407+357 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894969 | |||||||
| chr9:124894970 | T | A | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1407+3579A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894970 | |||||||
| chr9:124895115 | A | T | 8 | a0002c0003t0001g0022 a0002c0003t0001g0187 a0002c0003t0001g0188 others(5): Show |
9 | HG00438.hp1 HG00621.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+3434T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895115 | |||||||
| chr9:124895150 | TCTCCACA others(9): Show |
T | 1 | a0002c0002t0001g0262 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1407+3383_1407+339 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895150 | |||||||
| chr9:124895268 | ATCCACAA others(140): Show |
A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+3134_1407+328 others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895268 | |||||||
| chr9:124895302 | CTCCACAA others(10): Show |
C | 1 | a0002c0002t0001g0274 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1407+3230_1407+324 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895302 | |||||||
| chr9:124895348 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1407+3201T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895348 | |||||||
| chr9:124895365 | TCTCCACA others(42): Show |
T | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1407+3135_1407+318 others(53): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895365 | |||||||
| chr9:124895445 | A | AACCCTCC others(26): Show |
1 | a0002c0002t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1407+3071_1407+310 others(37): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895445 | |||||||
| chr9:124895567 | C | T | 1 | a0002c0003t0001g0216 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1407+2982G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895567 | |||||||
| chr9:124895624 | G | GGAGCCTC others(9): Show |
1 | a0001c0001t0002g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1407+2909_1407+292 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895624 | |||||||
| chr9:124895795 | T | A | 1 | a0002c0003t0014g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1407+2754A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895795 | |||||||
| chr9:124895806 | GACCCTCC others(10): Show |
G | 7 | a0001c0001t0002g0159 a0001c0001t0003g0056 a0001c0001t0003g0057 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+2726_1407+274 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895806 | |||||||
| chr9:124895859 | C | T | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1407+2690G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895859 | |||||||
| chr9:124895862 | TCCACAAC others(10): Show |
T | 6 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(3): Show |
6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+2670_1407+268 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895862 | |||||||
| chr9:124895896 | CCCACAAC others(10): Show |
C | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+2636_1407+265 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895896 | |||||||
| chr9:124895900 | CAACAGAG others(42): Show |
C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+2600_1407+264 others(53): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895900 | |||||||
| chr9:124895939 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1407+2610T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895939 | |||||||
| chr9:124895947 | T | C | 1 | a0002c0002t0001g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1407+2602A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895947 | |||||||
| chr9:124895948 | A | G | 90 | a0001c0001t0008g0042 a0002c0002t0001g0002 a0002c0002t0001g0004 others(87): Show |
106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1407+2601T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895948 | |||||||
| chr9:124895949 | T | TAACAGAG others(10): Show |
1 | a0002c0002t0001g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1407+2583_1407+259 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895949 | |||||||
| chr9:124895968 | A | G | 1 | a0001c0001t0003g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1407+2581T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895968 | |||||||
| chr9:124896014 | C | T | 2 | a0001c0001t0003g0051 a0001c0001t0003g0067 |
2 | HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1407+2535G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896014 | |||||||
| chr9:124896191 | A | G | 90 | a0001c0001t0008g0042 a0002c0002t0001g0002 a0002c0002t0001g0004 others(87): Show |
106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1407+2358T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896191 | |||||||
| chr9:124896284 | C | T | 84 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(81): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1407+2265G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896284 | |||||||
| chr9:124896319 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1407+2230T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896319 | |||||||
| chr9:124896606 | C | A | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+1943G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896606 | |||||||
| chr9:124896756 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1407+1793T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896756 | |||||||
| chr9:124896890 | C | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+1659G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896890 | |||||||
| chr9:124896931 | CA | C | 6 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(3): Show |
9 | HG00558.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+1617delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896931 | |||||||
| chr9:124896997 | C | T | 1 | a0002c0003t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1407+1552G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896997 | |||||||
| chr9:124897067 | T | C | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1407+1482A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897067 | |||||||
| chr9:124897120 | T | C | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1407+1429A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897120 | |||||||
| chr9:124897132 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+1417A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897132 | |||||||
| chr9:124897513 | G | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1407+1036C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897513 | |||||||
| chr9:124897623 | G | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0052 others(4): Show |
9 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+926C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897623 | |||||||
| chr9:124897703 | T | C | 1 | a0002c0002t0001g0288 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1407+846A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897703 | |||||||
| chr9:124897796 | A | C | 1 | a0001c0001t0017g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1407+753T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897796 | |||||||
| chr9:124897808 | G | T | 1 | a0002c0003t0001g0213 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1407+741C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897808 | |||||||
| chr9:124897931 | G | T | 161 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(158): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1407+618C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897931 | |||||||
| chr9:124897985 | T | G | 32 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0113 others(29): Show |
34 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1407+564A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897985 | |||||||
| chr9:124898068 | T | C | 10 | a0002c0002t0001g0005 a0002c0002t0001g0304 a0002c0002t0001g0305 others(7): Show |
12 | HG00438.hp2 HG02080.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+481A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898068 | |||||||
| chr9:124898129 | C | G | 71 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(68): Show |
76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1407+420G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898129 | |||||||
| chr9:124898233 | C | T | 2 | a0002c0002t0001g0300 a0002c0002t0001g0301 |
2 | NA18965.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1407+316G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898233 | |||||||
| chr9:124898354 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+195C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898354 | |||||||
| chr9:124898414 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1407+135C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898414 | |||||||
| chr9:124898424 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1407+125T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898424 | |||||||
| chr9:124898792 | G | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-148C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898792 | |||||||
| chr9:124898914 | G | A | 1 | a0002c0002t0001g0313 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1312-270C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898914 | |||||||
| chr9:124898929 | C | G | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1312-285G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898929 | |||||||
| chr9:124898952 | T | G | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-308A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898952 | |||||||
| chr9:124898990 | G | A | 1 | a0009c0013t0002g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1311+339C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898990 | |||||||
| chr9:124899021 | C | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+308G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899021 | |||||||
| chr9:124899128 | C | T | 3 | a0003c0004t0006g0101 a0003c0004t0006g0106 a0003c0004t0006g0107 |
3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1311+201G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899128 | |||||||
| chr9:124899242 | T | C | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1311+87A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899242 | |||||||
| chr9:124899247 | A | C | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1311+82T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899247 | |||||||
| chr9:124899262 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1311+67G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899262 | |||||||
| chr9:124899294 | C | T | 1 | a0002c0002t0020g0326 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1311+35G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899294 | |||||||
| chr9:124899483 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG00597.hp2 | splice_region_variant&intron_variant | LOW | c.1162-5C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899483 | |||||||
| chr9:124899618 | C | A | 1 | a0002c0003t0001g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1162-140G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899618 | |||||||
| chr9:124899850 | C | G | 163 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(160): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1162-372G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899850 | |||||||
| chr9:124899874 | A | G | 3 | a0003c0004t0006g0101 a0003c0004t0006g0106 a0003c0004t0006g0107 |
3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1162-396T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899874 | |||||||
| chr9:124899881 | G | A | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-403C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899881 | |||||||
| chr9:124899882 | G | C | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-404C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899882 | |||||||
| chr9:124899883 | C | A | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-405G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899883 | |||||||
| chr9:124899886 | C | T | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-408G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899886 | |||||||
| chr9:124899896 | G | T | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-418C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899896 | |||||||
| chr9:124899950 | T | A | 1 | a0002c0002t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1162-472A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899950 | |||||||
| chr9:124900027 | G | A | 1 | a0002c0002t0001g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1161+425C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900027 | |||||||
| chr9:124900057 | T | C | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1161+395A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900057 | |||||||
| chr9:124900146 | G | T | 109 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(106): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1161+306C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900146 | |||||||
| chr9:124900217 | G | T | 1 | a0001c0001t0003g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1161+235C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900217 | |||||||
| chr9:124900269 | C | G | 135 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(132): Show |
157 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1161+183G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900269 | |||||||
