| geneid | 3617 |
|---|---|
| ensemblid | ENSG00000112706.12 |
| hgncid | 6055 |
| symbol | IMPG1 |
| name | interphotoreceptor matrix proteoglycan 1 |
| refseq_nuc | NM_001563.4 |
| refseq_prot | NP_001554.2 |
| ensembl_nuc | ENST00000369950.8 |
| ensembl_prot | ENSP00000358966.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 75921114 |
| end | 76072662 |
| strand | - |
| ver | v1.2 |
| region | chr6:75921114-76072662 |
| region5000 | chr6:75916114-76077662 |
| regionname0 | IMPG1_chr6_75921114_76072662 |
| regionname5000 | IMPG1_chr6_75916114_76077662 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 797 | 89 | 31 | 8 | 45 | 0 | 5 | 31 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002 | 1/0 | 797 | 57 | 23 | 9 | 14 | 3 | 7 | 11 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003 | 0/0 | 797 | 37 | 7 | 12 | 14 | 1 | 3 | 12 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0004 | 0/0 | 797 | 19 | 0 | 0 | 19 | 0 | 0 | 13 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0005 | 0/1 | 797 | 14 | 0 | 8 | 1 | 2 | 2 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006 | 0/0 | 797 | 14 | 0 | 3 | 8 | 1 | 2 | 6 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0007 | 0/0 | 797 | 13 | 6 | 6 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0008 | 0/0 | 797 | 11 | 0 | 4 | 7 | 0 | 0 | 6 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0009 | 0/0 | 797 | 10 | 3 | 0 | 7 | 0 | 0 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0010 | 0/0 | 797 | 8 | 0 | 3 | 4 | 1 | 0 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0011 | 0/0 | 797 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0012 | 0/0 | 797 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0013 | 0/0 | 797 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0014 | 0/0 | 797 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0015 | 0/0 | 797 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0016 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0017 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0018 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0019 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0020 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0021 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0022 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0023 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0024 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0025 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2394 | 84 | 26 | 8 | 45 | 0 | 5 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0002 | 1/0 | 2394 | 57 | 23 | 9 | 14 | 3 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0003 | 0/0 | 2394 | 35 | 5 | 12 | 14 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0004 | 0/0 | 2394 | 19 | 0 | 0 | 19 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0005 | 0/0 | 2394 | 14 | 0 | 3 | 8 | 1 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0006 | 0/1 | 2394 | 14 | 0 | 8 | 1 | 2 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0007 | 0/0 | 2394 | 13 | 6 | 6 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0008 | 0/0 | 2394 | 11 | 0 | 4 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0009 | 0/0 | 2394 | 10 | 3 | 0 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0010 | 0/0 | 2394 | 8 | 0 | 3 | 4 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0011 | 0/0 | 2394 | 6 | 0 | 2 | 0 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0012 | 0/0 | 2394 | 5 | 1 | 3 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0013 | 0/0 | 2394 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0014 | 0/0 | 2394 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0015 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0016 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0017 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0018 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0019 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0020 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0021 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0022 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0023 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0024 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0025 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0026 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0027 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0028 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| c0029 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1150 | 211 | 48 | 35 | 107 | 6 | 14 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0002 | 0/0 | 1146 | 25 | 0 | 0 | 25 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0003 | 0/1 | 1150 | 20 | 0 | 10 | 1 | 3 | 5 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0004 | 0/0 | 1150 | 18 | 7 | 9 | 0 | 1 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0005 | 0/0 | 1154 | 13 | 12 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0006 | 0/0 | 1150 | 3 | 2 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0007 | 0/0 | 1150 | 3 | 3 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0008 | 0/0 | 1150 | 3 | 0 | 0 | 0 | 0 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0009 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0010 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0011 | 0/0 | 1150 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0012 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0013 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| t0014 | 0/0 | 1150 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2394 | 84 | 26 | 8 | 45 | 0 | 5 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0016 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0018 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0026 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002c0002 | 1/0 | 2394 | 57 | 23 | 9 | 14 | 3 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003 | 0/0 | 2394 | 35 | 5 | 12 | 14 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0015 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0004c0004 | 0/0 | 2394 | 19 | 0 | 0 | 19 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0005c0006 | 0/1 | 2394 | 14 | 0 | 8 | 1 | 2 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005 | 0/0 | 2394 | 14 | 0 | 3 | 8 | 1 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0007c0007 | 0/0 | 2394 | 13 | 6 | 6 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0008c0008 | 0/0 | 2394 | 11 | 0 | 4 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0009c0009 | 0/0 | 2394 | 10 | 3 | 0 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0010c0010 | 0/0 | 2394 | 8 | 0 | 3 | 4 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0011c0011 | 0/0 | 2394 | 6 | 0 | 2 | 0 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0012c0012 | 0/0 | 2394 | 5 | 1 | 3 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0013c0013 | 0/0 | 2394 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0014c0014 | 0/0 | 2394 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0015c0017 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0016c0019 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0017c0029 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0018c0020 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0019c0021 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0020c0024 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0021c0022 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0022c0023 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0023c0025 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0024c0027 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0025c0028 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3543 | 71 | 16 | 7 | 44 | 0 | 4 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0001t0005 | 0/0 | 3547 | 10 | 9 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0001t0009 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0001t0010 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0001t0012 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0016t0005 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0018t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0001c0026t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002c0002t0001 | 1/0 | 3543 | 53 | 19 | 9 | 14 | 3 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002c0002t0005 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002c0002t0007 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0002c0002t0013 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003t0001 | 0/0 | 3543 | 29 | 3 | 11 | 13 | 1 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003t0002 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003t0006 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003t0008 | 0/0 | 3543 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0003t0014 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0003c0015t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0004c0004t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0004c0004t0002 | 0/0 | 3539 | 18 | 0 | 0 | 18 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0005c0006t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0005c0006t0003 | 0/1 | 3543 | 13 | 0 | 8 | 1 | 2 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005t0001 | 0/0 | 3543 | 6 | 0 | 1 | 3 | 1 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005t0002 | 0/0 | 3539 | 5 | 0 | 0 | 5 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005t0006 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005t0008 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0006c0005t0011 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0007c0007t0004 | 0/0 | 3543 | 13 | 6 | 6 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0008c0008t0001 | 0/0 | 3543 | 11 | 0 | 4 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0009c0009t0001 | 0/0 | 3543 | 9 | 2 | 0 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0009c0009t0007 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0010c0010t0001 | 0/0 | 3543 | 8 | 0 | 3 | 4 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0011c0011t0003 | 0/0 | 3543 | 6 | 0 | 2 | 0 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0012c0012t0004 | 0/0 | 3543 | 5 | 1 | 3 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0013c0013t0001 | 0/0 | 3543 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0014c0014t0001 | 0/0 | 3543 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0015c0017t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0016c0019t0003 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0017c0029t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0018c0020t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0019c0021t0002 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0020c0024t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0021c0022t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0022c0023t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0023c0025t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0024c0027t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| a0025c0028t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | copy fasta | chr6 | 75916114 | 76077662 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0001t0012g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0016t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0016t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0018t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0018t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0001c0026t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0002c0002t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0008g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0003t0014g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0015t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0003c0015t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0004c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0005c0006t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0008g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0006c0005t0011g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0007c0007t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0008c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0009c0009t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0010c0010t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0011c0011t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0012c0012t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0012c0012t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0012c0012t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0012c0012t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0012c0012t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0013c0013t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0013c0013t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0013c0013t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0013c0013t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0014c0014t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0014c0014t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0014c0014t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0015c0017t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0015c0017t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0016c0019t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0017c0029t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0018c0020t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0019c0021t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0020c0024t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0021c0022t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0022c0023t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0023c0025t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0024c0027t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| a0025c0028t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0005 | c0006 | t0003 | g0090 | EUR | GBR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0152 | EUR | GBR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00423 | hp1 | a0004 | c0004 | t0002 | g0098 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00438 | hp2 | a0006 | c0005 | t0002 | g0108 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00558 | hp1 | a0004 | c0004 | t0002 | g0102 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00609 | hp1 | a0008 | c0008 | t0001 | g0123 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00609 | hp2 | a0004 | c0004 | t0002 | g0027 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00621 | hp1 | a0010 | c0010 | t0001 | g0185 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0159 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00735 | hp2 | a0008 | c0008 | t0001 | g0207 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0101 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00741 | hp1 | a0005 | c0006 | t0003 | g0085 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG00741 | hp2 | a0003 | c0003 | t0014 | g0083 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01070 | hp2 | a0007 | c0007 | t0004 | g0229 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01071 | hp1 | a0011 | c0011 | t0003 | g0122 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01071 | hp2 | a0007 | c0007 | t0004 | g0220 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0270 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01074 | hp2 | a0010 | c0010 | t0001 | g0172 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01081 | hp1 | a0005 | c0006 | t0003 | g0219 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0154 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01106 | hp1 | a0008 | c0008 | t0001 | g0209 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01109 | hp1 | a0007 | c0007 | t0004 | g0094 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01109 | hp2 | a0006 | c0005 | t0006 | g0222 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0163 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01167 | hp2 | a0005 | c0006 | t0003 | g0292 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01169 | hp1 | a0005 | c0006 | t0003 | g0228 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0180 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01192 | hp2 | a0012 | c0012 | t0004 | g0144 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01256 | hp1 | a0006 | c0005 | t0001 | g0171 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01256 | hp2 | a0007 | c0007 | t0004 | g0001 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01258 | hp2 | a0007 | c0007 | t0004 | g0001 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01261 | hp1 | a0007 | c0007 | t0004 | g0232 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01358 | hp1 | a0006 | c0005 | t0011 | g0149 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01433 | hp1 | a0011 | c0011 | t0003 | g0116 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01433 | hp2 | a0005 | c0006 | t0003 | g0204 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01496 | hp2 | a0010 | c0010 | t0001 | g0109 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0147 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01517 | hp2 | a0007 | c0007 | t0004 | g0200 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01884 | hp2 | a0015 | c0017 | t0001 | g0294 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01928 | hp2 | a0008 | c0008 | t0001 | g0210 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01975 | hp1 | a0012 | c0012 | t0004 | g0165 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01978 | hp1 | a0005 | c0006 | t0003 | g0084 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0211 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01993 | hp1 | a0005 | c0006 | t0003 | g0268 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0155 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02015 | hp1 | a0023 | c0025 | t0001 | g0086 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02027 | hp2 | a0004 | c0004 | t0002 | g0055 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02071 | hp1 | a0025 | c0028 | t0001 | g0120 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02074 | hp2 | a0017 | c0029 | t0001 | g0135 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02083 | hp2 | a0006 | c0005 | t0002 | g0265 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02129 | hp2 | a0004 | c0004 | t0002 | g0118 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02148 | hp2 | a0008 | c0008 | t0001 | g0139 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02257 | hp1 | a0002 | c0002 | t0005 | g0080 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02273 | hp1 | a0010 | c0010 | t0001 | g0300 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02280 | hp1 | a0009 | c0009 | t0007 | g0255 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0239 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02300 | hp1 | a0005 | c0006 | t0003 | g0162 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02300 | hp2 | a0012 | c0012 | t0004 | g0164 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02523 | hp2 | a0004 | c0004 | t0002 | g0076 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02602 | hp1 | a0003 | c0003 | t0008 | g0137 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0261 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02622 | hp2 | a0007 | c0007 | t0004 | g0248 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02698 | hp2 | a0006 | c0005 | t0001 | g0143 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02735 | hp2 | a0011 | c0011 | t0003 | g0128 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02895 | hp2 | a0007 | c0007 | t0004 | g0246 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02897 | hp2 | a0007 | c0007 | t0004 | g0247 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02922 | hp2 | a0003 | c0015 | t0001 | g0014 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02965 | hp1 | a0003 | c0003 | t0006 | g0006 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0250 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03017 | hp1 | a0012 | c0012 | t0004 | g0148 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03041 | hp1 | a0009 | c0009 | t0001 | g0254 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03041 | hp2 | a0007 | c0007 | t0004 | g0245 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0079 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03098 | hp2 | a0001 | c0016 | t0005 | g0016 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03130 | hp1 | a0001 | c0018 | t0001 | g0107 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03130 | hp2 | a0009 | c0009 | t0001 | g0259 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0087 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03453 | hp2 | a0002 | c0002 | t0013 | g0008 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03486 | hp2 | a0001 | c0026 | t0001 | g0241 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03516 | hp1 | a0001 | c0016 | t0005 | g0015 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03540 | hp1 | a0007 | c0007 | t0004 | g0009 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03540 | hp2 | a0007 | c0007 | t0004 | g0058 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03704 | hp1 | a0001 | c0001 | t0012 | g0206 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03704 | hp2 | a0011 | c0011 | t0003 | g0126 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03710 | hp1 | a0006 | c0005 | t0008 | g0091 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03710 | hp2 | a0005 | c0006 | t0003 | g0282 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03831 | hp1 | a0016 | c0019 | t0003 | g0113 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0286 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0173 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04115 | hp1 | a0011 | c0011 | t0003 | g0129 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04184 | hp1 | a0005 | c0006 | t0001 | g0243 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04199 | hp1 | a0003 | c0003 | t0008 | g0178 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0256 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18522 | hp2 | a0001 | c0018 | t0001 | g0263 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18941 | hp1 | a0005 | c0006 | t0003 | g0032 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18944 | hp1 | a0004 | c0004 | t0002 | g0037 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18946 | hp2 | a0020 | c0024 | t0001 | g0136 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18947 | hp1 | a0013 | c0013 | t0001 | g0195 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18947 | hp2 | a0004 | c0004 | t0002 | g0075 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18948 | hp1 | a0022 | c0023 | t0001 | g0131 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18953 | hp2 | a0008 | c0008 | t0001 | g0127 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18954 | hp2 | a0013 | c0013 | t0001 | g0196 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18957 | hp2 | a0009 | c0009 | t0001 | g0117 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18960 | hp1 | a0010 | c0010 | t0001 | g0203 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18960 | hp2 | a0009 | c0009 | t0001 | g0169 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18962 | hp1 | a0008 | c0008 | t0001 | g0060 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18962 | hp2 | a0009 | c0009 | t0001 | g0068 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18965 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18965 | hp2 | a0006 | c0005 | t0002 | g0100 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18966 | hp2 | a0004 | c0004 | t0002 | g0236 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18969 | hp1 | a0006 | c0005 | t0001 | g0119 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18969 | hp2 | a0014 | c0014 | t0001 | g0041 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18971 | hp1 | a0010 | c0010 | t0001 | g0279 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18974 | hp1 | a0004 | c0004 | t0002 | g0176 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18974 | hp2 | a0008 | c0008 | t0001 | g0199 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18975 | hp1 | a0008 | c0008 | t0001 | g0215 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18975 | hp2 | a0004 | c0004 | t0002 | g0244 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18977 | hp1 | a0013 | c0013 | t0001 | g0183 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0170 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18982 | hp2 | a0019 | c0021 | t0002 | g0103 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18983 | hp1 | a0004 | c0004 | t0002 | g0025 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18983 | hp2 | a0018 | c0020 | t0001 | g0040 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18987 | hp1 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18989 | hp1 | a0006 | c0005 | t0001 | g0038 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18990 | hp2 | a0008 | c0008 | t0001 | g0216 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18993 | hp1 | a0006 | c0005 | t0002 | g0093 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18995 | hp1 | a0004 | c0004 | t0001 | g0234 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18995 | hp2 | a0004 | c0004 | t0002 | g0024 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18999 | hp1 | a0006 | c0005 | t0002 | g0202 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18999 | hp2 | a0014 | c0014 | t0001 | g0039 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19000 | hp2 | a0004 | c0004 | t0002 | g0168 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19003 | hp1 | a0009 | c0009 | t0001 | g0115 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19004 | hp1 | a0014 | c0014 | t0001 | g0050 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19004 | hp2 | a0004 | c0004 | t0002 | g0132 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19009 | hp2 | a0009 | c0009 | t0001 | g0106 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19010 | hp2 | a0006 | c0005 | t0001 | g0121 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19012 | hp2 | a0009 | c0009 | t0001 | g0096 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19043 | hp2 | a0015 | c0017 | t0001 | g0293 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19056 | hp2 | a0009 | c0009 | t0001 | g0104 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19057 | hp1 | a0004 | c0004 | t0002 | g0033 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0235 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19062 | hp2 | a0010 | c0010 | t0001 | g0028 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19063 | hp2 | a0013 | c0013 | t0001 | g0194 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19065 | hp2 | a0004 | c0004 | t0002 | g0077 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19077 | hp1 | a0021 | c0022 | t0001 | g0051 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19240 | hp1 | a0024 | c0027 | t0001 | g0064 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ASW | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20129 | hp2 | a0002 | c0002 | t0007 | g0062 | AFR | ASW | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20752 | hp1 | a0006 | c0005 | t0001 | g0157 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20752 | hp2 | a0011 | c0011 | t0003 | g0213 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20805 | hp1 | a0010 | c0010 | t0001 | g0201 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA20805 | hp2 | a0005 | c0006 | t0003 | g0110 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02559 | hp1 | a0003 | c0015 | t0001 | g0013 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG02559 | hp2 | a0012 | c0012 | t0004 | g0230 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0007 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | USA | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | USA | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18955 | hp1 | a0008 | c0008 | t0001 | g0081 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| NA18955 | hp2 | a0004 | c0004 | t0002 | g0092 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0006 | t0003 | g0182 | REF | REF | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0005 | REF | REF | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75922106
|
C | T | 4 | a0008a0010a0017others(1): Show | 21 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(18): Show |
missense_variant | MODERATE | c.2377G>A | p.Asp793Asn | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 2551/3543 | 2377/2394 | 793/797 | chr6 | 75922106 | ||
| chr6:75923668
|
C | T | 3 | a0005a0011a0016 | 21 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(18): Show |
missense_variant | MODERATE | c.2282G>A | p.Ser761Asn | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/17 | 2456/3543 | 2282/2394 | 761/797 | chr6 | 75923668 | ||
| chr6:75931064
|
C | T | 5 | a0003a0004a0006others(2): Show | 72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
missense_variant | MODERATE | c.2132G>A | p.Arg711His | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/17 | 2306/3543 | 2132/2394 | 711/797 | chr6 | 75931064 | ||
| chr6:75931086
|
G | A | 2 | a0007a0012 | 18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
missense_variant | MODERATE | c.2110C>T | p.Arg704Trp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/17 | 2284/3543 | 2110/2394 | 704/797 | chr6 | 75931086 | ||
| chr6:75950680
|
T | C | 5 | a0004a0009a0014others(2): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
missense_variant | MODERATE | c.1706A>G | p.Lys569Arg | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1880/3543 | 1706/2394 | 569/797 | chr6 | 75950680 | ||
| chr6:75950834
|
G | C | 13 | a0001a0003a0004others(10): Show | 198 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
missense_variant | MODERATE | c.1552C>G | p.His518Asp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1726/3543 | 1552/2394 | 518/797 | chr6 | 75950834 | ||
| chr6:75950998
|
C | A | 1 | a0024 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1388G>T | p.Gly463Val | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1562/3543 | 1388/2394 | 463/797 | chr6 | 75950998 | ||
| chr6:75951069
|
C | T | 1 | a0015 | 2 | HG01884.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1317G>A | p.Met439Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1491/3543 | 1317/2394 | 439/797 | chr6 | 75951069 | ||
| chr6:76002938
|
C | T | 3 | a0020a0021a0022 | 3 | NA18946.hp2 NA18948.hp1 NA19077.hp1 |
missense_variant | MODERATE | c.1271G>A | p.Gly424Glu | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/17 | 1445/3543 | 1271/2394 | 424/797 | chr6 | 76002938 | ||
| chr6:76002969
|
G | A | 1 | a0025 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1240C>T | p.Pro414Ser | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/17 | 1414/3543 | 1240/2394 | 414/797 | chr6 | 76002969 | ||
| chr6:76005322
|
T | C | 1 | a0013 | 4 | NA18947.hp1 NA18954.hp2 NA18977.hp1 others(1): Show |
missense_variant | MODERATE | c.1100A>G | p.Gln367Arg | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/17 | 1274/3543 | 1100/2394 | 367/797 | chr6 | 76005322 | ||
| chr6:76018807
|
C | T | 3 | a0014a0018a0019 | 5 | NA18969.hp2 NA18982.hp2 NA18983.hp2 others(2): Show |
missense_variant | MODERATE | c.718G>A | p.Val240Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/17 | 892/3543 | 718/2394 | 240/797 | chr6 | 76018807 | ||
| chr6:76022132
|
G | A | 1 | a0017 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.650C>T | p.Thr217Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/17 | 824/3543 | 650/2394 | 217/797 | chr6 | 76022132 | ||
| chr6:76042021
|
C | T | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.173G>A | p.Arg58Lys | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/17 | 347/3543 | 173/2394 | 58/797 | chr6 | 76042021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75947402
|
A | T | 1 | a0001c0018 | 2 | HG03130.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1956T>A | p.Ala652Ala | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/17 | 2130/3543 | 1956/2394 | 652/797 | chr6 | 75947402 | ||
| chr6:75950973
|
G | A | 1 | a0001c0026 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1413C>T | p.Asp471Asp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1587/3543 | 1413/2394 | 471/797 | chr6 | 75950973 | ||
| chr6:76025216
|
A | C | 2 | a0001c0016a0003c0015 | 4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.540T>G | p.Gly180Gly | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/17 | 714/3543 | 540/2394 | 180/797 | chr6 | 76025216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75921185
|
G | GAGAT | 3 | a0001c0001t0005a0001c0016t0005a0002c0002t0005 | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*900_*903dupATCT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 903 | chr6 | 75921185 | |||||
| chr6:75921224
|
A | G | 1 | a0002c0002t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 865 | chr6 | 75921224 | |||||
| chr6:75921279
|
T | C | 1 | a0006c0005t0011 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 810 | chr6 | 75921279 | |||||
| chr6:75921450
|
G | T | 2 | a0003c0003t0008a0006c0005t0008 | 3 | HG02602.hp1 HG03710.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 639 | chr6 | 75921450 | |||||
| chr6:75921530
|
C | T | 1 | a0001c0001t0010 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 559 | chr6 | 75921530 | |||||
| chr6:75921543
|
T | A | 1 | a0001c0001t0012 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 546 | chr6 | 75921543 | |||||
| chr6:75921572
|
T | C | 1 | a0002c0002t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 517 | chr6 | 75921572 | |||||
| chr6:75921666
|
C | T | 1 | a0001c0001t0009 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 423 | chr6 | 75921666 | |||||
| chr6:75921700
|
A | G | 2 | a0007c0007t0004a0012c0012t0004 | 18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*389T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 389 | chr6 | 75921700 | |||||
| chr6:75921758
|
C | T | 3 | a0005c0006t0003a0011c0011t0003a0016c0019t0003 | 20 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 331 | chr6 | 75921758 | |||||
| chr6:75921800
|
G | A | 1 | a0003c0003t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 289 | chr6 | 75921800 | |||||
| chr6:75921875
|
GGTTT | G | 4 | a0003c0003t0002a0004c0004t0002a0006c0005t0002others(1): Show | 25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*213delAAAC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 210 | chr6 | 75921875 | |||||
| chr6:75921888
|
A | G | 2 | a0002c0002t0007a0009c0009t0007 | 3 | HG02280.hp1 NA18522.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 201 | chr6 | 75921888 | |||||
| chr6:75921978
|
A | G | 2 | a0003c0003t0006a0006c0005t0006 | 3 | HG01109.hp2 HG02965.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 111 | chr6 | 75921978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75922244
|
A | G | 3 | a0001c0001t0001g0043a0009c0009t0001g0104a0025c0028t0001g0120 | 3 | HG02071.hp1 NA19003.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2317-78T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922244 | ||||||
| chr6:75922309
|
A | G | 2 | a0007c0007t0004g0220a0007c0007t0004g0229 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2317-143T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922309 | ||||||
| chr6:75922353
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2317-187G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922353 | ||||||
| chr6:75922630
|
T | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2317-464A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922630 | ||||||
| chr6:75922662
|
G | A | 1 | a0003c0003t0006g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-496C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922662 | ||||||
| chr6:75922903
|
A | AT | 10 | a0001c0018t0001g0107a0002c0002t0001g0227a0003c0003t0001g0152others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2316+730dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922903 | ||||||
| chr6:75923102
|
TGTAAAAT others(12): Show |
T | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2316+513_2316+531d others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923102 | ||||||
| chr6:75923288
|
G | C | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2316+346C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923288 | ||||||
| chr6:75923406
|
A | G | 1 | a0002c0002t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2316+228T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923406 | ||||||
| chr6:75923418
|
A | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(77): Show | 82 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.2316+216T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923418 | ||||||
| chr6:75923487
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2316+147T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923487 | ||||||
| chr6:75923826
|
T | C | 1 | a0002c0002t0001g0290 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2244-120A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923826 | ||||||
| chr6:75923841
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0226a0009c0009t0001g0254others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-135G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923841 | ||||||
| chr6:75923893
|
T | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244-187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923893 | ||||||
| chr6:75924103
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2244-397A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924103 | ||||||
| chr6:75924242
|
TATCTATC others(213): Show |
T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-756_2244-537d others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924242 | ||||||
| chr6:75924444
|
AATATAAC others(6): Show |
A | 4 | a0001c0001t0001g0114a0001c0001t0001g0226a0009c0009t0001g0254others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-751_2244-739d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924444 | ||||||
| chr6:75924451
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0018t0001g0263others(3): Show | 6 | HG02723.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-745G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924451 | ||||||
| chr6:75924451
|
CAT | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(19): Show | 22 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2244-747_2244-746d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924451 | ||||||
| chr6:75924468
|
A | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-762T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924468 | ||||||
| chr6:75924481
|
A | G | 1 | a0011c0011t0003g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2244-775T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924481 | ||||||
| chr6:75924482
|
T | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-776A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924482 | ||||||
| chr6:75924488
|
TATA | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(6): Show | 9 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2244-785_2244-783d others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924488 | ||||||
| chr6:75924499
|
T | C | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2244-793A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924499 | ||||||
| chr6:75924500
|
A | ATATAATA others(20): Show |
12 | a0007c0007t0004g0001a0007c0007t0004g0009a0007c0007t0004g0058others(9): Show | 13 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2244-821_2244-795d others(29): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924500 | ||||||
| chr6:75924504
|
A | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-798T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924504 | ||||||
| chr6:75924508
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(60): Show | 64 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2244-802A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924508 | ||||||
| chr6:75924509
|
A | G | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-803T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924509 | ||||||
| chr6:75924513
|
A | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-807T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924513 | ||||||
| chr6:75924527
|
T | A | 2 | a0004c0004t0002g0102a0004c0004t0002g0168 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2244-821A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924527 | ||||||
| chr6:75924527
|
TTATAATA others(6): Show |
T | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-834_2244-822d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924527 | ||||||
| chr6:75924528
|
TATAATAT others(178): Show |
T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-1007_2244-823 others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924528 | ||||||
| chr6:75924529
|
A | ATAATATA others(15): Show |
4 | a0002c0002t0001g0140a0009c0009t0001g0068a0009c0009t0001g0106others(1): Show | 4 | NA18962.hp2 NA18977.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-845_2244-824d others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924529 | ||||||
| chr6:75924530
|
TA | T | 69 | a0001c0001t0001g0056a0001c0001t0001g0057a0003c0003t0001g0017others(66): Show | 69 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2244-825delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924530 | ||||||
| chr6:75924531
|
A | AATTAATA others(14): Show |
2 | a0003c0003t0001g0044a0003c0003t0001g0045 | 2 | NA18959.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2244-826_2244-825i others(23): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924531 | ||||||
| chr6:75924544
|
A | AATATAAT others(19): Show |
2 | a0007c0007t0004g0220a0007c0007t0004g0229 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2244-839_2244-838i others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924544 | ||||||
| chr6:75924544
|
A | AATATAAT others(19): Show |
1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2244-864_2244-839d others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924544 | ||||||
| chr6:75924550
|
A | T | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-844T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924550 | ||||||
| chr6:75924552
|
TA | T | 3 | a0001c0001t0001g0054a0002c0002t0001g0048a0014c0014t0001g0050 | 3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2244-847delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924552 | ||||||
| chr6:75924554
|
A | AT | 82 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-849dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924554 | ||||||
| chr6:75924557
|
TA | T | 4 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0151others(1): Show | 4 | HG01175.hp2 NA18985.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-852delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924557 | ||||||
| chr6:75924558
|
A | AT | 82 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-853_2244-852i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924558 | ||||||
| chr6:75924558
|
A | C | 1 | a0004c0004t0002g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2244-852T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924558 | ||||||
| chr6:75924561
|
T | A | 86 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-855A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924561 | ||||||
| chr6:75924566
|
ATTAT | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(17): Show | 20 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2244-864_2244-861d others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924566 | ||||||
| chr6:75924568
|
T | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.2244-862A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924568 | ||||||
| chr6:75924568
|
T | TATATATA others(32): Show |
2 | a0004c0004t0002g0102a0004c0004t0002g0168 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2244-863_2244-862i others(41): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924568 | ||||||
| chr6:75924569
|
ATATATAA others(1): Show |
A | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-871_2244-864d others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924569 | ||||||
| chr6:75924571
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0264 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2244-865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924571 | ||||||
| chr6:75924575
|
AAT | A | 86 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-871_2244-870d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924575 | ||||||
| chr6:75924578
|
T | A | 2 | a0002c0002t0001g0069a0002c0002t0001g0270 | 2 | HG01074.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2244-872A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924578 | ||||||
| chr6:75924579
|
A | T | 2 | a0002c0002t0001g0069a0002c0002t0001g0270 | 2 | HG01074.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2244-873T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924579 | ||||||
| chr6:75924583
|
TA | T | 86 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-878delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924583 | ||||||
| chr6:75924593
|
T | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0275a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-887A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924593 | ||||||
| chr6:75924593
|
TTA | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 60 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2244-889_2244-888d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924593 | ||||||
| chr6:75924594
|
T | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(17): Show | 20 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2244-888A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924594 | ||||||
| chr6:75924595
|
A | ATATAATT others(29): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0009g0261 | 3 | HG02622.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2244-890_2244-889i others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924595 | ||||||
| chr6:75924598
|
T | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0275a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-892A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924598 | ||||||
| chr6:75924599
|
