Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3268 |
| ensemblid | ENSG00000106351.13 |
| hgncid | 5177 |
| symbol | AGFG2 |
| name | ArfGAP with FG repeats 2 |
| refseq_nuc | NM_006076.5 |
| refseq_prot | NP_006067.3 |
| ensembl_nuc | ENST00000300176.9 |
| ensembl_prot | ENSP00000300176.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 100539203 |
| end | 100568220 |
| strand | + |
| ver | v1.2 |
| region | chr7:100539203-100568220 |
| region5000 | chr7:100534203-100573220 |
| regionname0 | AGFG2_chr7_100539203_100568220 |
| regionname5000 | AGFG2_chr7_100534203_100573220 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 481 | 178 | 33 | 27 | 75 | 10 | 31 | 55 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0002 | 0/0 | 481 | 38 | 20 | 8 | 1 | 3 | 6 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0003 | 0/0 | 481 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0004 | 0/0 | 481 | 10 | 0 | 0 | 8 | 1 | 1 | 5 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0005 | 0/0 | 481 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0006 | 0/0 | 481 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0007 | 0/0 | 481 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0008 | 0/0 | 481 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0009 | 0/0 | 481 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| a0010 | 0/0 | 481 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | MVMAA others(476): Show |
chr7 | 100534203 | 100573220 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1443 | 172 | 29 | 26 | 75 | 10 | 30 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0001c0005 | 0/0 | 1443 | 3 | 3 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0001c0011 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0001c0012 | 0/0 | 1443 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0001c0013 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0002c0002 | 0/0 | 1443 | 38 | 20 | 8 | 1 | 3 | 6 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0003c0003 | 0/0 | 1443 | 13 | 13 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0003c0007 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0004c0004 | 0/0 | 1443 | 10 | 0 | 0 | 8 | 1 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0005c0008 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0006c0010 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0007c0006 | 0/0 | 1443 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0008c0014 | 0/0 | 1443 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0009c0015 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 | ||
| a0010c0009 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | ATGGT others(1438): Show |
chr7 | 100534203 | 100573220 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4818 | 155 | 24 | 25 | 71 | 10 | 24 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0002 | 0/0 | 4818 | 6 | 3 | 1 | 1 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0005 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0006 | 1/0 | 4819 | 2 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4814): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0009 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0010 | 0/0 | 4818 | 2 | 0 | 0 | 1 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0013 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0014 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0016 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0001t0021 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0005t0005 | 0/0 | 4818 | 3 | 3 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0011t0017 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0012t0001 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0001c0013t0001 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0001 | 0/0 | 4818 | 16 | 11 | 4 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0003 | 0/0 | 4817 | 12 | 0 | 4 | 1 | 3 | 4 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0004 | 0/0 | 4817 | 5 | 5 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0006 | 0/0 | 4819 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4814): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0012 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0015 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0002c0002t0020 | 0/0 | 4817 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0003c0003t0004 | 0/0 | 4817 | 4 | 4 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0003c0003t0007 | 0/0 | 4817 | 4 | 4 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0003c0003t0008 | 0/0 | 4817 | 3 | 3 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0003c0003t0018 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0003c0003t0019 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0003c0007t0004 | 0/0 | 4817 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0004c0004t0002 | 0/0 | 4818 | 9 | 0 | 0 | 8 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0004c0004t0011 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0005c0008t0001 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0006c0010t0009 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4812): Show |
chr7 | 100534203 | 100573220 |
| a0007c0006t0002 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0008c0014t0001 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0009c0015t0001 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| a0010c0009t0001 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | GGTGG others(4813): Show |
chr7 | 100534203 | 100573220 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0006g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0001t0021g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0005t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0005t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0011t0017g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0001c0013t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0002c0002t0020g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0018g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0003t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0003c0007t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0004c0004t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0005c0008t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0006c0010t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0007c0006t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0008c0014t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0009c0015t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| a0010c0009t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00140 | hp1 | a0004 | c0004 | t0011 | g0066 | EUR | GBR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0114 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0044 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0157 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0175 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0043 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01258 | hp1 | a0005 | c0008 | t0001 | g0152 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01433 | hp1 | a0001 | c0011 | t0017 | g0052 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0029 | EUR | IBS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02040 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0101 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02071 | hp2 | a0006 | c0010 | t0009 | g0198 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02074 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02257 | hp1 | a0001 | c0005 | t0005 | g0147 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02257 | hp2 | a0003 | c0007 | t0004 | g0036 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02451 | hp2 | a0003 | c0003 | t0004 | g0104 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0003 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02615 | hp2 | a0003 | c0003 | t0008 | g0047 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02698 | hp1 | a0007 | c0006 | t0002 | g0067 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0028 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0095 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0113 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02738 | hp2 | a0001 | c0012 | t0001 | g0078 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02809 | hp1 | a0002 | c0002 | t0006 | g0179 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02818 | hp1 | a0002 | c0002 | t0006 | g0180 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02886 | hp2 | a0003 | c0003 | t0008 | g0042 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02895 | hp1 | a0003 | c0003 | t0007 | g0057 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0105 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0106 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02965 | hp2 | a0003 | c0003 | t0007 | g0033 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0037 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0064 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03139 | hp1 | a0001 | c0005 | t0005 | g0007 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03225 | hp1 | a0003 | c0003 | t0007 | g0035 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03239 | hp1 | a0002 | c0002 | t0020 | g0099 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03486 | hp1 | a0003 | c0003 | t0018 | g0108 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03486 | hp2 | a0003 | c0003 | t0007 | g0034 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03579 | hp1 | a0003 | c0003 | t0008 | g0046 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03579 | hp2 | a0002 | c0002 | t0015 | g0174 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0041 | SAS | PJL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0045 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03834 | hp1 | a0008 | c0014 | t0001 | g0063 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0005 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG04228 | hp2 | a0004 | c0004 | t0002 | g0070 | SAS | STU | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18522 | hp2 | a0001 | c0005 | t0005 | g0007 | AFR | YRI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18612 | hp1 | a0004 | c0004 | t0002 | g0072 | EAS | CHB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18747 | hp2 | a0004 | c0004 | t0002 | g0069 | EAS | CHB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | YRI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | YRI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18948 | hp1 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18950 | hp2 | a0004 | c0004 | t0002 | g0024 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18960 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18975 | hp2 | a0009 | c0015 | t0001 | g0200 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18978 | hp1 | a0004 | c0004 | t0002 | g0023 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18999 | hp1 | a0004 | c0004 | t0002 | g0068 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19030 | hp2 | a0010 | c0009 | t0001 | g0058 | AFR | LWK | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | LWK | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19074 | hp2 | a0004 | c0004 | t0002 | g0071 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20129 | hp2 | a0003 | c0003 | t0004 | g0168 | AFR | ASW | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0107 | EUR | TSI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0176 | EUR | TSI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0100 | SAS | GIH | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG02486 | hp2 | a0002 | c0002 | t0012 | g0021 | AFR | ACB | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0121 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG03471 | hp2 | a0003 | c0003 | t0019 | g0038 | AFR | MSL | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| HG06807 | hp2 | a0003 | c0003 | t0004 | g0196 | AFR | USA | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0051 | REF | REF | AGFG2_chr7_100534203_100573220 | AGFG2 | chr7 | 100534203 | 100573220 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100539462 | G | C | 2 | a0004 a0007 |
11 | HG00140.hp1 HG02040.hp2 HG02698.hp1 others(8): Show |
missense_variant | MODERATE | c.116G>C | p.Cys39Ser | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/12 | 260/4819 | 116/1446 | 39/481 | chr7 | 100539462 | |||
| chr7:100539498 | C | T | 1 | a0009 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.152C>T | p.Ala51Val | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/12 | 296/4819 | 152/1446 | 51/481 | chr7 | 100539498 | |||
| chr7:100548833 | A | G | 1 | a0008 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.233A>G | p.Asn78Ser | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/12 | 377/4819 | 233/1446 | 78/481 | chr7 | 100548833 | |||
| chr7:100554096 | G | A | 1 | a0003 | 14 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(11): Show |
missense_variant | MODERATE | c.589G>A | p.Val197Ile | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/12 | 733/4819 | 589/1446 | 197/481 | chr7 | 100554096 | |||
| chr7:100562274 | C | T | 1 | a0007 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.893C>T | p.Thr298Ile | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/12 | 1037/4819 | 893/1446 | 298/481 | chr7 | 100562274 | |||
| chr7:100562303 | G | A | 1 | a0005 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.922G>A | p.Ala308Thr | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/12 | 1066/4819 | 922/1446 | 308/481 | chr7 | 100562303 | |||
| chr7:100562363 | G | C | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.982G>C | p.Ala328Pro | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/12 | 1126/4819 | 982/1446 | 328/481 | chr7 | 100562363 | |||
| chr7:100562641 | T | C | 3 | a0002 a0003 a0010 |
53 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
missense_variant | MODERATE | c.1046T>C | p.Met349Thr | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 8/12 | 1190/4819 | 1046/1446 | 349/481 | chr7 | 100562641 | |||
| chr7:100562655 | G | A | 1 | a0006 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.1060G>A | p.Gly354Ser | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 8/12 | 1204/4819 | 1060/1446 | 354/481 | chr7 | 100562655 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100555665 | C | T | 1 | a0003c0007 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.807C>T | p.Pro269Pro | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/12 | 951/4819 | 807/1446 | 269/481 | chr7 | 100555665 | |||
| chr7:100555710 | G | T | 1 | a0001c0013 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.852G>T | p.Ser284Ser | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/12 | 996/4819 | 852/1446 | 284/481 | chr7 | 100555710 | |||
| chr7:100562302 | C | T | 1 | a0001c0005 | 3 | HG02257.hp1 HG03139.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.921C>T | p.Pro307Pro | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/12 | 1065/4819 | 921/1446 | 307/481 | chr7 | 100562302 | |||
| chr7:100562651 | C | T | 1 | a0001c0012 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1056C>T | p.Gly352Gly | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 8/12 | 1200/4819 | 1056/1446 | 352/481 | chr7 | 100562651 | |||
| chr7:100563934 | G | A | 1 | a0001c0011 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1272G>A | p.Pro424Pro | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 10/12 | 1416/4819 | 1272/1446 | 424/481 | chr7 | 100563934 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100539224 | C | T | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/12 | 123 | chr7 | 100539224 | ||||||
| chr7:100539241 | C | G | 9 | a0002c0002t0003 a0002c0002t0004 a0002c0002t0020 others(6): Show |
32 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-106C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/12 | 106 | chr7 | 100539241 | ||||||
| chr7:100539253 | A | T | 1 | a0002c0002t0020 | 1 | HG03239.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/12 | chr7 | 100539253 | |||||||
| chr7:100565107 | A | G | 1 | a0001c0011t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 116 | chr7 | 100565107 | ||||||
| chr7:100565294 | C | T | 2 | a0001c0001t0005 a0001c0005t0005 |
5 | HG02257.hp1 HG03139.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*303C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 303 | chr7 | 100565294 | ||||||
| chr7:100565313 | C | T | 1 | a0003c0003t0008 | 3 | HG02615.hp2 HG02886.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 322 | chr7 | 100565313 | ||||||
| chr7:100565492 | G | A | 4 | a0001c0001t0002 a0004c0004t0002 a0004c0004t0011 others(1): Show |
17 | HG00140.hp1 HG01081.hp1 HG02040.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 501 | chr7 | 100565492 | ||||||
| chr7:100565615 | T | C | 1 | a0002c0002t0012 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 624 | chr7 | 100565615 | ||||||
| chr7:100565889 | CT | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(21): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*917delT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 917 | INFO_REALIGN_3_PRIME | chr7 | 100565889 | |||||
| chr7:100565889 | CTT | C | 9 | a0001c0001t0009 a0002c0002t0003 a0002c0002t0004 others(6): Show |
32 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*916_*917delTT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 916 | INFO_REALIGN_3_PRIME | chr7 | 100565889 | |||||
| chr7:100565908 | T | C | 1 | a0001c0001t0013 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 917 | chr7 | 100565908 | ||||||
| chr7:100566186 | G | A | 1 | a0001c0001t0014 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1195G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 1195 | chr7 | 100566186 | ||||||
| chr7:100566366 | C | T | 3 | a0001c0001t0016 a0002c0002t0003 a0002c0002t0020 |
14 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1375C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 1375 | chr7 | 100566366 | ||||||