| chr9:124900305 | T | C | 51 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(48): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1161+147A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900305 | |||||||
| chr9:124900370 | C | T | 1 | a0002c0002t0001g0303 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1161+82G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900370 | |||||||
| chr9:124900377 | A | G | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+75T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900377 | |||||||
| chr9:124900556 | G | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1066-9C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900556 | |||||||
| chr9:124900970 | A | AT | 20 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0154 others(17): Show |
22 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1066-424dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900970 | |||||||
| chr9:124900970 | AT | A | 52 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0086 others(49): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1066-424delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900970 | |||||||
| chr9:124900994 | T | C | 323 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(320): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1066-447A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900994 | |||||||
| chr9:124901037 | T | C | 121 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(118): Show |
130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1066-490A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901037 | |||||||
| chr9:124901072 | C | T | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-525G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901072 | |||||||
| chr9:124901246 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1066-699G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901246 | |||||||
| chr9:124901272 | A | AT | 10 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0010g0241 others(7): Show |
10 | HG01109.hp2 HG02559.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1066-726dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901272 | |||||||
| chr9:124901272 | AT | A | 64 | a0001c0001t0003g0052 a0002c0002t0001g0002 a0002c0002t0001g0004 others(61): Show |
75 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1066-726delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901272 | |||||||
| chr9:124901356 | C | T | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-809G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901356 | |||||||
| chr9:124901419 | C | T | 135 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(132): Show |
157 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1066-872G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901419 | |||||||
| chr9:124901428 | G | A | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-881C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901428 | |||||||
| chr9:124901436 | A | AT | 91 | a0001c0001t0002g0121 a0001c0001t0002g0126 a0001c0001t0002g0128 others(88): Show |
107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1066-890dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901436 | |||||||
| chr9:124901436 | A | ATT | 53 | a0001c0001t0002g0201 a0001c0001t0003g0049 a0002c0002t0001g0250 others(50): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1066-891_1066-890d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901436 | |||||||
| chr9:124901492 | T | C | 1 | a0002c0002t0001g0310 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1066-945A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901492 | |||||||
| chr9:124901521 | A | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0087 a0001c0001t0002g0088 others(10): Show |
14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-974T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901521 | |||||||
| chr9:124901523 | C | T | 3 | a0002c0002t0001g0266 a0002c0002t0001g0325 a0008c0017t0004g0085 |
3 | HG02132.hp1 HG02683.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1066-976G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901523 | |||||||
| chr9:124901547 | A | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0087 a0001c0001t0002g0088 others(10): Show |
14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-1000T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901547 | |||||||
| chr9:124901567 | TA | T | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1066-1021delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901567 | |||||||
| chr9:124901605 | T | A | 1 | a0003c0004t0006g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1066-1058A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901605 | |||||||
| chr9:124901687 | G | C | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1066-1140C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901687 | |||||||
| chr9:124901757 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-1210C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901757 | |||||||
| chr9:124902134 | T | C | 318 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(315): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1066-1587A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902134 | |||||||
| chr9:124902180 | C | T | 2 | a0003c0004t0013g0079 a0011c0015t0013g0078 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1066-1633G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902180 | |||||||
| chr9:124902317 | T | C | 1 | a0002c0003t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1066-1770A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902317 | |||||||
| chr9:124902402 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1066-1855C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902402 | |||||||
| chr9:124902556 | G | A | 4 | a0003c0004t0009g0077 a0003c0004t0009g0100 a0003c0004t0009g0102 others(1): Show |
4 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-2009C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902556 | |||||||
| chr9:124902590 | C | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2043G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902590 | |||||||
| chr9:124902634 | C | T | 101 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(98): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1066-2087G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902634 | |||||||
| chr9:124902690 | C | T | 16 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(13): Show |
20 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1066-2143G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902690 | |||||||
| chr9:124902732 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1066-2185C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902732 | |||||||
| chr9:124902883 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1066-2336G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902883 | |||||||
| chr9:124902906 | A | G | 2 | a0002c0002t0001g0283 a0002c0002t0001g0297 |
2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1066-2359T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902906 | |||||||
| chr9:124902951 | C | T | 1 | a0002c0003t0001g0209 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1066-2404G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902951 | |||||||
| chr9:124903016 | G | C | 7 | a0002c0002t0001g0005 a0002c0002t0001g0304 a0002c0002t0001g0305 others(4): Show |
9 | HG00438.hp2 HG02129.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1066-2469C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903016 | |||||||
| chr9:124903055 | T | C | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | NA19000.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1066-2508A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903055 | |||||||
| chr9:124903151 | T | C | 49 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(46): Show |
55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1066-2604A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903151 | |||||||
| chr9:124903179 | G | A | 1 | a0002c0003t0001g0209 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1066-2632C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903179 | |||||||
| chr9:124903180 | C | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-2633G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903180 | |||||||
| chr9:124903186 | T | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2639A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903186 | |||||||
| chr9:124903187 | C | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2640G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903187 | |||||||
| chr9:124903188 | C | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2641G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903188 | |||||||
| chr9:124903594 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1066-3047C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903594 | |||||||
| chr9:124903651 | C | CA | 82 | a0001c0001t0003g0055 a0001c0001t0008g0042 a0001c0005t0005g0006 others(79): Show |
101 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1066-3105dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | |||||||
| chr9:124903651 | C | CAA | 13 | a0002c0002t0001g0249 a0002c0002t0001g0265 a0002c0002t0001g0270 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1066-3106_1066-310 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | |||||||
| chr9:124903651 | CA | C | 203 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(200): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1066-3105delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | |||||||
| chr9:124903792 | T | C | 13 | a0001c0001t0002g0014 a0001c0001t0002g0087 a0001c0001t0002g0088 others(10): Show |
14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-3245A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903792 | |||||||
| chr9:124903817 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1066-3270C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903817 | |||||||
| chr9:124903862 | A | G | 103 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(100): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1066-3315T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903862 | |||||||
| chr9:124904072 | TA | T | 54 | a0001c0001t0002g0121 a0001c0001t0002g0201 a0001c0001t0003g0049 others(51): Show |
60 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1066-3526delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904072 | |||||||
| chr9:124904090 | T | G | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-3543A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904090 | |||||||
| chr9:124904093 | TA | T | 49 | a0001c0001t0002g0121 a0001c0001t0003g0007 a0001c0001t0003g0008 others(46): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1066-3547delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904093 | |||||||
| chr9:124904154 | T | C | 41 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(38): Show |
47 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1066-3607A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904154 | |||||||
| chr9:124904248 | G | A | 2 | a0003c0004t0013g0079 a0011c0015t0013g0078 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1066-3701C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904248 | |||||||
| chr9:124904256 | A | G | 6 | a0002c0002t0001g0005 a0002c0002t0001g0317 a0002c0002t0001g0318 others(3): Show |
8 | HG00438.hp2 HG02080.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1066-3709T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904256 | |||||||
| chr9:124904637 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1065+3740G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904637 | |||||||
| chr9:124904668 | G | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1065+3709C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904668 | |||||||
| chr9:124904677 | C | T | 1 | a0001c0001t0017g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1065+3700G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904677 | |||||||
| chr9:124904756 | A | G | 64 | a0001c0001t0002g0201 a0001c0001t0016g0045 a0002c0003t0001g0001 others(61): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1065+3621T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904756 | |||||||
| chr9:124904788 | A | C | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+3589T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904788 | |||||||
| chr9:124904877 | G | A | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065+3500C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904877 | |||||||
| chr9:124904897 | T | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0115 a0001c0001t0002g0122 others(4): Show |
8 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065+3480A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904897 | |||||||
| chr9:124904927 | G | C | 107 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(104): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1065+3450C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904927 | |||||||
| chr9:124904943 | C | CA | 305 | a0001c0001t0002g0014 a0001c0001t0002g0017 a0001c0001t0002g0018 others(302): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1065+3433dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904943 | |||||||