A | T | 6 | a0001c0001t0001g0175a0001c0001t0001g0275a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-893T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924599 | ||||||
| chr6:75924601
|
A | G | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-895T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924601 | ||||||
| chr6:75924603
|
T | TA | 6 | a0001c0001t0001g0175a0001c0001t0001g0275a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-898_2244-897i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924603 | ||||||
| chr6:75924603
|
T | TTAATA | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-898_2244-897i others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924603 | ||||||
| chr6:75924604
|
T | A | 4 | a0002c0002t0013g0008a0003c0003t0001g0159a0003c0003t0001g0163others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-898A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924604 | ||||||
| chr6:75924605
|
A | AT | 89 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(86): Show | 89 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2244-900_2244-899i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924605 | ||||||
| chr6:75924605
|
A | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-899T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924605 | ||||||
| chr6:75924608
|
T | G | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-902A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924608 | ||||||
| chr6:75924615
|
A | C | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-909T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924615 | ||||||
| chr6:75924615
|
A | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(16): Show | 19 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2244-909T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924615 | ||||||
| chr6:75924622
|
A | G | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-916T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924622 | ||||||
| chr6:75924624
|
TAAATTA | T | 92 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(89): Show | 92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-924_2244-919d others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924624 | ||||||
| chr6:75924625
|
A | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(21): Show | 24 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244-919T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924625 | ||||||
| chr6:75924629
|
T | TATATATA others(2): Show |
3 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-924_2244-923i others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924629 | ||||||
| chr6:75924636
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-930A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | ||||||
| chr6:75924636
|
T | C | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-930A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | ||||||
| chr6:75924636
|
T | G | 92 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(89): Show | 92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-930A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | ||||||
| chr6:75924637
|
A | T | 1 | a0004c0004t0002g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2244-931T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924637 | ||||||
| chr6:75924643
|
A | C | 92 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(89): Show | 92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-937T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924643 | ||||||
| chr6:75924643
|
A | G | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-937T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924643 | ||||||
| chr6:75924645
|
T | TA | 93 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(90): Show | 93 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.2244-940_2244-939i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924645 | ||||||
| chr6:75924645
|
T | TATA | 3 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-940_2244-939i others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924645 | ||||||
| chr6:75924646
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-940A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924646 | ||||||
| chr6:75924647
|
A | AT | 3 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-942_2244-941i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924647 | ||||||
| chr6:75924647
|
A | T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-941T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924647 | ||||||
| chr6:75924654
|
T | TAC | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-949_2244-948i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924654 | ||||||
| chr6:75924656
|
T | TCA | 3 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-951_2244-950i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924656 | ||||||
| chr6:75924657
|
A | ATG | 66 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2244-952_2244-951i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | ||||||
| chr6:75924657
|
A | ATGATATA others(2): Show |
3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-952_2244-951i others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | ||||||
| chr6:75924657
|
A | G | 15 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(12): Show | 15 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2244-951T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | ||||||
| chr6:75924657
|
A | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(110): Show | 113 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.2244-951T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | ||||||
| chr6:75924658
|
A | T | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-952T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924658 | ||||||
| chr6:75924659
|
T | C | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-953A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924659 | ||||||
| chr6:75924664
|
A | AAT | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-960_2244-959d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924664
|
A | AATAT | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-959_2244-958i others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924664
|
A | AATTATAT others(1): Show |
3 | a0007c0007t0004g0009a0007c0007t0004g0094a0012c0012t0004g0230 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-959_2244-958i others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924664
|
A | C | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-958T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924664
|
A | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-958T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924664
|
A | T | 81 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(78): Show | 81 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2244-958T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | ||||||
| chr6:75924667
|
A | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-961T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924667 | ||||||
| chr6:75924668
|
A | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(262): Show | 267 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.2244-962T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924668 | ||||||
| chr6:75924669
|
A | T | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-963T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924669 | ||||||
| chr6:75924670
|
T | A | 93 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(90): Show | 93 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.2244-964A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | ||||||
| chr6:75924670
|
T | TAATA | 64 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2244-965_2244-964i others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | ||||||
| chr6:75924670
|
T | TTA | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-966_2244-965d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | ||||||
| chr6:75924671
|
T | A | 27 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(24): Show | 28 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.2244-965A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | ||||||
| chr6:75924671
|
T | C | 6 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-965A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | ||||||
| chr6:75924671
|
T | TATATATA | 68 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(65): Show | 69 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2244-966_2244-965i others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | ||||||
| chr6:75924671
|
TA | T | 92 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(89): Show | 92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-966delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | ||||||
| chr6:75924673
|
T | A | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-967A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924673 | ||||||
| chr6:75924675
|
T | TA | 6 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-970dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924675 | ||||||
| chr6:75924678
|
T | A | 4 | a0001c0001t0010g0003a0002c0002t0013g0008a0003c0003t0001g0179others(1): Show | 4 | HG01261.hp1 HG02015.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-972A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | ||||||
| chr6:75924678
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244-972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | ||||||
| chr6:75924678
|
T | G | 125 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(122): Show | 125 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2244-972A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | ||||||
| chr6:75924682
|
T | TATAATTA | 3 | a0001c0001t0001g0175a0001c0001t0001g0275a0006c0005t0011g0149 | 3 | HG01358.hp1 NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-977_2244-976i others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924682 | ||||||
| chr6:75924684
|
T | A | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-978A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924684 | ||||||
| chr6:75924684
|
T | TCA | 39 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(36): Show | 39 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.2244-979_2244-978i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924684 | ||||||
| chr6:75924685
|
T | A | 3 | a0003c0003t0001g0159a0003c0003t0001g0163a0003c0003t0001g0180 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-979A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | ||||||
| chr6:75924685
|
T | C | 118 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(115): Show | 118 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2244-979A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | ||||||
| chr6:75924685
|
T | G | 1 | a0001c0001t0010g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2244-979A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | ||||||
| chr6:75924689
|
TATAAATA | T | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-990_2244-984d others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924689 | ||||||
| chr6:75924690
|
ATAAATAA others(6): Show |
A | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-997_2244-985d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924690 | ||||||
| chr6:75924690
|
ATAAATAA others(8): Show |
A | 82 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-999_2244-985d others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924690 | ||||||
| chr6:75924691
|
T | A | 10 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0069others(7): Show | 10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-985A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924691 | ||||||
| chr6:75924691
|
T | TC | 7 | a0002c0002t0001g0140a0003c0003t0001g0159a0003c0003t0001g0163others(4): Show | 7 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244-986_2244-985i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924691 | ||||||
| chr6:75924692
|
A | AT | 28 | a0001c0001t0001g0175a0001c0001t0001g0275a0003c0003t0002g0170others(25): Show | 28 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.2244-987_2244-986i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924692 | ||||||
| chr6:75924692
|
A | T | 10 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0069others(7): Show | 10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-986T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924692 | ||||||
| chr6:75924693
|
A | AT | 4 | a0001c0018t0001g0263a0007c0007t0004g0009a0007c0007t0004g0094others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-988_2244-987i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | ||||||
| chr6:75924693
|
A | ATATATCA others(1): Show |
42 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(39): Show | 42 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.2244-988_2244-987i others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | ||||||
| chr6:75924693
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0275a0006c0005t0011g0149 | 3 | HG01358.hp1 NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-987T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | ||||||
| chr6:75924693
|
A | T | 17 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0069others(14): Show | 17 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2244-987T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | ||||||
| chr6:75924694
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(107): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2244-988T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924694 | ||||||
| chr6:75924695
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-989A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924695 | ||||||
| chr6:75924695
|
TA | T | 10 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0069others(7): Show | 10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-990delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924695 | ||||||
| chr6:75924696
|
A | AT | 112 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(109): Show | 113 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2244-991_2244-990i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924696 | ||||||
| chr6:75924696
|
A | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-990T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924696 | ||||||
| chr6:75924697
|
AT | A | 4 | a0002c0002t0001g0140a0009c0009t0001g0068a0009c0009t0001g0106others(1): Show | 4 | NA18962.hp2 NA18977.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-992delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924697 | ||||||
| chr6:75924698
|
T | A | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-992A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924698 | ||||||
| chr6:75924699
|
T | A | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-993A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | ||||||
| chr6:75924699
|
T | C | 38 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2244-993A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | ||||||
| chr6:75924699
|
T | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-993A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | ||||||
| chr6:75924701
|
T | TATGATAT others(3): Show |
3 | a0007c0007t0004g0009a0007c0007t0004g0094a0012c0012t0004g0230 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-996_2244-995i others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924701 | ||||||
| chr6:75924703
|
T | TA | 25 | a0003c0003t0002g0170a0004c0004t0002g0024a0004c0004t0002g0025others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2244-998dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924703 | ||||||
| chr6:75924705
|
T | A | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-999A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924705 | ||||||
| chr6:75924706
|
A | AATATATA others(8): Show |
2 | a0003c0003t0001g0193a0004c0004t0001g0234 | 2 | NA18957.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2244-1001_2244-100 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | ||||||
| chr6:75924706
|
A | AATATATC others(7): Show |
1 | a0002c0002t0001g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2244-1001_2244-100 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | ||||||
| chr6:75924706
|
A | AATATATC others(8): Show |
37 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(34): Show | 37 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2244-1001_2244-100 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | ||||||
| chr6:75924706
|
A | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.2244-1000T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | ||||||
| chr6:75924707
|
A | AT | 3 | a0007c0007t0004g0009a0007c0007t0004g0094a0012c0012t0004g0230 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-1002dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924707 | ||||||
| chr6:75924707
|
A | T | 83 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(80): Show | 83 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.2244-1001T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924707 | ||||||
| chr6:75924708
|
T | C | 1 | a0001c0001t0010g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2244-1002A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924708 | ||||||
| chr6:75924710
|
T | TA | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-1005dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924710 | ||||||
| chr6:75924711
|
ATAATAT | A | 6 | a0001c0001t0001g0054a0002c0002t0001g0048a0002c0002t0001g0069others(3): Show | 6 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-1011_2244-100 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924711 | ||||||
| chr6:75924713
|
A | AATTATAT others(1): Show |
9 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(6): Show | 9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | AATTATAT others(17): Show |
1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1008_2244-100 others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | AATTATAT others(16): Show |
37 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(34): Show | 38 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(27): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | AATTATAT others(65): Show |
13 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0088others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(76): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | AATTATAT others(63): Show |
27 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0258others(24): Show | 28 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(74): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | AATTATAT others(57): Show |
6 | a0005c0006t0003g0084a0005c0006t0003g0085a0005c0006t0003g0090others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(68): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2244-1007T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0275 | 2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-1007T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924713
|
A | T | 127 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(124): Show | 127 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.2244-1007T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | ||||||
| chr6:75924717
|
T | TA | 10 | a0001c0018t0001g0263a0003c0003t0001g0079a0003c0003t0001g0159others(7): Show | 10 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1012dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924717 | ||||||
| chr6:75924719
|
T | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-1013A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924719 | ||||||
| chr6:75924720
|
A | C | 51 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(48): Show | 51 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2244-1014T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | ||||||
| chr6:75924720
|
A | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(31): Show | 34 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2244-1014T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | ||||||
| chr6:75924720
|
AATATAAT others(29): Show |
A | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-1050_2244-101 others(40): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | ||||||
| chr6:75924724
|
TA | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(33): Show | 36 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2244-1019delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924724 | ||||||
| chr6:75924725
|
A | AATTATAT | 79 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(76): Show | 79 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2244-1026_2244-102 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924725 | ||||||
| chr6:75924727
|
T | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0275 | 2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-1021A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924727 | ||||||
| chr6:75924728
|
T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(22): Show | 25 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2244-1022A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | ||||||
| chr6:75924728
|
T | TATATATA | 59 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.2244-1029_2244-102 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | ||||||
| chr6:75924728
|
T | TATATATA others(7): Show |
1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2244-1036_2244-102 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | ||||||
| chr6:75924728
|
TATATATA others(7): Show |
T | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-1036_2244-102 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | ||||||
| chr6:75924735
|
A | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-1029T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924735 | ||||||
| chr6:75924735
|
A | T | 35 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(32): Show | 35 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2244-1029T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924735 | ||||||
| chr6:75924737
|
T | TATATA | 3 | a0005c0006t0001g0243a0005c0006t0003g0282a0011c0011t0003g0126 | 3 | HG03704.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2244-1036_2244-103 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924737 | ||||||
| chr6:75924739
|
T | TA | 10 | a0003c0003t0001g0079a0003c0003t0001g0159a0003c0003t0001g0163others(7): Show | 10 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1034dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924739 | ||||||
| chr6:75924741
|
T | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-1035A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924741 | ||||||
| chr6:75924742
|
A | AATATAAT others(1): Show |
65 | a0002c0002t0001g0140a0003c0003t0001g0017a0003c0003t0001g0023others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2244-1037_2244-103 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | ||||||
| chr6:75924742
|
A | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(27): Show | 30 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2244-1036T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | ||||||
| chr6:75924742
|
AATATATA others(7): Show |
A | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-1050_2244-103 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | ||||||
| chr6:75924743
|
A | ATATAAT | 9 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(6): Show | 9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1038_2244-103 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924743 | ||||||
| chr6:75924749
|
A | G | 9 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(6): Show | 9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1043T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924749 | ||||||
| chr6:75924756
|
C | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(236): Show | 241 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.2244-1050G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924756
|
C | CATATAAT others(37): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(29): Show | 32 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2244-1051_2244-105 others(48): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924756
|
C | CATATAAT others(59): Show |
1 | a0006c0005t0011g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(70): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924756
|
C | CATATAAT others(51): Show |
7 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(4): Show | 7 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2244-1051_2244-105 others(62): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924756
|
C | CATATAAT others(71): Show |
1 | a0002c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(82): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924756
|
C | CATATAAT others(58): Show |
1 | a0011c0011t0003g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(69): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | ||||||
| chr6:75924763
|
T | A | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1057A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924763 | ||||||
| chr6:75924774
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2244-1068T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924774 | ||||||
| chr6:75925162
|
C | T | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1456G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925162 | ||||||
| chr6:75925208
|
A | G | 3 | a0005c0006t0001g0243a0005c0006t0003g0282a0011c0011t0003g0126 | 3 | HG03704.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2244-1502T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925208 | ||||||
| chr6:75925247
|
CAGTT | C | 71 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(68): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2244-1545_2244-154 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925247 | ||||||
| chr6:75925494
|
T | A | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1788A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925494 | ||||||
| chr6:75925624
|
C | T | 3 | a0002c0002t0001g0297a0002c0002t0001g0298a0009c0009t0001g0169 | 3 | NA18945.hp1 NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2244-1918G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925624 | ||||||
| chr6:75925669
|
A | ATTTG | 8 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(5): Show | 8 | HG02257.hp1 HG02615.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244-1967_2244-196 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925669 | ||||||
| chr6:75925669
|
A | ATTTGTTT others(1): Show |
189 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(186): Show | 189 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.2244-1971_2244-196 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925669 | ||||||
| chr6:75925805
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(77): Show | 82 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.2244-2099T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925805 | ||||||
| chr6:75925822
|
C | T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-2116G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925822 | ||||||
| chr6:75925861
|
T | C | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-2155A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925861 | ||||||
| chr6:75925890
|
T | A | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-2184A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925890 | ||||||
| chr6:75925897
|
C | T | 1 | a0005c0006t0003g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2244-2191G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925897 | ||||||
| chr6:75926026
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(77): Show | 82 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.2244-2320G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926026 | ||||||
| chr6:75926200
|
G | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2244-2494C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926200 | ||||||
| chr6:75926305
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2244-2599G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926305 | ||||||
| chr6:75926316
|
C | A | 1 | a0005c0006t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2244-2610G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926316 | ||||||
| chr6:75926434
|
G | A | 1 | a0004c0004t0002g0236 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2244-2728C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926434 | ||||||
| chr6:75926667
|
T | C | 88 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(85): Show | 88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2244-2961A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926667 | ||||||
| chr6:75926706
|
A | T | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-3000T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926706 | ||||||
| chr6:75926707
|
T | A | 1 | a0002c0002t0001g0297 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-3001A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926707 | ||||||
| chr6:75926713
|
C | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-3007G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926713 | ||||||
| chr6:75926728
|
C | CA | 68 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(65): Show | 68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2244-3023dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926728 | ||||||
| chr6:75926790
|
C | A | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2244-3084G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926790 | ||||||
| chr6:75926814
|
GGAGTA | G | 72 | a0001c0018t0001g0263a0003c0003t0001g0017a0003c0003t0001g0023others(69): Show | 72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2244-3113_2244-310 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926814 | ||||||
| chr6:75926962
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-3256G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926962 | ||||||
| chr6:75926973
|
C | T | 2 | a0004c0004t0002g0098a0006c0005t0002g0265 | 2 | HG00423.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2244-3267G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926973 | ||||||
| chr6:75927085
|
G | GA | 6 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-3380dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927085 | ||||||
| chr6:75927401
|
T | C | 17 | a0007c0007t0004g0001a0007c0007t0004g0009a0007c0007t0004g0058others(14): Show | 18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+3552A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927401 | ||||||
| chr6:75927427
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2243+3526T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927427 | ||||||
| chr6:75927680
|
C | A | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2243+3273G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927680 | ||||||
| chr6:75927715
|
T | TTCCC | 4 | a0001c0018t0001g0107a0002c0002t0001g0298a0009c0009t0001g0117others(1): Show | 4 | HG03130.hp1 NA18945.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243+3234_2243+323 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927715 | ||||||
| chr6:75927731
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+3222G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927731 | ||||||
| chr6:75927789
|
T | G | 25 | a0003c0003t0002g0170a0004c0004t0002g0024a0004c0004t0002g0025others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2243+3164A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927789 | ||||||
| chr6:75927790
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 39 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2243+3163C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927790 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4778): Show |
1 | a0013c0013t0001g0183 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4789): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4775): Show |
2 | a0001c0001t0001g0099a0002c0002t0001g0072 | 2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4786): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4776): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0205others(2): Show | 5 | HG00621.hp2 HG02027.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4787): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4777): Show |
9 | a0001c0001t0001g0026a0001c0001t0001g0174a0001c0001t0001g0175others(6): Show | 9 | HG00438.hp1 NA18941.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4788): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4778): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0134others(1): Show | 4 | HG00597.hp1 HG01928.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4789): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4777): Show |
1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4788): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927807
|
C | CAAAAATG others(4779): Show |
1 | a0001c0001t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4790): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | ||||||
| chr6:75927842
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2243+3111G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927842 | ||||||
| chr6:75927843
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0099a0002c0002t0001g0072 | 3 | HG00673.hp1 HG02129.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2243+3110C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927843 | ||||||
| chr6:75927852
|
T | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2243+3101A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927852 | ||||||
| chr6:75927907
|
G | A | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243+3046C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927907 | ||||||
| chr6:75927981
|
T | C | 1 | a0004c0004t0002g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2243+2972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927981 | ||||||
| chr6:75928104
|
A | G | 89 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(86): Show | 89 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2243+2849T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928104 | ||||||
| chr6:75928207
|
C | CT | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+2745dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928207 | ||||||
| chr6:75928211
|
T | C | 2 | a0006c0005t0002g0093a0006c0005t0002g0100 | 2 | NA18965.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2243+2742A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928211 | ||||||
| chr6:75928239
|
G | A | 1 | a0001c0001t0005g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2243+2714C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928239 | ||||||
| chr6:75928308
|
T | G | 2 | a0007c0007t0004g0009a0012c0012t0004g0230 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2243+2645A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928308 | ||||||
| chr6:75928410
|
G | A | 17 | a0007c0007t0004g0001a0007c0007t0004g0009a0007c0007t0004g0058others(14): Show | 18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+2543C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928410 | ||||||
| chr6:75928419
|
C | A | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+2534G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928419 | ||||||
| chr6:75928481
|
C | T | 2 | a0002c0002t0007g0062a0002c0002t0007g0256 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2243+2472G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928481 | ||||||
| chr6:75928567
|
A | C | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+2386T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928567 | ||||||
| chr6:75928601
|
T | A | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+2352A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928601 | ||||||
| chr6:75928859
|
A | G | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2243+2094T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928859 | ||||||
| chr6:75928895
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(60): Show | 64 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2243+2058T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928895 | ||||||
| chr6:75928939
|
C | A | 1 | a0011c0011t0003g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2243+2014G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928939 | ||||||
| chr6:75929011
|
A | G | 165 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(162): Show | 165 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.2243+1942T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929011 | ||||||
| chr6:75929166
|
A | G | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+1787T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929166 | ||||||
| chr6:75929167
|
T | TAATG | 17 | a0007c0007t0004g0001a0007c0007t0004g0009a0007c0007t0004g0058others(14): Show | 18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+1782_2243+178 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929167 | ||||||
| chr6:75929233
|
T | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(107): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2243+1720A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929233 | ||||||
| chr6:75929385
|
T | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+1568A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929385 | ||||||
| chr6:75929455
|
A | G | 1 | a0005c0006t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2243+1498T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929455 | ||||||
| chr6:75929536
|
C | G | 3 | a0001c0001t0001g0054a0002c0002t0001g0048a0014c0014t0001g0050 | 3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2243+1417G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929536 | ||||||
| chr6:75929603
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(28): Show | 31 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2243+1350C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929603 | ||||||
| chr6:75929739
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2243+1214T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929739 | ||||||
| chr6:75929748
|
G | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2243+1205C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929748 | ||||||
| chr6:75929754
|
TA | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(22): Show | 25 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2243+1198delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929754 | ||||||
| chr6:75929996
|
G | C | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2243+957C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929996 | ||||||
| chr6:75930054
|
C | A | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2243+899G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930054 | ||||||
| chr6:75930071
|
C | T | 2 | a0002c0002t0007g0062a0002c0002t0007g0256 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2243+882G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930071 | ||||||
| chr6:75930138
|
C | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(28): Show | 31 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2243+815G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930138 | ||||||
| chr6:75930504
|
C | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+449G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930504 | ||||||
| chr6:75930535
|
G | A | 1 | a0006c0005t0001g0038 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2243+418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930535 | ||||||
| chr6:75930641
|
G | A | 7 | a0002c0002t0001g0242a0002c0002t0001g0262a0002c0002t0007g0062others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2243+312C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930641 | ||||||
| chr6:75930658
|
T | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+295A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930658 | ||||||
| chr6:75930679
|
G | A | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+274C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930679 | ||||||
| chr6:75930833
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2243+120T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930833 | ||||||
| chr6:75930883
|
C | G | 3 | a0004c0004t0002g0075a0004c0004t0002g0132a0019c0021t0002g0103 | 3 | NA18947.hp2 NA18982.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2243+70G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930883 | ||||||
| chr6:75931177
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2045-26G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931177 | ||||||
| chr6:75931244
|
A | G | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-93T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931244 | ||||||
| chr6:75931311
|
T | C | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045-160A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931311 | ||||||
| chr6:75931393
|
A | C | 9 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045-242T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931393 | ||||||
| chr6:75931426
|
C | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-275G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931426 | ||||||
| chr6:75931579
|
GT | G | 74 | a0001c0018t0001g0263a0002c0002t0013g0008a0003c0003t0001g0017others(71): Show | 74 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2045-429delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931579 | ||||||
| chr6:75931625
|
T | G | 3 | a0013c0013t0001g0194a0013c0013t0001g0195a0013c0013t0001g0196 | 3 | NA18947.hp1 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2045-474A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931625 | ||||||
| chr6:75931706
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0010g0003others(1): Show | 4 | HG00673.hp1 HG02129.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-555C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931706 | ||||||
| chr6:75931964
|
T | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-813A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931964 | ||||||
| chr6:75932213
|
G | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-1062C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932213 | ||||||
| chr6:75932244
|
G | A | 20 | a0005c0006t0001g0243a0005c0006t0003g0032a0005c0006t0003g0084others(17): Show | 20 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2045-1093C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932244 | ||||||
| chr6:75932288
|
C | T | 1 | a0011c0011t0003g0122 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2045-1137G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932288 | ||||||
| chr6:75932289
|
T | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.2045-1138A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932289 | ||||||
| chr6:75932301
|
C | T | 1 | a0002c0002t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2045-1150G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932301 | ||||||
| chr6:75932413
|
G | T | 1 | a0002c0002t0001g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2045-1262C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932413 | ||||||
| chr6:75932567
|
A | C | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-1416T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932567 | ||||||
| chr6:75932756
|
A | C | 1 | a0006c0005t0011g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2045-1605T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932756 | ||||||
| chr6:75932770
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2045-1619T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932770 | ||||||
| chr6:75932809
|
T | C | 1 | a0005c0006t0003g0282 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2045-1658A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932809 | ||||||
| chr6:75932815
|
C | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-1664G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932815 | ||||||
| chr6:75932820
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(74): Show | 79 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.2045-1669G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932820 | ||||||
| chr6:75932906
|
G | T | 8 | a0007c0007t0004g0001a0007c0007t0004g0058a0007c0007t0004g0200others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2045-1755C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932906 | ||||||
| chr6:75933033
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2045-1882T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933033 | ||||||
| chr6:75933169
|
A | G | 1 | a0004c0004t0002g0132 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2045-2018T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933169 | ||||||
| chr6:75933186
|
C | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2035G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933186 | ||||||
| chr6:75933193
|
A | G | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2045-2042T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933193 | ||||||
| chr6:75933337
|
A | G | 1 | a0009c0009t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2045-2186T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933337 | ||||||
| chr6:75933364
|
G | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2213C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933364 | ||||||
| chr6:75933411
|
A | T | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2045-2260T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933411 | ||||||
| chr6:75933450
|
A | G | 44 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(41): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2045-2299T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933450 | ||||||
| chr6:75933657
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 39 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2045-2506T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933657 | ||||||
| chr6:75933681
|
C | T | 1 | a0003c0003t0001g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2045-2530G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933681 | ||||||
| chr6:75933725
|
A | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2574T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933725 | ||||||
| chr6:75933839
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2045-2688G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933839 | ||||||
| chr6:75933864
|
T | G | 1 | a0005c0006t0003g0085 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2045-2713A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933864 | ||||||