| chr7:100566771 | T | C | 1 | a0002c0002t0012 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 1780 | chr7 | 100566771 | ||||||
| chr7:100566785 | T | C | 1 | a0003c0003t0018 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 1794 | chr7 | 100566785 | ||||||
| chr7:100567476 | G | A | 1 | a0002c0002t0015 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2485G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 2485 | chr7 | 100567476 | ||||||
| chr7:100567507 | A | C | 1 | a0001c0001t0010 | 2 | HG02074.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2516A>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 2516 | chr7 | 100567507 | ||||||
| chr7:100567512 | G | A | 1 | a0002c0002t0015 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2521G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 2521 | chr7 | 100567512 | ||||||
| chr7:100567626 | C | T | 1 | a0004c0004t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2635C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 2635 | chr7 | 100567626 | ||||||
| chr7:100567885 | A | C | 1 | a0003c0003t0018 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894A>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 2894 | chr7 | 100567885 | ||||||
| chr7:100568154 | G | A | 1 | a0003c0003t0007 | 4 | HG02895.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3163G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 12/12 | 3163 | chr7 | 100568154 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100539803 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.221+236G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100539803 | |||||||
| chr7:100540025 | A | C | 6 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG01952.hp2 HG02027.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+458A>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540025 | |||||||
| chr7:100540050 | C | T | 1 | a0003c0003t0004g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.221+483C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540050 | |||||||
| chr7:100540119 | T | TA | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0002c0002t0001g0022 others(3): Show |
6 | HG01934.hp2 HG02486.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+568dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100540119 | ||||||
| chr7:100540119 | TA | T | 12 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(9): Show |
14 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.221+568delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100540119 | ||||||
| chr7:100540137 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.221+570C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540137 | |||||||
| chr7:100540145 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.221+578C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540145 | |||||||
| chr7:100540348 | G | T | 15 | a0002c0002t0001g0008 a0002c0002t0001g0177 a0002c0002t0001g0178 others(12): Show |
17 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.221+781G>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540348 | |||||||
| chr7:100540739 | C | T | 2 | a0002c0002t0003g0175 a0002c0002t0003g0176 |
2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.221+1172C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540739 | |||||||
| chr7:100540751 | C | T | 1 | a0002c0002t0015g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221+1184C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540751 | |||||||
| chr7:100540780 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.221+1213G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100540780 | |||||||
| chr7:100541010 | C | CA | 5 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0003g0028 others(2): Show |
5 | HG00639.hp1 HG01517.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1465dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100541010 | ||||||
| chr7:100541010 | CA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.221+1465delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100541010 | ||||||
| chr7:100541010 | CAA | C | 7 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG02451.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+1464_221+1465d others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100541010 | ||||||
| chr7:100541501 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221+1934C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100541501 | |||||||
| chr7:100541647 | C | T | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221+2080C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100541647 | |||||||
| chr7:100541711 | C | T | 1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+2144C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100541711 | |||||||
| chr7:100541744 | C | G | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.221+2177C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100541744 | |||||||
| chr7:100541766 | C | CA | 9 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
9 | HG02572.hp1 HG02572.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+2215dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100541766 | ||||||
| chr7:100541766 | CA | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0164 others(10): Show |
20 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.221+2215delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100541766 | ||||||
| chr7:100542084 | C | T | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221+2517C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542084 | |||||||
| chr7:100542089 | C | T | 1 | a0003c0003t0007g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.221+2522C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542089 | |||||||
| chr7:100542165 | G | A | 1 | a0008c0014t0001g0063 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.221+2598G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542165 | |||||||
| chr7:100542208 | G | A | 15 | a0002c0002t0001g0008 a0002c0002t0001g0177 a0002c0002t0001g0178 others(12): Show |
17 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.221+2641G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542208 | |||||||
| chr7:100542212 | T | C | 3 | a0002c0002t0001g0022 a0002c0002t0015g0174 a0010c0009t0001g0058 |
3 | HG03453.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.221+2645T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542212 | |||||||
| chr7:100542510 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18947.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.221+2943A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542510 | |||||||
| chr7:100542581 | T | G | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.221+3014T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542581 | |||||||
| chr7:100542618 | T | C | 1 | a0002c0002t0004g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.221+3051T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542618 | |||||||
| chr7:100542766 | T | C | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221+3199T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542766 | |||||||
| chr7:100542845 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG03239.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+3278C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542845 | |||||||
| chr7:100542875 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221+3308G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542875 | |||||||
| chr7:100542930 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221+3363G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542930 | |||||||
| chr7:100542944 | A | T | 1 | a0002c0002t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221+3377A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542944 | |||||||
| chr7:100542964 | A | G | 15 | a0002c0002t0001g0008 a0002c0002t0001g0177 a0002c0002t0001g0178 others(12): Show |
17 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.221+3397A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100542964 | |||||||
| chr7:100543070 | A | AT | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+3514dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100543070 | ||||||
| chr7:100543071 | T | A | 10 | a0004c0004t0002g0012 a0004c0004t0002g0023 a0004c0004t0002g0024 others(7): Show |
11 | HG00140.hp1 HG02040.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+3504T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543071 | |||||||
| chr7:100543511 | C | T | 1 | a0002c0002t0003g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.221+3944C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543511 | |||||||
| chr7:100543578 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.221+4011G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543578 | |||||||
| chr7:100543634 | T | C | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221+4067T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543634 | |||||||
| chr7:100543680 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.221+4113C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543680 | |||||||