| chr9:124904954 | A | AT | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0126 others(6): Show |
11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1065+3422_1065+342 others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904954 | |||||||
| chr9:124904956 | T | A | 16 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(13): Show |
19 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1065+3421A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904956 | |||||||
| chr9:124904992 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1065+3385T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904992 | |||||||
| chr9:124905149 | AAAT | A | 84 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(81): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1065+3225_1065+322 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905149 | |||||||
| chr9:124905415 | T | C | 2 | a0002c0002t0001g0281 a0002c0002t0001g0316 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1065+2962A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905415 | |||||||
| chr9:124905649 | T | C | 1 | a0002c0002t0001g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1065+2728A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905649 | |||||||
| chr9:124905890 | C | T | 1 | a0001c0001t0004g0230 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1065+2487G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905890 | |||||||
| chr9:124905965 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1065+2412A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905965 | |||||||
| chr9:124905972 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1065+2405C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905972 | |||||||
| chr9:124905973 | C | T | 1 | a0002c0002t0001g0294 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1065+2404G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905973 | |||||||
| chr9:124905994 | T | C | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1065+2383A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905994 | |||||||
| chr9:124906116 | A | AAAAT | 9 | a0001c0001t0004g0027 a0001c0001t0004g0237 a0001c0001t0004g0238 others(6): Show |
10 | HG01123.hp1 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065+2257_1065+226 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | |||||||
| chr9:124906116 | A | AAAATAAA others(1): Show |
19 | a0001c0001t0004g0229 a0001c0001t0016g0045 a0002c0002t0001g0256 others(16): Show |
20 | HG00733.hp1 HG01081.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.1065+2253_1065+226 others(12): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | |||||||
| chr9:124906116 | A | AAAATAAA others(5): Show |
90 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0028 others(87): Show |
109 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1065+2249_1065+226 others(16): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | |||||||
| chr9:124906116 | A | AAAATAAA others(9): Show |
23 | a0002c0002t0001g0005 a0002c0002t0001g0249 a0002c0002t0001g0260 others(20): Show |
25 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1065+2245_1065+226 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | |||||||
| chr9:124906116 | AAAAT | A | 168 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(165): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1065+2257_1065+226 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | |||||||
| chr9:124906262 | C | T | 1 | a0002c0003t0001g0195 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1065+2115G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906262 | |||||||
| chr9:124906305 | C | T | 1 | a0002c0002t0001g0288 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1065+2072G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906305 | |||||||
| chr9:124906345 | C | T | 9 | a0002c0003t0001g0184 a0002c0003t0001g0191 a0002c0003t0001g0193 others(6): Show |
9 | HG02027.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065+2032G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906345 | |||||||
| chr9:124906419 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG01975.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1065+1958T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906419 | |||||||
| chr9:124906425 | T | C | 318 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(315): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1065+1952A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906425 | |||||||
| chr9:124906461 | C | G | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065+1916G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906461 | |||||||
| chr9:124906526 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1065+1851C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906526 | |||||||
| chr9:124906612 | C | T | 164 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(161): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1065+1765G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906612 | |||||||
| chr9:124907194 | A | T | 1 | a0002c0003t0001g0223 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1065+1183T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907194 | |||||||
| chr9:124907204 | A | G | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1065+1173T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907204 | |||||||
| chr9:124907255 | A | G | 146 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(143): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1065+1122T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907255 | |||||||
| chr9:124907556 | G | C | 6 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(3): Show |
6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065+821C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907556 | |||||||
| chr9:124907724 | T | C | 1 | a0002c0002t0001g0294 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1065+653A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907724 | |||||||
| chr9:124907737 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1065+640A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907737 | |||||||
| chr9:124907758 | C | G | 142 | a0001c0001t0002g0292 a0001c0001t0008g0042 a0002c0002t0001g0002 others(139): Show |
164 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1065+619G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907758 | |||||||
| chr9:124907822 | G | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065+555C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907822 | |||||||
| chr9:124907871 | G | A | 1 | a0002c0002t0001g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1065+506C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907871 | |||||||
| chr9:124908098 | A | G | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1065+279T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908098 | |||||||
| chr9:124908099 | A | G | 318 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(315): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1065+278T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908099 | |||||||
| chr9:124908294 | C | T | 1 | a0004c0007t0007g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1065+83G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908294 | |||||||
| chr9:124908527 | T | A | 1 | a0002c0003t0001g0223 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.970-55A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908527 | |||||||
| chr9:124908668 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.970-196T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908668 | |||||||
| chr9:124908743 | G | A | 89 | a0001c0001t0002g0292 a0002c0002t0001g0002 a0002c0002t0001g0004 others(86): Show |
105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.970-271C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908743 | |||||||
| chr9:124908757 | C | T | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.970-285G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908757 | |||||||
| chr9:124908802 | G | C | 1 | a0001c0001t0002g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.970-330C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908802 | |||||||
| chr9:124908804 | G | A | 1 | a0002c0002t0001g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.970-332C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908804 | |||||||
| chr9:124908850 | C | T | 1 | a0002c0002t0001g0290 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970-378G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908850 | |||||||
| chr9:124908861 | G | A | 159 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(156): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.970-389C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908861 | |||||||
| chr9:124909048 | A | C | 51 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(48): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.970-576T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909048 | |||||||
| chr9:124909120 | G | A | 1 | a0003c0004t0006g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.970-648C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909120 | |||||||
| chr9:124909146 | C | T | 3 | a0002c0002t0001g0033 a0002c0002t0001g0309 a0002c0002t0001g0310 |
4 | HG00140.hp2 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-674G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909146 | |||||||
| chr9:124909311 | T | TA | 15 | a0001c0001t0003g0071 a0002c0002t0001g0030 a0002c0002t0001g0032 others(12): Show |
18 | HG00673.hp1 HG02040.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.970-840dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909311 | |||||||
| chr9:124909311 | TA | T | 9 | a0001c0001t0003g0046 a0002c0003t0001g0184 a0002c0003t0001g0191 others(6): Show |
9 | HG02027.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.970-840delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909311 | |||||||
| chr9:124909373 | C | T | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.970-901G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909373 | |||||||
| chr9:124909608 | C | CA | 7 | a0001c0001t0002g0165 a0001c0001t0002g0172 a0001c0001t0003g0049 others(4): Show |
7 | HG01981.hp2 HG02074.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.970-1137dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | |||||||
| chr9:124909608 | C | CAAA | 10 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.970-1139_970-1137d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | |||||||
| chr9:124909608 | CA | C | 130 | a0001c0001t0002g0087 a0001c0001t0002g0143 a0002c0002t0001g0002 others(127): Show |
152 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.970-1137delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | |||||||
| chr9:124909608 | CAA | C | 9 | a0002c0002t0001g0246 a0002c0003t0001g0189 a0002c0003t0001g0192 others(6): Show |
9 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.970-1138_970-1137d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | |||||||
| chr9:124909625 | A | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.970-1153T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909625 | |||||||
| chr9:124909734 | G | C | 1 | a0001c0001t0002g0142 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.970-1262C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909734 | |||||||
| chr9:124909804 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0175 |
3 | NA18970.hp2 NA18989.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.970-1332C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909804 | |||||||
| chr9:124909870 | T | C | 163 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(160): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.970-1398A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909870 | |||||||
| chr9:124909898 | G | A | 88 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(85): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.970-1426C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909898 | |||||||
| chr9:124909968 | G | A | 1 | a0002c0002t0001g0290 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970-1496C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909968 | |||||||
| chr9:124910146 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.970-1674C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910146 | |||||||
| chr9:124910319 | C | A | 102 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(99): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.969+1582G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910319 | |||||||
| chr9:124910501 | T | C | 1 | a0002c0002t0001g0299 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.969+1400A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910501 | |||||||
| chr9:124910583 | T | C | 1 | a0002c0002t0001g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.969+1318A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910583 | |||||||
| chr9:124910939 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.969+962G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910939 | |||||||
| chr9:124910953 | C | G | 318 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(315): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.969+948G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910953 | |||||||
| chr9:124910999 | C | A | 1 | a0002c0003t0001g0224 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.969+902G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910999 | |||||||
| chr9:124911046 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0052 |