| chr6:75933885
|
A | G | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-2734T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933885 | ||||||
| chr6:75933925
|
G | A | 19 | a0005c0006t0001g0243a0005c0006t0003g0032a0005c0006t0003g0084others(16): Show | 19 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2045-2774C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933925 | ||||||
| chr6:75933926
|
G | A | 1 | a0006c0005t0002g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2045-2775C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933926 | ||||||
| chr6:75934021
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2045-2870A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934021 | ||||||
| chr6:75934139
|
G | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0273 | 2 | NA18959.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2045-2988C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934139 | ||||||
| chr6:75934144
|
C | A | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2045-2993G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934144 | ||||||
| chr6:75934166
|
A | G | 1 | a0002c0002t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2045-3015T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934166 | ||||||
| chr6:75934315
|
C | A | 1 | a0002c0002t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2045-3164G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934315 | ||||||
| chr6:75934416
|
G | A | 25 | a0003c0003t0002g0170a0004c0004t0002g0024a0004c0004t0002g0025others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2045-3265C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934416 | ||||||
| chr6:75934512
|
T | C | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-3361A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934512 | ||||||
| chr6:75934554
|
C | T | 2 | a0001c0001t0012g0206a0002c0002t0001g0061 | 2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2045-3403G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934554 | ||||||
| chr6:75934577
|
T | G | 13 | a0001c0001t0005g0011a0001c0001t0005g0018a0001c0001t0005g0019others(10): Show | 13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-3426A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934577 | ||||||
| chr6:75934631
|
A | G | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-3480T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934631 | ||||||
| chr6:75934662
|
T | G | 1 | a0009c0009t0001g0096 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2045-3511A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934662 | ||||||
| chr6:75934668
|
C | T | 71 | a0001c0001t0001g0010a0002c0002t0013g0008a0003c0003t0001g0017others(68): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2045-3517G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934668 | ||||||
| chr6:75934691
|
A | C | 2 | a0005c0006t0003g0085a0005c0006t0003g0090 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2045-3540T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934691 | ||||||
| chr6:75934720
|
C | T | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2045-3569G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934720 | ||||||
| chr6:75934795
|
C | G | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2045-3644G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934795 | ||||||
| chr6:75934801
|
C | G | 1 | a0005c0006t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2045-3650G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934801 | ||||||
| chr6:75934810
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.2045-3659G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934810 | ||||||
| chr6:75934868
|
C | T | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-3717G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934868 | ||||||
| chr6:75934999
|
A | C | 1 | a0010c0010t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2045-3848T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934999 | ||||||
| chr6:75935291
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2045-4140G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935291 | ||||||
| chr6:75935443
|
A | G | 1 | a0005c0006t0003g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2045-4292T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935443 | ||||||
| chr6:75935492
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2045-4341G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935492 | ||||||
| chr6:75935691
|
C | T | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-4540G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935691 | ||||||
| chr6:75935837
|
G | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2045-4686C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935837 | ||||||
| chr6:75936086
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(61): Show | 65 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2045-4935G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936086 | ||||||
| chr6:75936106
|
C | G | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2045-4955G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936106 | ||||||
| chr6:75936117
|
C | T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-4966G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936117 | ||||||
| chr6:75936140
|
AT | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0296a0022c0023t0001g0131 | 3 | HG00597.hp1 NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2045-4990delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936140 | ||||||
| chr6:75936241
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2045-5090T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936241 | ||||||
| chr6:75936368
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(69): Show | 73 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2045-5217A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936368 | ||||||
| chr6:75936518
|
A | T | 1 | a0011c0011t0003g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2045-5367T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936518 | ||||||
| chr6:75936762
|
G | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(61): Show | 65 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2045-5611C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936762 | ||||||
| chr6:75936823
|
T | C | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2045-5672A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936823 | ||||||
| chr6:75936941
|
G | A | 1 | a0002c0002t0001g0138 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2045-5790C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936941 | ||||||
| chr6:75936944
|
A | G | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-5793T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936944 | ||||||
| chr6:75936954
|
A | G | 5 | a0008c0008t0001g0139a0008c0008t0001g0207a0008c0008t0001g0209others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-5803T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936954 | ||||||
| chr6:75937054
|
G | A | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2045-5903C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937054 | ||||||
| chr6:75937099
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2045-5948C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937099 | ||||||
| chr6:75937323
|
G | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-6172C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937323 | ||||||
| chr6:75937391
|
T | C | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2045-6240A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937391 | ||||||
| chr6:75937469
|
GGC | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2045-6320_2045-631 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937469 | ||||||
| chr6:75937483
|
G | A | 88 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0074others(85): Show | 88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2045-6332C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937483 | ||||||
| chr6:75937504
|
G | A | 1 | a0001c0001t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2045-6353C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937504 | ||||||
| chr6:75937597
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2045-6446G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937597 | ||||||
| chr6:75937644
|
T | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(41): Show | 45 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2045-6493A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937644 | ||||||
| chr6:75937672
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2045-6521T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937672 | ||||||
| chr6:75937693
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(61): Show | 65 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2045-6542T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937693 | ||||||
| chr6:75937800
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0010g0003 | 3 | HG00673.hp1 NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2045-6649C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937800 | ||||||
| chr6:75937859
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(157): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2045-6708G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937859 | ||||||
| chr6:75937890
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(157): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2045-6739A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937890 | ||||||
| chr6:75937927
|
A | T | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2045-6776T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937927 | ||||||
| chr6:75937991
|
G | A | 68 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0029others(65): Show | 68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2045-6840C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937991 | ||||||
| chr6:75937999
|
T | C | 3 | a0007c0007t0004g0009a0007c0007t0004g0094a0012c0012t0004g0230 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2045-6848A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937999 | ||||||
| chr6:75938001
|
G | A | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2045-6850C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938001 | ||||||
| chr6:75938365
|
C | A | 2 | a0009c0009t0001g0068a0013c0013t0001g0183 | 2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2045-7214G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938365 | ||||||
| chr6:75938366
|
C | G | 2 | a0009c0009t0001g0068a0013c0013t0001g0183 | 2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2045-7215G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938366 | ||||||
| chr6:75938469
|
A | G | 3 | a0007c0007t0004g0009a0007c0007t0004g0094a0012c0012t0004g0230 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2045-7318T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938469 | ||||||
| chr6:75938523
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2045-7372G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938523 | ||||||
| chr6:75938573
|
G | A | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7422C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938573 | ||||||
| chr6:75938695
|
A | C | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2045-7544T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938695 | ||||||
| chr6:75938730
|
T | C | 2 | a0002c0002t0001g0197a0002c0002t0001g0212 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2045-7579A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938730 | ||||||
| chr6:75938744
|
C | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2045-7593G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938744 | ||||||
| chr6:75938810
|
T | TCAAAA | 154 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0043others(151): Show | 155 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.2045-7664_2045-766 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | ||||||
| chr6:75938810
|
T | TCAAAACA others(3): Show |
82 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2045-7669_2045-766 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | ||||||
| chr6:75938810
|
T | TCAAAACA others(8): Show |
1 | a0001c0001t0001g0275 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2045-7674_2045-766 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | ||||||
| chr6:75938810
|
T | TCAAAACA others(13): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0065 | 3 | HG03209.hp2 HG03579.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2045-7679_2045-766 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | ||||||
| chr6:75938810
|
TCAAAA | T | 27 | a0001c0018t0001g0263a0003c0003t0001g0079a0003c0003t0002g0170others(24): Show | 27 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2045-7664_2045-766 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | ||||||
| chr6:75938831
|
CAAAACAA others(13): Show |
C | 5 | a0007c0007t0004g0232a0007c0007t0004g0245a0007c0007t0004g0246others(2): Show | 5 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-7700_2045-768 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938831 | ||||||
| chr6:75938851
|
A | C | 8 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(5): Show | 8 | HG01109.hp1 HG02293.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2045-7700T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938851 | ||||||
| chr6:75938887
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2045-7736G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938887 | ||||||
| chr6:75938912
|
C | T | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7761G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938912 | ||||||
| chr6:75938923
|
T | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 164 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2045-7772A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938923 | ||||||
| chr6:75938981
|
G | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-7830C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938981 | ||||||
| chr6:75939082
|
A | C | 2 | a0002c0002t0001g0146a0002c0002t0001g0147 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2045-7931T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939082 | ||||||
| chr6:75939109
|
G | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-7958C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939109 | ||||||
| chr6:75939119
|
G | A | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7968C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939119 | ||||||
| chr6:75939209
|
A | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 164 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2045-8058T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939209 | ||||||
| chr6:75939247
|
G | A | 1 | a0002c0002t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+8067C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939247 | ||||||
| chr6:75939350
|
T | TC | 27 | a0003c0003t0001g0233a0003c0003t0002g0170a0004c0004t0002g0024others(24): Show | 27 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2044+7963dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939350 | ||||||
| chr6:75939355
|
C | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(106): Show | 109 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2044+7959G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939355 | ||||||
| chr6:75939355
|
C | T | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+7959G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939355 | ||||||
| chr6:75939841
|
G | C | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+7473C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939841 | ||||||
| chr6:75939888
|
C | T | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044+7426G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939888 | ||||||
| chr6:75940193
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(68): Show | 72 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2044+7121G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940193 | ||||||
| chr6:75940331
|
A | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0226a0002c0002t0001g0059others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044+6983T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940331 | ||||||
| chr6:75940342
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 164 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2044+6972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940342 | ||||||
| chr6:75940436
|
C | T | 4 | a0004c0004t0002g0075a0004c0004t0002g0132a0004c0004t0002g0244others(1): Show | 4 | NA18947.hp2 NA18975.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+6878G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940436 | ||||||
| chr6:75940494
|
T | C | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+6820A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940494 | ||||||
| chr6:75940602
|
T | G | 10 | a0003c0003t0001g0105a0003c0003t0001g0188a0003c0003t0001g0233others(7): Show | 10 | HG01256.hp1 HG01358.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.2044+6712A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940602 | ||||||
| chr6:75940744
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2044+6570T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940744 | ||||||
| chr6:75940759
|
C | T | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+6555G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940759 | ||||||
| chr6:75940760
|
G | A | 72 | a0001c0001t0001g0258a0003c0003t0001g0017a0003c0003t0001g0023others(69): Show | 72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2044+6554C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940760 | ||||||
| chr6:75940767
|
T | G | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+6547A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940767 | ||||||
| chr6:75940964
|
T | G | 7 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(4): Show | 7 | HG02615.hp2 HG03098.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044+6350A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940964 | ||||||
| chr6:75941117
|
T | TG | 89 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0005g0018others(86): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2044+6196dupC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941117 | ||||||
| chr6:75941124
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2044+6190C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941124 | ||||||
| chr6:75941169
|
G | A | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2044+6145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941169 | ||||||
| chr6:75941196
|
T | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044+6118A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941196 | ||||||
| chr6:75941361
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2044+5953C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941361 | ||||||
| chr6:75941550
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2044+5764G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941550 | ||||||
| chr6:75941629
|
T | G | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+5685A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941629 | ||||||
| chr6:75941660
|
ACT | A | 3 | a0003c0003t0001g0079a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+5652_2044+565 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941660 | ||||||
| chr6:75941688
|
G | A | 1 | a0005c0006t0003g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2044+5626C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941688 | ||||||
| chr6:75941736
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(70): Show | 74 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.2044+5578G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941736 | ||||||
| chr6:75941938
|
G | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.2044+5376C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941938 | ||||||
| chr6:75941981
|
C | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.2044+5333G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941981 | ||||||
| chr6:75942046
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2044+5268G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942046 | ||||||
| chr6:75942110
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0226a0009c0009t0001g0254others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044+5204A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942110 | ||||||
| chr6:75942145
|
C | T | 3 | a0010c0010t0001g0109a0010c0010t0001g0172a0010c0010t0001g0201 | 3 | HG01074.hp2 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2044+5169G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942145 | ||||||
| chr6:75942175
|
A | G | 1 | a0011c0011t0003g0213 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2044+5139T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942175 | ||||||
| chr6:75942494
|
G | C | 3 | a0001c0001t0001g0054a0002c0002t0001g0048a0014c0014t0001g0050 | 3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2044+4820C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942494 | ||||||
| chr6:75942546
|
C | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.2044+4768G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942546 | ||||||
| chr6:75942594
|
T | C | 19 | a0005c0006t0001g0243a0005c0006t0003g0032a0005c0006t0003g0084others(16): Show | 19 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2044+4720A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942594 | ||||||
| chr6:75942726
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(41): Show | 45 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2044+4588G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942726 | ||||||
| chr6:75942781
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+4533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942781 | ||||||
| chr6:75942836
|
A | G | 1 | a0002c0002t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2044+4478T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942836 | ||||||
| chr6:75943119
|
G | A | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+4195C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943119 | ||||||
| chr6:75943138
|
G | C | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+4176C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943138 | ||||||
| chr6:75943204
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(160): Show | 165 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2044+4110G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943204 | ||||||
| chr6:75943278
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2044+4036A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943278 | ||||||
| chr6:75943284
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0065a0003c0003t0001g0079others(2): Show | 5 | HG02559.hp1 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+4030T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943284 | ||||||
| chr6:75943378
|
G | A | 88 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0074others(85): Show | 88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2044+3936C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943378 | ||||||
| chr6:75943628
|
A | C | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+3686T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943628 | ||||||
| chr6:75943990
|
C | T | 2 | a0001c0001t0001g0010a0002c0002t0013g0008 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2044+3324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943990 | ||||||
| chr6:75944136
|
C | T | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+3178G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944136 | ||||||
| chr6:75944137
|
G | A | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+3177C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944137 | ||||||
| chr6:75944255
|
C | T | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+3059G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944255 | ||||||
| chr6:75944302
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(19): Show | 22 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2044+3012G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944302 | ||||||
| chr6:75944693
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+2621G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944693 | ||||||
| chr6:75944705
|
T | A | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+2609A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944705 | ||||||
| chr6:75944915
|
CTT | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0021others(240): Show | 245 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.2044+2397_2044+239 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944915 | ||||||
| chr6:75945037
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2044+2277T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945037 | ||||||
| chr6:75945208
|
G | A | 3 | a0003c0003t0006g0006a0003c0003t0006g0007a0006c0005t0006g0222 | 3 | HG01109.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2044+2106C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945208 | ||||||
| chr6:75945253
|
G | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044+2061C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945253 | ||||||
| chr6:75945358
|
C | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+1956G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945358 | ||||||
| chr6:75945358
|
CT | C | 43 | a0001c0001t0001g0273a0003c0003t0001g0017a0003c0003t0001g0029others(40): Show | 43 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2044+1955delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945358 | ||||||
| chr6:75945359
|
T | C | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+1955A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945359 | ||||||
| chr6:75945552
|
T | A | 24 | a0004c0004t0002g0024a0004c0004t0002g0025a0004c0004t0002g0027others(21): Show | 24 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2044+1762A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945552 | ||||||
| chr6:75945722
|
G | A | 9 | a0001c0001t0001g0156a0001c0001t0001g0272a0001c0001t0001g0274others(6): Show | 9 | HG01081.hp2 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2044+1592C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945722 | ||||||
| chr6:75945882
|
G | T | 10 | a0002c0002t0005g0080a0007c0007t0004g0001a0007c0007t0004g0058others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+1432C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945882 | ||||||
| chr6:75945989
|
G | A | 2 | a0001c0018t0001g0107a0001c0018t0001g0263 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+1325C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945989 | ||||||
| chr6:75946055
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 50 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2044+1259A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946055 | ||||||
| chr6:75946253
|
G | T | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2044+1061C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946253 | ||||||
| chr6:75946604
|
A | G | 8 | a0007c0007t0004g0009a0007c0007t0004g0094a0007c0007t0004g0232others(5): Show | 8 | HG01109.hp1 HG01261.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2044+710T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946604 | ||||||
| chr6:75946877
|
AT | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044+436delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946877 | ||||||
| chr6:75946974
|
C | T | 1 | a0003c0003t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2044+340G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946974 | ||||||
| chr6:75946994
|
T | G | 2 | a0002c0002t0001g0059a0002c0002t0001g0150 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2044+320A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946994 | ||||||
| chr6:75947023
|
T | C | 172 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0056others(169): Show | 173 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.2044+291A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947023 | ||||||
| chr6:75947098
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+216C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947098 | ||||||
| chr6:75947148
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2044+166G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947148 | ||||||
| chr6:75947261
|
AT | A | 171 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0056others(168): Show | 171 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.2044+52delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947261 | ||||||
| chr6:75947646
|
T | G | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1825-113A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947646 | ||||||
| chr6:75947747
|
G | T | 30 | a0003c0003t0001g0017a0003c0003t0001g0023a0003c0003t0001g0087others(27): Show | 30 | HG00140.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1825-214C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947747 | ||||||
| chr6:75947825
|
A | G | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-292T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947825 | ||||||
| chr6:75947857
|
TA | T | 131 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(128): Show | 132 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1825-325delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947857 | ||||||
| chr6:75947857
|
TAA | T | 6 | a0007c0007t0004g0232a0007c0007t0004g0245a0007c0007t0004g0246others(3): Show | 6 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-326_1825-325d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947857 | ||||||
| chr6:75947871
|
C | A | 18 | a0005c0006t0001g0243a0005c0006t0003g0084a0005c0006t0003g0085others(15): Show | 18 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1825-338G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947871 | ||||||
| chr6:75947981
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(201): Show | 206 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1825-448G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947981 | ||||||
| chr6:75948182
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02896.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825-649A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948182 | ||||||
| chr6:75948251
|
T | C | 4 | a0001c0018t0001g0263a0002c0002t0001g0231a0002c0002t0005g0080others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-718A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948251 | ||||||
| chr6:75948355
|
GGCTCTGA others(2): Show |
G | 7 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(4): Show | 7 | HG02615.hp2 HG02922.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-831_1825-823d others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948355 | ||||||
| chr6:75948369
|
GC | G | 8 | a0001c0001t0001g0010a0002c0002t0013g0008a0007c0007t0004g0009others(5): Show | 8 | HG01261.hp1 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-837delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948369 | ||||||
| chr6:75948536
|
G | T | 43 | a0001c0001t0001g0134a0001c0001t0001g0174a0001c0001t0001g0175others(40): Show | 43 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1825-1003C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948536 | ||||||
| chr6:75948700
|
G | A | 2 | a0002c0002t0001g0242a0002c0002t0001g0262 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1825-1167C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948700 | ||||||
| chr6:75948876
|
C | T | 1 | a0005c0006t0003g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1825-1343G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948876 | ||||||
| chr6:75948909
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1825-1376A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948909 | ||||||
| chr6:75948941
|
G | A | 1 | a0006c0005t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1825-1408C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948941 | ||||||
| chr6:75949001
|
A | G | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1825-1468T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949001 | ||||||
| chr6:75949101
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0226others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+1461T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949101 | ||||||
| chr6:75949438
|
A | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1824+1124T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949438 | ||||||
| chr6:75949660
|
C | T | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1824+902G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949660 | ||||||
| chr6:75949733
|
ATGGTG | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0003c0003t0001g0087 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1824+824_1824+828d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949733 | ||||||
| chr6:75949798
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1824+764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949798 | ||||||
| chr6:75949844
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1824+718C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949844 | ||||||
| chr6:75950102
|
T | C | 1 | a0003c0003t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1824+460A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950102 | ||||||
| chr6:75950123
|
G | T | 2 | a0012c0012t0004g0164a0012c0012t0004g0165 | 2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1824+439C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950123 | ||||||
| chr6:75950139
|
C | G | 3 | a0001c0026t0001g0241a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1824+423G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950139 | ||||||
| chr6:75950247
|
T | C | 1 | a0024c0027t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1824+315A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950247 | ||||||
| chr6:75950417
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1824+145G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950417 | ||||||
| chr6:75950418
|
T | C | 31 | a0004c0004t0001g0234a0004c0004t0002g0024a0004c0004t0002g0025others(28): Show | 31 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1824+144A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950418 | ||||||
| chr6:75950465
|
A | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0226others(3): Show | 6 | HG01261.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+97T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950465 | ||||||
| chr6:75950554
|
C | T | 6 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(3): Show | 6 | HG01070.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1824+8G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950554 | ||||||
| chr6:75951223
|
A | AT | 81 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(78): Show | 83 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1292-130dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951223 | ||||||
| chr6:75951223
|
AT | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(71): Show | 74 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1292-130delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951223 | ||||||
| chr6:75951236
|
T | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-142A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951236 | ||||||
| chr6:75951590
|
G | GA | 46 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1292-497dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951590 | ||||||
| chr6:75951635
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(166): Show | 171 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1292-541C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951635 | ||||||
| chr6:75951684
|
T | G | 76 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-590A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951684 | ||||||
| chr6:75951796
|
G | C | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1292-702C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951796 | ||||||
| chr6:75951814
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0226others(3): Show | 6 | HG01261.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-720G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951814 | ||||||
| chr6:75951872
|
G | A | 3 | a0001c0001t0001g0258a0001c0018t0001g0263a0007c0007t0004g0009 | 3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-778C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951872 | ||||||
| chr6:75951891
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 164 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1292-797C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951891 | ||||||
| chr6:75951914
|
C | T | 76 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-820G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951914 | ||||||
| chr6:75951943
|
AAAT | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(289): Show | 294 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(291): Show |
intron_variant | MODIFIER | c.1292-852_1292-850d others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951943 | ||||||
| chr6:75951960
|
A | C | 2 | a0004c0004t0002g0118a0009c0009t0001g0117 | 2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1292-866T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951960 | ||||||
| chr6:75952004
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-910G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952004 | ||||||
| chr6:75952062
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1292-968G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952062 | ||||||
| chr6:75952177
|
C | A | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1083G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952177 | ||||||
| chr6:75952341
|
G | C | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1247C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952341 | ||||||
| chr6:75952365
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1292-1271G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952365 | ||||||
| chr6:75952453
|
C | A | 1 | a0004c0004t0002g0236 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1292-1359G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952453 | ||||||
| chr6:75952630
|
G | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-1536C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952630 | ||||||
| chr6:75952675
|
A | G | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-1581T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952675 | ||||||
| chr6:75952764
|
G | A | 2 | a0002c0002t0001g0140a0007c0007t0004g0232 | 2 | HG01261.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1292-1670C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952764 | ||||||
| chr6:75953062
|
T | A | 150 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(147): Show | 151 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1292-1968A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953062 | ||||||
| chr6:75953069
|
T | TTCTTATG others(6): Show |
4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1988_1292-197 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953069 | ||||||
| chr6:75953095
|
C | T | 1 | a0002c0002t0001g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1292-2001G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953095 | ||||||
| chr6:75953096
|
G | A | 76 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-2002C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953096 | ||||||
| chr6:75953781
|
A | G | 146 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(143): Show | 147 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1292-2687T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953781 | ||||||
| chr6:75953909
|
A | C | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-2815T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953909 | ||||||
| chr6:75953937
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1292-2843A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953937 | ||||||
| chr6:75954094
|
G | T | 34 | a0004c0004t0001g0234a0004c0004t0002g0024a0004c0004t0002g0025others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1292-3000C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954094 | ||||||
| chr6:75954183
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-3089C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954183 | ||||||
| chr6:75954229
|
A | G | 30 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(27): Show | 31 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1292-3135T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954229 | ||||||
| chr6:75954260
|
C | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0264 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1292-3166G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954260 | ||||||
| chr6:75954281
|
T | C | 162 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 163 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1292-3187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954281 | ||||||
| chr6:75954323
|
T | C | 1 | a0007c0007t0004g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1292-3229A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954323 | ||||||
| chr6:75954398
|
G | A | 1 | a0001c0001t0009g0261 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1292-3304C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954398 | ||||||
| chr6:75954420
|
A | C | 17 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(14): Show | 17 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1292-3326T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954420 | ||||||
| chr6:75954438
|
T | C | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-3344A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954438 | ||||||
| chr6:75954623
|
T | C | 11 | a0002c0002t0001g0072a0002c0002t0001g0097a0002c0002t0001g0138others(8): Show | 11 | HG01261.hp2 HG01496.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-3529A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954623 | ||||||
| chr6:75954913
|
A | T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1292-3819T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954913 | ||||||
| chr6:75955317
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-4223C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955317 | ||||||
| chr6:75955406
|
T | G | 2 | a0001c0001t0001g0192a0010c0010t0001g0185 | 2 | HG00621.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1292-4312A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955406 | ||||||
| chr6:75955869
|
T | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(32): Show | 36 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-4775A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955869 | ||||||
| chr6:75955919
|
T | C | 1 | a0002c0002t0001g0133 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1292-4825A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955919 | ||||||
| chr6:75956004
|
G | A | 1 | a0011c0011t0003g0213 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1292-4910C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956004 | ||||||
| chr6:75956106
|
C | T | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-5012G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956106 | ||||||
| chr6:75956146
|
T | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(26): Show | 30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-5052A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956146 | ||||||
| chr6:75956203
|
T | C | 2 | a0002c0002t0001g0150a0002c0002t0005g0080 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1292-5109A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956203 | ||||||
| chr6:75956248
|
T | A | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-5154A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956248 | ||||||
| chr6:75956489
|
T | C | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1292-5395A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956489 | ||||||
| chr6:75956510
|
G | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(26): Show | 30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-5416C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956510 | ||||||
| chr6:75956584
|
C | T | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5490G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956584 | ||||||
| chr6:75956725
|
C | A | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5631G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956725 | ||||||
| chr6:75956951
|
G | A | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5857C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956951 | ||||||
| chr6:75956964
|
A | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-5870T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956964 | ||||||
| chr6:75957119
|
C | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1292-6025G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957119 | ||||||
| chr6:75957217
|
C | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1292-6123G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957217 | ||||||
| chr6:75957252
|
G | T | 1 | a0003c0003t0001g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1292-6158C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957252 | ||||||
| chr6:75957435
|
C | G | 1 | a0003c0003t0001g0271 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1292-6341G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957435 | ||||||
| chr6:75957480
|
T | C | 1 | a0016c0019t0003g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1292-6386A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957480 | ||||||
| chr6:75957548
|
C | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(26): Show | 30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-6454G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957548 | ||||||
| chr6:75957948
|
A | T | 76 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-6854T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957948 | ||||||
| chr6:75958034
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-6940G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958034 | ||||||
| chr6:75958058
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-6964G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958058 | ||||||
| chr6:75958618
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-7524A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958618 | ||||||