| chr7:100543691 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.221+4124G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543691 | |||||||
| chr7:100543824 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.221+4257A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100543824 | |||||||
| chr7:100544238 | T | G | 15 | a0002c0002t0001g0008 a0002c0002t0001g0177 a0002c0002t0001g0178 others(12): Show |
17 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-4584T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544238 | |||||||
| chr7:100544358 | A | G | 15 | a0002c0002t0001g0008 a0002c0002t0001g0177 a0002c0002t0001g0178 others(12): Show |
17 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-4464A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544358 | |||||||
| chr7:100544694 | G | A | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222-4128G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544694 | |||||||
| chr7:100544724 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.222-4098C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544724 | |||||||
| chr7:100544725 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
5 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-4097G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544725 | |||||||
| chr7:100544747 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.222-4075G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544747 | |||||||
| chr7:100544748 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0001c0001t0001g0079 others(1): Show |
4 | HG00642.hp1 HG01934.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-4074G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544748 | |||||||
| chr7:100544810 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222-4012G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100544810 | |||||||
| chr7:100545195 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-3627A>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545195 | |||||||
| chr7:100545231 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222-3591G>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545231 | |||||||
| chr7:100545238 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0080 |
2 | HG00558.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.222-3584T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545238 | |||||||
| chr7:100545462 | C | A | 3 | a0002c0002t0001g0022 a0002c0002t0001g0177 a0010c0009t0001g0058 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222-3360C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545462 | |||||||
| chr7:100545582 | T | C | 4 | a0003c0003t0007g0033 a0003c0003t0007g0034 a0003c0003t0007g0035 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3240T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545582 | |||||||
| chr7:100545678 | C | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222-3144C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545678 | |||||||
| chr7:100545918 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.222-2904C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545918 | |||||||
| chr7:100545926 | T | C | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222-2896T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100545926 | |||||||
| chr7:100546115 | C | A | 8 | a0003c0003t0004g0037 a0003c0003t0004g0196 a0003c0003t0007g0033 others(5): Show |
8 | HG02257.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.222-2707C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100546115 | |||||||
| chr7:100546160 | G | A | 1 | a0002c0002t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.222-2662G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100546160 | |||||||
| chr7:100546166 | C | G | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222-2656C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100546166 | |||||||
| chr7:100546737 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-2085G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100546737 | |||||||
| chr7:100547048 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0083 |
4 | NA18948.hp2 NA18962.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-1774G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547048 | |||||||
| chr7:100547111 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.222-1711G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547111 | |||||||
| chr7:100547201 | G | A | 1 | a0002c0002t0015g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.222-1621G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547201 | |||||||
| chr7:100547341 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.222-1481G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547341 | |||||||
| chr7:100547406 | A | AT | 16 | a0001c0001t0001g0055 a0002c0002t0001g0008 a0002c0002t0001g0177 others(13): Show |
18 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-1404dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100547406 | ||||||
| chr7:100547767 | C | T | 1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-1055C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547767 | |||||||
| chr7:100547847 | A | G | 1 | a0003c0003t0019g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.222-975A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547847 | |||||||
| chr7:100547871 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-951T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100547871 | |||||||
| chr7:100548052 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.222-770G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548052 | |||||||
| chr7:100548145 | C | G | 1 | a0002c0002t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.222-677C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548145 | |||||||
| chr7:100548240 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.222-582G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548240 | |||||||
| chr7:100548305 | T | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(23): Show |
37 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.222-517T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548305 | |||||||
| chr7:100548321 | G | T | 1 | a0002c0002t0001g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.222-501G>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548321 | |||||||
| chr7:100548818 | A | G | 3 | a0002c0002t0001g0022 a0002c0002t0001g0177 a0010c0009t0001g0058 |
3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.222-4A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 1/11 | chr7 | 100548818 | |||||||
| chr7:100548949 | A | AC | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+36dupC | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 100548949 | ||||||
| chr7:100548996 | C | T | 8 | a0003c0003t0004g0037 a0003c0003t0004g0196 a0003c0003t0007g0033 others(5): Show |
8 | HG02257.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.315+81C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100548996 | |||||||
| chr7:100549141 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18950.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.315+226G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549141 | |||||||
| chr7:100549283 | T | C | 1 | a0002c0002t0015g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.315+368T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549283 | |||||||
| chr7:100549675 | G | GTTTA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0150 others(11): Show |
14 | HG01167.hp2 HG01258.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-695_316-692dup others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 100549675 | ||||||
| chr7:100549675 | GTTTATTT others(5): Show |
G | 1 | a0002c0002t0015g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316-703_316-692del others(12): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 100549675 | ||||||
| chr7:100549714 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.316-682G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549714 | |||||||
| chr7:100549732 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
5 | NA18948.hp2 NA18960.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-664A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549732 | |||||||
| chr7:100549753 | T | C | 51 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(48): Show |
53 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.316-643T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549753 | |||||||
| chr7:100549883 | G | T | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.316-513G>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100549883 | |||||||
| chr7:100550128 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.316-268G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100550128 | |||||||
| chr7:100550282 | G | A | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.316-114G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | chr7 | 100550282 | |||||||
| chr7:100550305 | C | CA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0060 others(8): Show |