3 | NA18955.hp1 NA18962.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.969+855A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911046 | |||||||
| chr9:124911106 | A | C | 163 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(160): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.969+795T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911106 | |||||||
| chr9:124911190 | C | T | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.969+711G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911190 | |||||||
| chr9:124911210 | C | G | 1 | a0001c0001t0002g0142 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.969+691G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911210 | |||||||
| chr9:124911321 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.969+580C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911321 | |||||||
| chr9:124911518 | G | A | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.969+383C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911518 | |||||||
| chr9:124911598 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.969+303G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911598 | |||||||
| chr9:124911670 | C | T | 160 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(157): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.969+231G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911670 | |||||||
| chr9:124911697 | CT | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+203delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911697 | |||||||
| chr9:124911725 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.969+176G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911725 | |||||||
| chr9:124911761 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+140C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911761 | |||||||
| chr9:124911812 | C | G | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.969+89G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911812 | |||||||
| chr9:124911870 | C | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+31G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911870 | |||||||
| chr9:124912110 | T | C | 1 | a0002c0002t0001g0320 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.844-84A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912110 | |||||||
| chr9:124912552 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.844-526A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912552 | |||||||
| chr9:124912554 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.844-528C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912554 | |||||||
| chr9:124912566 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.844-540C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912566 | |||||||
| chr9:124912575 | C | G | 1 | a0001c0001t0002g0025 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.844-549G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912575 | |||||||
| chr9:124912605 | C | T | 48 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.844-579G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912605 | |||||||
| chr9:124912606 | G | A | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-580C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912606 | |||||||
| chr9:124912667 | C | T | 22 | a0001c0001t0002g0020 a0001c0001t0002g0160 a0001c0001t0002g0167 others(19): Show |
23 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-641G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912667 | |||||||
| chr9:124912845 | C | CT | 10 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.844-820dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912845 | |||||||
| chr9:124913093 | G | A | 1 | a0002c0002t0001g0290 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.844-1067C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913093 | |||||||
| chr9:124913246 | G | A | 1 | a0003c0004t0013g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.844-1220C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913246 | |||||||
| chr9:124913299 | T | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1273A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913299 | |||||||
| chr9:124913385 | G | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1359C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913385 | |||||||
| chr9:124913514 | G | C | 1 | a0003c0004t0006g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.844-1488C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913514 | |||||||
| chr9:124913541 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844-1515T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913541 | |||||||
| chr9:124913542 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-1516G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913542 | |||||||
| chr9:124913596 | G | A | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-1570C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913596 | |||||||
| chr9:124913613 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.844-1587T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913613 | |||||||
| chr9:124913750 | C | A | 324 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(321): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.844-1724G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913750 | |||||||
| chr9:124914054 | T | G | 3 | a0002c0003t0001g0225 a0002c0003t0001g0226 a0002c0003t0001g0227 |
3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.844-2028A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914054 | |||||||
| chr9:124914154 | G | A | 2 | a0001c0005t0005g0037 a0001c0005t0005g0327 |
3 | HG02451.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-2128C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914154 | |||||||
| chr9:124914255 | T | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.844-2229A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914255 | |||||||
| chr9:124914546 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.844-2520C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914546 | |||||||
| chr9:124914635 | G | C | 1 | a0001c0001t0003g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.844-2609C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914635 | |||||||
| chr9:124914639 | G | A | 14 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0118 others(11): Show |
16 | HG00280.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.844-2613C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914639 | |||||||
| chr9:124914953 | T | C | 91 | a0001c0001t0002g0292 a0001c0001t0008g0042 a0002c0002t0001g0002 others(88): Show |
107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.844-2927A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914953 | |||||||
| chr9:124914995 | G | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.844-2969C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914995 | |||||||
| chr9:124915027 | A | T | 1 | a0002c0002t0001g0028 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.844-3001T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915027 | |||||||
| chr9:124915121 | T | C | 4 | a0002c0002t0001g0272 a0002c0002t0001g0285 a0002c0002t0001g0286 others(1): Show |
4 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-3095A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915121 | |||||||
| chr9:124915319 | G | A | 53 | a0001c0001t0002g0201 a0001c0001t0016g0045 a0002c0003t0001g0001 others(50): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.844-3293C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915319 | |||||||
| chr9:124915522 | T | C | 2 | a0001c0001t0002g0110 a0001c0001t0002g0116 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.844-3496A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915522 | |||||||
| chr9:124915639 | C | T | 29 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0113 others(26): Show |
31 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.844-3613G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915639 | |||||||
| chr9:124915733 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.844-3707G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915733 | |||||||
| chr9:124915742 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.844-3716C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915742 | |||||||
| chr9:124915873 | G | A | 1 | a0001c0001t0017g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.844-3847C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915873 | |||||||
| chr9:124916012 | G | T | 2 | a0002c0002t0011g0034 a0002c0002t0011g0312 |
3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844-3986C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916012 | |||||||
| chr9:124916101 | C | CTAAA | 104 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0183 others(101): Show |
124 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.844-4079_844-4076d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | |||||||
| chr9:124916101 | C | CTAAATAA others(1): Show |
11 | a0001c0001t0004g0235 a0002c0002t0001g0314 a0002c0003t0001g0184 others(8): Show |
11 | HG02027.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.844-4083_844-4076d others(10): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | |||||||
| chr9:124916101 | C | CTAAATAA others(5): Show |
26 | a0001c0001t0016g0045 a0001c0001t0017g0236 a0002c0003t0001g0001 others(23): Show |
30 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-4087_844-4076d others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | |||||||
| chr9:124916101 | C | CTAAATAA others(9): Show |
19 | a0001c0001t0002g0201 a0002c0002t0001g0248 a0002c0003t0001g0023 others(16): Show |
21 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-4091_844-4076d others(18): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | |||||||
| chr9:124916120 | A | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0052 others(4): Show |
9 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-4094T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916120 | |||||||
| chr9:124916124 | A | AATAAATA others(5): Show |
1 | a0002c0003t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.844-4099_844-4098i others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916124 | |||||||
| chr9:124916128 | A | AATAAATA others(5): Show |
1 | a0002c0003t0014g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844-4103_844-4102i others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916128 | |||||||
| chr9:124916178 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.844-4152G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916178 | |||||||
| chr9:124916399 | T | G | 1 | a0002c0002t0001g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.844-4373A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916399 | |||||||
| chr9:124916600 | A | G | 2 | a0002c0002t0001g0266 a0002c0002t0001g0325 |
2 | HG02132.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.843+4529T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916600 | |||||||
| chr9:124916652 | T | C | 14 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(11): Show |
17 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+4477A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916652 | |||||||
| chr9:124916715 | A | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0116 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.843+4414T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916715 | |||||||
| chr9:124916867 | C | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+4262G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916867 | |||||||
| chr9:124916871 | G | GAC | 4 | a0002c0003t0001g0024 a0002c0003t0001g0187 a0002c0003t0001g0225 others(1): Show |
5 | HG03130.hp2 NA18906.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+4256_843+4257d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916871 | |||||||
| chr9:124916877 | C | CA | 139 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(136): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.843+4251dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916877 | |||||||
| chr9:124916877 | C | CAA | 50 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0092 others(47): Show |
58 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.843+4250_843+4251d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916877 | |||||||
| chr9:124916878 | A | AC | 21 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0041 others(18): Show |
24 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.843+4250_843+4251i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916878 | |||||||
| chr9:124916879 | A | C | 35 | a0001c0001t0002g0139 a0001c0001t0002g0159 a0001c0001t0003g0007 others(32): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+4250T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916879 | |||||||
| chr9:124916880 | A | C | 15 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0041 others(12): Show |
17 | HG00738.hp1 HG01167.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+4249T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916880 | |||||||
| chr9:124916881 | A | C | 30 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(27): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.843+4248T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916881 | |||||||
| chr9:124916882 | A | C | 1 | a0001c0001t0003g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.843+4247T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916882 | |||||||