| chr6:75958716
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(11): Show | 14 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-7622C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958716 | ||||||
| chr6:75958854
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1292-7760G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958854 | ||||||
| chr6:75958932
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.1292-7838G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958932 | ||||||
| chr6:75959062
|
G | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-7968C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959062 | ||||||
| chr6:75959088
|
A | G | 162 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 163 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1292-7994T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959088 | ||||||
| chr6:75959475
|
C | G | 76 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-8381G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959475 | ||||||
| chr6:75959485
|
G | T | 1 | a0002c0002t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1292-8391C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959485 | ||||||
| chr6:75959684
|
A | C | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1292-8590T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959684 | ||||||
| chr6:75959761
|
A | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | NA18986.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1292-8667T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959761 | ||||||
| chr6:75959789
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1292-8695C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959789 | ||||||
| chr6:75959954
|
G | A | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1292-8860C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959954 | ||||||
| chr6:75959978
|
C | G | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-8884G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959978 | ||||||
| chr6:75960125
|
C | T | 2 | a0005c0006t0003g0084a0005c0006t0003g0162 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1292-9031G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960125 | ||||||
| chr6:75960189
|
G | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-9095C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960189 | ||||||
| chr6:75960286
|
C | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-9192G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960286 | ||||||
| chr6:75960314
|
C | T | 4 | a0001c0001t0005g0239a0001c0001t0005g0240a0002c0002t0001g0158others(1): Show | 4 | HG02145.hp2 HG02293.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-9220G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960314 | ||||||
| chr6:75960365
|
A | C | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-9271T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960365 | ||||||
| chr6:75960369
|
C | T | 64 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(61): Show | 65 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1292-9275G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960369 | ||||||
| chr6:75960400
|
A | T | 146 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(143): Show | 147 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1292-9306T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960400 | ||||||
| chr6:75960503
|
A | C | 3 | a0001c0026t0001g0241a0003c0015t0001g0013a0003c0015t0001g0014 | 3 | HG02559.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1292-9409T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960503 | ||||||
| chr6:75960613
|
C | T | 64 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(61): Show | 65 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1292-9519G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960613 | ||||||
| chr6:75960642
|
ATAT | A | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-9551_1292-954 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960642 | ||||||
| chr6:75960819
|
T | C | 3 | a0001c0001t0001g0258a0001c0018t0001g0263a0007c0007t0004g0009 | 3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-9725A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960819 | ||||||
| chr6:75960861
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1292-9767C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960861 | ||||||
| chr6:75961012
|
T | A | 78 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0065others(75): Show | 78 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1292-9918A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961012 | ||||||
| chr6:75961449
|
A | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-10355T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961449 | ||||||
| chr6:75961693
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-10599C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961693 | ||||||
| chr6:75961856
|
C | T | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1292-10762G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961856 | ||||||
| chr6:75961991
|
CT | C | 66 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(63): Show | 67 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1292-10898delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961991 | ||||||
| chr6:75962013
|
G | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-10919C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962013 | ||||||
| chr6:75962102
|
C | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-11008G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962102 | ||||||
| chr6:75962130
|
TG | T | 149 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1292-11037delC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962130 | ||||||
| chr6:75962131
|
G | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-11037C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962131 | ||||||
| chr6:75962179
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1292-11085C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962179 | ||||||
| chr6:75962294
|
A | T | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11200T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962294 | ||||||
| chr6:75962325
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-11231G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962325 | ||||||
| chr6:75962360
|
C | T | 2 | a0002c0002t0007g0062a0002c0002t0007g0256 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1292-11266G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962360 | ||||||
| chr6:75962603
|
C | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0238others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-11509G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962603 | ||||||
| chr6:75962630
|
C | A | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-11536G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962630 | ||||||
| chr6:75962633
|
C | T | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11539G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962633 | ||||||
| chr6:75962634
|
G | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(63): Show | 67 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1292-11540C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962634 | ||||||
| chr6:75962724
|
C | T | 150 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(147): Show | 151 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1292-11630G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962724 | ||||||
| chr6:75962753
|
T | A | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11659A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962753 | ||||||
| chr6:75962858
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1292-11764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962858 | ||||||
| chr6:75962961
|
A | G | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-11867T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962961 | ||||||
| chr6:75962997
|
C | G | 18 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-11903G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962997 | ||||||
| chr6:75963032
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1292-11938G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963032 | ||||||
| chr6:75963044
|
G | GA | 41 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0021others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-11951dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963044 | ||||||
| chr6:75963285
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1292-12191T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963285 | ||||||
| chr6:75963379
|
C | T | 2 | a0001c0001t0001g0010a0007c0007t0004g0232 | 2 | HG01261.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1292-12285G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963379 | ||||||
| chr6:75963457
|
TTTTTA | T | 108 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(105): Show | 109 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1292-12368_1292-12 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963457 | ||||||
| chr6:75963744
|
G | A | 1 | a0004c0004t0002g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1292-12650C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963744 | ||||||
| chr6:75963913
|
T | G | 35 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(32): Show | 36 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-12819A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963913 | ||||||
| chr6:75963946
|
A | C | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-12852T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963946 | ||||||
| chr6:75963987
|
T | G | 1 | a0024c0027t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1292-12893A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963987 | ||||||
| chr6:75964170
|
C | A | 3 | a0001c0001t0001g0258a0001c0018t0001g0263a0007c0007t0004g0009 | 3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-13076G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964170 | ||||||
| chr6:75964207
|
C | T | 1 | a0010c0010t0001g0300 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1292-13113G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964207 | ||||||
| chr6:75964227
|
A | T | 1 | a0008c0008t0001g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1292-13133T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964227 | ||||||
| chr6:75964338
|
CAAT | C | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-13247_1292-13 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964338 | ||||||
| chr6:75964675
|
C | CA | 23 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1292-13582dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | ||||||
| chr6:75964675
|
C | CAA | 10 | a0001c0001t0001g0004a0001c0001t0005g0011a0001c0001t0005g0160others(7): Show | 10 | HG01169.hp2 HG01993.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-13583_1292-13 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | ||||||
| chr6:75964675
|
C | CAAA | 90 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0052others(87): Show | 91 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1292-13584_1292-13 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | ||||||
| chr6:75964675
|
C | CAAAAA | 11 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0114others(8): Show | 11 | HG01261.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-13586_1292-13 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | ||||||
| chr6:75964675
|
CAA | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-13583_1292-13 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | ||||||
| chr6:75965144
|
T | C | 1 | a0009c0009t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1292-14050A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965144 | ||||||
| chr6:75965365
|
CT | C | 173 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(170): Show | 174 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1292-14272delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965365 | ||||||
| chr6:75965523
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1292-14429T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965523 | ||||||
| chr6:75965604
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1292-14510A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965604 | ||||||
| chr6:75965606
|
C | CT | 20 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(17): Show | 20 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-14513dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | ||||||
| chr6:75965606
|
C | CTT | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1292-14514_1292-14 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | ||||||
| chr6:75965606
|
C | CTTT | 21 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0001g0257others(18): Show | 21 | HG01099.hp2 HG01175.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-14515_1292-14 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | ||||||
| chr6:75965677
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(201): Show | 206 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1292-14583A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965677 | ||||||
| chr6:75965678
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-14584C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965678 | ||||||
| chr6:75965678
|
G | C | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1292-14584C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965678 | ||||||
| chr6:75965682
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1292-14588A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965682 | ||||||
| chr6:75965695
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-14601C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965695 | ||||||
| chr6:75965707
|
A | G | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-14613T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965707 | ||||||
| chr6:75965756
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0059others(1): Show | 4 | HG02896.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-14662A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965756 | ||||||
| chr6:75965761
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0059others(1): Show | 4 | HG02896.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-14667A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965761 | ||||||
| chr6:75965780
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1292-14686A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965780 | ||||||
| chr6:75965798
|
A | G | 1 | a0002c0002t0001g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1292-14704T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965798 | ||||||
| chr6:75965828
|
C | A | 27 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.1292-14734G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965828 | ||||||
| chr6:75965849
|
T | C | 1 | a0002c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1292-14755A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965849 | ||||||
| chr6:75965854
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1292-14760C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965854 | ||||||
| chr6:75965875
|
A | G | 1 | a0005c0006t0003g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1292-14781T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965875 | ||||||
| chr6:75965884
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1292-14790C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965884 | ||||||
| chr6:75965887
|
A | G | 2 | a0003c0003t0001g0152a0003c0003t0014g0083 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1292-14793T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965887 | ||||||
| chr6:75965889
|
G | A | 2 | a0003c0003t0001g0152a0003c0003t0014g0083 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1292-14795C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965889 | ||||||
| chr6:75966026
|
G | A | 1 | a0003c0003t0008g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1292-14932C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966026 | ||||||
| chr6:75966094
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-15000C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966094 | ||||||
| chr6:75966179
|
A | G | 1 | a0025c0028t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1292-15085T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966179 | ||||||
| chr6:75966491
|
C | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(82): Show | 86 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1292-15397G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966491 | ||||||
| chr6:75966591
|
T | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-15497A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966591 | ||||||
| chr6:75966733
|
A | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(52): Show | 56 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1292-15639T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966733 | ||||||
| chr6:75966762
|
GAAGA | G | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-15672_1292-15 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966762 | ||||||
| chr6:75966767
|
A | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-15673T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966767 | ||||||
| chr6:75966853
|
C | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-15759G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966853 | ||||||
| chr6:75966885
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-15791T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966885 | ||||||
| chr6:75966899
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1292-15805G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966899 | ||||||
| chr6:75966937
|
T | G | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1292-15843A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966937 | ||||||
| chr6:75966946
|
G | C | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1292-15852C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966946 | ||||||
| chr6:75966998
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(19): Show | 22 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1292-15904G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966998 | ||||||
| chr6:75967089
|
G | T | 2 | a0002c0002t0001g0291a0006c0005t0001g0143 | 2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1292-15995C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967089 | ||||||
| chr6:75967176
|
A | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(57): Show | 60 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1292-16082T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967176 | ||||||
| chr6:75967177
|
T | TA | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-16084dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967177 | ||||||
| chr6:75967253
|
C | G | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-16159G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967253 | ||||||
| chr6:75967296
|
T | C | 3 | a0013c0013t0001g0194a0013c0013t0001g0195a0013c0013t0001g0196 | 3 | NA18947.hp1 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1292-16202A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967296 | ||||||
| chr6:75967381
|
A | G | 2 | a0002c0002t0001g0150a0002c0002t0005g0080 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1292-16287T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967381 | ||||||
| chr6:75967612
|
A | G | 1 | a0006c0005t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1292-16518T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967612 | ||||||
| chr6:75967615
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1292-16521T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967615 | ||||||
| chr6:75967791
|
A | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-16697T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967791 | ||||||
| chr6:75967927
|
T | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-16833A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967927 | ||||||
| chr6:75968122
|
A | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-17028T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968122 | ||||||
| chr6:75968142
|
G | T | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-17048C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968142 | ||||||
| chr6:75968274
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1292-17180T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968274 | ||||||
| chr6:75968317
|
C | T | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-17223G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968317 | ||||||
| chr6:75968380
|
T | C | 3 | a0001c0001t0001g0258a0002c0002t0013g0008a0007c0007t0004g0009 | 3 | HG03453.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1292-17286A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968380 | ||||||
| chr6:75968465
|
A | AAGTAGAA others(4): Show |
2 | a0002c0002t0013g0008a0007c0007t0004g0009 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1292-17372_1292-17 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968465 | ||||||
| chr6:75968510
|
T | A | 174 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1292-17416A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968510 | ||||||
| chr6:75968581
|
C | CT | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-17488dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968581 | ||||||
| chr6:75968651
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1292-17557C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968651 | ||||||
| chr6:75968956
|
A | G | 2 | a0001c0001t0001g0275a0005c0006t0003g0032 | 2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1292-17862T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968956 | ||||||
| chr6:75969090
|
G | C | 59 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(56): Show | 59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-17996C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969090 | ||||||
| chr6:75969261
|
G | A | 174 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1292-18167C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969261 | ||||||
| chr6:75969377
|
A | G | 2 | a0001c0001t0001g0275a0005c0006t0003g0032 | 2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1292-18283T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969377 | ||||||
| chr6:75969630
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0296 | 2 | HG00597.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1292-18536C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969630 | ||||||
| chr6:75969731
|
A | AAAAC | 19 | a0001c0001t0001g0042a0002c0002t0001g0061a0002c0002t0001g0133others(16): Show | 19 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-18641_1292-18 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | ||||||
| chr6:75969731
|
AAAAC | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0043others(19): Show | 22 | HG01070.hp1 HG01516.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.1292-18641_1292-18 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | ||||||
| chr6:75969731
|
AAAACAAA others(5): Show |
A | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1292-18649_1292-18 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | ||||||
| chr6:75969939
|
T | TA | 3 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147 | 3 | HG01070.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1292-18846dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969939 | ||||||
| chr6:75969965
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1292-18871A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969965 | ||||||
| chr6:75970082
|
T | A | 1 | a0002c0002t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1292-18988A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970082 | ||||||
| chr6:75970380
|
C | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0238others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-19286G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970380 | ||||||
| chr6:75970491
|
T | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-19397A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970491 | ||||||
| chr6:75970573
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0021others(157): Show | 161 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1292-19479A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970573 | ||||||
| chr6:75970653
|
C | T | 3 | a0001c0026t0001g0241a0002c0002t0001g0082a0002c0002t0001g0161 | 3 | HG02273.hp2 HG03017.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1292-19559G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970653 | ||||||
| chr6:75970654
|
G | A | 1 | a0014c0014t0001g0039 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1292-19560C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970654 | ||||||
| chr6:75970704
|
A | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0021others(157): Show | 161 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1292-19610T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970704 | ||||||
| chr6:75970727
|
T | C | 7 | a0002c0002t0001g0072a0002c0002t0001g0097a0002c0002t0001g0138others(4): Show | 7 | HG01261.hp2 HG01496.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-19633A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970727 | ||||||
| chr6:75970882
|
A | G | 1 | a0002c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1292-19788T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970882 | ||||||
| chr6:75971031
|
C | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-19937G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971031 | ||||||
| chr6:75971066
|
C | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-19972G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971066 | ||||||
| chr6:75971079
|
C | A | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1292-19985G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971079 | ||||||
| chr6:75971146
|
T | C | 2 | a0002c0002t0001g0291a0006c0005t0001g0143 | 2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1292-20052A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971146 | ||||||
| chr6:75971211
|
C | T | 59 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(56): Show | 59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-20117G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971211 | ||||||
| chr6:75971215
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1292-20121G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971215 | ||||||
| chr6:75971239
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1292-20145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971239 | ||||||
| chr6:75971274
|
T | C | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-20180A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971274 | ||||||
| chr6:75971276
|
C | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-20182G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971276 | ||||||
| chr6:75971299
|
C | G | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-20205G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971299 | ||||||
| chr6:75971331
|
G | C | 33 | a0001c0001t0001g0056a0001c0001t0001g0057a0004c0004t0001g0234others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.1292-20237C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971331 | ||||||
| chr6:75971369
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-20275C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971369 | ||||||
| chr6:75971418
|
C | T | 30 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-20324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971418 | ||||||
| chr6:75971474
|
TA | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-20381delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971474 | ||||||
| chr6:75971477
|
A | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1292-20383T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971477 | ||||||
| chr6:75971627
|
C | A | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1292-20533G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971627 | ||||||
| chr6:75971836
|
G | A | 1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1292-20742C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971836 | ||||||
| chr6:75971894
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1292-20800G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971894 | ||||||
| chr6:75971912
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1292-20818C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971912 | ||||||
| chr6:75971951
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG02071.hp2 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-20857A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971951 | ||||||
| chr6:75971955
|
A | T | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-20861T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971955 | ||||||
| chr6:75972175
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0035others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1292-21081G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972175 | ||||||
| chr6:75972261
|
C | A | 59 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(56): Show | 59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-21167G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972261 | ||||||
| chr6:75972279
|
A | G | 3 | a0001c0001t0001g0258a0002c0002t0013g0008a0007c0007t0004g0009 | 3 | HG03453.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1292-21185T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972279 | ||||||
| chr6:75972404
|
C | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-21310G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972404 | ||||||
| chr6:75972485
|
C | A | 1 | a0003c0003t0014g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1292-21391G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972485 | ||||||
| chr6:75972512
|
G | A | 3 | a0001c0016t0005g0015a0001c0016t0005g0016a0007c0007t0004g0232 | 3 | HG01261.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-21418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972512 | ||||||
| chr6:75972535
|
T | C | 174 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1292-21441A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972535 | ||||||
| chr6:75972538
|
G | A | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1292-21444C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972538 | ||||||
| chr6:75972608
|
T | A | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-21514A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972608 | ||||||
| chr6:75972702
|
G | A | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-21608C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972702 | ||||||
| chr6:75972784
|
A | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(57): Show | 60 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1292-21690T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972784 | ||||||
| chr6:75972829
|
T | C | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-21735A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972829 | ||||||
| chr6:75972935
|
G | T | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-21841C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972935 | ||||||
| chr6:75973123
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(105): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1292-22029T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973123 | ||||||
| chr6:75973172
|
T | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-22078A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973172 | ||||||
| chr6:75973242
|
A | AGTGTCCG others(47): Show |
2 | a0001c0018t0001g0107a0003c0003t0001g0079 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1292-22149_1292-22 others(60): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973242 | ||||||
| chr6:75973246
|
T | TCCGGATT others(20): Show |
44 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0043others(41): Show | 44 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1292-22179_1292-22 others(33): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973246 | ||||||
| chr6:75973246
|
T | TCCGGATT others(47): Show |
1 | a0001c0001t0001g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1292-22153_1292-22 others(60): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973246 | ||||||
| chr6:75973292
|
T | TC | 114 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0034others(111): Show | 115 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1292-22199dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973292 | ||||||
| chr6:75973299
|
C | CT | 4 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0296others(1): Show | 4 | HG00597.hp1 NA18987.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-22206_1292-22 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973299 | ||||||
| chr6:75973349
|
G | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-22255C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973349 | ||||||
| chr6:75973912
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0278 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1292-22818C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973912 | ||||||
| chr6:75973918
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.1292-22824A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973918 | ||||||
| chr6:75973929
|
A | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1292-22835T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973929 | ||||||
| chr6:75974045
|
T | C | 1 | a0004c0004t0001g0234 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1292-22951A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974045 | ||||||
| chr6:75974115
|
C | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0022others(36): Show | 40 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1292-23021G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974115 | ||||||
| chr6:75974245
|
ACTTT | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-23155_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974245 | ||||||
| chr6:75974258
|
CTT | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(19): Show | 22 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-23166_1292-23 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974258 | ||||||
| chr6:75974274
|
TTCTC | T | 5 | a0003c0003t0006g0006a0003c0003t0006g0007a0009c0009t0001g0254others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23184_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974274 | ||||||
| chr6:75974296
|
TTTC | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23205_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974296 | ||||||
| chr6:75974330
|
C | CCTTT | 19 | a0002c0002t0001g0048a0002c0002t0001g0066a0002c0002t0001g0111others(16): Show | 19 | HG00558.hp2 HG00609.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1292-23240_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
C | CCTTTCTT others(1): Show |
14 | a0001c0001t0001g0065a0002c0002t0001g0078a0002c0002t0001g0124others(11): Show | 14 | HG01074.hp1 HG01106.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-23244_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
C | CCTTTCTT others(5): Show |
2 | a0006c0005t0002g0093a0013c0013t0001g0196 | 2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1292-23248_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
CCTTT | C | 25 | a0002c0002t0001g0063a0002c0002t0001g0073a0002c0002t0001g0130others(22): Show | 25 | HG00735.hp1 HG01070.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1292-23240_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
CCTTTCTT others(1): Show |
C | 19 | a0002c0002t0001g0067a0002c0002t0001g0249a0002c0002t0001g0252others(16): Show | 19 | HG00438.hp2 HG00558.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-23244_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
CCTTTCTT others(5): Show |
C | 13 | a0001c0001t0001g0260a0001c0001t0001g0264a0002c0002t0001g0059others(10): Show | 13 | HG00423.hp1 HG01261.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23248_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
CCTTTCTT others(9): Show |
C | 3 | a0001c0001t0001g0056a0002c0002t0001g0125a0009c0009t0001g0068 | 3 | HG03579.hp1 NA18962.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1292-23252_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974330
|
CCTTTCTT others(13): Show |
C | 6 | a0001c0001t0001g0238a0001c0001t0005g0011a0001c0001t0009g0261others(3): Show | 6 | HG02015.hp1 HG02622.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-23256_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | ||||||
| chr6:75974343
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-23259_1292-23 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974343 | ||||||
| chr6:75974356
|
TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0001g0283a0007c0007t0004g0094 | 2 | HG01109.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974356 | ||||||
| chr6:75974359
|
C | CTT | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1292-23267_1292-23 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974359 | ||||||
| chr6:75974360
|
TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0001g0267a0001c0001t0001g0278 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1292-23277_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | ||||||
| chr6:75974360
|
TTTCTTTC others(8): Show |
T | 6 | a0001c0001t0001g0002a0001c0001t0001g0276a0001c0001t0001g0281others(3): Show | 7 | HG00673.hp2 HG02056.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | ||||||
| chr6:75974360
|
TTTCTTTC others(12): Show |
T | 9 | a0001c0001t0001g0022a0001c0001t0001g0266a0001c0001t0001g0274others(6): Show | 9 | HG00140.hp2 HG01074.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-23285_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | ||||||
| chr6:75974360
|
TTTCTTTC others(16): Show |
T | 1 | a0003c0003t0014g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1292-23289_1292-23 others(29): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | ||||||
| chr6:75974364
|
TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0001g0287a0005c0006t0003g0282 | 2 | HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974364 | ||||||
| chr6:75974364
|
TTTCTTTC others(8): Show |
T | 2 | a0001c0001t0001g0288a0005c0006t0003g0292 | 2 | HG01167.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1292-23285_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974364 | ||||||
| chr6:75974367
|
C | CT | 4 | a0003c0015t0001g0014a0004c0004t0002g0075a0014c0014t0001g0039others(1): Show | 4 | HG02922.hp2 NA18947.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23274dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974367 | ||||||
| chr6:75974368
|
TTTC | T | 4 | a0001c0001t0001g0218a0007c0007t0004g0220a0007c0007t0004g0229others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23277_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974368 | ||||||
| chr6:75974368
|
TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0001g0089a0003c0003t0001g0087 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1292-23293_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974368 | ||||||
| chr6:75974372
|
TTTCTTTC others(8): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1292-23293_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974372 | ||||||
| chr6:75974375
|
C | CT | 8 | a0003c0003t0001g0105a0003c0003t0001g0179a0005c0006t0003g0084others(5): Show | 8 | HG00741.hp1 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23282dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974375 | ||||||
| chr6:75974379
|
C | CT | 18 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0175others(15): Show | 18 | HG00140.hp1 HG00609.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-23286dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974379 | ||||||
| chr6:75974379
|
C | CTTTCT | 20 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0074others(17): Show | 21 | HG01106.hp1 HG01256.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-23290_1292-23 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974379 | ||||||
| chr6:75974380
|
T | C | 2 | a0001c0001t0001g0280a0003c0015t0001g0013 | 2 | HG02559.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1292-23286A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974380 | ||||||
| chr6:75974382
|
T | TTCTTTCC others(3): Show |
1 | a0009c0009t0001g0259 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1292-23289_1292-23 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974382 | ||||||
| chr6:75974383
|
C | CT | 5 | a0001c0001t0001g0190a0001c0001t0005g0239a0001c0026t0001g0241others(2): Show | 5 | HG01099.hp1 HG01169.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-23290dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974383 | ||||||
| chr6:75974384
|
T | C | 11 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0280others(8): Show | 11 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-23290A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974384 | ||||||
| chr6:75974384
|
TTTCTTTC others(5): Show |
T | 1 | a0011c0011t0003g0122 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1292-23302_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974384 | ||||||
| chr6:75974386
|
T | C | 2 | a0009c0009t0001g0254a0009c0009t0001g0259 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-23292A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974386 | ||||||
| chr6:75974388
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0218a0001c0001t0001g0267others(23): Show | 27 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1292-23294A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974388 | ||||||
| chr6:75974390
|
T | C | 2 | a0009c0009t0001g0254a0009c0009t0001g0259 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-23296A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974390 | ||||||
| chr6:75974391
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0034others(26): Show | 29 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-23297G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974391 | ||||||
| chr6:75974391
|
CT | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0035others(46): Show | 50 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1292-23298delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974391 | ||||||
| chr6:75974392
|
T | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0034others(36): Show | 39 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1292-23298A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | ||||||
| chr6:75974392
|
T | TTTC | 8 | a0001c0001t0001g0190a0001c0001t0005g0239a0003c0003t0001g0044others(5): Show | 8 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | ||||||
| chr6:75974392
|
T | TTTCTTTC others(4): Show |
1 | a0003c0003t0001g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1292-23299_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | ||||||
| chr6:75974392
|
T | TTTCTTTC others(5): Show |
2 | a0003c0003t0001g0030a0007c0007t0004g0200 | 2 | HG01517.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | ||||||
| chr6:75974392
|
T | TTTCTTTT others(1): Show |
5 | a0001c0001t0001g0198a0001c0001t0001g0225a0003c0003t0001g0101others(2): Show | 5 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | ||||||
| chr6:75974393
|
T | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0218others(31): Show | 35 | HG00140.hp2 HG00673.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-23299A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCC | 13 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0174others(10): Show | 13 | HG01261.hp1 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCCTTCC | 12 | a0001c0001t0001g0184a0001c0018t0001g0107a0003c0003t0001g0017others(9): Show | 13 | HG00609.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(13): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCCTTCC others(4): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0299a0005c0006t0003g0090others(4): Show | 7 | HG00140.hp1 HG01106.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCCTTCC others(20): Show |
1 | a0005c0006t0003g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(33): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCTTTCC others(4): Show |
1 | a0008c0008t0001g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCTTTCC others(24): Show |
1 | a0005c0006t0003g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(37): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCTTTCC others(28): Show |
1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(41): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974393
|
T | TTCTTTTC others(33): Show |
1 | a0001c0001t0001g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(46): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | ||||||
| chr6:75974395
|
T | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0275a0001c0001t0012g0206others(5): Show | 8 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23301A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974395 | ||||||
| chr6:75974395
|
T | G | 1 | a0003c0015t0001g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1292-23301A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974395 | ||||||
| chr6:75974396
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1292-23302G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974396 | ||||||
| chr6:75974397
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(81): Show | 86 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1292-23303A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974397 | ||||||
| chr6:75974397
|
T | TTCCTTCC others(12): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0275 | 2 | NA18945.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1292-23304_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974397 | ||||||
| chr6:75974399
|
T | C | 4 | a0001c0001t0012g0206a0003c0003t0001g0049a0003c0003t0006g0006others(1): Show | 4 | HG01433.hp2 HG02965.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-23305A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974399 | ||||||
| chr6:75974401
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(93): Show | 98 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1292-23307A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTCCTTCC others(8): Show |
4 | a0001c0001t0012g0206a0003c0003t0001g0049a0003c0003t0006g0006others(1): Show | 4 | HG01433.hp2 HG02965.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCCTTC others(17): Show |