13 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-66dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 100550305 | ||||||
| chr7:100550305 | CA | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0096 others(37): Show |
42 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.316-66delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 100550305 | ||||||
| chr7:100550845 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.431+334T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100550845 | |||||||
| chr7:100550863 | A | AT | 7 | a0001c0001t0001g0056 a0001c0001t0001g0094 a0001c0001t0001g0111 others(4): Show |
7 | HG01361.hp1 HG02071.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+367dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100550863 | ||||||
| chr7:100551030 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0110 a0001c0001t0001g0116 |
3 | HG02040.hp1 NA18944.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.431+519T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551030 | |||||||
| chr7:100551030 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.431+519_431+520ins others(11): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551030 | |||||||
| chr7:100551030 | T | TATATATA others(6): Show |
1 | a0001c0005t0005g0007 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.431+519_431+520ins others(13): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551030 | |||||||
| chr7:100551030 | T | TATATATA others(8): Show |
1 | a0004c0004t0002g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.431+519_431+520ins others(15): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551030 | |||||||
| chr7:100551030 | T | TATATATA others(10): Show |
1 | a0004c0004t0002g0012 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.431+519_431+520ins others(17): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551030 | |||||||
| chr7:100551030 | T | TTA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(35): Show |
39 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.431+555_431+556dup others(2): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(9): Show |
13 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.431+553_431+556dup others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATA | 16 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0018 others(13): Show |
18 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.431+551_431+556dup others(6): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(1): Show |
9 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0001c0001t0001g0130 others(6): Show |
9 | HG00099.hp2 HG02027.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.431+549_431+556dup others(8): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(3): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0055 others(5): Show |
9 | HG02486.hp1 HG02738.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.431+547_431+556dup others(10): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(5): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0134 a0001c0001t0002g0142 others(1): Show |
4 | HG00642.hp2 HG01081.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+545_431+556dup others(12): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(7): Show |
12 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(9): Show |
12 | HG00280.hp1 HG00735.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+543_431+556dup others(14): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(9): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(5): Show |
9 | HG00621.hp1 HG01517.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+541_431+556dup others(16): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(11): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0050 others(9): Show |
12 | HG00140.hp1 HG00741.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431+539_431+556dup others(18): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+537_431+556dup others(20): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0032 a0001c0001t0001g0088 a0001c0001t0001g0155 others(1): Show |
4 | HG00140.hp2 HG00558.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+535_431+556dup others(22): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(17): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0126 others(2): Show |
5 | HG00609.hp1 HG03831.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+533_431+556dup others(24): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0092 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.431+531_431+556dup others(26): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(21): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0086 |
2 | HG03491.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.431+529_431+556dup others(28): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0004 a0001c0001t0013g0095 |
2 | HG00597.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.431+527_431+556dup others(30): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(25): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0002c0002t0020g0099 |
3 | HG02071.hp1 HG03239.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.431+525_431+556dup others(32): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.431+523_431+556dup others(34): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.431+550_431+551ins others(36): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATA | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0040 others(6): Show |
10 | HG01074.hp2 HG01099.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.431+553_431+556del others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATA | T | 4 | a0001c0001t0001g0059 a0002c0002t0001g0177 a0002c0002t0004g0101 others(1): Show |
4 | HG02055.hp2 HG03225.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+551_431+556del others(6): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATAT others(1): Show |
T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0145 a0001c0001t0001g0149 others(3): Show |
6 | HG02451.hp1 HG02818.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+549_431+556del others(8): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0010g0002 others(1): Show |
5 | HG02074.hp1 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+547_431+556del others(10): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATAT others(9): Show |
T | 4 | a0003c0003t0008g0042 a0003c0003t0008g0046 a0003c0003t0008g0047 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+541_431+556del others(16): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATAT others(11): Show |
T | 2 | a0001c0013t0001g0121 a0007c0006t0002g0067 |
2 | HG02698.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.431+539_431+556del others(18): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551030 | TTATATAT others(17): Show |
T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0076 others(2): Show |
8 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+533_431+556del others(24): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551030 | ||||||
| chr7:100551032 | A | T | 3 | a0002c0002t0001g0022 a0002c0002t0015g0174 a0010c0009t0001g0058 |
3 | HG03453.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.431+521A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551032 | |||||||
| chr7:100551034 | A | T | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.431+523A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551034 | |||||||
| chr7:100551036 | A | T | 1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431+525A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551036 | |||||||
| chr7:100551049 | TATATATA others(10): Show |
T | 1 | a0004c0004t0002g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431+539_431+555del others(17): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551049 | |||||||
| chr7:100551058 | A | ATATATAT others(11): Show |
1 | a0001c0001t0005g0007 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.431+556_431+557ins others(18): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551058 | ||||||
| chr7:100551060 | A | T | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.431+549A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551060 | |||||||
| chr7:100551062 | A | T | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.431+551A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551062 | |||||||
| chr7:100551062 | ATATAT | A | 2 | a0002c0002t0001g0008 a0002c0002t0001g0189 |
4 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+553_431+557del others(5): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551062 | ||||||
| chr7:100551064 | A | T | 6 | a0002c0002t0001g0022 a0002c0002t0001g0181 a0002c0002t0001g0182 others(3): Show |
6 | HG02486.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+553A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551064 | |||||||
| chr7:100551066 | A | ATATATAT others(27): Show |
1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431+556_431+557ins others(34): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551066 | ||||||