| chr9:124916883 | A | C | 5 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0052 others(2): Show |
7 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+4246T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916883 | |||||||
| chr9:124916909 | C | CA | 8 | a0001c0001t0003g0008 a0001c0001t0003g0046 a0001c0001t0003g0048 others(5): Show |
9 | HG03654.hp1 NA18944.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+4219dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916909 | |||||||
| chr9:124917295 | C | A | 1 | a0002c0002t0001g0295 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.843+3834G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917295 | |||||||
| chr9:124917535 | CATT | C | 5 | a0001c0001t0002g0019 a0001c0001t0002g0117 a0001c0001t0002g0162 others(2): Show |
6 | HG02055.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+3591_843+3593d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917535 | |||||||
| chr9:124917581 | C | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+3548G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917581 | |||||||
| chr9:124917762 | C | T | 1 | a0002c0002t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843+3367G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917762 | |||||||
| chr9:124917856 | T | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+3273A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917856 | |||||||
| chr9:124917857 | A | T | 47 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(44): Show |
53 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+3272T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917857 | |||||||
| chr9:124917859 | A | T | 50 | a0001c0001t0002g0201 a0002c0002t0001g0263 a0002c0003t0001g0001 others(47): Show |
56 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.843+3270T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917859 | |||||||
| chr9:124917860 | T | TA | 3 | a0001c0005t0005g0328 a0002c0002t0001g0261 a0002c0003t0001g0044 |
3 | HG02145.hp1 HG02723.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.843+3268_843+3269i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917860 | |||||||
| chr9:124917861 | T | A | 181 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(178): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.843+3268A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917861 | |||||||
| chr9:124917863 | T | A | 8 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0245 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+3266A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917863 | |||||||
| chr9:124918066 | G | A | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+3063C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918066 | |||||||
| chr9:124918072 | G | A | 1 | a0002c0002t0001g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.843+3057C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918072 | |||||||
| chr9:124918146 | C | T | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+2983G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918146 | |||||||
| chr9:124918160 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.843+2969T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918160 | |||||||
| chr9:124918226 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+2903A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918226 | |||||||
| chr9:124918746 | A | T | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+2383T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918746 | |||||||
| chr9:124918875 | T | G | 164 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(161): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.843+2254A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918875 | |||||||
| chr9:124918886 | G | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+2243C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918886 | |||||||
| chr9:124919015 | G | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+2114C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919015 | |||||||
| chr9:124919066 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.843+2063A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919066 | |||||||
| chr9:124919132 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.843+1997G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919132 | |||||||
| chr9:124919232 | G | A | 4 | a0001c0001t0004g0027 a0001c0001t0004g0229 a0001c0001t0004g0237 others(1): Show |
5 | HG01123.hp1 HG01255.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1897C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919232 | |||||||
| chr9:124919262 | A | G | 1 | a0002c0002t0001g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.843+1867T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919262 | |||||||
| chr9:124919705 | A | T | 189 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(186): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.843+1424T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919705 | |||||||
| chr9:124919719 | G | A | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+1410C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919719 | |||||||
| chr9:124919740 | C | T | 2 | a0001c0001t0003g0051 a0001c0001t0003g0067 |
2 | HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.843+1389G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919740 | |||||||
| chr9:124919936 | A | ATATT | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+1189_843+1192d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | |||||||
| chr9:124919936 | A | T | 1 | a0001c0001t0002g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843+1193T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | |||||||
| chr9:124919936 | ATATT | A | 8 | a0002c0003t0001g0023 a0002c0003t0001g0186 a0002c0003t0001g0189 others(5): Show |
9 | HG00558.hp1 HG00597.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+1189_843+1192d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | |||||||
| chr9:124919978 | CAG | C | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+1149_843+1150d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919978 | |||||||
| chr9:124919981 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0128 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843+1148T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919981 | |||||||
| chr9:124920007 | T | A | 1 | a0001c0001t0002g0292 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.843+1122A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920007 | |||||||
| chr9:124920013 | G | A | 1 | a0001c0001t0019g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.843+1116C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920013 | |||||||
| chr9:124920090 | A | AG | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+1038_843+1039i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920090 | |||||||
| chr9:124920286 | AT | A | 57 | a0001c0001t0002g0128 a0001c0001t0002g0136 a0001c0001t0002g0201 others(54): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.843+842delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920286 | |||||||
| chr9:124920308 | G | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0307 |
2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.843+821C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920308 | |||||||
| chr9:124920332 | CAT | C | 141 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(138): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.843+795_843+796del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920332 | |||||||
| chr9:124920434 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.843+695A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920434 | |||||||
| chr9:124920659 | G | C | 4 | a0002c0002t0001g0029 a0002c0002t0001g0036 a0002c0002t0001g0256 others(1): Show |
6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+470C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920659 | |||||||
| chr9:124920680 | A | C | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.843+449T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920680 | |||||||
| chr9:124920751 | T | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+378A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920751 | |||||||
| chr9:124920855 | G | GA | 53 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(50): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.843+273dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920855 | |||||||
| chr9:124920855 | GA | G | 56 | a0001c0001t0002g0099 a0001c0001t0002g0121 a0001c0001t0002g0157 others(53): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.843+273delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920855 | |||||||
| chr9:124921035 | G | T | 1 | a0002c0002t0001g0264 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843+94C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124921035 | |||||||
| chr9:124921105 | G | A | 2 | a0003c0004t0013g0079 a0011c0015t0013g0078 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.843+24C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124921105 | |||||||
| chr9:124921373 | C | T | 1 | a0001c0001t0003g0008 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.732-133G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921373 | |||||||
| chr9:124921497 | G | C | 1 | a0002c0003t0001g0219 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.731+226C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921497 | |||||||
| chr9:124921619 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.731+104G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921619 | |||||||
| chr9:124921976 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-84G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124921976 | |||||||
| chr9:124921993 | T | G | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-101A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124921993 | |||||||
| chr9:124922044 | A | G | 1 | a0002c0003t0001g0189 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.562-152T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922044 | |||||||
| chr9:124922153 | G | A | 1 | a0002c0003t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.562-261C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922153 | |||||||
| chr9:124922409 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-517G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922409 | |||||||
| chr9:124922423 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0092 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.562-531G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922423 | |||||||
| chr9:124922550 | C | CA | 6 | a0001c0001t0002g0125 a0001c0001t0003g0073 a0001c0001t0004g0238 others(3): Show |
6 | HG01257.hp2 HG03831.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+544dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922550 | |||||||
| chr9:124922861 | A | C | 2 | a0001c0001t0002g0139 a0001c0001t0002g0142 |
2 | NA19055.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.561+234T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922861 | |||||||
| chr9:124922884 | C | G | 7 | a0002c0002t0001g0002 a0002c0002t0001g0258 a0002c0002t0001g0259 others(4): Show |
10 | NA18954.hp2 NA18957.hp2 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.561+211G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922884 | |||||||
| chr9:124923014 | G | T | 4 | a0003c0004t0009g0077 a0003c0004t0009g0100 a0003c0004t0009g0102 others(1): Show |
4 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+81C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124923014 | |||||||
| chr9:124923227 | T | C | 24 | a0001c0001t0002g0020 a0001c0001t0002g0167 a0001c0001t0002g0168 others(21): Show |
25 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.433-4A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923227 | |||||||
| chr9:124923231 | A | G | 53 | a0001c0001t0002g0201 a0001c0001t0016g0045 a0002c0003t0001g0001 others(50): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
splice_region_variant&intron_variant | LOW | c.433-8T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923231 | |||||||
| chr9:124923237 | G | A | 2 | a0002c0002t0001g0293 a0002c0002t0001g0321 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.433-14C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923237 | |||||||
| chr9:124923282 | G | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-59C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923282 | |||||||
| chr9:124923383 | C | T | 5 | a0002c0002t0001g0035 a0002c0002t0001g0252 a0002c0002t0001g0313 others(2): Show |
6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-160G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923383 | |||||||
| chr9:124923537 | T | C | 2 | a0001c0001t0002g0110 a0001c0001t0002g0116 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.433-314A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923537 | |||||||
| chr9:124923662 | T | C | 1 | a0002c0002t0001g0322 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.433-439A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923662 | |||||||
| chr9:124923781 | G | A | 9 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(6): Show |
13 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.433-558C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923781 | |||||||
| chr9:124923847 | C | T | 244 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(241): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.433-624G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923847 | |||||||