1 | a0005c0006t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCCTTC others(21): Show |
1 | a0001c0001t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(34): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(5): Show |
3 | a0001c0001t0005g0018a0001c0001t0005g0223a0004c0004t0002g0024 | 3 | HG02615.hp2 HG02717.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(9): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0273 | 2 | HG02074.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(25): Show |
1 | a0001c0001t0001g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(17): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0296 | 2 | HG00597.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(25): Show |
1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
T | TTTCTTTC others(29): Show |
1 | a0003c0003t0001g0044 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(42): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974401
|
TTTCC | T | 3 | a0004c0004t0002g0118a0009c0009t0001g0117a0011c0011t0003g0213 | 3 | HG02129.hp2 NA18957.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1292-23311_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | ||||||
| chr6:75974404
|
C | CCTTCCTT others(13): Show |
1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1292-23311_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | ||||||
| chr6:75974404
|
C | CCTTCCTT others(9): Show |
1 | a0008c0008t0001g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1292-23311_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | ||||||
| chr6:75974404
|
C | CTTTCCTT others(17): Show |
4 | a0001c0001t0001g0214a0003c0003t0001g0045a0010c0010t0001g0201others(1): Show | 4 | HG00423.hp2 HG02273.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23311_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | ||||||
| chr6:75974404
|
C | G | 19 | a0001c0001t0001g0042a0001c0001t0001g0299a0004c0004t0002g0027others(16): Show | 19 | HG00140.hp1 HG00609.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-23310G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | ||||||
| chr6:75974405
|
C | T | 35 | a0001c0001t0001g0054a0001c0001t0001g0156a0001c0001t0001g0181others(32): Show | 35 | HG00423.hp1 HG00558.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1292-23311G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974405 | ||||||
| chr6:75974408
|
C | CCTTCCTT others(9): Show |
8 | a0001c0001t0001g0198a0001c0001t0001g0205a0003c0003t0001g0030others(5): Show | 8 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23315_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | ||||||
| chr6:75974408
|
C | CCTTCCTT others(5): Show |
10 | a0001c0001t0001g0026a0001c0001t0001g0099a0001c0001t0001g0187others(7): Show | 10 | HG00438.hp1 HG00673.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-23315_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | ||||||
| chr6:75974408
|
C | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0184others(11): Show | 15 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1292-23314G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | ||||||
| chr6:75974409
|
C | T | 2 | a0004c0004t0002g0118a0009c0009t0001g0117 | 2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1292-23315G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974409 | ||||||
| chr6:75974412
|
C | CCTTCCTT others(5): Show |
9 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0166others(6): Show | 9 | HG00621.hp1 HG01993.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-23319_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | ||||||
| chr6:75974412
|
C | CCTTCCTT others(1): Show |
3 | a0001c0001t0001g0034a0001c0001t0010g0003a0003c0003t0001g0023 | 3 | HG01928.hp1 HG01952.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1292-23319_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | ||||||
| chr6:75974412
|
C | G | 13 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0001g0175others(10): Show | 13 | HG01261.hp1 HG02015.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1292-23318G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | ||||||
| chr6:75974416
|
C | CCTTCCTT others(1): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0043a0003c0003t0001g0155 | 3 | HG01993.hp2 HG02145.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1292-23323_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974416 | ||||||
| chr6:75974416
|
C | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG01099.hp1 HG02293.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-23322G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974416 | ||||||
| chr6:75974424
|
C | G | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-23330G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974424 | ||||||
| chr6:75974428
|
G | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1292-23334C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
G | GCTTCCTT others(5): Show |
3 | a0003c0003t0001g0163a0003c0003t0001g0180a0003c0003t0001g0211 | 3 | HG01167.hp1 HG01169.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1292-23346_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
G | GCTTCCTT others(9): Show |
9 | a0001c0001t0001g0054a0001c0001t0001g0156a0001c0001t0001g0181others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-23350_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
G | GCTTCCTT others(13): Show |
13 | a0004c0004t0001g0234a0004c0004t0002g0037a0004c0004t0002g0055others(10): Show | 13 | HG00423.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23354_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
G | GCTTCCTT others(17): Show |
6 | a0004c0004t0002g0076a0004c0004t0002g0092a0004c0004t0002g0102others(3): Show | 6 | HG00558.hp1 HG02523.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-23358_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
G | GCTTCCTT others(25): Show |
1 | a0009c0009t0001g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1292-23335_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974428
|
GCTTCCTT others(9): Show |
G | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-23350_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | ||||||
| chr6:75974451
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-23357A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974451 | ||||||
| chr6:75974508
|
C | T | 2 | a0002c0002t0001g0066a0002c0002t0001g0067 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1292-23414G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974508 | ||||||
| chr6:75974813
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-23719C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974813 | ||||||
| chr6:75974923
|
C | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020 | 3 | HG02717.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1292-23829G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974923 | ||||||
| chr6:75975383
|
G | A | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-24289C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975383 | ||||||
| chr6:75975433
|
C | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0160a0001c0001t0005g0221others(2): Show | 5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-24339G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975433 | ||||||
| chr6:75975553
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-24459C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975553 | ||||||
| chr6:75975594
|
C | G | 8 | a0002c0002t0001g0289a0002c0002t0001g0290a0004c0004t0002g0132others(5): Show | 8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-24500G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975594 | ||||||
| chr6:75975595
|
T | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(31): Show | 34 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1292-24501A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975595 | ||||||
| chr6:75975760
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-24666C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975760 | ||||||
| chr6:75975998
|
C | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(21): Show | 24 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1292-24904G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975998 | ||||||
| chr6:75976153
|
A | G | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-25059T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976153 | ||||||
| chr6:75976232
|
A | G | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1292-25138T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976232 | ||||||
| chr6:75976293
|
G | A | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-25199C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976293 | ||||||
| chr6:75976417
|
C | T | 2 | a0003c0003t0001g0030a0003c0003t0001g0101 | 2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1292-25323G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976417 | ||||||
| chr6:75976431
|
G | A | 1 | a0012c0012t0004g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1292-25337C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976431 | ||||||
| chr6:75976439
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0001g0156a0001c0001t0001g0181others(8): Show | 11 | HG01081.hp2 HG01099.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-25345C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976439 | ||||||
| chr6:75976626
|
C | A | 10 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(7): Show | 10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-25532G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976626 | ||||||
| chr6:75976696
|
G | A | 62 | a0001c0001t0001g0134a0002c0002t0001g0048a0002c0002t0001g0061others(59): Show | 62 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1292-25602C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976696 | ||||||
| chr6:75976738
|
C | G | 2 | a0001c0018t0001g0263a0007c0007t0004g0094 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-25644G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976738 | ||||||
| chr6:75976873
|
C | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-25779G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976873 | ||||||
| chr6:75976884
|
T | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1292-25790A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976884 | ||||||
| chr6:75976887
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-25793C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976887 | ||||||
| chr6:75976909
|
TA | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1292-25816delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976909 | ||||||
| chr6:75977043
|
C | T | 5 | a0001c0001t0001g0010a0007c0007t0004g0245a0007c0007t0004g0246others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+25875G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977043 | ||||||
| chr6:75977044
|
G | A | 5 | a0003c0003t0006g0006a0003c0003t0006g0007a0009c0009t0001g0254others(2): Show | 5 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+25874C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977044 | ||||||
| chr6:75977094
|
A | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1291+25824T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977094 | ||||||
| chr6:75977144
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1291+25774A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977144 | ||||||
| chr6:75977154
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+25764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977154 | ||||||
| chr6:75977385
|
C | T | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1291+25533G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977385 | ||||||
| chr6:75977456
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+25462C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977456 | ||||||
| chr6:75977501
|
C | T | 10 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(7): Show | 10 | HG01192.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291+25417G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977501 | ||||||
| chr6:75977587
|
C | CA | 11 | a0001c0001t0001g0099a0001c0001t0009g0261a0002c0002t0001g0066others(8): Show | 11 | HG00673.hp1 HG00738.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+25330dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977587 | ||||||
| chr6:75977587
|
CA | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(169): Show | 174 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1291+25330delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977587 | ||||||
| chr6:75977590
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+25328T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977590 | ||||||
| chr6:75977597
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+25321T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977597 | ||||||
| chr6:75977602
|
C | A | 1 | a0006c0005t0002g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1291+25316G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977602 | ||||||
| chr6:75977611
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1291+25307T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977611 | ||||||
| chr6:75977665
|
A | C | 1 | a0001c0001t0005g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1291+25253T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977665 | ||||||
| chr6:75977716
|
G | A | 20 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0145others(17): Show | 20 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291+25202C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977716 | ||||||
| chr6:75977822
|
C | T | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1291+25096G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977822 | ||||||
| chr6:75978037
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+24881C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978037 | ||||||
| chr6:75978129
|
T | TTATATAC others(3): Show |
2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+24779_1291+24 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978129 | ||||||
| chr6:75978253
|
T | C | 1 | a0011c0011t0003g0122 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1291+24665A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978253 | ||||||
| chr6:75978323
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1291+24595G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978323 | ||||||
| chr6:75978463
|
A | G | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+24455T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978463 | ||||||
| chr6:75978474
|
TG | T | 10 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(7): Show | 10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+24443delC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978474 | ||||||
| chr6:75978803
|
T | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+24115A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978803 | ||||||
| chr6:75979006
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1291+23912C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979006 | ||||||
| chr6:75979089
|
C | T | 1 | a0002c0002t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1291+23829G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979089 | ||||||
| chr6:75979153
|
G | A | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1291+23765C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979153 | ||||||
| chr6:75979197
|
G | A | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+23721C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979197 | ||||||
| chr6:75979211
|
C | T | 1 | a0025c0028t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1291+23707G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979211 | ||||||
| chr6:75979583
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1291+23335G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979583 | ||||||
| chr6:75979597
|
A | T | 1 | a0014c0014t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1291+23321T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979597 | ||||||
| chr6:75979631
|
C | A | 1 | a0002c0002t0001g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291+23287G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979631 | ||||||
| chr6:75979716
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+23202C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979716 | ||||||
| chr6:75979736
|
G | C | 1 | a0024c0027t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1291+23182C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979736 | ||||||
| chr6:75979817
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1291+23101T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979817 | ||||||
| chr6:75979892
|
A | G | 6 | a0004c0004t0002g0075a0014c0014t0001g0039a0014c0014t0001g0041others(3): Show | 6 | NA18947.hp2 NA18969.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+23026T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979892 | ||||||
| chr6:75979922
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+22996A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979922 | ||||||
| chr6:75980135
|
A | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+22783T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980135 | ||||||
| chr6:75980322
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1291+22596G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980322 | ||||||
| chr6:75980344
|
A | G | 6 | a0001c0026t0001g0241a0003c0003t0006g0006a0003c0003t0006g0007others(3): Show | 6 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+22574T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980344 | ||||||
| chr6:75980414
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1291+22504G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980414 | ||||||
| chr6:75980583
|
G | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1291+22335C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980583 | ||||||
| chr6:75980596
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+22322T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980596 | ||||||
| chr6:75980710
|
C | A | 1 | a0010c0010t0001g0109 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1291+22208G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980710 | ||||||
| chr6:75980884
|
G | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+22034C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980884 | ||||||
| chr6:75981107
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+21811T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981107 | ||||||
| chr6:75981148
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(9): Show | 12 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+21770G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981148 | ||||||
| chr6:75981195
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+21723C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981195 | ||||||
| chr6:75981238
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(7): Show | 10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+21680G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981238 | ||||||
| chr6:75981626
|
C | T | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1291+21292G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981626 | ||||||
| chr6:75981819
|
G | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+21099C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981819 | ||||||
| chr6:75981836
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1291+21082A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981836 | ||||||
| chr6:75982059
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1291+20859G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982059 | ||||||
| chr6:75982196
|
C | A | 2 | a0003c0003t0006g0006a0003c0003t0006g0007 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+20722G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982196 | ||||||
| chr6:75982293
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1291+20625A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982293 | ||||||
| chr6:75982321
|
T | A | 1 | a0009c0009t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1291+20597A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982321 | ||||||
| chr6:75982397
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1291+20521G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982397 | ||||||
| chr6:75982464
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1291+20454G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982464 | ||||||
| chr6:75982511
|
G | A | 66 | a0001c0001t0001g0099a0001c0001t0001g0134a0001c0001t0001g0174others(63): Show | 66 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1291+20407C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982511 | ||||||
| chr6:75982536
|
T | A | 1 | a0004c0004t0002g0176 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1291+20382A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982536 | ||||||
| chr6:75982541
|
A | ATATC | 5 | a0001c0001t0001g0010a0009c0009t0001g0254a0009c0009t0001g0259others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+20373_1291+20 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
A | ATATCTAT others(1): Show |
130 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1291+20369_1291+20 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
A | ATATCTAT others(5): Show |
13 | a0001c0001t0001g0054a0001c0001t0001g0281a0001c0001t0001g0299others(10): Show | 13 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291+20365_1291+20 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
A | ATATCTAT others(9): Show |
1 | a0002c0002t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1291+20361_1291+20 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
A | ATATCTAT others(13): Show |
3 | a0001c0001t0005g0221a0002c0002t0001g0227a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1291+20357_1291+20 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
A | ATATCTAT others(17): Show |
1 | a0004c0004t0002g0037 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1291+20376_1291+20 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982541
|
ATATC | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257 | 3 | HG02257.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1291+20373_1291+20 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | ||||||
| chr6:75982586
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1291+20332C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | ||||||
| chr6:75982586
|
GATATATA others(11): Show |
G | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+20314_1291+20 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | ||||||
| chr6:75982586
|
GATATATA others(29): Show |
G | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+20296_1291+20 others(42): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | ||||||
| chr6:75982698
|
A | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+20220T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982698 | ||||||
| chr6:75982829
|
G | C | 2 | a0003c0003t0006g0006a0003c0003t0006g0007 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+20089C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982829 | ||||||
| chr6:75983048
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.1291+19870A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983048 | ||||||
| chr6:75983772
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+19146C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983772 | ||||||
| chr6:75983826
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+19092C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983826 | ||||||
| chr6:75983870
|
GC | G | 12 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(9): Show | 12 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+19047delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983870 | ||||||
| chr6:75984229
|
G | C | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+18689C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984229 | ||||||
| chr6:75984785
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+18133A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984785 | ||||||
| chr6:75984922
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(8): Show | 11 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+17996A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984922 | ||||||
| chr6:75984938
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+17980C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984938 | ||||||
| chr6:75984956
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+17962G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984956 | ||||||
| chr6:75984957
|
C | A | 1 | a0002c0002t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+17961G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984957 | ||||||
| chr6:75985038
|
A | G | 2 | a0002c0002t0001g0289a0002c0002t0001g0290 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1291+17880T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985038 | ||||||
| chr6:75985109
|
A | G | 9 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+17809T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985109 | ||||||
| chr6:75985284
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1291+17634C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985284 | ||||||
| chr6:75985332
|
C | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+17586G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985332 | ||||||
| chr6:75985481
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(190): Show | 195 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1291+17437T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985481 | ||||||
| chr6:75985548
|
GA | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+17369delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985548 | ||||||
| chr6:75985583
|
C | T | 1 | a0003c0003t0001g0211 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1291+17335G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985583 | ||||||
| chr6:75985599
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1291+17319G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985599 | ||||||
| chr6:75985606
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+17312A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985606 | ||||||
| chr6:75985697
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1291+17221C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985697 | ||||||
| chr6:75985928
|
T | C | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1291+16990A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985928 | ||||||
| chr6:75985984
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1291+16934T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985984 | ||||||
| chr6:75986004
|
A | T | 10 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+16914T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986004 | ||||||
| chr6:75986080
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(148): Show | 153 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1291+16838A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986080 | ||||||
| chr6:75986186
|
G | A | 1 | a0016c0019t0003g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1291+16732C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986186 | ||||||
| chr6:75986251
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+16667G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986251 | ||||||
| chr6:75986482
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+16436G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986482 | ||||||
| chr6:75986519
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291+16399A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986519 | ||||||
| chr6:75986745
|
GA | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+16172delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986745 | ||||||
| chr6:75986810
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1291+16108C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986810 | ||||||
| chr6:75986826
|
CA | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257 | 3 | HG02257.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1291+16091delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986826 | ||||||
| chr6:75987037
|
G | A | 1 | a0002c0002t0001g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291+15881C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987037 | ||||||
| chr6:75987048
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+15870G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987048 | ||||||
| chr6:75987301
|
C | CT | 116 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(113): Show | 117 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1291+15616dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987301 | ||||||
| chr6:75987301
|
CT | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(26): Show | 30 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1291+15616delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987301 | ||||||
| chr6:75987343
|
T | C | 16 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00621.hp1 HG01175.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291+15575A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987343 | ||||||
| chr6:75987354
|
C | T | 1 | a0005c0006t0003g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1291+15564G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987354 | ||||||
| chr6:75987373
|
T | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+15545A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987373 | ||||||
| chr6:75987453
|
C | CG | 4 | a0001c0001t0001g0114a0002c0002t0001g0295a0015c0017t0001g0293others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+15464_1291+15 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987453 | ||||||
| chr6:75987454
|
T | C | 5 | a0001c0001t0001g0114a0002c0002t0001g0295a0013c0013t0001g0183others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+15464A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | ||||||
| chr6:75987454
|
T | G | 6 | a0001c0001t0001g0226a0001c0001t0001g0257a0001c0001t0005g0160others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+15464A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | ||||||
| chr6:75987454
|
T | TC | 40 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 40 | HG00621.hp1 HG00738.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1291+15463dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | ||||||
| chr6:75987471
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1291+15447G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987471 | ||||||
| chr6:75987600
|
T | C | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1291+15318A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987600 | ||||||
| chr6:75987647
|
C | CT | 148 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(145): Show | 150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1291+15270dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987647 | ||||||
| chr6:75987685
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+15233G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987685 | ||||||
| chr6:75987745
|
C | T | 8 | a0002c0002t0001g0289a0002c0002t0001g0290a0004c0004t0002g0132others(5): Show | 8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291+15173G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987745 | ||||||
| chr6:75987805
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+15113G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987805 | ||||||
| chr6:75987866
|
T | C | 5 | a0007c0007t0004g0232a0007c0007t0004g0245a0007c0007t0004g0246others(2): Show | 5 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+15052A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987866 | ||||||
| chr6:75987898
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+15020G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987898 | ||||||
| chr6:75987972
|
T | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 154 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291+14946A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987972 | ||||||
| chr6:75987991
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1291+14927G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987991 | ||||||
| chr6:75988017
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+14901T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988017 | ||||||
| chr6:75988021
|
T | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+14897A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988021 | ||||||
| chr6:75988242
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+14676A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988242 | ||||||
| chr6:75988307
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+14611G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988307 | ||||||
| chr6:75988345
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(201): Show | 206 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1291+14573G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988345 | ||||||
| chr6:75988442
|
A | G | 63 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0095others(60): Show | 64 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1291+14476T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988442 | ||||||
| chr6:75988450
|
C | G | 2 | a0003c0003t0006g0006a0003c0003t0006g0007 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+14468G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988450 | ||||||
| chr6:75988485
|
T | G | 1 | a0025c0028t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1291+14433A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988485 | ||||||
| chr6:75988751
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 154 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291+14167A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988751 | ||||||
| chr6:75988757
|
T | C | 1 | a0006c0005t0008g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1291+14161A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988757 | ||||||
| chr6:75988775
|
A | C | 1 | a0005c0006t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1291+14143T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988775 | ||||||
| chr6:75988955
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+13963T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988955 | ||||||
| chr6:75989049
|
C | CA | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+13868_1291+13 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989049 | ||||||
| chr6:75989366
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1291+13552T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989366 | ||||||
| chr6:75989425
|
T | C | 13 | a0002c0002t0001g0048a0002c0002t0001g0061a0002c0002t0001g0073others(10): Show | 13 | HG02135.hp2 HG02602.hp2 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291+13493A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989425 | ||||||
| chr6:75989443
|
T | C | 2 | a0002c0002t0001g0153a0003c0003t0001g0152 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1291+13475A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989443 | ||||||
| chr6:75989550
|
A | G | 1 | a0011c0011t0003g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291+13368T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989550 | ||||||
| chr6:75989564
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02896.hp1 HG03209.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+13354G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989564 | ||||||
| chr6:75989599
|
T | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+13319A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989599 | ||||||
| chr6:75989900
|
A | C | 1 | a0008c0008t0001g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1291+13018T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989900 | ||||||
| chr6:75990182
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+12736C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990182 | ||||||
| chr6:75990259
|
A | C | 4 | a0001c0001t0001g0095a0004c0004t0002g0055a0004c0004t0002g0098others(1): Show | 4 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+12659T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990259 | ||||||
| chr6:75990579
|
C | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(151): Show | 156 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1291+12339G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990579 | ||||||
| chr6:75990588
|
T | TAC | 46 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(43): Show | 47 | HG00673.hp2 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1291+12328_1291+12 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990588
|
T | TACAC | 16 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0264others(13): Show | 17 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+12326_1291+12 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990588
|
T | TACACAC | 33 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+12324_1291+12 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990588
|
T | TACACACA others(1): Show |
83 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1291+12322_1291+12 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990588
|
T | TACACACA others(3): Show |
17 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0190others(14): Show | 17 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+12320_1291+12 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990588
|
T | TACACACA others(5): Show |
12 | a0001c0001t0001g0198a0003c0003t0001g0029a0003c0003t0001g0030others(9): Show | 12 | HG00140.hp1 HG00597.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+12318_1291+12 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | ||||||
| chr6:75990773
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+12145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990773 | ||||||
| chr6:75990793
|
CA | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+12124delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990793 | ||||||
| chr6:75990873
|
T | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+12045A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990873 | ||||||
| chr6:75991007
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0003c0003t0001g0087 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1291+11911T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991007 | ||||||
| chr6:75991059
|
T | G | 1 | a0002c0002t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1291+11859A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991059 | ||||||
| chr6:75991106
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+11812A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991106 | ||||||
| chr6:75991233
|
T | C | 3 | a0001c0001t0005g0011a0001c0001t0005g0221a0001c0001t0005g0224 | 3 | HG03453.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1291+11685A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991233 | ||||||
| chr6:75991315
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+11603G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991315 | ||||||
| chr6:75991349
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1291+11569G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991349 | ||||||
| chr6:75991382
|
C | G | 10 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+11536G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991382 | ||||||
| chr6:75991396
|
T | TA | 13 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(10): Show | 13 | HG01884.hp2 HG02027.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1291+11521dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991396 | ||||||
| chr6:75991396
|
TAA | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+11520_1291+11 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991396 | ||||||
| chr6:75991567
|
A | G | 2 | a0002c0002t0007g0062a0002c0002t0007g0256 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1291+11351T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991567 | ||||||
| chr6:75991649
|
G | A | 1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+11269C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991649 | ||||||
| chr6:75991743
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+11175A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991743 | ||||||
| chr6:75992072
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+10846C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992072 | ||||||
| chr6:75992164
|
C | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+10754G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992164 | ||||||
| chr6:75992450
|
C | T | 3 | a0004c0004t0002g0075a0018c0020t0001g0040a0019c0021t0002g0103 | 3 | NA18947.hp2 NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1291+10468G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992450 | ||||||
| chr6:75992581
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1291+10337G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992581 | ||||||
| chr6:75992711
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+10207G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992711 | ||||||
| chr6:75992758
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+10160G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992758 | ||||||
| chr6:75992801
|
T | G | 117 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(114): Show | 118 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1291+10117A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992801 | ||||||
| chr6:75992834
|
G | A | 1 | a0007c0007t0004g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1291+10084C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992834 | ||||||
| chr6:75992993
|
C | T | 1 | a0001c0001t0012g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1291+9925G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992993 | ||||||
| chr6:75993298
|
C | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(24): Show | 28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+9620G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993298 | ||||||
| chr6:75993479
|
AGAGAGAA others(3): Show |
A | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+9429_1291+943 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993479 | ||||||
| chr6:75993499
|
GGAGAGAG others(11): Show |
G | 1 | a0004c0004t0002g0037 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1291+9401_1291+941 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993499 | ||||||
| chr6:75993660
|
T | A | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+9258A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993660 | ||||||
| chr6:75993715
|
A | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+9203T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993715 | ||||||
| chr6:75993797
|
T | TAAAAGTT others(1586): Show |
1 | a0010c0010t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1291+9120_1291+912 others(1597): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993797 | ||||||
| chr6:75993847
|
T | C | 1 | a0017c0029t0001g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1291+9071A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993847 | ||||||
| chr6:75993864
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+9054T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993864 | ||||||
| chr6:75993948
|
T | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+8970A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993948 | ||||||
| chr6:75993993
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1291+8925A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993993 | ||||||
| chr6:75994179
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+8739C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994179 | ||||||
| chr6:75994334
|
T | C | 1 | a0006c0005t0002g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1291+8584A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994334 | ||||||
| chr6:75994411
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1291+8507G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994411 | ||||||
| chr6:75994597
|
G | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+8321C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994597 | ||||||
| chr6:75994772
|
G | A | 2 | a0002c0002t0007g0062a0002c0002t0007g0256 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1291+8146C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994772 | ||||||
| chr6:75994956
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+7962C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994956 | ||||||
| chr6:75995037
|
C | T | 1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+7881G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995037 | ||||||
| chr6:75995363
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1291+7555C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995363 | ||||||
| chr6:75995374
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0036others(2): Show | 5 | HG00597.hp1 HG02074.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+7544G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995374 | ||||||
| chr6:75995385
|
T | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+7533A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995385 | ||||||
| chr6:75995486
|
C | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(24): Show | 28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+7432G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995486 | ||||||
| chr6:75995594
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+7324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995594 | ||||||
| chr6:75996045
|
T | C | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+6873A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996045 | ||||||
| chr6:75996159
|
G | T | 109 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(106): Show | 110 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1291+6759C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996159 | ||||||
| chr6:75996160
|
C | T | 21 | a0001c0001t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(18): Show | 21 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1291+6758G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996160 | ||||||
| chr6:75996316
|
C | A | 1 | a0005c0006t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1291+6602G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996316 | ||||||
| chr6:75996567
|