| chr7:100551066 | A | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0178 a0002c0002t0001g0181 others(4): Show |
7 | HG02486.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+555A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551066 | |||||||
| chr7:100551067 | T | TA | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0009g0114 |
3 | HG00438.hp1 HG02040.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.431+556_431+557ins others(1): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551067 | |||||||
| chr7:100551067 | T | TATATATA others(2): Show |
4 | a0003c0003t0007g0033 a0003c0003t0007g0034 a0003c0003t0007g0035 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+556_431+557ins others(9): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551067 | |||||||
| chr7:100551067 | T | TATATATA others(6): Show |
1 | a0003c0003t0004g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.431+556_431+557ins others(13): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551067 | |||||||
| chr7:100551067 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0150 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.431+556_431+557ins others(19): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551067 | |||||||
| chr7:100551068 | T | A | 6 | a0001c0001t0006g0113 a0002c0002t0001g0190 a0002c0002t0001g0191 others(3): Show |
6 | HG02738.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+557T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551068 | |||||||
| chr7:100551069 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.431+558T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551069 | |||||||
| chr7:100551069 | T | C | 1 | a0004c0004t0002g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431+558T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551069 | |||||||
| chr7:100551070 | C | A | 5 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 others(2): Show |
5 | HG02922.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+559C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551070 | |||||||
| chr7:100551070 | C | T | 21 | a0001c0001t0001g0082 a0002c0002t0001g0008 a0002c0002t0001g0022 others(18): Show |
23 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.431+559C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551070 | |||||||
| chr7:100551071 | T | A | 1 | a0002c0002t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.431+560T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551071 | |||||||
| chr7:100551071 | T | C | 8 | a0001c0001t0001g0082 a0003c0003t0004g0037 a0003c0003t0004g0196 others(5): Show |
8 | HG02257.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.431+560T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551071 | |||||||
| chr7:100551071 | T | TATATATA others(8): Show |
3 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 |
3 | HG02970.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431+560_431+561ins others(15): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551071 | |||||||
| chr7:100551072 | T | A | 2 | a0002c0002t0001g0193 a0002c0002t0001g0194 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.431+561T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551072 | |||||||
| chr7:100551073 | T | A | 3 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 |
3 | HG02970.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431+562T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551073 | |||||||
| chr7:100551074 | T | A | 2 | a0002c0002t0001g0193 a0002c0002t0001g0194 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.431+563T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551074 | |||||||
| chr7:100551098 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.431+587C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551098 | |||||||
| chr7:100551100 | C | T | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.431+589C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551100 | |||||||
| chr7:100551131 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.431+620G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551131 | |||||||
| chr7:100551174 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0149 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.431+663A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551174 | |||||||
| chr7:100551304 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0144 |
2 | HG00099.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.431+793C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551304 | |||||||
| chr7:100551818 | C | A | 1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431+1307C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100551818 | |||||||
| chr7:100551885 | C | CA | 47 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0049 others(44): Show |
47 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.431+1400dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551885 | ||||||
| chr7:100551885 | C | CAA | 9 | a0002c0002t0003g0028 a0002c0002t0003g0175 a0002c0002t0004g0101 others(6): Show |
9 | HG00741.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.431+1399_431+1400d others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551885 | ||||||
| chr7:100551885 | CA | C | 23 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0149 others(20): Show |
25 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.431+1400delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 100551885 | ||||||
| chr7:100552010 | G | A | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.432-1337G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552010 | |||||||
| chr7:100552252 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.432-1095A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552252 | |||||||
| chr7:100552283 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.432-1064A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552283 | |||||||
| chr7:100552355 | G | A | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.432-992G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552355 | |||||||
| chr7:100552740 | C | T | 4 | a0003c0003t0007g0033 a0003c0003t0007g0034 a0003c0003t0007g0035 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-607C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552740 | |||||||
| chr7:100552741 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0077 |
2 | HG00642.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.432-606G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552741 | |||||||
| chr7:100552892 | G | A | 1 | a0002c0002t0004g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.432-455G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100552892 | |||||||
| chr7:100553033 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432-314G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100553033 | |||||||
| chr7:100553113 | A | C | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-234A>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100553113 | |||||||
| chr7:100553253 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432-94T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 3/11 | chr7 | 100553253 | |||||||
| chr7:100553560 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.585+60T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 4/11 | chr7 | 100553560 | |||||||
| chr7:100553670 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.585+170T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 4/11 | chr7 | 100553670 | |||||||
| chr7:100554011 | C | T | 2 | a0002c0002t0001g0181 a0002c0002t0001g0182 |
2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.586-82C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 4/11 | chr7 | 100554011 | |||||||
| chr7:100554555 | G | A | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.751+297G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100554555 | |||||||
| chr7:100554709 | C | T | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.751+451C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100554709 | |||||||
| chr7:100554926 | A | G | 3 | a0003c0003t0008g0042 a0003c0003t0008g0046 a0003c0003t0008g0047 |
3 | HG02615.hp2 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.751+668A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100554926 | |||||||
| chr7:100554937 | C | CA | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.752-648dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100554937 | ||||||
| chr7:100554937 | C | CAA | 8 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG02055.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-649_752-648dup others(2): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100554937 | ||||||
| chr7:100554937 | CA | C | 8 | a0002c0002t0001g0022 a0003c0003t0004g0037 a0003c0003t0004g0196 others(5): Show |
8 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.752-648delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100554937 | ||||||
| chr7:100555263 | G | GT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
108 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.752-319dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100555263 | ||||||