| chr9:124924136 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.433-913C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924136 | |||||||
| chr9:124924370 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.433-1147G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924370 | |||||||
| chr9:124924440 | C | T | 100 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(97): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.433-1217G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924440 | |||||||
| chr9:124924636 | C | CA | 217 | a0001c0001t0002g0014 a0001c0001t0002g0017 a0001c0001t0002g0018 others(214): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.433-1414dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924636 | |||||||
| chr9:124924636 | C | CAA | 21 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(18): Show |
27 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.433-1415_433-1414d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924636 | |||||||
| chr9:124924655 | A | T | 1 | a0002c0002t0020g0326 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433-1432T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924655 | |||||||
| chr9:124924691 | C | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0126 others(6): Show |
11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1468G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924691 | |||||||
| chr9:124924756 | G | T | 5 | a0002c0002t0001g0035 a0002c0002t0001g0252 a0002c0002t0001g0313 others(2): Show |
6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1533C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924756 | |||||||
| chr9:124924921 | T | C | 3 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0245 |
3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.433-1698A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924921 | |||||||
| chr9:124924932 | T | A | 4 | a0001c0001t0002g0018 a0001c0001t0002g0154 a0001c0001t0002g0155 others(1): Show |
5 | HG01106.hp1 HG01123.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-1709A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924932 | |||||||
| chr9:124925103 | C | T | 1 | a0002c0002t0001g0255 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.432+1606G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925103 | |||||||
| chr9:124925156 | T | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0245 |
3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.432+1553A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925156 | |||||||
| chr9:124925221 | AT | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.432+1487delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925221 | |||||||
| chr9:124925285 | T | C | 23 | a0001c0001t0002g0020 a0001c0001t0002g0167 a0001c0001t0002g0168 others(20): Show |
24 | HG00408.hp1 HG00609.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.432+1424A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925285 | |||||||
| chr9:124925359 | AT | A | 188 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(185): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.432+1349delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925359 | |||||||
| chr9:124925359 | ATT | A | 49 | a0001c0001t0002g0201 a0001c0001t0003g0067 a0002c0003t0001g0001 others(46): Show |
55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.432+1348_432+1349d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925359 | |||||||
| chr9:124925457 | C | T | 2 | a0003c0004t0013g0079 a0011c0015t0013g0078 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.432+1252G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925457 | |||||||
| chr9:124925735 | C | T | 46 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+974G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925735 | |||||||
| chr9:124925937 | T | C | 4 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
4 | HG01175.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+772A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925937 | |||||||
| chr9:124926148 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.432+561C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926148 | |||||||
| chr9:124926174 | A | G | 3 | a0004c0007t0007g0013 a0004c0007t0007g0075 a0004c0007t0007g0076 |
4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+535T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926174 | |||||||
| chr9:124926265 | C | T | 1 | a0003c0004t0009g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432+444G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926265 | |||||||
| chr9:124926267 | A | G | 46 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(43): Show |
51 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.432+442T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926267 | |||||||
| chr9:124926335 | A | G | 38 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0021 others(35): Show |
41 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.432+374T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926335 | |||||||
| chr9:124926398 | A | G | 2 | a0001c0001t0002g0090 a0001c0010t0002g0091 |
2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.432+311T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926398 | |||||||
| chr9:124926415 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.432+294C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926415 | |||||||
| chr9:124926688 | C | T | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+21G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926688 | |||||||
| chr9:124926890 | G | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.400-149C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124926890 | |||||||
| chr9:124927040 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.400-299G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927040 | |||||||
| chr9:124927249 | G | A | 1 | a0002c0002t0001g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.400-508C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927249 | |||||||
| chr9:124927348 | G | T | 2 | a0002c0003t0001g0223 a0002c0003t0001g0224 |
2 | NA19054.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.400-607C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927348 | |||||||
| chr9:124927375 | C | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.400-634G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927375 | |||||||
| chr9:124927407 | T | C | 2 | a0002c0003t0001g0223 a0002c0003t0001g0224 |
2 | NA19054.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.400-666A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927407 | |||||||
| chr9:124927442 | A | T | 1 | a0002c0002t0001g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-701T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927442 | |||||||
| chr9:124927540 | ACT | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0170 a0001c0001t0002g0171 others(5): Show |
9 | HG00609.hp2 HG02074.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+646_399+647del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927540 | |||||||
| chr9:124927632 | T | C | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+556A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927632 | |||||||
| chr9:124927709 | G | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+479C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927709 | |||||||
| chr9:124927876 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.399+312A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927876 | |||||||
| chr9:124928005 | A | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.399+183T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124928005 | |||||||
| chr9:124928050 | A | C | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.399+138T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124928050 | |||||||
| chr9:124928332 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.302-47G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928332 | |||||||
| chr9:124928523 | T | C | 1 | a0002c0002t0001g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.302-238A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928523 | |||||||
| chr9:124928546 | GT | G | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.302-262delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928546 | |||||||
| chr9:124928643 | A | G | 1 | a0001c0001t0003g0048 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.302-358T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928643 | |||||||
| chr9:124928773 | T | C | 1 | a0002c0002t0001g0299 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.301+443A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928773 | |||||||
| chr9:124928840 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.301+376T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928840 | |||||||
| chr9:124928905 | T | TCCAGACC others(111): Show |
1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.301+193_301+310dup others(118): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928905 | |||||||
| chr9:124929090 | A | T | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301+126T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124929090 | |||||||
| chr9:124929524 | GC | G | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-235delG | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929524 | |||||||
| chr9:124929672 | C | T | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-382G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929672 | |||||||
| chr9:124929710 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-420G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929710 | |||||||
| chr9:124929781 | A | C | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-491T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929781 | |||||||
| chr9:124929821 | C | T | 1 | a0002c0003t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.227-531G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929821 | |||||||
| chr9:124929959 | T | C | 4 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(1): Show |
4 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-669A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929959 | |||||||
| chr9:124930152 | C | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-862G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930152 | |||||||
| chr9:124930167 | C | T | 4 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(1): Show |
4 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-877G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930167 | |||||||
| chr9:124930181 | T | C | 5 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-891A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930181 | |||||||
| chr9:124930259 | C | A | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.227-969G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930259 | |||||||
| chr9:124930322 | A | G | 164 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(161): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.226+994T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930322 | |||||||
| chr9:124930399 | C | T | 1 | a0002c0002t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.226+917G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930399 | |||||||
| chr9:124930558 | T | C | 4 | a0002c0002t0001g0247 a0002c0002t0001g0300 a0002c0002t0001g0301 others(1): Show |
4 | HG00558.hp2 NA18965.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+758A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930558 | |||||||
| chr9:124930840 | A | G | 1 | a0002c0003t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.226+476T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930840 | |||||||
| chr9:124930969 | T | C | 189 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(186): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.226+347A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930969 | |||||||
| chr9:124931021 | A | G | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+295T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931021 | |||||||
| chr9:124931111 | T | A | 1 | a0002c0002t0001g0303 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.226+205A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931111 | |||||||
| chr9:124931201 | A | T | 1 | a0001c0001t0003g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226+115T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931201 | |||||||
| chr9:124931428 | A | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-22T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931428 | |||||||
| chr9:124931568 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-162G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931568 | |||||||
| chr9:124931596 | G | C | 1 | a0001c0001t0003g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-190C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931596 | |||||||
| chr9:124931786 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-380C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931786 | |||||||
| chr9:124931850 | C | T | 1 | a0002c0003t0014g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-444G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931850 | |||||||
| chr9:124931930 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136-524C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931930 | |||||||