G | C | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+6351C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996567 | ||||||
| chr6:75996722
|
ATGTAATA others(12): Show |
A | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+6177_1291+619 others(23): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996722 | ||||||
| chr6:75997060
|
A | C | 1 | a0002c0002t0001g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1291+5858T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997060 | ||||||
| chr6:75997101
|
T | C | 3 | a0004c0004t0002g0118a0005c0006t0003g0032a0009c0009t0001g0117 | 3 | HG02129.hp2 NA18941.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1291+5817A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997101 | ||||||
| chr6:75997136
|
G | A | 1 | a0008c0008t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1291+5782C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997136 | ||||||
| chr6:75997318
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+5600G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997318 | ||||||
| chr6:75997353
|
T | C | 11 | a0001c0001t0001g0099a0002c0002t0001g0072a0002c0002t0001g0138others(8): Show | 11 | HG00673.hp1 HG00735.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+5565A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997353 | ||||||
| chr6:75997702
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291+5216C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997702 | ||||||
| chr6:75997714
|
A | T | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+5204T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997714 | ||||||
| chr6:75997723
|
T | C | 1 | a0022c0023t0001g0131 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1291+5195A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997723 | ||||||
| chr6:75997865
|
T | A | 4 | a0001c0001t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(1): Show | 4 | HG03139.hp2 HG03209.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+5053A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997865 | ||||||
| chr6:75997941
|
G | A | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+4977C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997941 | ||||||
| chr6:75998102
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1291+4816G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998102 | ||||||
| chr6:75998200
|
A | G | 8 | a0002c0002t0001g0289a0002c0002t0001g0290a0004c0004t0002g0132others(5): Show | 8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291+4718T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998200 | ||||||
| chr6:75998450
|
G | A | 1 | a0009c0009t0001g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1291+4468C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998450 | ||||||
| chr6:75998514
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+4404C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998514 | ||||||
| chr6:75998672
|
T | G | 1 | a0014c0014t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1291+4246A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998672 | ||||||
| chr6:75998717
|
C | T | 1 | a0006c0005t0008g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1291+4201G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998717 | ||||||
| chr6:75998743
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(24): Show | 28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+4175G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998743 | ||||||
| chr6:75998950
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+3968T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998950 | ||||||
| chr6:75999077
|
G | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0226a0001c0001t0001g0257others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+3841C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999077 | ||||||
| chr6:75999089
|
TC | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+3828delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999089 | ||||||
| chr6:75999165
|
T | A | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1291+3753A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999165 | ||||||
| chr6:75999237
|
T | C | 1 | a0003c0003t0001g0188 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1291+3681A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999237 | ||||||
| chr6:75999261
|
A | ACATACCA others(300): Show |
4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+3656_1291+365 others(311): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999261 | ||||||
| chr6:75999275
|
T | C | 1 | a0013c0013t0001g0194 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1291+3643A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999275 | ||||||
| chr6:75999501
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+3417C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999501 | ||||||
| chr6:75999506
|
G | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+3412C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999506 | ||||||
| chr6:75999551
|
C | T | 1 | a0008c0008t0001g0127 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1291+3367G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999551 | ||||||
| chr6:75999555
|
G | A | 1 | a0004c0004t0002g0236 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1291+3363C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999555 | ||||||
| chr6:75999607
|
G | A | 1 | a0002c0002t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1291+3311C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999607 | ||||||
| chr6:75999807
|
C | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(202): Show | 207 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1291+3111G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999807 | ||||||
| chr6:75999857
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1291+3061T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999857 | ||||||
| chr6:75999919
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+2999G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999919 | ||||||
| chr6:75999931
|
T | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+2987A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999931 | ||||||
| chr6:76000081
|
C | T | 1 | a0003c0003t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1291+2837G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000081 | ||||||
| chr6:76000438
|
A | G | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1291+2480T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000438 | ||||||
| chr6:76000624
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0266others(20): Show | 24 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1291+2294G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000624 | ||||||
| chr6:76000755
|
A | C | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1291+2163T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000755 | ||||||
| chr6:76000759
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+2159G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000759 | ||||||
| chr6:76000760
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+2158G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000760 | ||||||
| chr6:76000830
|
G | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+2088C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000830 | ||||||
| chr6:76000958
|
A | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1960T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000958 | ||||||
| chr6:76001074
|
C | A | 2 | a0002c0002t0001g0242a0002c0002t0001g0262 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1291+1844G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001074 | ||||||
| chr6:76001145
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+1773A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001145 | ||||||
| chr6:76001253
|
T | C | 2 | a0002c0002t0013g0008a0007c0007t0004g0009 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1291+1665A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001253 | ||||||
| chr6:76001332
|
C | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+1586G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001332 | ||||||
| chr6:76001812
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+1106A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001812 | ||||||
| chr6:76001894
|
A | G | 1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+1024T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001894 | ||||||
| chr6:76002054
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.1291+864C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002054 | ||||||
| chr6:76002092
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0005g0018a0001c0001t0005g0019others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+826T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002092 | ||||||
| chr6:76002372
|
G | C | 1 | a0006c0005t0011g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1291+546C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002372 | ||||||
| chr6:76002648
|
C | T | 26 | a0001c0001t0001g0043a0002c0002t0001g0097a0003c0003t0001g0105others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.1291+270G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002648 | ||||||
| chr6:76002718
|
C | T | 6 | a0003c0003t0006g0006a0003c0003t0006g0007a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+200G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002718 | ||||||
| chr6:76002735
|
T | C | 2 | a0002c0002t0001g0249a0002c0002t0001g0250 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1291+183A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002735 | ||||||
| chr6:76002751
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1291+167G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002751 | ||||||
| chr6:76002813
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+105G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002813 | ||||||
| chr6:76003248
|
C | T | 1 | a0025c0028t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1213-252G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003248 | ||||||
| chr6:76003453
|
C | T | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1212+421G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003453 | ||||||
| chr6:76003545
|
T | C | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1212+329A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003545 | ||||||
| chr6:76003816
|
T | C | 1 | a0002c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1212+58A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003816 | ||||||
| chr6:76004037
|
C | T | 114 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(111): Show | 115 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1136-87G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004037 | ||||||
| chr6:76004038
|
G | A | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1136-88C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004038 | ||||||
| chr6:76004065
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1136-115G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004065 | ||||||
| chr6:76004138
|
A | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136-188T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004138 | ||||||
| chr6:76004185
|
G | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1136-235C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004185 | ||||||
| chr6:76004297
|
A | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(23): Show | 26 | HG02145.hp1 HG02280.hp1 HG02293.hp2 others(23): Show |
intron_variant | MODIFIER | c.1136-347T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004297 | ||||||
| chr6:76004462
|
C | T | 1 | a0003c0003t0001g0188 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1136-512G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004462 | ||||||
| chr6:76004463
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136-513C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004463 | ||||||
| chr6:76004532
|
C | T | 1 | a0010c0010t0001g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1136-582G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004532 | ||||||
| chr6:76004647
|
C | A | 114 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(111): Show | 115 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1135+640G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004647 | ||||||
| chr6:76004852
|
T | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+435A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004852 | ||||||
| chr6:76004880
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135+407G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004880 | ||||||
| chr6:76004997
|
C | G | 2 | a0002c0002t0001g0186a0003c0003t0001g0173 | 2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1135+290G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004997 | ||||||
| chr6:76005016
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(142): Show | 146 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1135+271A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005016 | ||||||
| chr6:76005024
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1135+263G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005024 | ||||||
| chr6:76005079
|
T | C | 5 | a0001c0001t0001g0012a0002c0002t0007g0062a0002c0002t0013g0008others(2): Show | 5 | HG01109.hp1 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135+208A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005079 | ||||||
| chr6:76005209
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1135+78G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005209 | ||||||
| chr6:76005222
|
A | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1135+65T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005222 | ||||||
| chr6:76005582
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.888-48C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005582 | ||||||
| chr6:76005825
|
T | A | 3 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147 | 3 | HG01070.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.888-291A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005825 | ||||||
| chr6:76005827
|
TTTTC | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(20): Show | 23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.888-297_888-294del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005827 | ||||||
| chr6:76006133
|
C | G | 3 | a0020c0024t0001g0136a0021c0022t0001g0051a0022c0023t0001g0131 | 3 | NA18946.hp2 NA18948.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.888-599G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006133 | ||||||
| chr6:76006183
|
T | C | 4 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(1): Show | 4 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.888-649A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006183 | ||||||
| chr6:76006209
|
G | A | 100 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0134others(97): Show | 100 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.888-675C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006209 | ||||||
| chr6:76006348
|
A | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.888-814T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006348 | ||||||
| chr6:76006455
|
TGTGTATA others(15): Show |
T | 128 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0065others(125): Show | 129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.888-943_888-922del others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006455 | ||||||
| chr6:76006519
|
G | T | 1 | a0001c0001t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887+961C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006519 | ||||||
| chr6:76006520
|
G | A | 1 | a0001c0001t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887+960C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006520 | ||||||
| chr6:76006529
|
C | CGT | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.887+949_887+950dup others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006529 | ||||||
| chr6:76006550
|
A | G | 3 | a0002c0002t0013g0008a0007c0007t0004g0009a0007c0007t0004g0094 | 3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.887+930T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006550 | ||||||
| chr6:76006551
|
T | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.887+929A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006551 | ||||||
| chr6:76006568
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.887+912C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006568 | ||||||
| chr6:76006683
|
C | T | 100 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0134others(97): Show | 100 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.887+797G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006683 | ||||||
| chr6:76006907
|
A | G | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.887+573T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006907 | ||||||
| chr6:76007025
|
C | T | 119 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(116): Show | 120 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.887+455G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007025 | ||||||
| chr6:76007163
|
G | A | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.887+317C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007163 | ||||||
| chr6:76007184
|
C | T | 99 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0134others(96): Show | 99 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.887+296G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007184 | ||||||
| chr6:76007275
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG02027.hp2 HG02071.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+205T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007275 | ||||||
| chr6:76007300
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.887+180C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007300 | ||||||
| chr6:76007302
|
A | AT | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.887+177dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007302 | ||||||
| chr6:76007302
|
AT | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(27): Show | 31 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.887+177delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007302 | ||||||
| chr6:76007440
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(26): Show | 30 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.887+40G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007440 | ||||||
| chr6:76007552
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867-52C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007552 | ||||||
| chr6:76007691
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.867-191C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007691 | ||||||
| chr6:76007818
|
G | A | 1 | a0004c0004t0002g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.867-318C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007818 | ||||||
| chr6:76007832
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.867-332G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007832 | ||||||
| chr6:76007832
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.867-332G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007832 | ||||||
| chr6:76008046
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0065others(125): Show | 129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.867-546C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008046 | ||||||
| chr6:76008290
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.867-790G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008290 | ||||||
| chr6:76008566
|
G | A | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.867-1066C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008566 | ||||||
| chr6:76008797
|
C | T | 112 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(109): Show | 113 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.867-1297G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008797 | ||||||
| chr6:76008861
|
C | T | 1 | a0010c0010t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.867-1361G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008861 | ||||||
| chr6:76009088
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867-1588A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009088 | ||||||
| chr6:76009294
|
G | C | 1 | a0002c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867-1794C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009294 | ||||||
| chr6:76009542
|
G | A | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.866+1624C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009542 | ||||||
| chr6:76009702
|
T | TA | 3 | a0002c0002t0001g0231a0003c0003t0001g0079a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.866+1463dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009702 | ||||||
| chr6:76009978
|
T | G | 23 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0181others(20): Show | 23 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.866+1188A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009978 | ||||||
| chr6:76010054
|
A | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0205others(27): Show | 31 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.866+1112T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010054 | ||||||
| chr6:76010294
|
G | A | 1 | a0001c0018t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.866+872C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010294 | ||||||
| chr6:76010382
|
T | C | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.866+784A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010382 | ||||||
| chr6:76010384
|
T | C | 3 | a0002c0002t0001g0231a0003c0003t0001g0079a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.866+782A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010384 | ||||||
| chr6:76010487
|
C | T | 21 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(18): Show | 21 | HG01070.hp1 HG01358.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.866+679G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010487 | ||||||
| chr6:76010548
|
C | G | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.866+618G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010548 | ||||||
| chr6:76010577
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.866+589C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010577 | ||||||
| chr6:76010633
|
G | A | 1 | a0010c0010t0001g0279 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.866+533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010633 | ||||||
| chr6:76010779
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.866+387G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010779 | ||||||
| chr6:76010835
|
C | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(271): Show | 276 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.866+331G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010835 | ||||||
| chr6:76010867
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.866+299G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010867 | ||||||
| chr6:76010888
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.866+278G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010888 | ||||||
| chr6:76011034
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(142): Show | 146 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.866+132G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76011034 | ||||||
| chr6:76011057
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0005g0011 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.866+109C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76011057 | ||||||
| chr6:76011242
|
TTTGTAAA others(6): Show |
T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.808-31_808-19delGA others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011242 | ||||||
| chr6:76011273
|
A | T | 113 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(110): Show | 114 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.808-49T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011273 | ||||||
| chr6:76011394
|
T | C | 4 | a0001c0001t0001g0237a0003c0003t0001g0233a0003c0003t0001g0235others(1): Show | 4 | NA18970.hp1 NA18987.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-170A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011394 | ||||||
| chr6:76011508
|
G | A | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-284C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011508 | ||||||
| chr6:76011736
|
T | C | 1 | a0011c0011t0003g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.808-512A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011736 | ||||||
| chr6:76011737
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.808-513G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011737 | ||||||
| chr6:76011910
|
T | A | 1 | a0002c0002t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808-686A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011910 | ||||||
| chr6:76011981
|
A | G | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-757T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011981 | ||||||
| chr6:76012003
|
C | G | 3 | a0006c0005t0001g0171a0011c0011t0003g0128a0011c0011t0003g0129 | 3 | HG01256.hp1 HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.808-779G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012003 | ||||||
| chr6:76012040
|
TTATC | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(20): Show | 23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-820_808-817del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012040 | ||||||
| chr6:76012068
|
A | G | 1 | a0002c0002t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.808-844T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012068 | ||||||
| chr6:76012084
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0005g0011 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.808-860C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012084 | ||||||
| chr6:76012128
|
T | G | 2 | a0004c0004t0002g0244a0009c0009t0001g0115 | 2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.808-904A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012128 | ||||||
| chr6:76012550
|
C | A | 1 | a0006c0005t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.808-1326G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012550 | ||||||
| chr6:76012600
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0231others(3): Show | 6 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1376C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012600 | ||||||
| chr6:76012634
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(20): Show | 23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-1410C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012634 | ||||||
| chr6:76012758
|
C | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(20): Show | 23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-1534G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012758 | ||||||
| chr6:76012998
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0278 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.808-1774A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012998 | ||||||
| chr6:76013109
|
G | T | 1 | a0009c0009t0001g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.808-1885C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013109 | ||||||
| chr6:76013294
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0065others(125): Show | 129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.808-2070G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013294 | ||||||
| chr6:76013338
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.808-2114G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013338 | ||||||
| chr6:76013469
|
T | C | 1 | a0003c0003t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.808-2245A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013469 | ||||||
| chr6:76013698
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.808-2474A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013698 | ||||||
| chr6:76013905
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.808-2681G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013905 | ||||||
| chr6:76013980
|
G | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.808-2756C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013980 | ||||||
| chr6:76014023
|
G | A | 120 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(117): Show | 121 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.808-2799C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014023 | ||||||
| chr6:76014218
|
C | T | 1 | a0004c0004t0002g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.808-2994G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014218 | ||||||
| chr6:76014285
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.808-3061G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014285 | ||||||
| chr6:76014486
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.808-3262C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014486 | ||||||
| chr6:76014838
|
T | C | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-3614A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014838 | ||||||
| chr6:76014967
|
C | T | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.808-3743G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014967 | ||||||
| chr6:76015018
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.807+3700G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015018 | ||||||
| chr6:76015459
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3259C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015459 | ||||||
| chr6:76015484
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3234A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015484 | ||||||
| chr6:76015487
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0231others(3): Show | 6 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+3231C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015487 | ||||||
| chr6:76015499
|
C | T | 1 | a0003c0003t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.807+3219G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015499 | ||||||
| chr6:76015534
|
C | T | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.807+3184G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015534 | ||||||
| chr6:76015549
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.807+3169G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015549 | ||||||
| chr6:76015567
|
G | A | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.807+3151C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015567 | ||||||
| chr6:76015598
|
C | T | 6 | a0001c0001t0001g0099a0002c0002t0001g0097a0004c0004t0002g0092others(3): Show | 6 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+3120G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015598 | ||||||
| chr6:76015634
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3084G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015634 | ||||||
| chr6:76015753
|
T | C | 1 | a0004c0004t0002g0037 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.807+2965A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015753 | ||||||
| chr6:76015800
|
C | CA | 102 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(99): Show | 103 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.807+2917dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | ||||||
| chr6:76015800
|
C | CAA | 9 | a0001c0001t0001g0198a0003c0003t0001g0029a0003c0003t0001g0045others(6): Show | 9 | HG00597.hp2 HG01169.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.807+2916_807+2917d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | ||||||
| chr6:76015800
|
CA | C | 96 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0095others(93): Show | 96 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.807+2917delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | ||||||
| chr6:76015800
|
CAA | C | 11 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(8): Show | 11 | HG01099.hp1 HG02135.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+2916_807+2917d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | ||||||
| chr6:76015800
|
CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.807+2909_807+2917d others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | ||||||
| chr6:76015892
|
C | G | 132 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(129): Show | 133 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.807+2826G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015892 | ||||||
| chr6:76015935
|
T | TTC | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+2781_807+2782d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015935 | ||||||
| chr6:76016025
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+2693T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016025 | ||||||
| chr6:76016027
|
C | G | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+2691G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016027 | ||||||
| chr6:76016491
|
T | C | 1 | a0005c0006t0003g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.807+2227A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016491 | ||||||
| chr6:76016808
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.807+1910G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016808 | ||||||
| chr6:76016928
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.807+1790G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016928 | ||||||
| chr6:76016979
|
G | A | 1 | a0007c0007t0004g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.807+1739C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016979 | ||||||
| chr6:76017195
|
CA | C | 132 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(129): Show | 133 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.807+1522delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017195 | ||||||
| chr6:76017370
|
T | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807+1348A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017370 | ||||||
| chr6:76017437
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.807+1281G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017437 | ||||||
| chr6:76017591
|
C | T | 22 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0181others(19): Show | 22 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.807+1127G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017591 | ||||||
| chr6:76017898
|
G | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.807+820C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017898 | ||||||
| chr6:76017989
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.807+729G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017989 | ||||||
| chr6:76018020
|
G | A | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.807+698C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018020 | ||||||
| chr6:76018210
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+508T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018210 | ||||||
| chr6:76018229
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+489G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018229 | ||||||
| chr6:76018329
|
C | T | 26 | a0001c0001t0001g0065a0001c0018t0001g0263a0002c0002t0001g0059others(23): Show | 26 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.807+389G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018329 | ||||||
| chr6:76018375
|
A | G | 1 | a0006c0005t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.807+343T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018375 | ||||||
| chr6:76018489
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+229C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018489 | ||||||
| chr6:76018609
|
A | T | 3 | a0005c0006t0003g0204a0007c0007t0004g0001a0007c0007t0004g0200 | 4 | HG01256.hp2 HG01258.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+109T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018609 | ||||||
| chr6:76018618
|
A | T | 1 | a0010c0010t0001g0201 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.807+100T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018618 | ||||||
| chr6:76018637
|
C | T | 6 | a0003c0003t0006g0006a0003c0003t0006g0007a0007c0007t0004g0245others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+81G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018637 | ||||||
| chr6:76018640
|
C | T | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+78G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018640 | ||||||
| chr6:76018641
|
G | A | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.807+77C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018641 | ||||||
| chr6:76018661
|
G | A | 1 | a0009c0009t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.807+57C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018661 | ||||||
| chr6:76018866
|
T | TA | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-9dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76018866 | ||||||
| chr6:76018866
|
TA | T | 13 | a0001c0001t0001g0272a0001c0001t0001g0285a0002c0002t0001g0295others(10): Show | 13 | HG00558.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.667-9delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76018866 | ||||||
| chr6:76019240
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(25): Show | 29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-382T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019240 | ||||||
| chr6:76019332
|
G | A | 1 | a0010c0010t0001g0279 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.667-474C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019332 | ||||||
| chr6:76019402
|
C | T | 3 | a0002c0002t0013g0008a0007c0007t0004g0009a0007c0007t0004g0094 | 3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667-544G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019402 | ||||||
| chr6:76019586
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.667-728G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019586 | ||||||
| chr6:76019616
|
G | A | 3 | a0002c0002t0013g0008a0007c0007t0004g0009a0007c0007t0004g0094 | 3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667-758C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019616 | ||||||
| chr6:76019822
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0231others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-964T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019822 | ||||||
| chr6:76019867
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.667-1009T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019867 | ||||||
| chr6:76019891
|
A | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.667-1033T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019891 | ||||||
| chr6:76019949
|
A | G | 2 | a0001c0001t0001g0166a0009c0009t0001g0169 | 2 | NA18960.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.667-1091T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019949 | ||||||
| chr6:76020017
|
A | G | 20 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0258others(17): Show | 20 | HG01109.hp1 HG01884.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.667-1159T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020017 | ||||||
| chr6:76020208
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.667-1350T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020208 | ||||||
| chr6:76020257
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.667-1399G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020257 | ||||||
| chr6:76020337
|
G | T | 1 | a0008c0008t0001g0127 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.667-1479C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020337 | ||||||
| chr6:76020476
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.667-1618C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020476 | ||||||
| chr6:76020568
|
C | T | 50 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0052others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.666+1548G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020568 | ||||||
| chr6:76020698
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+1418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020698 | ||||||
| chr6:76020716
|
A | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0273 | 2 | NA18959.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.666+1400T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020716 | ||||||
| chr6:76020800
|
G | A | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+1316C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020800 | ||||||
| chr6:76020997
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.666+1119G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020997 | ||||||
| chr6:76021004
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.666+1112T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021004 | ||||||
| chr6:76021160
|
G | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.666+956C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021160 | ||||||
| chr6:76021479
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+637G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021479 | ||||||
| chr6:76021480
|
G | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0001g0231others(9): Show | 12 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.666+636C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021480 | ||||||
| chr6:76021641
|
A | T | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.666+475T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021641 | ||||||
| chr6:76021665
|
G | A | 3 | a0002c0002t0001g0231a0003c0003t0001g0079a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.666+451C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021665 | ||||||
| chr6:76021694
|
T | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+422A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021694 | ||||||
| chr6:76021725
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(161): Show | 165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.666+391A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021725 | ||||||
| chr6:76021751
|
G | C | 8 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142others(5): Show | 8 | NA18947.hp1 NA18954.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.666+365C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021751 | ||||||
| chr6:76021778
|
C | CATATATA others(1): Show |
4 | a0002c0002t0001g0295a0005c0006t0003g0228a0015c0017t0001g0293others(1): Show | 4 | HG01169.hp1 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+330_666+337dup others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(3): Show |
6 | a0001c0001t0005g0160a0001c0026t0001g0241a0007c0007t0004g0232others(3): Show | 6 | HG01261.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+328_666+337dup others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(5): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0226others(13): Show | 16 | HG00438.hp2 HG02071.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+326_666+337dup others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(7): Show |
46 | a0001c0001t0001g0099a0001c0001t0001g0184a0001c0001t0001g0191others(43): Show | 47 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.666+324_666+337dup others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(9): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0034others(42): Show | 46 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.666+322_666+337dup others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(11): Show |
93 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0056others(90): Show | 93 | HG00597.hp2 HG00609.hp2 HG01071.hp1 others(90): Show |
intron_variant | MODIFIER | c.666+320_666+337dup others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(13): Show |
76 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.666+318_666+337dup others(20): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(15): Show |
4 | a0001c0001t0001g0192a0001c0001t0001g0276a0002c0002t0001g0151others(1): Show | 4 | HG01175.hp2 NA18947.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+316_666+337dup others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(17): Show |
1 | a0002c0002t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.666+314_666+337dup others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(19): Show |
2 | a0002c0002t0001g0112a0002c0002t0001g0186 | 2 | HG00738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.666+337_666+338ins others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021778
|
C | CATATATA others(23): Show |
2 | a0003c0003t0001g0023a0008c0008t0001g0139 | 2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.666+337_666+338ins others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | ||||||
| chr6:76021798
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.666+317_666+318ins others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021798 | ||||||
| chr6:76021853
|
G | A | 1 | a0005c0006t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.666+263C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021853 | ||||||
| chr6:76021869
|
G | A | 1 | a0004c0004t0002g0055 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.666+247C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021869 | ||||||
| chr6:76022035
|
T | C | 1 | a0009c0009t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.666+81A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76022035 | ||||||
| chr6:76022297
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.563-78A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022297 | ||||||
| chr6:76022364
|
G | A | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.563-145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022364 | ||||||
| chr6:76022371
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.563-152A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022371 | ||||||
| chr6:76022749
|
G | A | 3 | a0002c0002t0013g0008a0007c0007t0004g0009a0007c0007t0004g0094 | 3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.563-530C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022749 | ||||||
| chr6:76022823
|
A | G | 2 | a0001c0001t0001g0299a0010c0010t0001g0300 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.563-604T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022823 | ||||||
| chr6:76022892
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.563-673A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022892 | ||||||
| chr6:76022995
|
A | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0258others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.563-776T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022995 | ||||||