| chr7:100555263 | G | GTT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
16 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.752-320_752-319dup others(2): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100555263 | ||||||
| chr7:100555263 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.752-347G>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100555263 | |||||||
| chr7:100555263 | GT | G | 18 | a0002c0002t0001g0178 a0002c0002t0001g0189 a0002c0002t0001g0194 others(15): Show |
18 | HG00639.hp1 HG01255.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.752-319delT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100555263 | ||||||
| chr7:100555263 | GTT | G | 16 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(13): Show |
18 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.752-320_752-319del others(2): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100555263 | ||||||
| chr7:100555263 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.752-330_752-319del others(12): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 100555263 | ||||||
| chr7:100555325 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.752-285G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100555325 | |||||||
| chr7:100555553 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.752-57G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100555553 | |||||||
| chr7:100555569 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.752-41G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 5/11 | chr7 | 100555569 | |||||||
| chr7:100556004 | G | A | 1 | a0004c0004t0002g0068 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.877+269G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556004 | |||||||
| chr7:100556100 | G | A | 2 | a0002c0002t0006g0179 a0002c0002t0006g0180 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877+365G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556100 | |||||||
| chr7:100556187 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.877+452C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556187 | |||||||
| chr7:100556456 | A | T | 51 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(48): Show |
53 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.877+721A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556456 | |||||||
| chr7:100556583 | C | T | 3 | a0002c0002t0004g0064 a0002c0002t0004g0105 a0002c0002t0004g0106 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.877+848C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556583 | |||||||
| chr7:100556683 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.877+948G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556683 | |||||||
| chr7:100556805 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.877+1070G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556805 | |||||||
| chr7:100556871 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.877+1136G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556871 | |||||||
| chr7:100556967 | G | A | 3 | a0003c0003t0004g0037 a0003c0003t0004g0196 a0003c0007t0004g0036 |
3 | HG02257.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.877+1232G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100556967 | |||||||
| chr7:100557026 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.877+1291C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100557026 | |||||||
| chr7:100557066 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.877+1331C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100557066 | |||||||
| chr7:100557454 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.877+1719G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100557454 | |||||||
| chr7:100557580 | G | A | 1 | a0009c0015t0001g0200 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.877+1845G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100557580 | |||||||
| chr7:100557739 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.877+2004G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100557739 | |||||||
| chr7:100558072 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | NA18747.hp1 NA18982.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.877+2337G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558072 | |||||||
| chr7:100558215 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.877+2480G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558215 | |||||||
| chr7:100558221 | C | G | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.877+2486C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558221 | |||||||
| chr7:100558520 | CAG | C | 4 | a0003c0003t0007g0033 a0003c0003t0007g0034 a0003c0003t0007g0035 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+2788_877+2789d others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100558520 | ||||||
| chr7:100558545 | GT | G | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.877+2825delT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100558545 | ||||||
| chr7:100558564 | C | T | 3 | a0003c0003t0008g0042 a0003c0003t0008g0046 a0003c0003t0008g0047 |
3 | HG02615.hp2 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.877+2829C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558564 | |||||||
| chr7:100558565 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.877+2830G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558565 | |||||||
| chr7:100558713 | T | C | 1 | a0010c0009t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.877+2978T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558713 | |||||||
| chr7:100558732 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.877+2997A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558732 | |||||||
| chr7:100558815 | C | T | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.877+3080C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558815 | |||||||
| chr7:100558862 | G | A | 1 | a0003c0003t0018g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.877+3127G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558862 | |||||||
| chr7:100558867 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.877+3132G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100558867 | |||||||
| chr7:100559004 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.878-3255C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559004 | |||||||
| chr7:100559090 | C | T | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-3169C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559090 | |||||||
| chr7:100559124 | G | A | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.878-3135G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559124 | |||||||
| chr7:100559133 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.878-3126A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559133 | |||||||
| chr7:100559220 | T | C | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-3039T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559220 | |||||||
| chr7:100559395 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0159 |
3 | HG03239.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.878-2864G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559395 | |||||||
| chr7:100559600 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.878-2659T>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559600 | |||||||
| chr7:100559818 | C | CA | 18 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0120 others(15): Show |
20 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.878-2424dupA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100559818 | ||||||
| chr7:100559818 | C | CAA | 7 | a0002c0002t0001g0022 a0002c0002t0001g0190 a0002c0002t0001g0191 others(4): Show |
7 | HG02922.hp1 HG02970.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.878-2425_878-2424d others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100559818 | ||||||
| chr7:100559818 | CA | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0018 others(10): Show |
16 | HG00558.hp2 HG01099.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.878-2424delA | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100559818 | ||||||
| chr7:100559867 | G | A | 1 | a0002c0002t0003g0102 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.878-2392G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559867 | |||||||
| chr7:100559885 | G | A | 1 | a0001c0013t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.878-2374G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100559885 | |||||||
| chr7:100560304 | G | A | 2 | a0002c0002t0006g0179 a0002c0002t0006g0180 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.878-1955G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560304 | |||||||
| chr7:100560370 | G | A | 9 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
11 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.878-1889G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560370 | |||||||
| chr7:100560606 | A | G | 11 | a0003c0003t0004g0037 a0003c0003t0004g0196 a0003c0003t0007g0033 others(8): Show |