| chr9:124932352 | C | T | 52 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(49): Show |
58 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-946G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932352 | |||||||
| chr9:124932382 | A | G | 1 | a0002c0003t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136-976T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932382 | |||||||
| chr9:124932390 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-984A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932390 | |||||||
| chr9:124932395 | G | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-989C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932395 | |||||||
| chr9:124932494 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136-1088A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932494 | |||||||
| chr9:124932668 | T | C | 1 | a0003c0004t0006g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-1262A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932668 | |||||||
| chr9:124932881 | A | G | 1 | a0001c0005t0005g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.136-1475T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932881 | |||||||
| chr9:124932894 | T | C | 241 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(238): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.136-1488A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932894 | |||||||
| chr9:124932975 | T | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1569A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932975 | |||||||
| chr9:124932980 | A | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1574T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932980 | |||||||
| chr9:124932982 | A | T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1576T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932982 | |||||||
| chr9:124932983 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1577A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932983 | |||||||
| chr9:124932984 | A | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1578T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932984 | |||||||
| chr9:124932998 | A | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1592T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932998 | |||||||
| chr9:124933005 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1599A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933005 | |||||||
| chr9:124933025 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1619C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933025 | |||||||
| chr9:124933026 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1620A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933026 | |||||||
| chr9:124933030 | A | T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1624T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933030 | |||||||
| chr9:124933041 | T | G | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1635A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933041 | |||||||
| chr9:124933044 | T | G | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1638A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933044 | |||||||
| chr9:124933045 | T | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1639A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933045 | |||||||
| chr9:124933046 | A | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1640T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933046 | |||||||
| chr9:124933047 | T | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1641A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933047 | |||||||
| chr9:124933056 | G | T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1650C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933056 | |||||||
| chr9:124933058 | G | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1652C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933058 | |||||||
| chr9:124933065 | A | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1659T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933065 | |||||||
| chr9:124933066 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1660C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933066 | |||||||
| chr9:124933067 | G | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1661C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933067 | |||||||
| chr9:124933079 | G | GCAGTAGA others(3): Show |
1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1674_136-1673i others(12): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933079 | |||||||
| chr9:124933081 | C | T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1675G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933081 | |||||||
| chr9:124933084 | A | C | 55 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0025 others(52): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.136-1678T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933084 | |||||||
| chr9:124933275 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1869A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933275 | |||||||
| chr9:124933276 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1870A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933276 | |||||||
| chr9:124933277 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1871C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933277 | |||||||
| chr9:124933278 | G | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1872C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933278 | |||||||
| chr9:124933281 | C | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1875G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933281 | |||||||
| chr9:124933282 | T | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1876A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933282 | |||||||
| chr9:124933283 | T | G | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1877A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933283 | |||||||
| chr9:124933285 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1879C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933285 | |||||||
| chr9:124933286 | C | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1880G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933286 | |||||||
| chr9:124933287 | T | C | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1881A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933287 | |||||||
| chr9:124933297 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1891C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933297 | |||||||
| chr9:124933301 | T | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1895A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933301 | |||||||
| chr9:124933316 | G | A | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1910C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933316 | |||||||
| chr9:124933382 | G | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-1976C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933382 | |||||||
| chr9:124933413 | A | ATTAT | 20 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0122 others(17): Show |
23 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.136-2011_136-2008d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933413 | |||||||
| chr9:124933422 | TTATTTAT others(46): Show |
T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-2069_136-2017d others(55): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933422 | |||||||
| chr9:124933697 | G | A | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-2291C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933697 | |||||||
| chr9:124933794 | C | T | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0119 |
3 | NA18960.hp2 NA18969.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.136-2388G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933794 | |||||||
| chr9:124933914 | C | CTCATGCA others(52): Show |
1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-2509_136-2508i others(61): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933914 | |||||||
| chr9:124933920 | G | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-2514C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933920 | |||||||
| chr9:124934015 | T | A | 3 | a0002c0003t0001g0225 a0002c0003t0001g0226 a0002c0003t0001g0227 |
3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.136-2609A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934015 | |||||||
| chr9:124934019 | AGTCCTCC others(2306): Show |
A | 3 | a0002c0003t0001g0225 a0002c0003t0001g0226 a0002c0003t0001g0227 |
3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.135+2245_136-2614d others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934019 | |||||||
| chr9:124934112 | T | C | 1 | a0001c0014t0003g0066 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.136-2706A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934112 | |||||||
| chr9:124934231 | G | A | 12 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(9): Show |
12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-2825C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934231 | |||||||
| chr9:124934263 | G | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | NA18988.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.136-2857C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934263 | |||||||
| chr9:124934291 | G | A | 3 | a0004c0007t0007g0013 a0004c0007t0007g0075 a0004c0007t0007g0076 |
4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2885C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934291 | |||||||
| chr9:124934440 | G | C | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-3034C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934440 | |||||||
| chr9:124934520 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-3114C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934520 | |||||||
| chr9:124935175 | T | A | 2 | a0002c0002t0001g0281 a0002c0002t0001g0316 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.135+3402A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935175 | |||||||
| chr9:124935288 | G | A | 49 | a0001c0001t0002g0201 a0001c0001t0016g0045 a0002c0003t0001g0001 others(46): Show |
55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.135+3289C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935288 | |||||||
| chr9:124935615 | G | A | 4 | a0003c0004t0006g0101 a0003c0004t0006g0105 a0003c0004t0006g0106 others(1): Show |
4 | HG02258.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+2962C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935615 | |||||||
| chr9:124935763 | CA | C | 215 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(212): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.135+2813delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935763 | |||||||
| chr9:124935763 | CAA | C | 16 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(13): Show |
20 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+2812_135+2813d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935763 | |||||||
| chr9:124935781 | A | G | 1 | a0003c0004t0006g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+2796T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935781 | |||||||
| chr9:124935995 | A | G | 1 | a0002c0002t0001g0288 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.135+2582T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935995 | |||||||
| chr9:124936046 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.135+2531A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936046 | |||||||
| chr9:124936148 | C | T | 3 | a0001c0001t0003g0012 a0001c0001t0003g0058 a0001c0001t0003g0063 |
3 | HG00639.hp1 HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.135+2429G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936148 | |||||||
| chr9:124936155 | G | T | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+2422C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936155 | |||||||
| chr9:124936222 | TATTTCCT others(37): Show |
T | 1 | a0001c0005t0005g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+2311_135+2354d others(46): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936222 | |||||||
| chr9:124936260 | T | C | 3 | a0004c0007t0007g0013 a0004c0007t0007g0075 a0004c0007t0007g0076 |
4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+2317A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936260 | |||||||
| chr9:124936333 | T | C | 3 | a0002c0003t0001g0225 a0002c0003t0001g0226 a0002c0003t0001g0227 |
3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.135+2244A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936333 | |||||||
| chr9:124936410 | A | T | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2167T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936410 | |||||||
| chr9:124936444 | T | A | 1 | a0001c0001t0004g0239 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.135+2133A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936444 | |||||||
| chr9:124936609 | T | TA | 7 | a0001c0001t0003g0074 a0002c0002t0001g0308 a0002c0006t0003g0080 others(4): Show |
7 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+1967dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936609 | |||||||
| chr9:124936609 | TA | T | 6 | a0001c0001t0002g0121 a0001c0001t0003g0046 a0001c0001t0004g0229 others(3): Show |
6 | HG01993.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+1967delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936609 | |||||||