| chr6:76023027
|
A | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.563-808T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023027 | ||||||
| chr6:76023121
|
G | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.563-902C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023121 | ||||||
| chr6:76023205
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.563-986C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023205 | ||||||
| chr6:76023311
|
A | G | 3 | a0001c0001t0001g0099a0004c0004t0002g0098a0004c0004t0002g0102 | 3 | HG00423.hp1 HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.563-1092T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023311 | ||||||
| chr6:76023358
|
G | C | 1 | a0003c0003t0001g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-1139C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023358 | ||||||
| chr6:76023410
|
A | T | 4 | a0001c0016t0005g0015a0001c0016t0005g0016a0003c0015t0001g0013others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-1191T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023410 | ||||||
| chr6:76023858
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562+1336G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023858 | ||||||
| chr6:76023920
|
A | G | 116 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(113): Show | 117 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.562+1274T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023920 | ||||||
| chr6:76023962
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0003c0003t0001g0087 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.562+1232G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023962 | ||||||
| chr6:76024053
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562+1141A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024053 | ||||||
| chr6:76024173
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.562+1021C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024173 | ||||||
| chr6:76024205
|
C | T | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.562+989G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024205 | ||||||
| chr6:76024263
|
A | G | 1 | a0008c0008t0001g0210 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.562+931T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024263 | ||||||
| chr6:76024395
|
C | CTTAGA | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(161): Show | 165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.562+798_562+799ins others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024395 | ||||||
| chr6:76024398
|
T | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(161): Show | 165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.562+796A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024398 | ||||||
| chr6:76024655
|
TA | T | 15 | a0001c0001t0001g0218a0005c0006t0003g0084a0005c0006t0003g0085others(12): Show | 16 | HG00140.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.562+538delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024655 | ||||||
| chr6:76025111
|
A | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.562+83T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76025111 | ||||||
| chr6:76025119
|
T | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(33): Show | 37 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.562+75A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76025119 | ||||||
| chr6:76025348
|
A | G | 123 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0021others(120): Show | 124 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.498-90T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025348 | ||||||
| chr6:76025559
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(176): Show | 181 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.498-301C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025559 | ||||||
| chr6:76025743
|
T | C | 117 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(114): Show | 118 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.498-485A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025743 | ||||||
| chr6:76025839
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.498-581A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025839 | ||||||
| chr6:76026035
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-777C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026035 | ||||||
| chr6:76026040
|
G | T | 1 | a0002c0002t0001g0138 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.498-782C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026040 | ||||||
| chr6:76026085
|
ATGCGGGA others(21): Show |
A | 2 | a0002c0002t0001g0242a0002c0002t0001g0262 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.498-855_498-828del others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026085 | ||||||
| chr6:76026116
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0013g0008others(3): Show | 6 | HG01109.hp1 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-858G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026116 | ||||||
| chr6:76026260
|
C | A | 107 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0042others(104): Show | 108 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.498-1002G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026260 | ||||||
| chr6:76026306
|
C | T | 2 | a0002c0002t0001g0252a0002c0002t0001g0253 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.498-1048G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026306 | ||||||
| chr6:76026336
|
T | G | 1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.498-1078A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026336 | ||||||
| chr6:76026387
|
T | C | 1 | a0002c0002t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.498-1129A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026387 | ||||||
| chr6:76026411
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.498-1153G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026411 | ||||||
| chr6:76026434
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.498-1176G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026434 | ||||||
| chr6:76026435
|
T | A | 48 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0052others(45): Show | 48 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.498-1177A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026435 | ||||||
| chr6:76026451
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.498-1193G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026451 | ||||||
| chr6:76026470
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-1212C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026470 | ||||||
| chr6:76026527
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1269G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026527 | ||||||
| chr6:76026612
|
A | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.498-1354T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026612 | ||||||
| chr6:76026712
|
T | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1454A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026712 | ||||||
| chr6:76026868
|
G | A | 1 | a0010c0010t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.498-1610C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026868 | ||||||
| chr6:76026932
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0088others(23): Show | 27 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.498-1674A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026932 | ||||||
| chr6:76027112
|
G | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1854C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027112 | ||||||
| chr6:76027223
|
G | C | 3 | a0005c0006t0003g0228a0010c0010t0001g0201a0011c0011t0003g0213 | 3 | HG01169.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.498-1965C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027223 | ||||||
| chr6:76027277
|
T | C | 1 | a0002c0002t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.498-2019A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027277 | ||||||
| chr6:76027279
|
T | C | 123 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.498-2021A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027279 | ||||||
| chr6:76027280
|
C | T | 4 | a0002c0002t0001g0082a0002c0002t0001g0161a0002c0002t0001g0286others(1): Show | 4 | HG02273.hp2 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-2022G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027280 | ||||||
| chr6:76027445
|
T | C | 1 | a0001c0001t0005g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.498-2187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027445 | ||||||
| chr6:76027460
|
T | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.498-2202A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027460 | ||||||
| chr6:76027655
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.498-2397G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027655 | ||||||
| chr6:76027696
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(13): Show | 16 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.498-2438C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027696 | ||||||
| chr6:76027790
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2532C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027790 | ||||||
| chr6:76027854
|
T | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-2596A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027854 | ||||||
| chr6:76027990
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2732C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027990 | ||||||
| chr6:76028033
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2775G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028033 | ||||||
| chr6:76028256
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2998G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028256 | ||||||
| chr6:76028288
|
G | T | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.498-3030C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028288 | ||||||
| chr6:76028339
|
T | C | 72 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0156others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.498-3081A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028339 | ||||||
| chr6:76028395
|
C | T | 1 | a0008c0008t0001g0123 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.498-3137G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028395 | ||||||
| chr6:76028396
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.498-3138C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028396 | ||||||
| chr6:76028416
|
G | A | 2 | a0020c0024t0001g0136a0021c0022t0001g0051 | 2 | NA18946.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.498-3158C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028416 | ||||||
| chr6:76028570
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-3312G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028570 | ||||||
| chr6:76028595
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(13): Show | 16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-3337G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028595 | ||||||
| chr6:76028596
|
G | A | 1 | a0002c0002t0001g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.498-3338C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028596 | ||||||
| chr6:76028656
|
C | T | 8 | a0001c0016t0005g0015a0001c0016t0005g0016a0002c0002t0001g0295others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-3398G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028656 | ||||||
| chr6:76028657
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.498-3399C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028657 | ||||||
| chr6:76028900
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0238a0001c0001t0001g0260others(7): Show | 10 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-3642G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028900 | ||||||
| chr6:76028916
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-3658G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028916 | ||||||
| chr6:76028972
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0266others(20): Show | 24 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.498-3714G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028972 | ||||||
| chr6:76029249
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498-3991C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029249 | ||||||
| chr6:76029302
|
G | A | 1 | a0002c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.498-4044C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029302 | ||||||
| chr6:76029438
|
G | T | 27 | a0001c0001t0001g0099a0001c0001t0001g0166a0002c0002t0001g0097others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.498-4180C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029438 | ||||||
| chr6:76029701
|
G | T | 1 | a0002c0002t0001g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.498-4443C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029701 | ||||||
| chr6:76029763
|
C | G | 2 | a0007c0007t0004g0220a0007c0007t0004g0229 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.498-4505G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029763 | ||||||
| chr6:76030095
|
T | C | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.497+4220A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030095 | ||||||
| chr6:76030123
|
T | C | 1 | a0002c0002t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+4192A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030123 | ||||||
| chr6:76030178
|
A | G | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.497+4137T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030178 | ||||||
| chr6:76030179
|
C | G | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.497+4136G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030179 | ||||||
| chr6:76030185
|
G | A | 1 | a0002c0002t0007g0256 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497+4130C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030185 | ||||||
| chr6:76030462
|
TA | T | 3 | a0002c0002t0001g0231a0003c0003t0001g0079a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.497+3852delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030462 | ||||||
| chr6:76030553
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+3762C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030553 | ||||||
| chr6:76030657
|
A | C | 108 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0134others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.497+3658T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030657 | ||||||
| chr6:76030780
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.497+3535A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030780 | ||||||
| chr6:76030782
|
G | A | 11 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.497+3533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030782 | ||||||
| chr6:76030932
|
C | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0287a0003c0003t0001g0271others(1): Show | 4 | HG01175.hp1 HG01358.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+3383G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030932 | ||||||
| chr6:76030964
|
C | T | 3 | a0002c0002t0001g0111a0002c0002t0001g0112a0006c0005t0008g0091 | 3 | HG00738.hp1 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.497+3351G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030964 | ||||||
| chr6:76030996
|
C | T | 1 | a0001c0001t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497+3319G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030996 | ||||||
| chr6:76031100
|
T | C | 1 | a0006c0005t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.497+3215A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031100 | ||||||
| chr6:76031111
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+3204G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031111 | ||||||
| chr6:76031202
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+3113T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031202 | ||||||
| chr6:76031203
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+3112A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031203 | ||||||
| chr6:76031225
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0266others(20): Show | 24 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+3090A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031225 | ||||||
| chr6:76031342
|
T | C | 19 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0053others(16): Show | 19 | HG00621.hp1 HG02027.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.497+2973A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031342 | ||||||
| chr6:76031342
|
T | G | 3 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | NA18981.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.497+2973A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031342 | ||||||
| chr6:76031641
|
G | A | 1 | a0005c0006t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.497+2674C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031641 | ||||||
| chr6:76031734
|
C | T | 2 | a0012c0012t0004g0164a0012c0012t0004g0165 | 2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.497+2581G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031734 | ||||||
| chr6:76031861
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0005g0011 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.497+2454A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031861 | ||||||
| chr6:76031986
|
T | A | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497+2329A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031986 | ||||||
| chr6:76031992
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.497+2323G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031992 | ||||||
| chr6:76032260
|
T | G | 5 | a0001c0016t0005g0015a0001c0016t0005g0016a0003c0015t0001g0013others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+2055A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032260 | ||||||
| chr6:76032309
|
AT | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.497+2005delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032309 | ||||||
| chr6:76032467
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0005g0011 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.497+1848C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032467 | ||||||
| chr6:76032543
|
A | G | 3 | a0003c0015t0001g0013a0003c0015t0001g0014a0006c0005t0006g0222 | 3 | HG01109.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.497+1772T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032543 | ||||||
| chr6:76032875
|
T | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+1440A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032875 | ||||||
| chr6:76032938
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.497+1377G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032938 | ||||||
| chr6:76033002
|
C | G | 1 | a0010c0010t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.497+1313G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033002 | ||||||
| chr6:76033205
|
C | T | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.497+1110G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033205 | ||||||
| chr6:76033367
|
C | T | 5 | a0003c0003t0008g0137a0003c0003t0008g0178a0003c0003t0014g0083others(2): Show | 5 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+948G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033367 | ||||||
| chr6:76033399
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497+916T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033399 | ||||||
| chr6:76033452
|
A | G | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.497+863T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033452 | ||||||
| chr6:76033770
|
CTCT | C | 5 | a0001c0016t0005g0015a0001c0016t0005g0016a0003c0015t0001g0013others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+542_497+544del others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033770 | ||||||
| chr6:76033848
|
G | A | 2 | a0001c0001t0005g0223a0001c0001t0005g0224 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+467C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033848 | ||||||
| chr6:76033896
|
T | A | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+419A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033896 | ||||||
| chr6:76033943
|
G | T | 2 | a0001c0001t0001g0299a0010c0010t0001g0300 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.497+372C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033943 | ||||||
| chr6:76034142
|
T | C | 1 | a0003c0003t0001g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.497+173A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76034142 | ||||||
| chr6:76034264
|
T | G | 3 | a0003c0015t0001g0013a0003c0015t0001g0014a0006c0005t0006g0222 | 3 | HG01109.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.497+51A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76034264 | ||||||
| chr6:76034395
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0003c0003t0001g0087 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.469-52C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034395 | ||||||
| chr6:76034576
|
C | A | 3 | a0002c0002t0001g0231a0003c0003t0001g0079a0012c0012t0004g0230 | 3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.468+45G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034576 | ||||||
| chr6:76034581
|
C | T | 56 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0099others(53): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.468+40G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034581 | ||||||
| chr6:76034831
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0026others(29): Show | 32 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.302-44G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034831 | ||||||
| chr6:76034839
|
A | C | 1 | a0002c0002t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.302-52T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034839 | ||||||
| chr6:76034887
|
C | T | 1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.302-100G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034887 | ||||||
| chr6:76034892
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.302-105G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034892 | ||||||
| chr6:76035033
|
C | T | 115 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-246G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035033 | ||||||
| chr6:76035217
|
C | T | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.302-430G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035217 | ||||||
| chr6:76035238
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.302-451T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035238 | ||||||
| chr6:76035274
|
G | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-487C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035274 | ||||||
| chr6:76035277
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.302-490G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035277 | ||||||
| chr6:76035346
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-559T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035346 | ||||||
| chr6:76035360
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0005g0011 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.302-573C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035360 | ||||||
| chr6:76035447
|
C | T | 3 | a0007c0007t0004g0246a0007c0007t0004g0247a0007c0007t0004g0248 | 3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.302-660G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035447 | ||||||
| chr6:76035499
|
C | CA | 16 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0001g0264others(13): Show | 16 | HG02293.hp2 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.302-713dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | ||||||
| chr6:76035499
|
CA | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0021others(137): Show | 142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.302-713delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | ||||||
| chr6:76035499
|
CAA | C | 106 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0134others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.302-714_302-713del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | ||||||
| chr6:76035529
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.302-742T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035529 | ||||||
| chr6:76035535
|
G | A | 2 | a0002c0002t0001g0150a0002c0002t0005g0080 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.302-748C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035535 | ||||||
| chr6:76035623
|
C | T | 1 | a0003c0003t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.302-836G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035623 | ||||||
| chr6:76035635
|
A | G | 1 | a0004c0004t0002g0055 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.302-848T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035635 | ||||||
| chr6:76035734
|
A | C | 1 | a0001c0001t0005g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302-947T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035734 | ||||||
| chr6:76035740
|
C | G | 1 | a0002c0002t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-953G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035740 | ||||||
| chr6:76035774
|
C | G | 1 | a0002c0002t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-987G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035774 | ||||||
| chr6:76035830
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.302-1043C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035830 | ||||||
| chr6:76035853
|
G | A | 1 | a0008c0008t0001g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302-1066C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035853 | ||||||
| chr6:76036222
|
A | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-1435T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036222 | ||||||
| chr6:76036278
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.302-1491G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036278 | ||||||
| chr6:76036334
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.302-1547G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036334 | ||||||
| chr6:76036686
|
T | C | 5 | a0002c0002t0001g0138a0002c0002t0001g0197a0002c0002t0001g0212others(2): Show | 5 | HG00735.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-1899A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036686 | ||||||
| chr6:76036787
|
GAGTGGCT others(72): Show |
G | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(178): Show | 182 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.302-2079_302-2001d others(81): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036787 | ||||||
| chr6:76036828
|
C | T | 2 | a0003c0003t0001g0030a0003c0003t0001g0101 | 2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.302-2041G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036828 | ||||||
| chr6:76036909
|
A | C | 26 | a0001c0001t0001g0065a0001c0018t0001g0263a0002c0002t0001g0063others(23): Show | 26 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.302-2122T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036909 | ||||||
| chr6:76036944
|
A | G | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.302-2157T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036944 | ||||||
| chr6:76037021
|
T | C | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.302-2234A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037021 | ||||||
| chr6:76037068
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.302-2281C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037068 | ||||||
| chr6:76037233
|
G | C | 162 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.302-2446C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037233 | ||||||
| chr6:76037761
|
A | G | 1 | a0005c0006t0003g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.302-2974T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037761 | ||||||
| chr6:76037853
|
C | T | 1 | a0012c0012t0004g0165 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.302-3066G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037853 | ||||||
| chr6:76037866
|
A | T | 1 | a0002c0002t0001g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.302-3079T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037866 | ||||||
| chr6:76037914
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.302-3127A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037914 | ||||||
| chr6:76037927
|
C | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-3140G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037927 | ||||||
| chr6:76037948
|
T | A | 2 | a0001c0001t0001g0192a0003c0003t0001g0193 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.302-3161A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037948 | ||||||
| chr6:76037957
|
T | C | 1 | a0002c0002t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.302-3170A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037957 | ||||||
| chr6:76038045
|
C | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-3258G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038045 | ||||||
| chr6:76038106
|
A | G | 2 | a0008c0008t0001g0215a0008c0008t0001g0216 | 2 | NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.302-3319T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038106 | ||||||
| chr6:76038179
|
G | A | 2 | a0002c0002t0001g0158a0006c0005t0001g0157 | 2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.302-3392C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038179 | ||||||
| chr6:76038227
|
A | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(187): Show | 191 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.302-3440T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038227 | ||||||
| chr6:76038476
|
G | A | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.301+3417C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038476 | ||||||
| chr6:76038753
|
C | T | 1 | a0006c0005t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.301+3140G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038753 | ||||||
| chr6:76038828
|
C | T | 298 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(295): Show | 300 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.301+3065G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038828 | ||||||
| chr6:76039098
|
C | T | 1 | a0025c0028t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301+2795G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039098 | ||||||
| chr6:76039356
|
G | GT | 42 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0181others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+2536dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039356 | ||||||
| chr6:76039356
|
GT | G | 103 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.301+2536delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039356 | ||||||
| chr6:76039365
|
T | C | 2 | a0001c0001t0005g0223a0001c0001t0005g0224 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301+2528A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039365 | ||||||
| chr6:76039402
|
A | C | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.301+2491T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039402 | ||||||
| chr6:76039501
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | NA18941.hp2 NA18974.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+2392C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039501 | ||||||
| chr6:76039542
|
G | A | 3 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | NA18981.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.301+2351C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039542 | ||||||
| chr6:76039750
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.301+2143G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039750 | ||||||
| chr6:76039909
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.301+1984T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039909 | ||||||
| chr6:76039955
|
T | G | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+1938A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039955 | ||||||
| chr6:76040168
|
T | G | 1 | a0002c0002t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.301+1725A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040168 | ||||||
| chr6:76040184
|
A | G | 1 | a0011c0011t0003g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+1709T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040184 | ||||||
| chr6:76040196
|
A | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.301+1697T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040196 | ||||||
| chr6:76040412
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.301+1481A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040412 | ||||||
| chr6:76040674
|
C | G | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.301+1219G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040674 | ||||||
| chr6:76040871
|
T | C | 2 | a0012c0012t0004g0164a0012c0012t0004g0165 | 2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.301+1022A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040871 | ||||||
| chr6:76040971
|
G | T | 2 | a0002c0002t0001g0291a0006c0005t0001g0143 | 2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.301+922C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040971 | ||||||
| chr6:76041028
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(22): Show | 26 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.301+865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041028 | ||||||
| chr6:76041042
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.301+851C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041042 | ||||||
| chr6:76041137
|
T | C | 1 | a0006c0005t0008g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.301+756A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041137 | ||||||
| chr6:76041163
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.301+730C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041163 | ||||||
| chr6:76041243
|
T | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0238others(18): Show | 21 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.301+650A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041243 | ||||||
| chr6:76041312
|
A | AACC | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.301+578_301+580dup others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041312 | ||||||
| chr6:76041356
|
A | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+537T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041356 | ||||||
| chr6:76041496
|
T | A | 1 | a0003c0003t0001g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.301+397A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041496 | ||||||
| chr6:76042175
|
A | G | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-49T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042175 | ||||||
| chr6:76042329
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-203C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042329 | ||||||
| chr6:76042346
|
A | G | 1 | a0003c0003t0001g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-220T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042346 | ||||||
| chr6:76042449
|
G | C | 1 | a0001c0001t0005g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-323C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042449 | ||||||
| chr6:76042608
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(22): Show | 26 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-482T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042608 | ||||||
| chr6:76042943
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-817G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042943 | ||||||
| chr6:76042960
|
A | C | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-834T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042960 | ||||||
| chr6:76043184
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68-1058G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043184 | ||||||
| chr6:76043215
|
T | A | 85 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.68-1089A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043215 | ||||||
| chr6:76043269
|
G | A | 6 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1143C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043269 | ||||||
| chr6:76043308
|
G | T | 1 | a0002c0002t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.68-1182C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043308 | ||||||
| chr6:76043384
|
G | T | 1 | a0004c0004t0002g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.68-1258C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043384 | ||||||
| chr6:76043481
|
GT | G | 123 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.68-1356delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043481 | ||||||
| chr6:76043517
|
A | G | 1 | a0009c0009t0001g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.68-1391T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043517 | ||||||
| chr6:76043563
|
C | T | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.68-1437G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043563 | ||||||
| chr6:76043595
|
T | C | 116 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.68-1469A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043595 | ||||||
| chr6:76043736
|
A | G | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-1610T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043736 | ||||||
| chr6:76043897
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0238others(18): Show | 21 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.68-1771C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043897 | ||||||
| chr6:76043921
|
A | G | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-1795T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043921 | ||||||
| chr6:76043940
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-1814G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043940 | ||||||
| chr6:76043971
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-1845G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043971 | ||||||
| chr6:76044087
|
A | C | 4 | a0001c0016t0005g0015a0001c0016t0005g0016a0003c0015t0001g0013others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1961T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044087 | ||||||
| chr6:76044094
|
C | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-1968G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044094 | ||||||
| chr6:76044272
|
A | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2146T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044272 | ||||||
| chr6:76044548
|
T | C | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.68-2422A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044548 | ||||||
| chr6:76044897
|
C | G | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2771G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044897 | ||||||
| chr6:76045024
|
C | T | 4 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(1): Show | 4 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2898G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045024 | ||||||
| chr6:76045065
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2939A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045065 | ||||||
| chr6:76045259
|
C | T | 23 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(20): Show | 23 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-3133G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045259 | ||||||
| chr6:76045344
|
G | A | 2 | a0001c0001t0005g0160a0005c0006t0003g0090 | 2 | HG00140.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-3218C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045344 | ||||||
| chr6:76045418
|
T | C | 2 | a0004c0004t0002g0244a0009c0009t0001g0115 | 2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.68-3292A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045418 | ||||||
| chr6:76045441
|
C | CT | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(84): Show | 88 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.68-3316dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045441 | ||||||
| chr6:76045441
|
C | CTT | 83 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.68-3317_68-3316dup others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045441 | ||||||
| chr6:76045479
|
G | A | 1 | a0024c0027t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-3353C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045479 | ||||||
| chr6:76045504
|
G | A | 112 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.68-3378C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045504 | ||||||
| chr6:76045604
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.68-3478A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045604 | ||||||
| chr6:76045994
|
A | C | 1 | a0001c0001t0005g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.68-3868T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045994 | ||||||
| chr6:76046090
|
GA | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(152): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.68-3965delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046090 | ||||||
| chr6:76046186
|
C | T | 1 | a0011c0011t0003g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-4060G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046186 | ||||||
| chr6:76046279
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-4153C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046279 | ||||||
| chr6:76046305
|
GA | G | 77 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0074others(74): Show | 77 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.68-4180delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046305 | ||||||
| chr6:76046320
|
G | A | 4 | a0002c0002t0001g0227a0002c0002t0001g0295a0015c0017t0001g0293others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4194C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046320 | ||||||
| chr6:76046472
|
G | A | 1 | a0002c0002t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.68-4346C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046472 | ||||||
| chr6:76046519
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68-4393A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046519 | ||||||
| chr6:76046529
|
A | G | 3 | a0002c0002t0001g0227a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-4403T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046529 | ||||||
| chr6:76046531
|
G | T | 4 | a0002c0002t0001g0227a0002c0002t0001g0295a0015c0017t0001g0293others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4405C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046531 | ||||||
| chr6:76046657
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.68-4531T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046657 | ||||||
| chr6:76046678
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-4552G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046678 | ||||||
| chr6:76046706
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-4580G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046706 | ||||||
| chr6:76046782
|
G | A | 1 | a0003c0003t0001g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-4656C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046782 | ||||||
| chr6:76046811
|
C | T | 2 | a0001c0001t0001g0088a0003c0003t0001g0087 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68-4685G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046811 | ||||||
| chr6:76046812
|
G | A | 2 | a0002c0002t0001g0153a0003c0003t0001g0152 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.68-4686C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046812 | ||||||
| chr6:76046991
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-4865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046991 | ||||||
| chr6:76047132
|
T | C | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-5006A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047132 | ||||||
| chr6:76047214
|
C | T | 38 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(35): Show | 38 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.68-5088G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047214 | ||||||
| chr6:76047249
|
G | A | 1 | a0003c0003t0006g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68-5123C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047249 | ||||||
| chr6:76047631
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5505G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047631 | ||||||
| chr6:76047674
|
TATTA | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5552_68-5549del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047674 | ||||||
| chr6:76047723
|
T | C | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-5597A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047723 | ||||||
| chr6:76047895
|
C | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0238others(2): Show | 5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-5769G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047895 | ||||||
| chr6:76048037
|
G | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(251): Show | 256 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.68-5911C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048037 | ||||||
| chr6:76048141
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-6015C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048141 | ||||||
| chr6:76048270
|
A | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-6144T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048270 | ||||||
| chr6:76048362
|
A | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6236T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048362 | ||||||
| chr6:76048363
|
G | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6237C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048363 | ||||||
| chr6:76048381
|
C | T | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-6255G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048381 | ||||||
| chr6:76048382
|
A | G | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6256T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048382 | ||||||
| chr6:76048449
|
A | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.68-6323T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048449 | ||||||
| chr6:76048460
|
C | A | 1 | a0005c0006t0003g0268 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.68-6334G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048460 | ||||||