11 | HG02257.hp2 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.878-1653A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560606 | |||||||
| chr7:100560660 | G | C | 1 | a0002c0002t0015g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.878-1599G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560660 | |||||||
| chr7:100560730 | A | G | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.878-1529A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560730 | |||||||
| chr7:100560736 | T | G | 1 | a0002c0002t0020g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.878-1523T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560736 | |||||||
| chr7:100560808 | C | CT | 37 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0001t0006g0113 others(34): Show |
37 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.878-1430dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100560808 | ||||||
| chr7:100560808 | C | CTT | 6 | a0002c0002t0001g0022 a0002c0002t0001g0177 a0002c0002t0001g0178 others(3): Show |
6 | HG02896.hp1 HG03225.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-1431_878-1430d others(4): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100560808 | ||||||
| chr7:100560808 | C | CTTT | 11 | a0002c0002t0001g0008 a0002c0002t0001g0181 a0002c0002t0001g0182 others(8): Show |
13 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.878-1432_878-1430d others(5): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100560808 | ||||||
| chr7:100560808 | CT | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0097 others(4): Show |
7 | HG02602.hp2 HG06807.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.878-1430delT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100560808 | ||||||
| chr7:100560810 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.878-1449T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560810 | |||||||
| chr7:100560905 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(23): Show |
37 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.878-1354G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560905 | |||||||
| chr7:100560961 | G | A | 1 | a0003c0003t0007g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.878-1298G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100560961 | |||||||
| chr7:100560978 | A | AT | 17 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0001c0001t0001g0131 others(14): Show |
19 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.878-1267dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100560978 | ||||||
| chr7:100561054 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.878-1205C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561054 | |||||||
| chr7:100561127 | C | CT | 33 | a0001c0001t0001g0085 a0001c0001t0001g0155 a0001c0001t0001g0165 others(30): Show |
33 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.878-1116dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 100561127 | ||||||
| chr7:100561149 | G | A | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.878-1110G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561149 | |||||||
| chr7:100561250 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0137 |
2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.878-1009C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561250 | |||||||
| chr7:100561274 | C | T | 1 | a0001c0011t0017g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.878-985C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561274 | |||||||
| chr7:100561331 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.878-928T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561331 | |||||||
| chr7:100561394 | T | G | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-865T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561394 | |||||||
| chr7:100561410 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.878-849A>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561410 | |||||||
| chr7:100561428 | A | G | 1 | a0002c0002t0012g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-831A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561428 | |||||||
| chr7:100561497 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0138 |
2 | HG02129.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.878-762A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561497 | |||||||
| chr7:100561498 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.878-761G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561498 | |||||||
| chr7:100561944 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.878-315A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100561944 | |||||||
| chr7:100562016 | G | A | 1 | a0002c0002t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.878-243G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100562016 | |||||||
| chr7:100562105 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.878-154G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 6/11 | chr7 | 100562105 | |||||||
| chr7:100562440 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.998+61G>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562440 | |||||||
| chr7:100562471 | A | G | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.998+92A>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562471 | |||||||
| chr7:100562481 | T | TC | 4 | a0001c0001t0001g0056 a0001c0001t0001g0092 a0001c0001t0001g0096 others(1): Show |
4 | HG01099.hp1 HG02735.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.998+106dupC | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 100562481 | ||||||
| chr7:100562486 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(24): Show |
38 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.998+107T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562486 | |||||||
| chr7:100562494 | C | G | 2 | a0002c0002t0001g0022 a0010c0009t0001g0058 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999-100C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562494 | |||||||
| chr7:100562496 | T | C | 19 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0177 others(16): Show |
21 | HG00639.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.999-98T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562496 | |||||||
| chr7:100562567 | TATGACTT others(9): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.999-26_999-11delAT others(14): Show |
AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 7/11 | chr7 | 100562567 | |||||||
| chr7:100562805 | G | A | 1 | a0004c0004t0002g0069 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1088-58G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 8/11 | chr7 | 100562805 | |||||||
| chr7:100563037 | C | T | 2 | a0003c0003t0004g0104 a0010c0009t0001g0058 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1171+91C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 9/11 | chr7 | 100563037 | |||||||
| chr7:100563082 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1171+136G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 9/11 | chr7 | 100563082 | |||||||
| chr7:100563624 | C | A | 1 | a0007c0006t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1172-210C>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 9/11 | chr7 | 100563624 | |||||||
| chr7:100564179 | C | T | 2 | a0002c0002t0003g0107 a0002c0002t0003g0157 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1301-39C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 10/11 | chr7 | 100564179 | |||||||
| chr7:100564396 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1386+93T>C | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564396 | |||||||
| chr7:100564420 | G | A | 1 | a0001c0013t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1386+117G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564420 | |||||||
| chr7:100564455 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1386+152C>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564455 | |||||||
| chr7:100564521 | C | CT | 20 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0167 others(17): Show |
23 | HG00639.hp1 HG00735.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1386+234dupT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 100564521 | ||||||
| chr7:100564521 | CT | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0094 others(3): Show |
7 | HG01074.hp2 HG01099.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+234delT | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 100564521 | ||||||
| chr7:100564534 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1386+231T>G | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564534 | |||||||
| chr7:100564572 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1386+269C>T | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564572 | |||||||
| chr7:100564659 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1387-273G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564659 | |||||||
| chr7:100564666 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1387-266G>A | AGFG2 | ENSG00000106351.13 | transcript | ENST00000300176.9 | protein_coding | 11/11 | chr7 | 100564666 |