| chr9:124936779 | T | C | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1798A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936779 | |||||||
| chr9:124936834 | T | C | 1 | a0001c0001t0016g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+1743A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936834 | |||||||
| chr9:124937009 | G | C | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.135+1568C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937009 | |||||||
| chr9:124937044 | G | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+1533C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937044 | |||||||
| chr9:124937092 | G | A | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.135+1485C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937092 | |||||||
| chr9:124937127 | T | TTA | 5 | a0002c0006t0003g0080 a0002c0006t0003g0081 a0002c0006t0003g0082 others(2): Show |
5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+1448_135+1449d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937127 | |||||||
| chr9:124937143 | C | T | 157 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(154): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.135+1434G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937143 | |||||||
| chr9:124937189 | C | T | 140 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(137): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.135+1388G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937189 | |||||||
| chr9:124937219 | C | T | 1 | a0002c0003t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.135+1358G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937219 | |||||||
| chr9:124937233 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.135+1344G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937233 | |||||||
| chr9:124937312 | C | T | 1 | a0002c0002t0001g0309 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.135+1265G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937312 | |||||||
| chr9:124937330 | T | A | 3 | a0003c0004t0006g0101 a0003c0004t0006g0106 a0003c0004t0006g0107 |
3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.135+1247A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937330 | |||||||
| chr9:124937331 | A | G | 5 | a0002c0002t0001g0035 a0002c0002t0001g0252 a0002c0002t0001g0313 others(2): Show |
6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+1246T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937331 | |||||||
| chr9:124937368 | G | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+1209C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937368 | |||||||
| chr9:124937421 | C | T | 3 | a0004c0007t0007g0013 a0004c0007t0007g0075 a0004c0007t0007g0076 |
4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1156G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937421 | |||||||
| chr9:124937435 | A | G | 140 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(137): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.135+1142T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937435 | |||||||
| chr9:124937488 | G | A | 3 | a0002c0002t0001g0033 a0002c0002t0001g0309 a0002c0002t0001g0310 |
4 | HG00140.hp2 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1089C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937488 | |||||||
| chr9:124937521 | C | T | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0119 others(1): Show |
4 | HG00423.hp1 NA18960.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1056G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937521 | |||||||
| chr9:124937552 | A | G | 1 | a0003c0016t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1025T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937552 | |||||||
| chr9:124937569 | T | A | 1 | a0008c0017t0004g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+1008A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937569 | |||||||
| chr9:124937592 | C | T | 1 | a0003c0004t0006g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.135+985G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937592 | |||||||
| chr9:124937630 | CA | C | 182 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(179): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.135+946delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937630 | |||||||
| chr9:124937682 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.135+895C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937682 | |||||||
| chr9:124937759 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0118 a0001c0001t0002g0178 |
4 | HG01081.hp2 HG01346.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+818A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937759 | |||||||
| chr9:124937904 | A | G | 182 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(179): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.135+673T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937904 | |||||||
| chr9:124937956 | A | G | 1 | a0003c0004t0009g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+621T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937956 | |||||||
| chr9:124937976 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02132.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.135+601C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937976 | |||||||
| chr9:124938037 | C | G | 1 | a0002c0002t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.135+540G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938037 | |||||||
| chr9:124938069 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.135+508G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938069 | |||||||
| chr9:124938082 | C | CAA | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+493_135+494dup others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938082 | |||||||
| chr9:124938082 | CA | C | 56 | a0001c0001t0002g0088 a0001c0001t0002g0201 a0001c0001t0004g0228 others(53): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.135+494delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938082 | |||||||
| chr9:124938098 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.135+479T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938098 | |||||||
| chr9:124938271 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.135+306G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938271 | |||||||
| chr9:124938382 | G | C | 99 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(96): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.135+195C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938382 | |||||||
| chr9:124938388 | AAT | A | 234 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(231): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.135+187_135+188del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938388 | |||||||
| chr9:124938399 | C | A | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+178G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938399 | |||||||
| chr9:124938437 | C | G | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.135+140G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938437 | |||||||
| chr9:124938497 | G | T | 1 | a0006c0011t0003g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+80C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938497 | |||||||
| chr9:124939028 | C | T | 1 | a0002c0002t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-155-162G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939028 | |||||||
| chr9:124939527 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-156+579G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939527 | |||||||
| chr9:124939538 | T | TTTTC | 16 | a0002c0002t0001g0005 a0002c0002t0001g0035 a0002c0002t0001g0036 others(13): Show |
21 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-156+564_-156+567d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939538 | |||||||
| chr9:124939546 | CTTTCTTT | C | 9 | a0003c0004t0006g0101 a0003c0004t0006g0104 a0003c0004t0006g0105 others(6): Show |
9 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156+553_-156+559d others(9): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939546 | |||||||
| chr9:124939550 | C | CT | 15 | a0001c0001t0008g0042 a0002c0002t0001g0004 a0002c0002t0001g0247 others(12): Show |
16 | HG00558.hp2 HG00738.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-156+555dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | |||||||
| chr9:124939550 | CTTT | C | 32 | a0001c0001t0002g0014 a0001c0001t0002g0087 a0001c0001t0002g0088 others(29): Show |
37 | HG00597.hp2 HG00621.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.-156+553_-156+555d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | |||||||
| chr9:124939550 | CTTTT | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(73): Show |
84 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-156+552_-156+555d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | |||||||
| chr9:124939550 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-156+545_-156+555d others(13): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | |||||||
| chr9:124939550 | CTTTTTTT others(5): Show |
C | 48 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+544_-156+555d others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | |||||||
| chr9:124939552 | T | TTC | 17 | a0001c0001t0002g0093 a0001c0001t0003g0008 a0001c0001t0003g0012 others(14): Show |
18 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-156+553_-156+554i others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939552 | |||||||
| chr9:124939553 | T | TC | 43 | a0001c0001t0002g0245 a0001c0001t0003g0007 a0001c0001t0003g0008 others(40): Show |
50 | HG00099.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.-156+552_-156+553i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939553 | |||||||
| chr9:124939554 | T | C | 3 | a0001c0001t0002g0110 a0001c0001t0003g0109 a0003c0016t0001g0108 |
3 | HG01109.hp2 HG01169.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-156+552A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939554 | |||||||
| chr9:124939556 | T | C | 2 | a0002c0003t0012g0111 a0002c0003t0012g0112 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-156+550A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939556 | |||||||
| chr9:124939557 | T | C | 20 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(17): Show |
24 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-156+549A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939557 | |||||||
| chr9:124939558 | T | C | 75 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(72): Show |
83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-156+548A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939558 | |||||||
| chr9:124939559 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02976.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-156+547A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939559 | |||||||
| chr9:124939560 | T | C | 1 | a0002c0002t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-156+546A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939560 | |||||||
| chr9:124939561 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-156+545A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939561 | |||||||
| chr9:124939563 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-156+543A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939563 | |||||||
| chr9:124939565 | T | C | 1 | a0002c0003t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-156+541A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939565 | |||||||
| chr9:124939566 | T | C | 48 | a0001c0001t0002g0201 a0002c0003t0001g0001 a0002c0003t0001g0022 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+540A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939566 | |||||||
| chr9:124939593 | G | A | 1 | a0001c0001t0002g0025 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-156+513C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939593 | |||||||
| chr9:124939596 | CTT | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0026 a0001c0001t0004g0027 others(12): Show |
19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-156+508_-156+509d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939596 | |||||||
| chr9:124939676 | C | G | 1 | a0001c0001t0010g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-156+430G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939676 | |||||||
| chr9:124939953 | T | C | 1 | a0002c0002t0001g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-156+153A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939953 | |||||||
| chr9:124940241 | G | A | 1 | a0003c0004t0006g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-205-86C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940241 | |||||||
| chr9:124940490 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-205-335A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940490 | |||||||
| chr9:124940681 | CAAAG | C | 5 | a0001c0005t0005g0006 a0001c0005t0005g0037 a0001c0005t0005g0327 others(2): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-206+286_-206+289d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940681 | |||||||
| chr9:124940722 | A | G | 236 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(233): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-206+249T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940722 | |||||||
| chr9:124940880 | G | A | 1 | a0002c0002t0001g0325 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-206+91C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940880 |