| chr6:76048461
|
G | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(10): Show | 13 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-6335C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048461 | ||||||
| chr6:76048509
|
G | T | 215 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.68-6383C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048509 | ||||||
| chr6:76048556
|
C | T | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-6430G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048556 | ||||||
| chr6:76048581
|
A | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-6455T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048581 | ||||||
| chr6:76048662
|
G | A | 7 | a0001c0001t0001g0156a0003c0003t0001g0070a0003c0003t0001g0071others(4): Show | 7 | HG01081.hp2 HG01099.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-6536C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048662 | ||||||
| chr6:76049001
|
T | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6875A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049001 | ||||||
| chr6:76049046
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6920G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049046 | ||||||
| chr6:76049088
|
C | T | 298 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(295): Show | 300 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.68-6962G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049088 | ||||||
| chr6:76049110
|
A | C | 1 | a0010c0010t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68-6984T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049110 | ||||||
| chr6:76049122
|
A | G | 1 | a0005c0006t0003g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.68-6996T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049122 | ||||||
| chr6:76049190
|
A | G | 111 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0088others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.68-7064T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049190 | ||||||
| chr6:76049308
|
A | G | 217 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0043others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.68-7182T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049308 | ||||||
| chr6:76049410
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.68-7284C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049410 | ||||||
| chr6:76049462
|
TTCTCTCT others(7): Show |
T | 2 | a0001c0001t0001g0257a0002c0002t0007g0256 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-7350_68-7337del others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049462 | ||||||
| chr6:76049482
|
C | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-7356G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049482 | ||||||
| chr6:76049590
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.68-7464G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049590 | ||||||
| chr6:76049608
|
A | G | 5 | a0002c0002t0001g0111a0002c0002t0001g0112a0005c0006t0003g0110others(2): Show | 5 | HG00738.hp1 HG01496.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-7482T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049608 | ||||||
| chr6:76049666
|
G | A | 1 | a0011c0011t0003g0213 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.68-7540C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049666 | ||||||
| chr6:76049695
|
A | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-7569T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049695 | ||||||
| chr6:76049822
|
A | G | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7696T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049822 | ||||||
| chr6:76049870
|
C | T | 1 | a0002c0002t0001g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.68-7744G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049870 | ||||||
| chr6:76050229
|
C | A | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8103G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050229 | ||||||
| chr6:76050312
|
G | A | 1 | a0003c0003t0001g0030 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.68-8186C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050312 | ||||||
| chr6:76050317
|
C | T | 9 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-8191G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050317 | ||||||
| chr6:76050325
|
C | A | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-8199G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050325 | ||||||
| chr6:76050350
|
T | G | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-8224A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050350 | ||||||
| chr6:76050357
|
C | T | 9 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-8231G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050357 | ||||||
| chr6:76050358
|
G | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0238others(2): Show | 5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-8232C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050358 | ||||||
| chr6:76050397
|
C | T | 1 | a0003c0003t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-8271G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050397 | ||||||
| chr6:76050398
|
G | A | 2 | a0002c0002t0001g0167a0004c0004t0002g0037 | 2 | NA18944.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.68-8272C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050398 | ||||||
| chr6:76050408
|
A | T | 1 | a0004c0004t0002g0092 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.68-8282T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050408 | ||||||
| chr6:76050440
|
CA | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0260a0001c0001t0001g0264others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-8315delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050440 | ||||||
| chr6:76050588
|
C | T | 111 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(108): Show | 112 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.68-8462G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050588 | ||||||
| chr6:76050678
|
G | A | 2 | a0002c0002t0001g0158a0006c0005t0001g0157 | 2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.68-8552C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050678 | ||||||
| chr6:76050726
|
C | T | 2 | a0003c0015t0001g0013a0003c0015t0001g0014 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-8600G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050726 | ||||||
| chr6:76050956
|
G | A | 2 | a0001c0016t0005g0015a0001c0016t0005g0016 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.68-8830C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050956 | ||||||
| chr6:76050959
|
G | A | 1 | a0003c0003t0001g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68-8833C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050959 | ||||||
| chr6:76050994
|
C | T | 2 | a0002c0002t0001g0242a0002c0002t0001g0262 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-8868G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050994 | ||||||
| chr6:76050999
|
A | G | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.68-8873T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050999 | ||||||
| chr6:76051072
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(10): Show | 13 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-8946A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051072 | ||||||
| chr6:76051192
|
T | C | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9066A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051192 | ||||||
| chr6:76051225
|
C | T | 1 | a0007c0007t0004g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.68-9099G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051225 | ||||||
| chr6:76051406
|
C | G | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9280G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051406 | ||||||
| chr6:76051444
|
T | C | 1 | a0001c0001t0005g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-9318A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051444 | ||||||
| chr6:76051536
|
A | G | 2 | a0002c0002t0001g0242a0002c0002t0001g0262 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-9410T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051536 | ||||||
| chr6:76051983
|
G | GA | 7 | a0001c0001t0001g0010a0001c0001t0001g0260a0001c0001t0001g0264others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-9858dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051983 | ||||||
| chr6:76052000
|
A | G | 1 | a0024c0027t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-9874T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052000 | ||||||
| chr6:76052247
|
T | A | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10121A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052247 | ||||||
| chr6:76052249
|
T | C | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10123A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052249 | ||||||
| chr6:76052291
|
T | C | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10165A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052291 | ||||||
| chr6:76052411
|
C | G | 6 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10285G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052411 | ||||||
| chr6:76052663
|
C | A | 1 | a0005c0006t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.68-10537G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052663 | ||||||
| chr6:76052743
|
G | A | 259 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.68-10617C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052743 | ||||||
| chr6:76052843
|
G | A | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10717C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052843 | ||||||
| chr6:76052844
|
A | T | 1 | a0013c0013t0001g0183 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.68-10718T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052844 | ||||||
| chr6:76052965
|
T | C | 2 | a0001c0001t0005g0239a0001c0001t0005g0240 | 2 | HG02293.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.68-10839A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052965 | ||||||
| chr6:76053149
|
A | G | 1 | a0002c0002t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.68-11023T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053149 | ||||||
| chr6:76053232
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.68-11106G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053232 | ||||||
| chr6:76053612
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-11486G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053612 | ||||||
| chr6:76053673
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-11547T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053673 | ||||||
| chr6:76053724
|
T | C | 1 | a0003c0003t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-11598A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053724 | ||||||
| chr6:76054179
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12053A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054179 | ||||||
| chr6:76054315
|
T | C | 3 | a0001c0001t0001g0214a0008c0008t0001g0215a0008c0008t0001g0216 | 3 | HG00423.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.68-12189A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054315 | ||||||
| chr6:76054456
|
T | C | 1 | a0002c0002t0001g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.68-12330A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054456 | ||||||
| chr6:76054473
|
T | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-12347A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054473 | ||||||
| chr6:76054474
|
T | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12348A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054474 | ||||||
| chr6:76054596
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12470A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054596 | ||||||
| chr6:76054602
|
A | T | 1 | a0007c0007t0004g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68-12476T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054602 | ||||||
| chr6:76054621
|
G | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.68-12495C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054621 | ||||||
| chr6:76054673
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-12547T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054673 | ||||||
| chr6:76054839
|
A | ACAAAGG | 86 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-12719_68-12714d others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054839 | ||||||
| chr6:76054858
|
G | T | 86 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-12732C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054858 | ||||||
| chr6:76055136
|
G | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.68-13010C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055136 | ||||||
| chr6:76055214
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.68-13088A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055214 | ||||||
| chr6:76055349
|
A | G | 86 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-13223T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055349 | ||||||
| chr6:76055399
|
T | C | 262 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.68-13273A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055399 | ||||||
| chr6:76055490
|
T | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.68-13364A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055490 | ||||||
| chr6:76055550
|
CA | C | 125 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.68-13425delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055550 | ||||||
| chr6:76055623
|
G | A | 7 | a0001c0001t0005g0160a0002c0002t0001g0082a0002c0002t0001g0161others(4): Show | 7 | HG00140.hp1 HG00741.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-13497C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055623 | ||||||
| chr6:76055675
|
A | AAGAAG | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13554_68-13550d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055675 | ||||||
| chr6:76055759
|
A | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(34): Show | 37 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.68-13633T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055759 | ||||||
| chr6:76055855
|
C | T | 1 | a0008c0008t0001g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.68-13729G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055855 | ||||||
| chr6:76056050
|
C | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13924G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056050 | ||||||
| chr6:76056051
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.68-13925C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056051 | ||||||
| chr6:76056083
|
G | GA | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13958dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056083 | ||||||
| chr6:76056219
|
G | T | 1 | a0002c0002t0001g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.68-14093C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056219 | ||||||
| chr6:76056283
|
G | A | 2 | a0005c0006t0003g0085a0005c0006t0003g0090 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.68-14157C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056283 | ||||||
| chr6:76056402
|
A | G | 1 | a0005c0006t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.68-14276T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056402 | ||||||
| chr6:76056502
|
C | CA | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14377dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056502 | ||||||
| chr6:76056588
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.68-14462T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056588 | ||||||
| chr6:76056644
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.68-14518G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056644 | ||||||
| chr6:76056652
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.68-14526T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056652 | ||||||
| chr6:76056683
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14557A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056683 | ||||||
| chr6:76056719
|
C | A | 1 | a0001c0001t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-14593G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056719 | ||||||
| chr6:76056790
|
A | T | 126 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.68-14664T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056790 | ||||||
| chr6:76056945
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-14819G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056945 | ||||||
| chr6:76057010
|
C | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14884G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057010 | ||||||
| chr6:76057117
|
G | A | 4 | a0001c0001t0005g0239a0001c0001t0005g0240a0003c0003t0001g0163others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-14991C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057117 | ||||||
| chr6:76057138
|
G | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-15012C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057138 | ||||||
| chr6:76057262
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.68-15136T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057262 | ||||||
| chr6:76057270
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-15144A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057270 | ||||||
| chr6:76057379
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.67+15043C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057379 | ||||||
| chr6:76057393
|
C | G | 2 | a0001c0001t0005g0239a0001c0001t0005g0240 | 2 | HG02293.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.67+15029G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057393 | ||||||
| chr6:76057447
|
A | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14975T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057447 | ||||||
| chr6:76057475
|
C | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14947G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057475 | ||||||
| chr6:76057507
|
G | A | 211 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.67+14915C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057507 | ||||||
| chr6:76057536
|
A | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14886T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057536 | ||||||
| chr6:76057619
|
C | T | 1 | a0003c0003t0001g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+14803G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057619 | ||||||
| chr6:76057641
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.67+14781T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057641 | ||||||
| chr6:76057741
|
T | C | 126 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.67+14681A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057741 | ||||||
| chr6:76057969
|
A | AAAAAT | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14448_67+14452d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057969 | ||||||
| chr6:76057969
|
AAAAAT | A | 211 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.67+14448_67+14452d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057969 | ||||||
| chr6:76058075
|
A | C | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0007g0256others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+14347T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058075 | ||||||
| chr6:76058093
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(12): Show | 15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+14329T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058093 | ||||||
| chr6:76058107
|
A | T | 2 | a0004c0004t0002g0092a0006c0005t0002g0093 | 2 | NA18955.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67+14315T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058107 | ||||||
| chr6:76058279
|
A | C | 1 | a0006c0005t0008g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+14143T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058279 | ||||||
| chr6:76058367
|
T | C | 3 | a0005c0006t0003g0219a0007c0007t0004g0220a0007c0007t0004g0229 | 3 | HG01070.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.67+14055A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058367 | ||||||
| chr6:76058542
|
C | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.67+13880G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058542 | ||||||
| chr6:76058784
|
A | G | 3 | a0009c0009t0001g0254a0009c0009t0001g0259a0009c0009t0007g0255 | 3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+13638T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058784 | ||||||
| chr6:76058804
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0007g0256 | 3 | HG02615.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67+13618A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058804 | ||||||
| chr6:76058829
|
T | G | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0007g0256others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+13593A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058829 | ||||||
| chr6:76059295
|
A | C | 4 | a0001c0018t0001g0263a0002c0002t0001g0295a0015c0017t0001g0293others(1): Show | 4 | HG01884.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+13127T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059295 | ||||||
| chr6:76059322
|
A | G | 1 | a0005c0006t0003g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67+13100T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059322 | ||||||
| chr6:76059331
|
G | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+13091C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059331 | ||||||
| chr6:76059357
|
A | T | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0007g0256others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+13065T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059357 | ||||||
| chr6:76059402
|
C | CT | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+13019dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059402 | ||||||
| chr6:76059402
|
CT | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+13019delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059402 | ||||||
| chr6:76059415
|
G | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.67+13007C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059415 | ||||||
| chr6:76059439
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.67+12983C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059439 | ||||||
| chr6:76059465
|
G | A | 2 | a0012c0012t0004g0164a0012c0012t0004g0165 | 2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67+12957C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059465 | ||||||
| chr6:76059481
|
T | C | 2 | a0002c0002t0001g0289a0002c0002t0001g0290 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.67+12941A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059481 | ||||||
| chr6:76059585
|
A | G | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12837T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059585 | ||||||
| chr6:76059680
|
C | A | 4 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12742G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059680 | ||||||
| chr6:76059768
|
A | T | 4 | a0001c0018t0001g0263a0002c0002t0001g0295a0015c0017t0001g0293others(1): Show | 4 | HG01884.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12654T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059768 | ||||||
| chr6:76059993
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+12429A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059993 | ||||||
| chr6:76060002
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+12420A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060002 | ||||||
| chr6:76060195
|
A | G | 2 | a0003c0003t0001g0233a0004c0004t0001g0234 | 2 | NA18987.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.67+12227T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060195 | ||||||
| chr6:76060349
|
G | A | 4 | a0001c0001t0005g0221a0001c0001t0005g0223a0001c0001t0005g0224others(1): Show | 4 | HG01109.hp2 HG02615.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12073C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060349 | ||||||
| chr6:76060403
|
A | T | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+12019T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060403 | ||||||
| chr6:76060528
|
C | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+11894G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060528 | ||||||
| chr6:76060543
|
A | G | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+11879T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060543 | ||||||
| chr6:76060784
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11638C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060784 | ||||||
| chr6:76060850
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+11572C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060850 | ||||||
| chr6:76061080
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0003c0003t0001g0087 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.67+11342G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061080 | ||||||
| chr6:76061208
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+11214T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061208 | ||||||
| chr6:76061256
|
A | G | 217 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.67+11166T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061256 | ||||||
| chr6:76061268
|
T | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.67+11154A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061268 | ||||||
| chr6:76061316
|
A | G | 1 | a0002c0002t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+11106T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061316 | ||||||
| chr6:76061418
|
C | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+11004G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061418 | ||||||
| chr6:76061581
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0034a0003c0003t0001g0023 | 3 | HG01928.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.67+10841G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061581 | ||||||
| chr6:76061635
|
A | G | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+10787T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061635 | ||||||
| chr6:76061643
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10779A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061643 | ||||||
| chr6:76061689
|
G | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10733C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061689 | ||||||
| chr6:76061722
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+10700T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061722 | ||||||
| chr6:76061737
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.67+10685G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061737 | ||||||
| chr6:76061861
|
T | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10561A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061861 | ||||||
| chr6:76061862
|
T | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(14): Show | 17 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+10560A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061862 | ||||||
| chr6:76062327
|
G | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+10095C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062327 | ||||||
| chr6:76062329
|
A | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10093T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062329 | ||||||
| chr6:76062414
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0007g0062others(1): Show | 4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+10008A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062414 | ||||||
| chr6:76062432
|
C | T | 1 | a0023c0025t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+9990G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062432 | ||||||
| chr6:76062443
|
A | C | 21 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(18): Show | 21 | HG00621.hp1 HG02055.hp1 HG03942.hp2 others(18): Show |
intron_variant | MODIFIER | c.67+9979T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062443 | ||||||
| chr6:76062848
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.67+9574T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062848 | ||||||
| chr6:76062855
|
GT | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(48): Show | 52 | HG00609.hp2 HG00673.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.67+9566delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | ||||||
| chr6:76062855
|
GTT | G | 204 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(201): Show | 205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.67+9565_67+9566del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | ||||||
| chr6:76062855
|
GTTT | G | 14 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0260others(11): Show | 14 | HG01884.hp2 HG01975.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+9564_67+9566del others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | ||||||
| chr6:76062872
|
T | C | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+9550A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062872 | ||||||
| chr6:76062896
|
G | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.67+9526C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062896 | ||||||
| chr6:76062915
|
T | C | 2 | a0001c0001t0001g0074a0002c0002t0001g0061 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+9507A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062915 | ||||||
| chr6:76062950
|
T | C | 5 | a0001c0001t0001g0166a0002c0002t0001g0167a0003c0003t0002g0170others(2): Show | 5 | NA18960.hp2 NA18979.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+9472A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062950 | ||||||
| chr6:76062952
|
C | T | 1 | a0002c0002t0001g0082 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.67+9470G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062952 | ||||||
| chr6:76063122
|
G | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+9300C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063122 | ||||||
| chr6:76063590
|
G | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8832C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063590 | ||||||
| chr6:76063748
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(12): Show | 15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+8674G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063748 | ||||||
| chr6:76063911
|
G | A | 1 | a0009c0009t0001g0259 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+8511C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063911 | ||||||
| chr6:76063932
|
G | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8490C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063932 | ||||||
| chr6:76063988
|
G | GT | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8433dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063988 | ||||||
| chr6:76064060
|
C | T | 9 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+8362G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064060 | ||||||
| chr6:76064068
|
C | G | 1 | a0008c0008t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.67+8354G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064068 | ||||||
| chr6:76064070
|
G | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+8352C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064070 | ||||||
| chr6:76064140
|
A | AAGGACAG others(20): Show |
1 | a0005c0006t0003g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+8255_67+8281dup others(27): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064140 | ||||||
| chr6:76064234
|
G | A | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+8188C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064234 | ||||||
| chr6:76064253
|
G | A | 1 | a0002c0002t0001g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67+8169C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064253 | ||||||
| chr6:76064303
|
G | A | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+8119C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064303 | ||||||
| chr6:76064360
|
A | AT | 32 | a0001c0001t0001g0002a0001c0001t0001g0260a0001c0001t0001g0266others(29): Show | 33 | HG00673.hp2 HG01167.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.67+8061dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064360 | ||||||
| chr6:76064370
|
C | T | 4 | a0001c0001t0001g0264a0002c0002t0001g0269a0002c0002t0001g0270others(1): Show | 4 | HG01074.hp1 HG01993.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+8052G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | ||||||
| chr6:76064370
|
CT | C | 241 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(238): Show | 242 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.67+8051delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | ||||||
| chr6:76064370
|
CTT | C | 6 | a0001c0001t0001g0238a0003c0003t0001g0180a0004c0004t0002g0033others(3): Show | 6 | HG01070.hp2 HG01169.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8050_67+8051del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | ||||||
| chr6:76064371
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.67+8051A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064371 | ||||||
| chr6:76064375
|
T | C | 2 | a0002c0002t0001g0231a0012c0012t0004g0230 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.67+8047A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064375 | ||||||
| chr6:76064504
|
A | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+7918T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064504 | ||||||
| chr6:76064554
|
A | T | 9 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+7868T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064554 | ||||||
| chr6:76064691
|
G | A | 1 | a0007c0007t0004g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.67+7731C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064691 | ||||||
| chr6:76064694
|
C | T | 3 | a0002c0002t0001g0078a0002c0002t0005g0080a0003c0003t0001g0079 | 3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67+7728G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064694 | ||||||
| chr6:76064768
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67+7654A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064768 | ||||||
| chr6:76064783
|
G | C | 1 | a0006c0005t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.67+7639C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064783 | ||||||
| chr6:76065176
|
A | G | 3 | a0004c0004t0002g0075a0004c0004t0002g0076a0004c0004t0002g0077 | 3 | HG02523.hp2 NA18947.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.67+7246T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065176 | ||||||
| chr6:76065206
|
T | G | 1 | a0005c0006t0003g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+7216A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065206 | ||||||
| chr6:76065251
|
T | A | 1 | a0002c0002t0007g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+7171A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065251 | ||||||
| chr6:76065254
|
A | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+7168T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065254 | ||||||
| chr6:76065275
|
A | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+7147T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065275 | ||||||
| chr6:76065424
|
A | G | 2 | a0001c0001t0001g0074a0002c0002t0001g0073 | 2 | HG02135.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+6998T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065424 | ||||||
| chr6:76065467
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+6955G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065467 | ||||||
| chr6:76065521
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+6901G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065521 | ||||||
| chr6:76065544
|
A | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+6878T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065544 | ||||||
| chr6:76065577
|
G | T | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.67+6845C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065577 | ||||||
| chr6:76065659
|
T | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+6763A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065659 | ||||||
| chr6:76065705
|
T | A | 1 | a0010c0010t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+6717A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065705 | ||||||
| chr6:76066419
|
C | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.67+6003G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066419 | ||||||
| chr6:76066515
|
C | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+5907G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066515 | ||||||
| chr6:76066706
|
C | T | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.67+5716G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066706 | ||||||
| chr6:76066780
|
A | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+5642T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066780 | ||||||
| chr6:76066980
|
T | TA | 5 | a0001c0001t0001g0237a0003c0003t0001g0233a0003c0003t0001g0235others(2): Show | 5 | NA18966.hp2 NA18970.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+5441dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066980 | ||||||
| chr6:76067013
|
C | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0007c0007t0004g0058 | 3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.67+5409G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067013 | ||||||
| chr6:76067214
|
T | TA | 9 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(6): Show | 9 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+5207dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067214 | ||||||
| chr6:76067507
|
T | C | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+4915A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067507 | ||||||
| chr6:76067633
|
TA | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0238others(2): Show | 5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4788delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067633 | ||||||
| chr6:76067716
|
C | T | 4 | a0007c0007t0004g0245a0007c0007t0004g0246a0007c0007t0004g0247others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+4706G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067716 | ||||||
| chr6:76067727
|
C | T | 1 | a0001c0018t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+4695G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067727 | ||||||
| chr6:76067807
|
G | T | 85 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(82): Show | 86 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.67+4615C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067807 | ||||||
| chr6:76067879
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+4543G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067879 | ||||||
| chr6:76067989
|
A | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4433T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067989 | ||||||
| chr6:76068181
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | NA18941.hp2 NA18974.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4241A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068181 | ||||||
| chr6:76068211
|
T | TA | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4210dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068211 | ||||||
| chr6:76068322
|
C | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4100G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068322 | ||||||
| chr6:76068505
|
C | G | 85 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(82): Show | 86 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.67+3917G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068505 | ||||||
| chr6:76068510
|
C | CT | 172 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.67+3911dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068510 | ||||||
| chr6:76068512
|
T | TTC | 27 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0272others(24): Show | 28 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+3909_67+3910ins others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068512 | ||||||
| chr6:76068591
|
C | T | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3831G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068591 | ||||||
| chr6:76068642
|
A | G | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+3780T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068642 | ||||||
| chr6:76068715
|
C | A | 1 | a0004c0004t0002g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.67+3707G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068715 | ||||||
| chr6:76068717
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.67+3705T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068717 | ||||||
| chr6:76068731
|
G | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3691C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068731 | ||||||
| chr6:76068802
|
C | G | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3620G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068802 | ||||||
| chr6:76068832
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+3590T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068832 | ||||||
| chr6:76068903
|
A | G | 1 | a0009c0009t0001g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.67+3519T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068903 | ||||||
| chr6:76069226
|
T | C | 1 | a0001c0026t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+3196A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069226 | ||||||
| chr6:76069423
|
C | T | 5 | a0001c0001t0001g0065a0002c0002t0001g0063a0002c0002t0001g0066others(2): Show | 5 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2999G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069423 | ||||||
| chr6:76069509
|
A | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0007g0062others(1): Show | 4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2913T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069509 | ||||||
| chr6:76069513
|
C | A | 1 | a0006c0005t0001g0038 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+2909G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069513 | ||||||
| chr6:76069736
|
T | C | 1 | a0002c0002t0001g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.67+2686A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069736 | ||||||
| chr6:76069745
|
CA | C | 229 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0042others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+2676delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069745 | ||||||
| chr6:76069745
|
CAA | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+2675_67+2676del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069745 | ||||||
| chr6:76069895
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02027.hp2 HG02071.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2527G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069895 | ||||||
| chr6:76069990
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0004c0004t0002g0037others(1): Show | 4 | HG02074.hp1 NA18944.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2432C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069990 | ||||||
| chr6:76070218
|
T | A | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0007g0256others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2204A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070218 | ||||||
| chr6:76070320
|
G | A | 8 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0009g0261others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2102C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070320 | ||||||
| chr6:76070370
|
A | T | 7 | a0001c0001t0001g0043a0002c0002t0001g0048a0003c0003t0001g0044others(4): Show | 7 | NA18953.hp1 NA18959.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2052T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070370 | ||||||
| chr6:76070623
|
C | T | 4 | a0001c0001t0001g0042a0014c0014t0001g0039a0014c0014t0001g0041others(1): Show | 4 | NA18969.hp2 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1799G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070623 | ||||||
| chr6:76070821
|
GA | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(8): Show | 11 | HG02145.hp1 HG02559.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+1600delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070821 | ||||||
| chr6:76070873
|
A | T | 2 | a0003c0003t0006g0006a0003c0003t0006g0007 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.67+1549T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070873 | ||||||
| chr6:76071278
|
A | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+1144T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071278 | ||||||
| chr6:76071351
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0005g0011others(12): Show | 15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+1071T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071351 | ||||||
| chr6:76071425
|
T | C | 1 | a0006c0005t0002g0265 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.67+997A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071425 | ||||||
| chr6:76071662
|
T | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(25): Show | 29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+760A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071662 | ||||||
| chr6:76071746
|
T | C | 3 | a0002c0002t0001g0295a0015c0017t0001g0293a0015c0017t0001g0294 | 3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+676A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071746 | ||||||
| chr6:76072026
|
T | C | 3 | a0001c0001t0001g0296a0002c0002t0001g0297a0002c0002t0001g0298 | 3 | NA18945.hp1 NA18987.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.67+396A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072026 | ||||||
| chr6:76072331
|
T | A | 2 | a0001c0001t0001g0299a0010c0010t0001g0300 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.67+91A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072331 | ||||||
| chr6:76072332
|
C | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.67+90G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072332 | ||||||
| chr6:76072349
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0010g0003 | 2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.67+73C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072349 |